Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54845 |
| ensemblid | ENSG00000104413.18 |
| hgncid | 25966 |
| symbol | ESRP1 |
| name | epithelial splicing regulatory protein 1 |
| refseq_nuc | NM_017697.4 |
| refseq_prot | NP_060167.2 |
| ensembl_nuc | ENST00000433389.8 |
| ensembl_prot | ENSP00000405738.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 94641174 |
| end | 94707466 |
| strand | + |
| ver | v1.2 |
| region | chr8:94641174-94707466 |
| region5000 | chr8:94636174-94712466 |
| regionname0 | ESRP1_chr8_94641174_94707466 |
| regionname5000 | ESRP1_chr8_94636174_94712466 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 681 | 371 | 95 | 68 | 156 | 9 | 41 | 116 | ESRP1_chr8_94636174_94712466 | ESRP1 | MTASP others(676): Show |
chr8 | 94636174 | 94712466 |
| a0002 | 0/0 | 681 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | MTASP others(676): Show |
chr8 | 94636174 | 94712466 |
| a0003 | 0/0 | 681 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | MTASP others(676): Show |
chr8 | 94636174 | 94712466 |
| a0004 | 0/0 | 681 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | MTASP others(676): Show |
chr8 | 94636174 | 94712466 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2043 | 217 | 74 | 34 | 90 | 5 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0002 | 0/0 | 2043 | 88 | 2 | 8 | 65 | 0 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0003 | 0/1 | 2043 | 39 | 8 | 19 | 0 | 2 | 9 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0004 | 0/0 | 2043 | 16 | 1 | 7 | 0 | 2 | 6 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0005 | 0/0 | 2043 | 4 | 4 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0006 | 0/0 | 2043 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0007 | 0/0 | 2043 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0008 | 0/0 | 2043 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0009 | 0/0 | 2043 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0001c0011 | 0/0 | 2043 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0002c0013 | 0/0 | 2043 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0003c0012 | 0/0 | 2043 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 | ||
| a0004c0010 | 0/0 | 2043 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | ATGAC others(2038): Show |
chr8 | 94636174 | 94712466 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3768 | 195 | 58 | 34 | 85 | 5 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0002 | 1/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0003 | 0/0 | 3768 | 6 | 6 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0004 | 0/0 | 3768 | 5 | 5 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0005 | 0/0 | 3768 | 4 | 0 | 0 | 4 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0006 | 0/0 | 3768 | 3 | 3 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0009 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0010 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0001t0011 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0002t0001 | 0/0 | 3768 | 4 | 1 | 2 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0002t0002 | 0/0 | 3768 | 80 | 0 | 6 | 61 | 0 | 13 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0002t0008 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0002t0012 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0002t0013 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0002t0014 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0003t0001 | 0/1 | 3768 | 39 | 8 | 19 | 0 | 2 | 9 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0004t0002 | 0/0 | 3768 | 15 | 1 | 7 | 0 | 2 | 5 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0004t0007 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0005t0001 | 0/0 | 3768 | 4 | 4 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0006t0001 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0007t0001 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0008t0001 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0009t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0001c0011t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0002c0013t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0003c0012t0002 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| a0004c0010t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | CTTTT others(3763): Show |
chr8 | 94636174 | 94712466 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0002g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0009g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0008g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0013g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0002t0014g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0129 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0003t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0004t0007g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0006t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0006t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0007t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0007t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0008t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0009t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0001c0011t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0002c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0003c0012t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| a0004c0010t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00140 | hp2 | a0002 | c0013 | t0001 | g0145 | EUR | GBR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0090 | EUR | FIN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0342 | EUR | FIN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0332 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0334 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0339 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0241 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0330 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0093 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0351 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0328 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0096 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01074 | hp1 | a0001 | c0004 | t0002 | g0095 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0325 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0348 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0324 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0369 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01168 | hp2 | a0001 | c0004 | t0002 | g0094 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01175 | hp2 | a0001 | c0003 | t0001 | g0337 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01243 | hp2 | a0001 | c0004 | t0002 | g0099 | AMR | PUR | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01256 | hp2 | a0001 | c0004 | t0002 | g0091 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0240 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01516 | hp1 | a0001 | c0004 | t0002 | g0101 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0088 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0341 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0303 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0307 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02080 | hp1 | a0001 | c0002 | t0014 | g0041 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02145 | hp1 | a0001 | c0009 | t0001 | g0150 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | CDX | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0007 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0350 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0183 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0335 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02735 | hp1 | a0001 | c0004 | t0002 | g0035 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0333 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0181 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0352 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0368 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02965 | hp1 | a0001 | c0006 | t0001 | g0345 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0319 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0349 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03130 | hp1 | a0001 | c0002 | t0012 | g0141 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0182 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0347 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0346 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0329 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0353 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03491 | hp2 | a0001 | c0004 | t0002 | g0034 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03492 | hp1 | a0001 | c0004 | t0002 | g0032 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ESN | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0340 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0021 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0331 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0336 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03710 | hp2 | a0001 | c0004 | t0002 | g0033 | SAS | PJL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03831 | hp1 | a0001 | c0004 | t0007 | g0031 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0371 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03927 | hp1 | a0001 | c0004 | t0002 | g0086 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0089 | SAS | BEB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0326 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0074 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0020 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0327 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04228 | hp1 | a0003 | c0012 | t0002 | g0122 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18522 | hp2 | a0001 | c0007 | t0001 | g0344 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0372 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0357 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18965 | hp2 | a0001 | c0008 | t0001 | g0277 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18968 | hp1 | a0001 | c0002 | t0008 | g0011 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0356 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18992 | hp1 | a0001 | c0002 | t0013 | g0017 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0354 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19240 | hp1 | a0004 | c0010 | t0001 | g0321 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ASW | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0184 | AFR | ASW | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0338 | EUR | TSI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | GIH | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01123 | hp1 | a0001 | c0004 | t0002 | g0092 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0239 | AMR | CLM | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0355 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0215 | AFR | MSL | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| NA21309 | hp2 | a0001 | c0011 | t0001 | g0251 | AFR | LWK | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0129 | REF | REF | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0271 | REF | REF | ESRP1_chr8_94636174_94712466 | ESRP1 | chr8 | 94636174 | 94712466 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94643357 | C | G | 1 | a0002 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.316C>G | p.Leu106Val | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/16 | 461/3768 | 316/2046 | 106/681 | chr8 | 94643357 | |||
| chr8:94646267 | G | A | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.475G>A | p.Ala159Thr | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/16 | 620/3768 | 475/2046 | 159/681 | chr8 | 94646267 | |||
| chr8:94646273 | A | G | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.481A>G | p.Met161Val | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/16 | 626/3768 | 481/2046 | 161/681 | chr8 | 94646273 | |||
| chr8:94667958 | A | G | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.941A>G | p.Asn314Ser | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/16 | 1086/3768 | 941/2046 | 314/681 | chr8 | 94667958 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94642060 | G | A | 1 | a0001c0008 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.237G>A | p.Ser79Ser | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/16 | 382/3768 | 237/2046 | 79/681 | chr8 | 94642060 | |||
| chr8:94643344 | G | A | 1 | a0001c0009 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.303G>A | p.Gly101Gly | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/16 | 448/3768 | 303/2046 | 101/681 | chr8 | 94643344 | |||
| chr8:94643368 | T | C | 1 | a0001c0004 | 16 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
synonymous_variant | LOW | c.327T>C | p.Asp109Asp | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/16 | 472/3768 | 327/2046 | 109/681 | chr8 | 94643368 | |||
| chr8:94646179 | A | G | 3 | a0001c0005 a0001c0006 a0001c0007 |
8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
synonymous_variant | LOW | c.387A>G | p.Leu129Leu | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/16 | 532/3768 | 387/2046 | 129/681 | chr8 | 94646179 | |||
| chr8:94668001 | C | T | 3 | a0001c0002 a0001c0004 a0003c0012 |
105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
synonymous_variant | LOW | c.984C>T | p.Val328Val | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/16 | 1129/3768 | 984/2046 | 328/681 | chr8 | 94668001 | |||
| chr8:94668229 | C | T | 2 | a0001c0007 a0001c0011 |
3 | HG03209.hp1 NA18522.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1212C>T | p.Ser404Ser | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/16 | 1357/3768 | 1212/2046 | 404/681 | chr8 | 94668229 | |||
| chr8:94678351 | T | C | 5 | a0001c0002 a0001c0003 a0001c0004 others(2): Show |
145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
synonymous_variant | LOW | c.1800T>C | p.Asn600Asn | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/16 | 1945/3768 | 1800/2046 | 600/681 | chr8 | 94678351 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94641201 | G | C | 1 | a0001c0004t0007 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-118G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/16 | 118 | chr8 | 94641201 | ||||||
| chr8:94641290 | C | T | 1 | a0001c0002t0014 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/16 | 29 | chr8 | 94641290 | ||||||
| chr8:94705982 | A | T | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9056 | chr8 | 94705982 | ||||||
| chr8:94706009 | G | C | 1 | a0001c0002t0008 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*120G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9083 | chr8 | 94706009 | ||||||
| chr8:94706086 | T | C | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
272 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*197T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9160 | chr8 | 94706086 | ||||||
| chr8:94706220 | T | C | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*331T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9294 | chr8 | 94706220 | ||||||
| chr8:94706227 | T | G | 1 | a0001c0001t0009 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9301 | chr8 | 94706227 | ||||||
| chr8:94706305 | T | C | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*416T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9379 | chr8 | 94706305 | ||||||
| chr8:94706306 | G | A | 1 | a0001c0001t0010 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*417G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9380 | chr8 | 94706306 | ||||||
| chr8:94706308 | A | G | 1 | a0001c0002t0013 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9382 | chr8 | 94706308 | ||||||
| chr8:94706401 | T | C | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*512T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9475 | chr8 | 94706401 | ||||||
| chr8:94706453 | T | C | 1 | a0001c0001t0011 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*564T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9527 | chr8 | 94706453 | ||||||
| chr8:94706505 | A | T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*616A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9579 | chr8 | 94706505 | ||||||
| chr8:94706670 | A | G | 1 | a0001c0001t0003 | 6 | HG02257.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*781A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9744 | chr8 | 94706670 | ||||||
| chr8:94706869 | A | G | 1 | a0001c0001t0005 | 4 | HG00423.hp1 HG02015.hp2 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*980A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 9943 | chr8 | 94706869 | ||||||
| chr8:94707065 | G | A | 1 | a0001c0001t0006 | 3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1176G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10139 | chr8 | 94707065 | ||||||
| chr8:94707099 | A | C | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1210A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10173 | chr8 | 94707099 | ||||||
| chr8:94707110 | A | T | 1 | a0001c0001t0004 | 5 | HG02109.hp1 HG02486.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1221A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10184 | chr8 | 94707110 | ||||||
| chr8:94707159 | A | T | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1270A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 16/16 | 10233 | chr8 | 94707159 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:94641516 | C | T | 1 | a0001c0002t0002g0372 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.132+66C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641516 | |||||||
| chr8:94641633 | C | T | 1 | a0001c0003t0001g0371 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.132+183C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641633 | |||||||
| chr8:94641716 | C | G | 1 | a0001c0001t0001g0370 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-240C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641716 | |||||||
| chr8:94641717 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(131): Show |
134 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.133-239G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641717 | |||||||
| chr8:94641804 | C | T | 12 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(9): Show |
12 | HG01167.hp2 HG02257.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-152C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641804 | |||||||
| chr8:94641815 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(133): Show |
136 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.133-141C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641815 | |||||||
| chr8:94641847 | C | T | 3 | a0001c0003t0001g0353 a0001c0003t0001g0354 a0001c0003t0001g0355 |
3 | HG02486.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.133-109C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641847 | |||||||
| chr8:94641861 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.133-95G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641861 | |||||||
| chr8:94641935 | C | G | 1 | a0001c0001t0011g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.133-21C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 1/15 | chr8 | 94641935 | |||||||
| chr8:94642119 | T | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.261+35T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642119 | |||||||
| chr8:94642206 | G | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261+122G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642206 | |||||||
| chr8:94642304 | A | G | 23 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(20): Show |
23 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.261+220A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642304 | |||||||
| chr8:94642347 | A | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(181): Show |
186 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.261+263A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642347 | |||||||
| chr8:94642400 | C | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0131 others(30): Show |
35 | HG00323.hp2 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.261+316C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642400 | |||||||
| chr8:94642495 | T | C | 316 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(313): Show |
318 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.261+411T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642495 | |||||||
| chr8:94642575 | C | T | 20 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(17): Show |
20 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.261+491C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642575 | |||||||
| chr8:94642658 | G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.261+574G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642658 | |||||||
| chr8:94642670 | G | T | 5 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(2): Show |
5 | HG00438.hp1 HG00609.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+586G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642670 | |||||||
| chr8:94642724 | GGCT | G | 16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(13): Show |
16 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.262-577_262-575del others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr8 | 94642724 | ||||||
| chr8:94642802 | G | T | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG02559.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.262-501G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642802 | |||||||
| chr8:94642822 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(274): Show |
279 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(276): Show |
intron_variant | MODIFIER | c.262-481A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642822 | |||||||
| chr8:94642978 | G | A | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-325G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94642978 | |||||||
| chr8:94643056 | A | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG01361.hp1 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.262-247A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643056 | |||||||
| chr8:94643109 | G | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262-194G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643109 | |||||||
| chr8:94643175 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-128C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643175 | |||||||
| chr8:94643187 | T | A | 122 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(119): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.262-116T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 2/15 | chr8 | 94643187 | |||||||
| chr8:94643525 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.375+109T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94643525 | |||||||
| chr8:94643727 | C | T | 8 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(5): Show |
8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+311C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94643727 | |||||||
| chr8:94643751 | A | ACT | 353 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(350): Show |
355 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.375+336_375+337dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94643751 | ||||||
| chr8:94644045 | G | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0274 others(45): Show |
48 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.375+629G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644045 | |||||||
| chr8:94644110 | A | T | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.375+694A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644110 | |||||||
| chr8:94644471 | T | C | 364 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(361): Show |
366 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.375+1055T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644471 | |||||||
| chr8:94644482 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.375+1066C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644482 | |||||||
| chr8:94644555 | C | A | 2 | a0001c0003t0001g0368 a0001c0003t0001g0369 |
2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.375+1139C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644555 | |||||||
| chr8:94644575 | T | C | 120 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(117): Show |
120 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.375+1159T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644575 | |||||||
| chr8:94644659 | C | T | 2 | a0001c0003t0001g0368 a0001c0003t0001g0369 |
2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.375+1243C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644659 | |||||||
| chr8:94644702 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.375+1286A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644702 | |||||||
| chr8:94644793 | G | A | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-1375G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644793 | |||||||
| chr8:94644934 | C | CAGAGCAT others(37377): Show |
1 | a0001c0005t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.376-1233_376-1232i others(37386): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94644934 | ||||||
| chr8:94644934 | CAA | C | 7 | a0001c0005t0001g0182 a0001c0005t0001g0183 a0001c0005t0001g0184 others(4): Show |
7 | HG02572.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.376-1232_376-1231d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94644934 | ||||||
| chr8:94644936 | A | C | 1 | a0001c0005t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.376-1232A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644936 | |||||||
| chr8:94644953 | G | A | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-1215G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94644953 | |||||||
| chr8:94645008 | A | C | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-1160A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645008 | |||||||
| chr8:94645427 | G | GA | 8 | a0001c0001t0001g0180 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-730dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94645427 | ||||||
| chr8:94645427 | GA | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(212): Show |
217 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.376-730delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94645427 | ||||||
| chr8:94645686 | AC | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(205): Show |
210 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.376-481delC | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645686 | |||||||
| chr8:94645728 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(205): Show |
210 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.376-440A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645728 | |||||||
| chr8:94645737 | G | A | 1 | a0004c0010t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.376-431G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645737 | |||||||
| chr8:94645744 | C | A | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-424C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645744 | |||||||
| chr8:94645811 | A | G | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-357A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645811 | |||||||
| chr8:94645831 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.376-337G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645831 | |||||||
| chr8:94645986 | A | C | 8 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(5): Show |
8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-182A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645986 | |||||||
| chr8:94645997 | G | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(205): Show |
210 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.376-171G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94645997 | |||||||
| chr8:94646042 | T | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(214): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.376-126T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94646042 | |||||||
| chr8:94646059 | A | AT | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(214): Show |
219 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.376-104dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr8 | 94646059 | ||||||
| chr8:94646068 | T | C | 8 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(5): Show |
8 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.376-100T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 3/15 | chr8 | 94646068 | |||||||
| chr8:94646298 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(206): Show |
211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.490+16T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646298 | |||||||
| chr8:94646334 | A | AAAAT | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(206): Show |
211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.490+52_490+53insAA others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646334 | |||||||
| chr8:94646477 | G | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490+195G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646477 | |||||||
| chr8:94646480 | C | T | 323 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(320): Show |
325 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.490+198C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646480 | |||||||
| chr8:94646515 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.490+233C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646515 | |||||||
| chr8:94646573 | A | G | 5 | a0001c0001t0001g0180 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+291A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646573 | |||||||
| chr8:94646597 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(153): Show |
158 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.490+315A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646597 | |||||||
| chr8:94646688 | C | T | 1 | a0003c0012t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.490+406C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646688 | |||||||
| chr8:94646709 | T | C | 1 | a0002c0013t0001g0145 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.490+427T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646709 | |||||||
| chr8:94646716 | G | A | 1 | a0001c0002t0002g0006 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.490+434G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646716 | |||||||
| chr8:94646724 | C | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
9 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+442C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646724 | |||||||
| chr8:94646731 | T | C | 7 | a0001c0001t0001g0247 a0001c0001t0001g0256 a0001c0001t0001g0257 others(4): Show |
7 | HG02559.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+449T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646731 | |||||||
| chr8:94646897 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.490+615A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94646897 | |||||||
| chr8:94647037 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.490+755A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647037 | |||||||
| chr8:94647123 | G | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0130 a0001c0001t0001g0131 others(103): Show |
106 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.490+841G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647123 | |||||||
| chr8:94647138 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.490+856T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647138 | |||||||
| chr8:94647161 | T | C | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+879T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647161 | |||||||
| chr8:94647201 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.490+919G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647201 | |||||||
| chr8:94647213 | C | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0193 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.490+931C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647213 | |||||||
| chr8:94647307 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490+1025C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647307 | |||||||
| chr8:94647408 | C | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(206): Show |
211 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.490+1126C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647408 | |||||||
| chr8:94647414 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(153): Show |
158 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.490+1132A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647414 | |||||||
| chr8:94647456 | T | C | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+1174T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647456 | |||||||
| chr8:94647621 | A | C | 323 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(320): Show |
325 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.490+1339A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647621 | |||||||
| chr8:94647672 | G | A | 1 | a0001c0004t0002g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.490+1390G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647672 | |||||||
| chr8:94647790 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.490+1508T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647790 | |||||||
| chr8:94647860 | G | T | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.490+1578G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94647860 | |||||||
| chr8:94648174 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(264): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.490+1892T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648174 | |||||||
| chr8:94648301 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.490+2019G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648301 | |||||||
| chr8:94648543 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.490+2261C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648543 | |||||||
| chr8:94648544 | C | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(260): Show |
265 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.490+2262C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648544 | |||||||
| chr8:94648574 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490+2292G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648574 | |||||||
| chr8:94648584 | A | C | 9 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
9 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+2302A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648584 | |||||||
| chr8:94648590 | C | T | 1 | a0001c0001t0004g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.490+2308C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648590 | |||||||
| chr8:94648611 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.490+2329G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648611 | |||||||
| chr8:94648737 | C | T | 6 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(3): Show |
6 | HG00423.hp2 NA18944.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+2455C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648737 | |||||||
| chr8:94648780 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.490+2498C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648780 | |||||||
| chr8:94648835 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0171 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.490+2553A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648835 | |||||||
| chr8:94648850 | G | A | 1 | a0001c0002t0002g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.490+2568G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648850 | |||||||
| chr8:94648924 | C | T | 347 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(344): Show |
349 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.490+2642C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648924 | |||||||
| chr8:94648963 | G | A | 1 | a0001c0002t0002g0009 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.490+2681G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648963 | |||||||
| chr8:94648984 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490+2702G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94648984 | |||||||
| chr8:94649047 | C | G | 1 | a0001c0002t0002g0120 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.490+2765C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649047 | |||||||
| chr8:94649050 | G | A | 19 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(16): Show |
19 | HG01257.hp1 HG02004.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+2768G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649050 | |||||||
| chr8:94649091 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.490+2809C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649091 | |||||||
| chr8:94649232 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(136): Show |
141 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.490+2950G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649232 | |||||||
| chr8:94649274 | T | C | 3 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 |
3 | HG01167.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.490+2992T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649274 | |||||||
| chr8:94649285 | C | G | 3 | a0001c0006t0001g0345 a0001c0007t0001g0344 a0001c0007t0001g0346 |
3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+3003C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649285 | |||||||
| chr8:94649349 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.490+3067C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649349 | |||||||
| chr8:94649356 | T | G | 1 | a0001c0001t0001g0274 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.490+3074T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649356 | |||||||
| chr8:94649440 | T | TCTC | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(264): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.490+3160_490+3161i others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94649440 | ||||||
| chr8:94649489 | C | T | 267 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(264): Show |
269 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.490+3207C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649489 | |||||||
| chr8:94649544 | C | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(137): Show |
142 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.490+3262C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649544 | |||||||
| chr8:94649598 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(54): Show |
57 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.490+3316C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649598 | |||||||
| chr8:94649613 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490+3331A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649613 | |||||||
| chr8:94649659 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.490+3377C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649659 | |||||||
| chr8:94649762 | C | A | 266 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(263): Show |
268 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.490+3480C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649762 | |||||||
| chr8:94649809 | G | A | 15 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(12): Show |
15 | HG01891.hp1 HG02559.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.490+3527G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94649809 | |||||||
| chr8:94649992 | CCTCTTCC others(14): Show |
C | 1 | a0001c0001t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.490+3712_490+3732d others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94649992 | ||||||
| chr8:94650111 | A | T | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.490+3829A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650111 | |||||||
| chr8:94650164 | T | C | 106 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(103): Show |
106 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.490+3882T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650164 | |||||||
| chr8:94650167 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.490+3885A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650167 | |||||||
| chr8:94650259 | TTTTG | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(90): Show |
94 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.490+3981_490+3984d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650259 | ||||||
| chr8:94650263 | G | GT | 143 | a0001c0001t0001g0042 a0001c0001t0001g0087 a0001c0001t0001g0123 others(140): Show |
144 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.490+3990dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650263 | ||||||
| chr8:94650263 | GT | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0193 others(47): Show |
50 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.490+3990delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650263 | ||||||
| chr8:94650352 | C | T | 24 | a0001c0003t0001g0001 a0001c0003t0001g0135 a0001c0003t0001g0239 others(21): Show |
25 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.490+4070C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650352 | |||||||
| chr8:94650408 | G | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(277): Show |
282 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(279): Show |
intron_variant | MODIFIER | c.490+4126G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650408 | |||||||
| chr8:94650488 | T | C | 1 | a0001c0002t0002g0010 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.490+4206T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650488 | |||||||
| chr8:94650558 | TGGTTTGT others(12): Show |
T | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG00438.hp2 NA18747.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+4291_490+4309d others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650558 | ||||||
| chr8:94650616 | T | C | 297 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(294): Show |
299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.490+4334T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650616 | |||||||
| chr8:94650678 | C | T | 11 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(8): Show |
11 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.490+4396C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650678 | |||||||
| chr8:94650721 | A | AT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(84): Show |
88 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.490+4448dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650721 | ||||||
| chr8:94650736 | G | A | 3 | a0001c0006t0001g0345 a0001c0007t0001g0344 a0001c0007t0001g0346 |
3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+4454G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650736 | |||||||
| chr8:94650770 | G | T | 1 | a0001c0001t0001g0315 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.490+4488G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650770 | |||||||
| chr8:94650802 | T | TC | 75 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0193 others(72): Show |
76 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.490+4522dupC | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94650802 | ||||||
| chr8:94650843 | C | G | 1 | a0001c0005t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.490+4561C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650843 | |||||||
| chr8:94650951 | C | T | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+4669C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94650951 | |||||||
| chr8:94651058 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.490+4776T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651058 | |||||||
| chr8:94651143 | A | G | 25 | a0001c0003t0001g0001 a0001c0003t0001g0135 a0001c0003t0001g0153 others(22): Show |
26 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.490+4861A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651143 | |||||||
| chr8:94651143 | A | T | 107 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.490+4861A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651143 | |||||||
| chr8:94651239 | C | CT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0117 others(92): Show |
95 | HG00140.hp2 HG00423.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.490+4979dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651239 | ||||||
| chr8:94651239 | CT | C | 110 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(107): Show |
110 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.490+4979delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651239 | ||||||
| chr8:94651271 | C | T | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+4989C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651271 | |||||||
| chr8:94651305 | G | A | 3 | a0001c0006t0001g0345 a0001c0007t0001g0344 a0001c0007t0001g0346 |
3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.490+5023G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651305 | |||||||
| chr8:94651378 | C | T | 25 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(22): Show |
26 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.490+5096C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651378 | |||||||
| chr8:94651397 | T | C | 1 | a0001c0008t0001g0277 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.490+5115T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651397 | |||||||
| chr8:94651441 | A | G | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.490+5159A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651441 | |||||||
| chr8:94651531 | T | C | 1 | a0001c0001t0001g0359 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.490+5249T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651531 | |||||||
| chr8:94651594 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(88): Show |
92 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.490+5312T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651594 | |||||||
| chr8:94651607 | G | C | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.490+5325G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651607 | |||||||
| chr8:94651616 | A | AT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(89): Show |
93 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.490+5343dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651616 | ||||||
| chr8:94651806 | T | A | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(279): Show |
283 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.490+5524T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651806 | |||||||
| chr8:94651922 | G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+5640G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94651922 | |||||||
| chr8:94651987 | C | CT | 60 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0161 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.490+5728dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | ||||||
| chr8:94651987 | C | CTT | 134 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0146 others(131): Show |
134 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.490+5727_490+5728d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | ||||||
| chr8:94651987 | C | CTTT | 87 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(84): Show |
88 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.490+5726_490+5728d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | ||||||
| chr8:94651987 | C | CTTTT | 17 | a0001c0001t0001g0087 a0001c0001t0001g0115 a0001c0001t0001g0118 others(14): Show |
17 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.490+5725_490+5728d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94651987 | ||||||
| chr8:94652010 | T | TTTTTTGA | 9 | a0001c0001t0001g0247 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
9 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+5728_490+5729i others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652010 | |||||||
| chr8:94652172 | G | C | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+5890G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652172 | |||||||
| chr8:94652239 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.490+5957C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652239 | |||||||
| chr8:94652275 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.490+5993A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652275 | |||||||
| chr8:94652290 | C | A | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+6008C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652290 | |||||||
| chr8:94652324 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490+6042G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652324 | |||||||
| chr8:94652441 | G | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+6159G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652441 | |||||||
| chr8:94652459 | T | C | 2 | a0001c0003t0001g0368 a0001c0003t0001g0369 |
2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.490+6177T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652459 | |||||||
| chr8:94652479 | G | GT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(89): Show |
93 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.490+6208dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94652479 | ||||||
| chr8:94652479 | G | GTT | 6 | a0001c0001t0001g0169 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG02559.hp1 HG02622.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+6207_490+6208d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94652479 | ||||||
| chr8:94652574 | A | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0193 others(62): Show |
65 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.490+6292A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652574 | |||||||
| chr8:94652601 | C | A | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+6319C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652601 | |||||||
| chr8:94652630 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(279): Show |
283 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.490+6348T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652630 | |||||||
| chr8:94652681 | C | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.490+6399C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652681 | |||||||
| chr8:94652737 | C | A | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+6455C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652737 | |||||||
| chr8:94652910 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.490+6628T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94652910 | |||||||
| chr8:94653009 | G | A | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG00438.hp2 NA18747.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+6727G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653009 | |||||||
| chr8:94653064 | T | C | 1 | a0001c0002t0002g0012 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.490+6782T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653064 | |||||||
| chr8:94653142 | G | GA | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(292): Show |
296 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.490+6869dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94653142 | ||||||
| chr8:94653198 | T | C | 1 | a0001c0001t0004g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.490+6916T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653198 | |||||||
| chr8:94653215 | TG | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.490+6939delG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94653215 | ||||||
| chr8:94653246 | A | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0103 others(97): Show |
101 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.490+6964A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653246 | |||||||
| chr8:94653545 | T | G | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+7263T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94653545 | |||||||
| chr8:94653802 | G | GAT | 106 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(103): Show |
106 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.490+7534_490+7535d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94653802 | ||||||
| chr8:94654140 | G | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+7858G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654140 | |||||||
| chr8:94654164 | C | CA | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(287): Show |
291 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.490+7886dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94654164 | ||||||
| chr8:94654176 | G | A | 6 | a0001c0003t0001g0001 a0001c0003t0001g0135 a0001c0003t0001g0324 others(3): Show |
7 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.490+7894G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654176 | |||||||
| chr8:94654189 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.490+7907G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654189 | |||||||
| chr8:94654259 | G | A | 1 | a0001c0001t0001g0360 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.490+7977G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654259 | |||||||
| chr8:94654275 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(274): Show |
278 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.490+7993A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654275 | |||||||
| chr8:94654393 | G | A | 277 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(274): Show |
278 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.491-7879G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654393 | |||||||
| chr8:94654406 | C | T | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(291): Show |
295 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.491-7866C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654406 | |||||||
| chr8:94654450 | CTT | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(83): Show |
87 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.491-7818_491-7817d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94654450 | ||||||
| chr8:94654494 | C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-7778C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654494 | |||||||
| chr8:94654495 | C | T | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-7777C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654495 | |||||||
| chr8:94654676 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-7596C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654676 | |||||||
| chr8:94654852 | G | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-7420G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94654852 | |||||||
| chr8:94654919 | C | CA | 35 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(32): Show |
36 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.491-7340dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94654919 | ||||||
| chr8:94655044 | CTG | C | 7 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0002g0014 others(4): Show |
7 | HG01943.hp2 HG01978.hp1 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-7225_491-7224d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655044 | ||||||
| chr8:94655060 | G | GTT | 9 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0001t0001g0304 others(6): Show |
9 | HG00738.hp2 HG01099.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-7207_491-7206d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | ||||||
| chr8:94655060 | G | GTTTT | 8 | a0001c0001t0004g0254 a0001c0002t0002g0069 a0001c0002t0002g0070 others(5): Show |
8 | HG02015.hp1 HG03540.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-7209_491-7206d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | ||||||
| chr8:94655060 | G | GTTTTT | 89 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(86): Show |
90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.491-7210_491-7206d others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | ||||||
| chr8:94655060 | G | GTTTTTT | 9 | a0001c0001t0001g0119 a0001c0001t0001g0189 a0001c0001t0001g0193 others(6): Show |
9 | HG00597.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-7211_491-7206d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655060 | ||||||
| chr8:94655063 | T | TTG | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02258.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.491-7208_491-7207i others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655063 | ||||||
| chr8:94655065 | T | G | 32 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(29): Show |
33 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.491-7207T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655065 | |||||||
| chr8:94655065 | T | TGTGTG | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02886.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.491-7207_491-7206i others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655065 | |||||||
| chr8:94655065 | T | TTGTG | 7 | a0001c0002t0002g0018 a0001c0002t0002g0019 a0001c0002t0002g0020 others(4): Show |
7 | HG00733.hp1 HG03654.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-7187_491-7184d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655065 | ||||||
| chr8:94655065 | T | TTTGTG | 4 | a0001c0001t0001g0149 a0001c0001t0011g0136 a0001c0002t0002g0024 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-7206_491-7205i others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655065 | ||||||
| chr8:94655065 | T | TTTTG | 87 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(84): Show |
87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.491-7206_491-7205i others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655065 | ||||||
| chr8:94655067 | G | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0103 others(168): Show |
172 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.491-7205G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655067 | |||||||
| chr8:94655069 | G | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0103 others(138): Show |
142 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.491-7203G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655069 | |||||||
| chr8:94655071 | G | T | 7 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0203 others(4): Show |
7 | HG02004.hp1 NA18949.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.491-7201G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655071 | |||||||
| chr8:94655087 | G | T | 13 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(10): Show |
13 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-7185G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655087 | |||||||
| chr8:94655106 | A | T | 3 | a0001c0002t0002g0020 a0001c0002t0002g0021 a0001c0002t0002g0022 |
3 | HG03654.hp2 HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.491-7166A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655106 | |||||||
| chr8:94655120 | C | T | 2 | a0001c0001t0001g0360 a0001c0001t0001g0367 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.491-7152C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655120 | |||||||
| chr8:94655352 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(59): Show |
62 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.491-6920G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655352 | |||||||
| chr8:94655388 | C | CT | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0103 others(163): Show |
167 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.491-6870dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655388 | ||||||
| chr8:94655444 | A | G | 3 | a0001c0006t0001g0345 a0001c0007t0001g0344 a0001c0007t0001g0346 |
3 | HG02965.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-6828A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655444 | |||||||
| chr8:94655466 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(59): Show |
62 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.491-6806G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655466 | |||||||
| chr8:94655603 | G | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(96): Show |
100 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.491-6669G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655603 | |||||||
| chr8:94655711 | T | C | 12 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(9): Show |
12 | HG01070.hp2 HG01081.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.491-6561T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655711 | |||||||
| chr8:94655727 | CA | C | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-6539delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94655727 | ||||||
| chr8:94655814 | C | T | 1 | a0001c0005t0001g0184 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-6458C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655814 | |||||||
| chr8:94655815 | C | T | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.491-6457C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655815 | |||||||
| chr8:94655889 | G | A | 1 | a0001c0002t0002g0023 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.491-6383G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655889 | |||||||
| chr8:94655996 | T | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.491-6276T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94655996 | |||||||
| chr8:94656003 | C | T | 59 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(56): Show |
59 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.491-6269C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656003 | |||||||
| chr8:94656087 | G | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(41): Show |
44 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.491-6185G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656087 | |||||||
| chr8:94656138 | C | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.491-6134C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656138 | |||||||
| chr8:94656145 | G | A | 2 | a0001c0002t0002g0025 a0001c0002t0002g0026 |
2 | HG02083.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.491-6127G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656145 | |||||||
| chr8:94656207 | C | CA | 74 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0001g0138 others(71): Show |
74 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.491-6043dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656207 | ||||||
| chr8:94656207 | C | CAA | 15 | a0001c0001t0001g0247 a0001c0001t0001g0249 a0001c0001t0001g0250 others(12): Show |
15 | HG02559.hp2 HG02630.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.491-6044_491-6043d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656207 | ||||||
| chr8:94656207 | CA | C | 28 | a0001c0001t0001g0245 a0001c0002t0001g0085 a0001c0002t0002g0009 others(25): Show |
29 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.491-6043delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656207 | ||||||
| chr8:94656229 | A | T | 30 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0231 others(27): Show |
31 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.491-6043A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656229 | |||||||
| chr8:94656230 | T | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0342 a0001c0001t0001g0343 others(2): Show |
5 | HG00323.hp1 HG00323.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-6042T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656230 | |||||||
| chr8:94656241 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491-6031C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656241 | |||||||
| chr8:94656311 | C | T | 6 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 others(3): Show |
6 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-5961C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656311 | |||||||
| chr8:94656364 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.491-5908G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656364 | |||||||
| chr8:94656410 | CG | C | 16 | a0001c0003t0001g0088 a0001c0003t0001g0153 a0001c0003t0001g0239 others(13): Show |
16 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.491-5857delG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94656410 | ||||||
| chr8:94656440 | C | T | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-5832C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656440 | |||||||
| chr8:94656511 | A | G | 2 | a0001c0001t0001g0238 a0001c0003t0001g0340 |
2 | HG03654.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.491-5761A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656511 | |||||||
| chr8:94656529 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(100): Show |
104 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.491-5743T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656529 | |||||||
| chr8:94656657 | G | A | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491-5615G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94656657 | |||||||
| chr8:94657034 | A | G | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.491-5238A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657034 | |||||||
| chr8:94657292 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.491-4980G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657292 | |||||||
| chr8:94657311 | T | G | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.491-4961T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657311 | |||||||
| chr8:94657414 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.491-4858C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657414 | |||||||
| chr8:94657472 | C | CGT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0149 others(32): Show |
35 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.491-4769_491-4768d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | CGTGT | 72 | a0001c0001t0001g0123 a0001c0001t0001g0130 a0001c0001t0001g0132 others(69): Show |
73 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.491-4771_491-4768d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | CGTGTGT | 126 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0087 others(123): Show |
127 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.491-4773_491-4768d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | CGTGTGTG others(1): Show |
29 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0228 others(26): Show |
29 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.491-4775_491-4768d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | CGTGTGTG others(3): Show |
18 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(15): Show |
18 | HG01070.hp2 HG01167.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-4777_491-4768d others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | CGTGTGTG others(5): Show |
4 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0003g0216 others(1): Show |
4 | HG02630.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-4779_491-4768d others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | CGTGTGTG others(7): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0190 |
2 | NA18946.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.491-4781_491-4768d others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.491-4800C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657472 | |||||||
| chr8:94657472 | CGT | C | 6 | a0001c0001t0001g0137 a0001c0001t0001g0180 a0001c0001t0001g0267 others(3): Show |
6 | HG00140.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-4769_491-4768d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | CGTGT | C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0212 a0001c0001t0001g0274 others(37): Show |
40 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.491-4771_491-4768d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | CGTGTGT | C | 3 | a0001c0001t0001g0285 a0001c0001t0001g0306 a0001c0008t0001g0277 |
3 | HG02738.hp2 HG04228.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.491-4773_491-4768d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657472 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.491-4781_491-4768d others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94657472 | ||||||
| chr8:94657522 | A | C | 1 | a0001c0004t0002g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.491-4750A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657522 | |||||||
| chr8:94657545 | A | T | 1 | a0001c0001t0001g0359 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.491-4727A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657545 | |||||||
| chr8:94657586 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.491-4686C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657586 | |||||||
| chr8:94657729 | C | A | 1 | a0001c0001t0001g0370 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.491-4543C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657729 | |||||||
| chr8:94657930 | C | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(295): Show |
299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.491-4342C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657930 | |||||||
| chr8:94657954 | G | A | 2 | a0001c0007t0001g0344 a0001c0007t0001g0346 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-4318G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94657954 | |||||||
| chr8:94658015 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-4257G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658015 | |||||||
| chr8:94658057 | G | A | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.491-4215G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658057 | |||||||
| chr8:94658073 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(42): Show |
45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.491-4199G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658073 | |||||||
| chr8:94658091 | T | C | 1 | a0001c0008t0001g0277 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.491-4181T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658091 | |||||||
| chr8:94658174 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-4098A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658174 | |||||||
| chr8:94658176 | GTGCTGGG others(18): Show |
G | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-4095_491-4071d others(27): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658176 | |||||||
| chr8:94658275 | G | A | 1 | a0001c0002t0002g0036 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-3997G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658275 | |||||||
| chr8:94658452 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 |
3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.491-3820A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658452 | |||||||
| chr8:94658483 | C | T | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.491-3789C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658483 | |||||||
| chr8:94658516 | T | C | 5 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-3756T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658516 | |||||||
| chr8:94658681 | A | G | 1 | a0001c0002t0002g0060 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.491-3591A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658681 | |||||||
| chr8:94658691 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0193 others(43): Show |
46 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.491-3581T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658691 | |||||||
| chr8:94658889 | A | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(295): Show |
299 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.491-3383A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658889 | |||||||
| chr8:94658959 | T | C | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.491-3313T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94658959 | |||||||
| chr8:94659002 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.491-3270G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659002 | |||||||
| chr8:94659109 | G | A | 2 | a0001c0007t0001g0344 a0001c0007t0001g0346 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.491-3163G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659109 | |||||||
| chr8:94659170 | C | T | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.491-3102C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659170 | |||||||
| chr8:94659190 | T | G | 1 | a0001c0003t0001g0347 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.491-3082T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659190 | |||||||
| chr8:94659195 | T | TA | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.491-3068dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94659195 | ||||||
| chr8:94659325 | G | A | 5 | a0001c0001t0001g0228 a0001c0001t0001g0231 a0001c0001t0001g0233 others(2): Show |
5 | HG00597.hp2 NA18612.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-2947G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659325 | |||||||
| chr8:94659342 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.491-2930C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659342 | |||||||
| chr8:94659428 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.491-2844C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659428 | |||||||
| chr8:94659429 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.491-2843G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659429 | |||||||
| chr8:94659577 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.491-2695A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659577 | |||||||
| chr8:94659614 | G | A | 2 | a0001c0003t0001g0368 a0001c0003t0001g0369 |
2 | HG01167.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.491-2658G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659614 | |||||||
| chr8:94659805 | T | C | 327 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(324): Show |
329 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.491-2467T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659805 | |||||||
| chr8:94659805 | T | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | NA18943.hp1 NA18957.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-2467T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94659805 | |||||||
| chr8:94660269 | T | C | 13 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-2003T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660269 | |||||||
| chr8:94660325 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.491-1947G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660325 | |||||||
| chr8:94660461 | G | A | 1 | a0001c0001t0001g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.491-1811G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660461 | |||||||
| chr8:94660709 | C | CA | 11 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0001t0001g0174 others(8): Show |
11 | HG00423.hp2 HG01123.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.491-1529dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | C | CAA | 9 | a0001c0001t0001g0165 a0001c0001t0001g0172 a0001c0001t0001g0173 others(6): Show |
9 | HG01261.hp2 HG02486.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-1530_491-1529d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | C | CAAA | 6 | a0001c0001t0001g0178 a0001c0003t0001g0339 a0001c0003t0001g0348 others(3): Show |
6 | HG00735.hp2 HG01070.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-1531_491-1529d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CA | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0157 others(12): Show |
15 | HG00140.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.491-1529delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAA | C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0139 a0001c0001t0006g0151 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-1530_491-1529d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAA | C | 13 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-1531_491-1529d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAA | C | 32 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0114 others(29): Show |
32 | HG00438.hp1 HG00438.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.491-1532_491-1529d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAA | C | 73 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0107 others(70): Show |
73 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.491-1533_491-1529d others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAAA | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0242 a0001c0001t0001g0247 others(14): Show |
18 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.491-1534_491-1529d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAAAA | C | 43 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0248 others(40): Show |
43 | HG00733.hp1 HG01109.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.491-1535_491-1529d others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAAAA others(1): Show |
C | 78 | a0001c0001t0001g0087 a0001c0001t0001g0212 a0001c0001t0001g0257 others(75): Show |
78 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.491-1536_491-1529d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAAAA others(2): Show |
C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0274 others(38): Show |
41 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.491-1537_491-1529d others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0278 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG00558.hp1 HG01928.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.491-1538_491-1529d others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660709 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.491-1540_491-1529d others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660709 | ||||||
| chr8:94660740 | A | C | 1 | a0001c0001t0001g0270 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.491-1532A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660740 | |||||||
| chr8:94660744 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.491-1528C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660744 | |||||||
| chr8:94660745 | C | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp2 HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.491-1527C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660745 | |||||||
| chr8:94660746 | A | AAAC | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 |
3 | HG02280.hp2 HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.491-1524_491-1523i others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660746 | ||||||
| chr8:94660746 | AAAACAAA others(1): Show |
A | 108 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.491-1514_491-1507d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr8 | 94660746 | ||||||
| chr8:94660805 | C | T | 1 | a0001c0002t0002g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.491-1467C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660805 | |||||||
| chr8:94660836 | G | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-1436G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94660836 | |||||||
| chr8:94661032 | C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.491-1240C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661032 | |||||||
| chr8:94661446 | A | C | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(343): Show |
348 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.491-826A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661446 | |||||||
| chr8:94661498 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.491-774G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661498 | |||||||
| chr8:94661651 | A | G | 5 | a0001c0002t0002g0045 a0001c0002t0002g0077 a0001c0002t0002g0273 others(2): Show |
5 | HG02074.hp2 NA18943.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-621A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661651 | |||||||
| chr8:94661657 | A | C | 13 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.491-615A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661657 | |||||||
| chr8:94661717 | A | G | 108 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0087 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.491-555A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661717 | |||||||
| chr8:94661897 | A | C | 1 | a0001c0001t0001g0320 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.491-375A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94661897 | |||||||
| chr8:94662025 | C | T | 2 | a0001c0002t0002g0019 a0001c0002t0002g0029 |
2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.491-247C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94662025 | |||||||
| chr8:94662204 | G | C | 107 | a0001c0001t0001g0042 a0001c0001t0001g0087 a0001c0002t0001g0013 others(104): Show |
107 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.491-68G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 4/15 | chr8 | 94662204 | |||||||
| chr8:94662380 | G | T | 4 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 others(1): Show |
4 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+10G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 5/15 | chr8 | 94662380 | |||||||
| chr8:94662382 | T | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00741.hp1 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+12T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 5/15 | chr8 | 94662382 | |||||||
| chr8:94662595 | G | GT | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(244): Show |
248 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.644+52dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94662595 | ||||||
| chr8:94662702 | G | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(249): Show |
254 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.644+147G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94662702 | |||||||
| chr8:94662733 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+178G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94662733 | |||||||
| chr8:94663017 | T | C | 4 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 others(1): Show |
4 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+462T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663017 | |||||||
| chr8:94663058 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.644+503A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663058 | |||||||
| chr8:94663127 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.644+572G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663127 | |||||||
| chr8:94663144 | G | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0087 others(169): Show |
172 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.644+589G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663144 | |||||||
| chr8:94663241 | C | CATTT | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+703_644+706dup others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94663241 | ||||||
| chr8:94663302 | G | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.644+747G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663302 | |||||||
| chr8:94663338 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.644+783C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663338 | |||||||
| chr8:94663460 | G | C | 2 | a0001c0007t0001g0344 a0001c0007t0001g0346 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.644+905G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663460 | |||||||
| chr8:94663723 | G | T | 17 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG01361.hp2 HG01928.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.645-974G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663723 | |||||||
| chr8:94663854 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.645-843T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663854 | |||||||
| chr8:94663992 | A | C | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.645-705A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94663992 | |||||||
| chr8:94664120 | C | CT | 37 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(34): Show |
37 | HG01070.hp2 HG01109.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.645-556dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | ||||||
| chr8:94664120 | C | CTT | 8 | a0001c0001t0001g0169 a0001c0001t0001g0256 a0001c0001t0001g0266 others(5): Show |
8 | HG00609.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-557_645-556dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | ||||||
| chr8:94664120 | CT | C | 105 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0157 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.645-556delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | ||||||
| chr8:94664120 | CTT | C | 8 | a0001c0002t0002g0030 a0001c0002t0002g0070 a0001c0002t0002g0078 others(5): Show |
8 | HG01167.hp2 HG01496.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.645-557_645-556del others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr8 | 94664120 | ||||||
| chr8:94664141 | T | TTTTTG | 24 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(21): Show |
25 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.645-556_645-555ins others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664141 | |||||||
| chr8:94664150 | G | C | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.645-547G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664150 | |||||||
| chr8:94664188 | A | G | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.645-509A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664188 | |||||||
| chr8:94664342 | G | C | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.645-355G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664342 | |||||||
| chr8:94664428 | T | A | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.645-269T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664428 | |||||||
| chr8:94664442 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0213 |
3 | HG02615.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.645-255T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664442 | |||||||
| chr8:94664557 | G | A | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.645-140G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664557 | |||||||
| chr8:94664633 | G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.645-64G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664633 | |||||||
| chr8:94664666 | C | G | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.645-31C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 6/15 | chr8 | 94664666 | |||||||
| chr8:94664904 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(250): Show |
255 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.756-23T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 7/15 | chr8 | 94664904 | |||||||
| chr8:94665352 | G | A | 1 | a0001c0006t0001g0345 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.931+156G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665352 | |||||||
| chr8:94665547 | G | A | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.931+351G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665547 | |||||||
| chr8:94665556 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.931+360A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665556 | |||||||
| chr8:94665566 | G | A | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.931+370G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665566 | |||||||
| chr8:94665570 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(212): Show |
216 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.931+374C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665570 | |||||||
| chr8:94665615 | C | T | 3 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 |
3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.931+419C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665615 | |||||||
| chr8:94665641 | G | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+445G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665641 | |||||||
| chr8:94665790 | G | A | 14 | a0001c0001t0001g0169 a0001c0001t0001g0247 a0001c0001t0001g0249 others(11): Show |
14 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.931+594G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665790 | |||||||
| chr8:94665812 | A | AT | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+616_931+617ins others(1): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665812 | |||||||
| chr8:94665813 | A | T | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+617A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665813 | |||||||
| chr8:94665814 | A | C | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.931+618A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665814 | |||||||
| chr8:94665853 | C | A | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.931+657C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94665853 | |||||||
| chr8:94666084 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(246): Show |
251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.931+888T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666084 | |||||||
| chr8:94666250 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.931+1054A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666250 | |||||||
| chr8:94666348 | G | A | 14 | a0001c0001t0001g0169 a0001c0001t0001g0247 a0001c0001t0001g0249 others(11): Show |
14 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.931+1152G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666348 | |||||||
| chr8:94666389 | A | G | 2 | a0001c0001t0011g0136 a0001c0009t0001g0150 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.931+1193A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666389 | |||||||
| chr8:94666568 | A | G | 1 | a0001c0002t0002g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.931+1372A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666568 | |||||||
| chr8:94666676 | G | T | 1 | a0001c0001t0001g0305 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.932-1273G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666676 | |||||||
| chr8:94666774 | A | C | 1 | a0001c0001t0001g0235 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.932-1175A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666774 | |||||||
| chr8:94666786 | GGTTGCT | G | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.932-1160_932-1155d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94666786 | ||||||
| chr8:94666950 | G | C | 331 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0042 others(328): Show |
333 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.932-999G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94666950 | |||||||
| chr8:94667040 | T | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00741.hp1 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-909T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667040 | |||||||
| chr8:94667043 | T | C | 34 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(31): Show |
35 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.932-906T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667043 | |||||||
| chr8:94667052 | A | G | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.932-897A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667052 | |||||||
| chr8:94667068 | G | GGGGGGTG others(13): Show |
4 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 others(1): Show |
4 | HG01167.hp2 HG02818.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-880_932-879ins others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGGGTG others(17): Show |
1 | a0001c0003t0001g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.932-880_932-879ins others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(7): Show |
10 | a0001c0003t0001g0001 a0001c0003t0001g0135 a0001c0003t0001g0327 others(7): Show |
11 | HG00642.hp2 HG01257.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.932-880_932-879ins others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(9): Show |
6 | a0001c0003t0001g0088 a0001c0003t0001g0153 a0001c0003t0001g0239 others(3): Show |
6 | HG00741.hp2 HG01123.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.932-880_932-879ins others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(11): Show |
1 | a0001c0003t0001g0338 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.932-880_932-879ins others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(13): Show |
1 | a0001c0003t0001g0355 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.932-880_932-879ins others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(17): Show |
3 | a0001c0003t0001g0349 a0001c0003t0001g0350 a0001c0003t0001g0351 |
3 | HG01070.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.932-880_932-879ins others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(19): Show |
1 | a0001c0003t0001g0353 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.932-880_932-879ins others(26): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGGGTGTG others(25): Show |
2 | a0001c0003t0001g0347 a0001c0003t0001g0348 |
2 | HG01081.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.932-880_932-879ins others(32): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGT | 5 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0004g0194 others(2): Show |
5 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.932-856_932-855dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGT | 98 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(95): Show |
99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.932-858_932-855dup others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGT | 91 | a0001c0001t0001g0105 a0001c0001t0001g0235 a0001c0001t0001g0246 others(88): Show |
91 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.932-860_932-855dup others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(1): Show |
20 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(17): Show |
20 | HG00597.hp1 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.932-862_932-855dup others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(3): Show |
13 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(10): Show |
13 | HG00735.hp2 HG02074.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.932-864_932-855dup others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(5): Show |
1 | a0001c0002t0002g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.932-866_932-855dup others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(7): Show |
46 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0267 others(43): Show |
46 | HG00140.hp1 HG00558.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.932-868_932-855dup others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(9): Show |
10 | a0001c0001t0001g0212 a0001c0001t0001g0298 a0001c0001t0001g0300 others(7): Show |
10 | HG00423.hp1 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.932-870_932-855dup others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(11): Show |
13 | a0001c0001t0001g0138 a0001c0001t0001g0169 a0001c0001t0001g0180 others(10): Show |
13 | HG02109.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.932-872_932-855dup others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(13): Show |
13 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 others(10): Show |
13 | HG02615.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.932-874_932-855dup others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(15): Show |
3 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0364 |
3 | HG02257.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.932-876_932-855dup others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GGTGTGTG others(17): Show |
3 | a0001c0001t0001g0363 a0001c0007t0001g0344 a0001c0007t0001g0346 |
3 | HG03209.hp1 HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.932-878_932-855dup others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667068 | ||||||
| chr8:94667068 | G | GTGTGTGT others(16): Show |
1 | a0001c0001t0001g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.932-881_932-880ins others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667068 | |||||||
| chr8:94667098 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG00438.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.932-851C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667098 | |||||||
| chr8:94667147 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02886.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.932-802G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667147 | |||||||
| chr8:94667173 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(213): Show |
217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.932-776G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667173 | |||||||
| chr8:94667217 | C | CA | 21 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(18): Show |
21 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.932-722dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667217 | ||||||
| chr8:94667217 | CA | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(107): Show |
111 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.932-722delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667217 | ||||||
| chr8:94667251 | C | T | 42 | a0001c0002t0002g0008 a0001c0002t0002g0010 a0001c0002t0002g0012 others(39): Show |
42 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.932-698C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667251 | |||||||
| chr8:94667393 | T | C | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.932-556T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667393 | |||||||
| chr8:94667435 | T | TA | 141 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(138): Show |
143 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.932-502dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667435 | ||||||
| chr8:94667435 | T | TAA | 108 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.932-503_932-502dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr8 | 94667435 | ||||||
| chr8:94667704 | C | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0103 others(51): Show |
55 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.932-245C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667704 | |||||||
| chr8:94667771 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.932-178A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667771 | |||||||
| chr8:94667772 | G | A | 1 | a0001c0001t0001g0370 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.932-177G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667772 | |||||||
| chr8:94667845 | C | T | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.932-104C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667845 | |||||||
| chr8:94667890 | C | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-59C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 9/15 | chr8 | 94667890 | |||||||
| chr8:94668431 | A | G | 9 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(6): Show |
9 | HG01167.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1233+181A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668431 | |||||||
| chr8:94668445 | G | A | 105 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1233+195G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668445 | |||||||
| chr8:94668528 | A | G | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1233+278A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668528 | |||||||
| chr8:94668601 | T | A | 5 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+351T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668601 | |||||||
| chr8:94668632 | A | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+382A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668632 | |||||||
| chr8:94668655 | T | A | 2 | a0001c0002t0002g0012 a0001c0002t0002g0066 |
2 | NA18965.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1233+405T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668655 | |||||||
| chr8:94668707 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1233+457G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668707 | |||||||
| chr8:94668788 | C | CGTGTGTG others(1): Show |
22 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(19): Show |
23 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1233+538_1233+539i others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | |||||||
| chr8:94668788 | C | CGTGTGTG others(3): Show |
1 | a0001c0003t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1233+538_1233+539i others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | |||||||
| chr8:94668788 | C | CGTGTGTG others(7): Show |
3 | a0001c0003t0001g0239 a0001c0003t0001g0240 a0001c0003t0001g0241 |
3 | HG00741.hp2 HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1233+538_1233+539i others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | |||||||
| chr8:94668788 | C | CGTGTGTG others(31): Show |
1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1233+538_1233+539i others(40): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668788 | |||||||
| chr8:94668789 | A | ATGTG | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+555_1233+558d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(7): Show |
1 | a0001c0002t0002g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1233+545_1233+558d others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(9): Show |
88 | a0001c0002t0001g0013 a0001c0002t0002g0006 a0001c0002t0002g0008 others(85): Show |
88 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1233+543_1233+558d others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(11): Show |
11 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(8): Show |
11 | HG00733.hp1 HG01943.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+541_1233+558d others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(13): Show |
4 | a0001c0002t0002g0039 a0001c0002t0002g0079 a0001c0002t0013g0017 others(1): Show |
4 | HG01243.hp2 NA18941.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(19): Show |
4 | a0001c0001t0001g0114 a0001c0001t0001g0230 a0001c0001t0004g0254 others(1): Show |
4 | HG03130.hp1 HG03540.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(28): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(21): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(30): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(23): Show |
13 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(10): Show |
13 | HG00741.hp1 HG02145.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(32): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(25): Show |
7 | a0001c0001t0001g0087 a0001c0001t0001g0123 a0001c0001t0001g0185 others(4): Show |
7 | HG01243.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(34): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(27): Show |
27 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(24): Show |
27 | HG00438.hp2 HG00609.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(36): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(29): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0110 a0001c0001t0001g0116 others(18): Show |
22 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(38): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(31): Show |
18 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(15): Show |
18 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(40): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(33): Show |
4 | a0001c0001t0001g0106 a0001c0001t0001g0154 a0001c0001t0001g0204 others(1): Show |
4 | HG03942.hp1 HG06807.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(42): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(35): Show |
8 | a0001c0001t0001g0042 a0001c0001t0001g0117 a0001c0001t0001g0190 others(5): Show |
8 | HG01891.hp1 HG02004.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+558_1233+559i others(44): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | ATGTGTGT others(37): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0201 |
2 | NA18974.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(46): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94668789 | ||||||
| chr8:94668789 | A | G | 27 | a0001c0001t0001g0197 a0001c0003t0001g0001 a0001c0003t0001g0088 others(24): Show |
28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1233+539A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668789 | |||||||
| chr8:94668808 | T | TGTGTGTG others(28): Show |
2 | a0001c0001t0001g0228 a0001c0001t0001g0246 |
2 | HG01934.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(37): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668808 | |||||||
| chr8:94668808 | T | TGTGTGTG others(30): Show |
3 | a0001c0001t0001g0234 a0001c0001t0001g0245 a0001c0001t0001g0343 |
3 | HG01255.hp2 HG01433.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1233+558_1233+559i others(39): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668808 | |||||||
| chr8:94668928 | C | T | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+678C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668928 | |||||||
| chr8:94668950 | A | G | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+700A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668950 | |||||||
| chr8:94668978 | A | G | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1233+728A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94668978 | |||||||
| chr8:94669196 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(234): Show |
239 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1233+946G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669196 | |||||||
| chr8:94669565 | C | G | 1 | a0001c0002t0002g0022 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1233+1315C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669565 | |||||||
| chr8:94669587 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(42): Show |
45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1233+1337C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669587 | |||||||
| chr8:94669712 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(242): Show |
247 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1233+1462A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669712 | |||||||
| chr8:94669725 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1233+1475G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94669725 | |||||||
| chr8:94669874 | C | CA | 24 | a0001c0001t0001g0042 a0001c0001t0001g0118 a0001c0001t0001g0119 others(21): Show |
24 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1234-1557dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | ||||||
| chr8:94669874 | C | CAA | 8 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0143 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1234-1558_1234-155 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | ||||||
| chr8:94669874 | CA | C | 46 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0146 others(43): Show |
47 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1234-1557delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | ||||||
| chr8:94669874 | CAAAAAAA others(1): Show |
C | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234-1564_1234-155 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr8 | 94669874 | ||||||
| chr8:94670065 | G | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-1388G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670065 | |||||||
| chr8:94670068 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(234): Show |
239 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.1234-1385G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670068 | |||||||
| chr8:94670354 | A | T | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1234-1099A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670354 | |||||||
| chr8:94670526 | G | C | 100 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(97): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1234-927G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670526 | |||||||
| chr8:94670548 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1234-905A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670548 | |||||||
| chr8:94670684 | A | G | 1 | a0001c0009t0001g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1234-769A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94670684 | |||||||
| chr8:94671040 | T | C | 1 | a0001c0002t0002g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1234-413T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671040 | |||||||
| chr8:94671041 | A | C | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1234-412A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671041 | |||||||
| chr8:94671211 | C | T | 5 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-242C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671211 | |||||||
| chr8:94671296 | C | T | 110 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(107): Show |
110 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1234-157C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671296 | |||||||
| chr8:94671333 | A | C | 10 | a0001c0003t0001g0001 a0001c0003t0001g0135 a0001c0003t0001g0324 others(7): Show |
11 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-120A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671333 | |||||||
| chr8:94671366 | C | T | 8 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(5): Show |
8 | HG02109.hp2 HG02572.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1234-87C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 10/15 | chr8 | 94671366 | |||||||
| chr8:94671700 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0278 a0001c0001t0001g0298 others(3): Show |
6 | HG00733.hp2 HG00738.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452+29T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94671700 | |||||||
| chr8:94671740 | G | GATATTAG others(21): Show |
2 | a0001c0001t0001g0298 a0001c0001t0001g0300 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1452+80_1452+107du others(29): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94671740 | ||||||
| chr8:94671953 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(92): Show |
96 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1452+282T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94671953 | |||||||
| chr8:94671975 | C | T | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+304C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94671975 | |||||||
| chr8:94672046 | T | C | 1 | a0001c0009t0001g0150 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1452+375T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672046 | |||||||
| chr8:94672143 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0212 others(42): Show |
45 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1452+472A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672143 | |||||||
| chr8:94672220 | T | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+549T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672220 | |||||||
| chr8:94672249 | A | T | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+578A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672249 | |||||||
| chr8:94672350 | C | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+679C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672350 | |||||||
| chr8:94672381 | A | G | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452+710A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672381 | |||||||
| chr8:94672520 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(240): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1452+849A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672520 | |||||||
| chr8:94672536 | C | CT | 12 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0149 others(9): Show |
12 | HG01109.hp1 HG02040.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1452+879dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94672536 | ||||||
| chr8:94672536 | CT | C | 9 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1452+879delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94672536 | ||||||
| chr8:94672551 | G | C | 34 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(31): Show |
35 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1452+880G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672551 | |||||||
| chr8:94672693 | C | T | 2 | a0001c0005t0001g0182 a0001c0005t0001g0183 |
2 | HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1452+1022C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672693 | |||||||
| chr8:94672820 | G | T | 105 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1452+1149G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672820 | |||||||
| chr8:94672871 | G | A | 1 | a0001c0002t0002g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1452+1200G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672871 | |||||||
| chr8:94672914 | T | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452+1243T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672914 | |||||||
| chr8:94672919 | A | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(137): Show |
142 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1452+1248A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94672919 | |||||||
| chr8:94672926 | A | AT | 369 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(366): Show |
371 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(368): Show |
intron_variant | MODIFIER | c.1452+1262dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr8 | 94672926 | ||||||
| chr8:94673113 | T | C | 2 | a0001c0001t0001g0206 a0001c0001t0001g0209 |
2 | NA18971.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1453-1195T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673113 | |||||||
| chr8:94673172 | A | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(227): Show |
231 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.1453-1136A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673172 | |||||||
| chr8:94673172 | A | T | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453-1136A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673172 | |||||||
| chr8:94673306 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1453-1002T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673306 | |||||||
| chr8:94673312 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1453-996C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673312 | |||||||
| chr8:94673359 | C | T | 113 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(110): Show |
113 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1453-949C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673359 | |||||||
| chr8:94673490 | A | G | 1 | a0001c0001t0004g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1453-818A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673490 | |||||||
| chr8:94673494 | A | T | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-814A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673494 | |||||||
| chr8:94673722 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1453-586A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673722 | |||||||
| chr8:94673832 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(108): Show |
112 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1453-476T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673832 | |||||||
| chr8:94673959 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1453-349C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673959 | |||||||
| chr8:94673986 | G | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0103 others(51): Show |
55 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1453-322G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94673986 | |||||||
| chr8:94674027 | C | A | 1 | a0001c0001t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1453-281C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674027 | |||||||
| chr8:94674030 | T | C | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1453-278T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674030 | |||||||
| chr8:94674051 | T | C | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1453-257T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674051 | |||||||
| chr8:94674058 | T | G | 10 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
10 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1453-250T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674058 | |||||||
| chr8:94674081 | T | C | 1 | a0001c0003t0001g0088 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1453-227T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674081 | |||||||
| chr8:94674094 | C | A | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453-214C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674094 | |||||||
| chr8:94674167 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0259 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1453-141G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 11/15 | chr8 | 94674167 | |||||||
| chr8:94674572 | G | A | 3 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0313 |
3 | HG01934.hp2 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1651+66G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94674572 | |||||||
| chr8:94674622 | A | G | 27 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(24): Show |
28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1651+116A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94674622 | |||||||
| chr8:94674739 | G | A | 13 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+233G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94674739 | |||||||
| chr8:94674948 | A | AT | 13 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+449dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94674948 | ||||||
| chr8:94675037 | A | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0252 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1651+531A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675037 | |||||||
| chr8:94675107 | C | T | 190 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(187): Show |
191 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.1651+601C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675107 | |||||||
| chr8:94675177 | GT | G | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1651+673delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94675177 | ||||||
| chr8:94675232 | T | C | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1651+726T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675232 | |||||||
| chr8:94675252 | A | C | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1651+746A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675252 | |||||||
| chr8:94675364 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1651+858G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675364 | |||||||
| chr8:94675506 | T | C | 3 | a0001c0007t0001g0344 a0001c0007t0001g0346 a0001c0011t0001g0251 |
3 | HG03209.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1651+1000T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675506 | |||||||
| chr8:94675776 | T | C | 27 | a0001c0001t0011g0136 a0001c0003t0001g0001 a0001c0003t0001g0088 others(24): Show |
28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1651+1270T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675776 | |||||||
| chr8:94675798 | C | T | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1651+1292C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675798 | |||||||
| chr8:94675848 | A | G | 2 | a0001c0007t0001g0344 a0001c0007t0001g0346 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1651+1342A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675848 | |||||||
| chr8:94675898 | G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1651+1392G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675898 | |||||||
| chr8:94675953 | G | A | 6 | a0001c0001t0001g0168 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1651+1447G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94675953 | |||||||
| chr8:94676059 | C | T | 13 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+1553C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676059 | |||||||
| chr8:94676086 | A | T | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651+1580A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676086 | |||||||
| chr8:94676132 | A | T | 1 | a0001c0001t0001g0191 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1651+1626A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676132 | |||||||
| chr8:94676171 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1651+1665G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676171 | |||||||
| chr8:94676230 | G | A | 3 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 |
3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1651+1724G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676230 | |||||||
| chr8:94676252 | T | A | 105 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(102): Show |
105 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1651+1746T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676252 | |||||||
| chr8:94676266 | T | C | 13 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1651+1760T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676266 | |||||||
| chr8:94676330 | C | G | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1651+1824C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676330 | |||||||
| chr8:94676333 | C | T | 1 | a0001c0002t0014g0041 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1651+1827C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676333 | |||||||
| chr8:94676343 | C | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1651+1837C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676343 | |||||||
| chr8:94676349 | C | CA | 166 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0207 others(163): Show |
167 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1652-1838dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94676349 | ||||||
| chr8:94676349 | C | CAA | 11 | a0001c0001t0001g0146 a0001c0001t0001g0359 a0001c0001t0004g0194 others(8): Show |
11 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.1652-1839_1652-183 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94676349 | ||||||
| chr8:94676349 | C | CAAA | 11 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(8): Show |
11 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1652-1840_1652-183 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr8 | 94676349 | ||||||
| chr8:94676422 | C | T | 3 | a0001c0007t0001g0344 a0001c0007t0001g0346 a0001c0011t0001g0251 |
3 | HG03209.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1652-1781C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676422 | |||||||
| chr8:94676499 | T | G | 1 | a0001c0001t0004g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1652-1704T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676499 | |||||||
| chr8:94676574 | G | A | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1652-1629G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676574 | |||||||
| chr8:94676749 | C | T | 12 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(9): Show |
12 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1652-1454C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676749 | |||||||
| chr8:94676777 | C | T | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1652-1426C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676777 | |||||||
| chr8:94676778 | G | A | 1 | a0001c0004t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1652-1425G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676778 | |||||||
| chr8:94676928 | A | G | 144 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(141): Show |
145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1652-1275A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676928 | |||||||
| chr8:94676929 | G | T | 1 | a0001c0003t0001g0001 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1652-1274G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676929 | |||||||
| chr8:94676939 | A | C | 9 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(6): Show |
9 | HG02109.hp2 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1652-1264A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676939 | |||||||
| chr8:94676999 | A | T | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1652-1204A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94676999 | |||||||
| chr8:94677084 | A | G | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1652-1119A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677084 | |||||||
| chr8:94677108 | C | G | 12 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(9): Show |
12 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1652-1095C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677108 | |||||||
| chr8:94677172 | G | A | 144 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(141): Show |
145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1652-1031G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677172 | |||||||
| chr8:94677198 | G | A | 2 | a0001c0001t0001g0360 a0001c0001t0001g0367 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1652-1005G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677198 | |||||||
| chr8:94677453 | T | G | 144 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(141): Show |
145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1652-750T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677453 | |||||||
| chr8:94677529 | G | A | 1 | a0001c0002t0002g0018 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1652-674G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677529 | |||||||
| chr8:94677594 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1652-609C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677594 | |||||||
| chr8:94677796 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1652-407G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677796 | |||||||
| chr8:94677918 | A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1652-285A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677918 | |||||||
| chr8:94677960 | T | C | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1652-243T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677960 | |||||||
| chr8:94677999 | C | A | 11 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(8): Show |
11 | HG01361.hp2 HG01928.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1652-204C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94677999 | |||||||
| chr8:94678033 | C | T | 12 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0348 others(9): Show |
12 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1652-170C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94678033 | |||||||
| chr8:94678100 | T | A | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1652-103T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 12/15 | chr8 | 94678100 | |||||||
| chr8:94678488 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1820+117A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678488 | |||||||
| chr8:94678601 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1820+230C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678601 | |||||||
| chr8:94678768 | A | C | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1820+397A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678768 | |||||||
| chr8:94678838 | T | C | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1820+467T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678838 | |||||||
| chr8:94678973 | T | A | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1820+602T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94678973 | |||||||
| chr8:94679188 | A | T | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG01109.hp1 HG02145.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+817A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679188 | |||||||
| chr8:94679497 | G | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+1126G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679497 | |||||||
| chr8:94679514 | A | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+1143A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679514 | |||||||
| chr8:94679571 | T | C | 2 | a0001c0002t0001g0085 a0001c0002t0001g0097 |
2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1820+1200T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679571 | |||||||
| chr8:94679596 | A | G | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1820+1225A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679596 | |||||||
| chr8:94679598 | G | T | 6 | a0001c0001t0001g0168 a0001c0001t0001g0185 a0001c0001t0001g0186 others(3): Show |
6 | HG02559.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+1227G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679598 | |||||||
| chr8:94679783 | C | T | 144 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(141): Show |
145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1820+1412C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679783 | |||||||
| chr8:94679862 | T | C | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+1491T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679862 | |||||||
| chr8:94679911 | T | C | 131 | a0001c0002t0001g0013 a0001c0002t0001g0085 a0001c0002t0001g0097 others(128): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1820+1540T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679911 | |||||||
| chr8:94679919 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1820+1548G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679919 | |||||||
| chr8:94679988 | A | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0198 others(43): Show |
46 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1820+1617A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94679988 | |||||||
| chr8:94680162 | A | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0125 others(278): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1820+1791A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680162 | |||||||
| chr8:94680166 | T | C | 1 | a0001c0002t0002g0314 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1820+1795T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680166 | |||||||
| chr8:94680568 | C | T | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1820+2197C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680568 | |||||||
| chr8:94680635 | G | A | 4 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+2264G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680635 | |||||||
| chr8:94680774 | A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1820+2403A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680774 | |||||||
| chr8:94680847 | G | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+2476G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680847 | |||||||
| chr8:94680926 | T | C | 123 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(120): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1820+2555T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680926 | |||||||
| chr8:94680956 | G | A | 123 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(120): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1820+2585G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680956 | |||||||
| chr8:94680999 | T | C | 123 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(120): Show |
123 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1820+2628T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94680999 | |||||||
| chr8:94681063 | C | T | 6 | a0001c0001t0001g0242 a0001c0001t0003g0214 a0001c0001t0003g0216 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820+2692C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681063 | |||||||
| chr8:94681064 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | NA19084.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1820+2693G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681064 | |||||||
| chr8:94681099 | A | G | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1820+2728A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681099 | |||||||
| chr8:94681107 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1820+2736C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681107 | |||||||
| chr8:94681110 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1820+2739G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681110 | |||||||
| chr8:94681126 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1820+2755C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681126 | |||||||
| chr8:94681140 | A | G | 5 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1820+2769A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681140 | |||||||
| chr8:94681141 | T | C | 2 | a0001c0002t0002g0071 a0001c0002t0002g0084 |
2 | NA18988.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1820+2770T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681141 | |||||||
| chr8:94681152 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1820+2781C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681152 | |||||||
| chr8:94681154 | T | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(86): Show |
90 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1820+2783T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681154 | |||||||
| chr8:94681161 | TA | T | 29 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0154 others(26): Show |
29 | HG01070.hp2 HG01081.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1820+2796delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681161 | ||||||
| chr8:94681198 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 |
3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1820+2827T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681198 | |||||||
| chr8:94681208 | C | A | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+2837C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681208 | |||||||
| chr8:94681225 | C | G | 1 | a0001c0005t0001g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1820+2854C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681225 | |||||||
| chr8:94681251 | G | A | 117 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(114): Show |
117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1820+2880G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681251 | |||||||
| chr8:94681283 | G | A | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1820+2912G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681283 | |||||||
| chr8:94681304 | T | C | 117 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(114): Show |
117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1820+2933T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681304 | |||||||
| chr8:94681325 | C | CA | 42 | a0001c0001t0001g0042 a0001c0001t0001g0123 a0001c0001t0001g0130 others(39): Show |
42 | HG00423.hp2 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1820+2982dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | C | CAA | 19 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(16): Show |
19 | HG00741.hp1 HG01346.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1820+2981_1820+298 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | C | CAAAAAA | 19 | a0001c0001t0001g0137 a0001c0001t0001g0140 a0001c0001t0001g0169 others(16): Show |
19 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.1820+2977_1820+298 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | C | CAAAAAAA | 28 | a0001c0001t0001g0003 a0001c0001t0001g0139 a0001c0001t0001g0144 others(25): Show |
28 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1820+2976_1820+298 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0143 a0001c0001t0001g0161 a0001c0001t0001g0167 others(5): Show |
8 | HG02004.hp1 HG02055.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+2975_1820+298 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0309 |
2 | HG01261.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.1820+2973_1820+298 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | CA | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0104 others(111): Show |
115 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1820+2982delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0234 a0001c0001t0001g0288 a0001c0001t0001g0313 |
3 | HG01934.hp2 HG02300.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1820+2969_1820+298 others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681325 | CAAAAAAA others(9): Show |
C | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+2967_1820+298 others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94681325 | ||||||
| chr8:94681435 | T | C | 117 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(114): Show |
117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1820+3064T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681435 | |||||||
| chr8:94681704 | C | T | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+3333C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681704 | |||||||
| chr8:94681721 | G | A | 9 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
9 | HG00597.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1820+3350G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681721 | |||||||
| chr8:94681742 | G | A | 102 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0002g0006 others(99): Show |
102 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1820+3371G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681742 | |||||||
| chr8:94681827 | C | T | 1 | a0001c0003t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1820+3456C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681827 | |||||||
| chr8:94681910 | G | T | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3539G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681910 | |||||||
| chr8:94681953 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3582T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681953 | |||||||
| chr8:94681981 | G | A | 2 | a0001c0002t0002g0040 a0001c0002t0002g0100 |
2 | NA19054.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1820+3610G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681981 | |||||||
| chr8:94681997 | G | A | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3626G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94681997 | |||||||
| chr8:94682041 | C | T | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+3670C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682041 | |||||||
| chr8:94682068 | A | G | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+3697A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682068 | |||||||
| chr8:94682072 | T | A | 156 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0161 others(153): Show |
156 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1820+3701T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682072 | |||||||
| chr8:94682096 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1820+3725G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682096 | |||||||
| chr8:94682316 | A | C | 1 | a0001c0002t0002g0050 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1820+3945A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682316 | |||||||
| chr8:94682364 | A | T | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+3993A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682364 | |||||||
| chr8:94682403 | A | G | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1820+4032A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682403 | |||||||
| chr8:94682639 | T | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4268T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682639 | |||||||
| chr8:94682641 | A | AATCCTCC | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4270_1820+427 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682641 | |||||||
| chr8:94682643 | A | AATGT | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4272_1820+427 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682643 | |||||||
| chr8:94682645 | G | C | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4274G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682645 | |||||||
| chr8:94682648 | T | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4277T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682648 | |||||||
| chr8:94682651 | GCCA | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4284_1820+428 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682651 | ||||||
| chr8:94682655 | C | T | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4284C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682655 | |||||||
| chr8:94682656 | C | A | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+4285C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682656 | |||||||
| chr8:94682683 | C | T | 1 | a0001c0001t0010g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1820+4312C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682683 | |||||||
| chr8:94682748 | C | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+4377C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682748 | |||||||
| chr8:94682869 | C | CAT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4507_1820+450 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682869 | ||||||
| chr8:94682888 | C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4517C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682888 | |||||||
| chr8:94682889 | A | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4518A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682889 | |||||||
| chr8:94682896 | T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4525T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682896 | |||||||
| chr8:94682897 | C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4526C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682897 | |||||||
| chr8:94682900 | T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4529T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682900 | |||||||
| chr8:94682901 | A | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4530A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682901 | |||||||
| chr8:94682902 | T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4531T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682902 | |||||||
| chr8:94682904 | T | A | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1820+4533T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682904 | |||||||
| chr8:94682904 | T | TTA | 18 | a0001c0001t0001g0115 a0001c0001t0001g0148 a0001c0001t0001g0225 others(15): Show |
19 | HG00323.hp2 HG00609.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1820+4561_1820+456 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0103 others(19): Show |
23 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1820+4559_1820+456 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATA | 8 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0199 others(5): Show |
8 | HG00438.hp1 HG01243.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+4557_1820+456 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(1): Show |
7 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0206 others(4): Show |
7 | HG01256.hp1 HG01258.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+4555_1820+456 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0218 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1820+4553_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(5): Show |
3 | a0001c0001t0001g0197 a0001c0001t0001g0310 a0001c0006t0001g0345 |
3 | HG02965.hp1 HG03195.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1820+4551_1820+456 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(7): Show |
1 | a0001c0003t0001g0368 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1820+4549_1820+456 others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0168 a0001c0001t0001g0186 |
2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1820+4545_1820+456 others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0187 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1820+4543_1820+456 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(34): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | TTA | T | 7 | a0001c0001t0001g0292 a0001c0004t0002g0086 a0001c0004t0002g0091 others(4): Show |
7 | HG01071.hp2 HG01074.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+4561_1820+456 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682904 | TTATATAT others(5): Show |
T | 1 | a0001c0003t0001g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1820+4551_1820+456 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682904 | ||||||
| chr8:94682906 | A | T | 7 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0002t0002g0025 others(4): Show |
7 | HG02083.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+4535A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682906 | |||||||
| chr8:94682908 | A | T | 2 | a0001c0001t0001g0360 a0001c0001t0001g0367 |
2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1820+4537A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682908 | |||||||
| chr8:94682921 | TATATATA others(4): Show |
T | 6 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(3): Show |
6 | HG01070.hp2 HG01081.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820+4551_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682921 | |||||||
| chr8:94682922 | ATATATAT others(4): Show |
A | 1 | a0001c0003t0001g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1820+4553_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682922 | ||||||
| chr8:94682922 | ATATATAT others(5): Show |
A | 1 | a0001c0003t0001g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1820+4553_1820+456 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682922 | ||||||
| chr8:94682924 | ATATATAT others(3): Show |
A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4555_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682924 | ||||||
| chr8:94682928 | A | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0004c0010t0001g0321 |
3 | HG01516.hp2 HG01517.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1820+4557A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682928 | |||||||
| chr8:94682930 | A | AT | 8 | a0001c0002t0002g0006 a0001c0002t0002g0014 a0001c0002t0002g0015 others(5): Show |
8 | HG01109.hp2 HG02040.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+4560dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682930 | ||||||
| chr8:94682930 | A | ATT | 5 | a0001c0002t0002g0012 a0001c0002t0002g0040 a0001c0002t0002g0283 others(2): Show |
5 | HG02451.hp1 HG03710.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+4560_1820+456 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682930 | ||||||
| chr8:94682930 | A | ATTTTTT | 4 | a0001c0001t0001g0155 a0001c0001t0001g0162 a0001c0001t0001g0171 others(1): Show |
4 | HG01255.hp1 HG01346.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4560_1820+456 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682930 | ||||||
| chr8:94682930 | A | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0256 others(4): Show |
7 | HG01516.hp2 HG01517.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1820+4559A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682930 | |||||||
| chr8:94682931 | TA | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0320 a0001c0002t0002g0064 others(1): Show |
4 | HG00741.hp1 HG02055.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4561delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682931 | |||||||
| chr8:94682932 | A | AT | 23 | a0001c0001t0001g0147 a0001c0001t0001g0180 a0001c0002t0001g0097 others(20): Show |
23 | HG00673.hp1 HG00733.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1820+4590dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATAT | 10 | a0001c0001t0001g0146 a0001c0001t0001g0226 a0001c0002t0002g0036 others(7): Show |
10 | HG00735.hp1 HG02015.hp1 HG03710.hp2 others(7): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATAT | 11 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0001t0001g0227 others(8): Show |
11 | HG01175.hp1 HG01433.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0268 a0001c0001t0001g0360 |
3 | HG02615.hp2 HG03579.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0202 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(17): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0247 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0358 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(31): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0366 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(27): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(30): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0365 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0272 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0362 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0367 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(19): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0359 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(13): Show |
1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0164 |
2 | HG01069.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0205 a0001c0001t0001g0229 |
3 | HG02004.hp2 HG02300.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0207 |
2 | NA18949.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | ATATTTT | 6 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0177 others(3): Show |
6 | HG02647.hp2 HG02717.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | A | T | 38 | a0001c0001t0001g0143 a0001c0001t0001g0155 a0001c0001t0001g0156 others(35): Show |
38 | HG01109.hp2 HG01255.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.1820+4561A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682932 | |||||||
| chr8:94682932 | AT | A | 11 | a0001c0001t0001g0165 a0001c0001t0001g0212 a0001c0001t0001g0284 others(8): Show |
11 | HG00423.hp1 HG00558.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1820+4590delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | ATT | A | 13 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0137 others(10): Show |
13 | HG00140.hp1 HG01934.hp2 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.1820+4589_1820+459 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | ATTT | A | 13 | a0001c0001t0001g0130 a0001c0001t0001g0133 a0001c0001t0001g0134 others(10): Show |
13 | HG00673.hp2 HG00738.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1820+4588_1820+459 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682932 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1820+4581_1820+459 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94682932 | ||||||
| chr8:94682933 | T | TA | 11 | a0001c0001t0001g0198 a0001c0001t0001g0220 a0001c0001t0001g0223 others(8): Show |
11 | HG00558.hp2 HG00609.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATA | 17 | a0001c0001t0001g0105 a0001c0001t0001g0116 a0001c0001t0001g0270 others(14): Show |
17 | HG00642.hp1 HG00735.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATA | 9 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0221 others(6): Show |
9 | HG00408.hp1 HG01891.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA | 7 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
7 | HG01167.hp2 NA18944.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0193 a0001c0001t0001g0364 a0001c0003t0001g0338 |
3 | HG02257.hp2 NA20300.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(13): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA others(4): Show |
3 | a0001c0001t0001g0179 a0001c0001t0001g0209 a0001c0001t0001g0259 |
3 | HG02165.hp2 HG02976.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA others(6): Show |
2 | a0001c0001t0001g0269 a0001c0003t0001g0334 |
2 | HG00642.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(17): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0149 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA others(12): Show |
2 | a0001c0001t0001g0072 a0001c0001t0001g0361 |
2 | NA18906.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1820+4562_1820+456 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682933 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0285 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1820+4562_1820+456 others(25): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682933 | |||||||
| chr8:94682934 | T | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0103 a0001c0001t0001g0126 others(35): Show |
40 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.1820+4563T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682934 | |||||||
| chr8:94682935 | T | A | 27 | a0001c0001t0001g0107 a0001c0001t0001g0128 a0001c0001t0001g0149 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1820+4564T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682935 | |||||||
| chr8:94682936 | T | A | 28 | a0001c0001t0001g0137 a0001c0001t0001g0168 a0001c0001t0001g0186 others(25): Show |
29 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1820+4565T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682936 | |||||||
| chr8:94682937 | T | A | 22 | a0001c0001t0001g0149 a0001c0001t0001g0185 a0001c0001t0001g0198 others(19): Show |
22 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1820+4566T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682937 | |||||||
| chr8:94682938 | T | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0186 a0001c0001t0001g0188 others(5): Show |
8 | HG00140.hp1 HG01928.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1820+4567T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682938 | |||||||
| chr8:94682939 | T | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0276 a0001c0001t0001g0284 others(1): Show |
4 | HG01109.hp1 HG02257.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4568T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682939 | |||||||
| chr8:94682940 | T | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0296 a0001c0003t0001g0368 others(1): Show |
4 | HG02818.hp2 HG02965.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4569T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682940 | |||||||
| chr8:94682941 | T | A | 1 | a0001c0001t0001g0364 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1820+4570T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682941 | |||||||
| chr8:94682942 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1820+4571T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682942 | |||||||
| chr8:94682943 | T | A | 1 | a0001c0001t0001g0364 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1820+4572T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682943 | |||||||
| chr8:94682944 | T | A | 1 | a0001c0001t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1820+4573T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682944 | |||||||
| chr8:94682946 | T | A | 1 | a0001c0001t0001g0243 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1820+4575T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682946 | |||||||
| chr8:94682961 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1820+4590T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682961 | |||||||
| chr8:94682967 | G | A | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4596G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94682967 | |||||||
| chr8:94683133 | G | A | 154 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(151): Show |
154 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1820+4762G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683133 | |||||||
| chr8:94683186 | C | T | 1 | a0001c0001t0001g0366 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1820+4815C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683186 | |||||||
| chr8:94683187 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1820+4816G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683187 | |||||||
| chr8:94683232 | C | T | 5 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+4861C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683232 | |||||||
| chr8:94683235 | C | T | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+4864C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683235 | |||||||
| chr8:94683252 | T | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+4881T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683252 | |||||||
| chr8:94683289 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+4918T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683289 | |||||||
| chr8:94683320 | A | G | 1 | a0001c0002t0002g0078 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1820+4949A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683320 | |||||||
| chr8:94683371 | G | T | 115 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(112): Show |
115 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1820+5000G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683371 | |||||||
| chr8:94683372 | G | A | 3 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 |
3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1820+5001G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683372 | |||||||
| chr8:94683385 | A | G | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1820+5014A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683385 | |||||||
| chr8:94683424 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1820+5053C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683424 | |||||||
| chr8:94683434 | G | T | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5063G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683434 | |||||||
| chr8:94683448 | A | G | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5077A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683448 | |||||||
| chr8:94683494 | C | T | 10 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(7): Show |
10 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1820+5123C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683494 | |||||||
| chr8:94683515 | A | G | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1820+5144A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683515 | |||||||
| chr8:94683607 | A | G | 1 | a0001c0003t0001g0354 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1820+5236A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683607 | |||||||
| chr8:94683654 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1820+5283C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683654 | |||||||
| chr8:94683725 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5354T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683725 | |||||||
| chr8:94683760 | A | G | 1 | a0001c0001t0001g0315 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1820+5389A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683760 | |||||||
| chr8:94683846 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5475T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683846 | |||||||
| chr8:94683902 | C | T | 201 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0161 others(198): Show |
201 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1820+5531C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94683902 | |||||||
| chr8:94684033 | G | A | 28 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(25): Show |
28 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1820+5662G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684033 | |||||||
| chr8:94684126 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+5755T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684126 | |||||||
| chr8:94684141 | A | C | 154 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(151): Show |
154 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1820+5770A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684141 | |||||||
| chr8:94684142 | C | CG | 153 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(150): Show |
153 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1820+5772dupG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94684142 | ||||||
| chr8:94684469 | C | T | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1820+6098C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684469 | |||||||
| chr8:94684533 | C | T | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1820+6162C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684533 | |||||||
| chr8:94684623 | T | C | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+6252T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684623 | |||||||
| chr8:94684643 | A | G | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+6272A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684643 | |||||||
| chr8:94684713 | A | G | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+6342A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684713 | |||||||
| chr8:94684863 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1820+6492C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684863 | |||||||
| chr8:94684965 | C | T | 6 | a0001c0003t0001g0001 a0001c0003t0001g0135 a0001c0003t0001g0324 others(3): Show |
7 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1820+6594C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94684965 | |||||||
| chr8:94685022 | TA | T | 149 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(146): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1820+6664delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94685022 | ||||||
| chr8:94685051 | A | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1820+6680A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685051 | |||||||
| chr8:94685130 | A | G | 1 | a0001c0001t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1820+6759A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685130 | |||||||
| chr8:94685205 | A | G | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(2): Show |
5 | HG02630.hp2 HG03041.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1820+6834A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685205 | |||||||
| chr8:94685236 | G | T | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1820+6865G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685236 | |||||||
| chr8:94685482 | T | A | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820+7111T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685482 | |||||||
| chr8:94685570 | G | A | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-7107G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685570 | |||||||
| chr8:94685662 | T | C | 4 | a0001c0003t0001g0324 a0001c0003t0001g0325 a0001c0003t0001g0332 others(1): Show |
4 | HG00642.hp1 HG01074.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-7015T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685662 | |||||||
| chr8:94685687 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | HG01261.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1821-6990C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685687 | |||||||
| chr8:94685786 | CA | C | 108 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(105): Show |
108 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1821-6880delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94685786 | ||||||
| chr8:94685797 | A | G | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-6880A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94685797 | |||||||
| chr8:94686001 | G | T | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-6676G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686001 | |||||||
| chr8:94686209 | A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1821-6468A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686209 | |||||||
| chr8:94686244 | T | G | 3 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 |
3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1821-6433T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686244 | |||||||
| chr8:94686254 | A | G | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-6423A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686254 | |||||||
| chr8:94686386 | C | T | 120 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(117): Show |
120 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1821-6291C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686386 | |||||||
| chr8:94686542 | C | T | 4 | a0001c0003t0001g0327 a0001c0003t0001g0328 a0001c0003t0001g0329 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-6135C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686542 | |||||||
| chr8:94686647 | A | G | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-6030A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686647 | |||||||
| chr8:94686724 | T | A | 1 | a0001c0002t0002g0040 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1821-5953T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686724 | |||||||
| chr8:94686991 | G | A | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-5686G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94686991 | |||||||
| chr8:94687093 | T | C | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1821-5584T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687093 | |||||||
| chr8:94687114 | C | G | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(2): Show |
5 | HG02630.hp2 HG03041.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-5563C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687114 | |||||||
| chr8:94687169 | C | A | 6 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0252 others(3): Show |
6 | HG02630.hp2 HG03041.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821-5508C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687169 | |||||||
| chr8:94687261 | A | T | 1 | a0001c0001t0001g0246 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1821-5416A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687261 | |||||||
| chr8:94687340 | G | A | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-5337G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687340 | |||||||
| chr8:94687350 | G | A | 1 | a0001c0002t0002g0009 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1821-5327G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687350 | |||||||
| chr8:94687400 | T | C | 28 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(25): Show |
28 | HG01261.hp2 HG02055.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1821-5277T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687400 | |||||||
| chr8:94687447 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-5230T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687447 | |||||||
| chr8:94687530 | A | G | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-5147A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94687530 | |||||||
| chr8:94688114 | G | A | 26 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(23): Show |
27 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1821-4563G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688114 | |||||||
| chr8:94688142 | C | T | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-4535C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688142 | |||||||
| chr8:94688175 | A | G | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-4502A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688175 | |||||||
| chr8:94688237 | AT | A | 154 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(151): Show |
154 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1821-4438delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94688237 | ||||||
| chr8:94688410 | T | C | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1821-4267T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688410 | |||||||
| chr8:94688460 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0125 others(273): Show |
277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1821-4217C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688460 | |||||||
| chr8:94688524 | A | T | 13 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(10): Show |
13 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1821-4153A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688524 | |||||||
| chr8:94688675 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1821-4002G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688675 | |||||||
| chr8:94688726 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1821-3951C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688726 | |||||||
| chr8:94688918 | G | A | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-3759G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688918 | |||||||
| chr8:94688989 | G | A | 1 | a0001c0002t0002g0023 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1821-3688G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94688989 | |||||||
| chr8:94689042 | G | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-3635G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689042 | |||||||
| chr8:94689173 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-3504T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689173 | |||||||
| chr8:94689236 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0137 a0001c0001t0001g0198 others(160): Show |
163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1821-3441G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689236 | |||||||
| chr8:94689249 | C | CA | 81 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0087 others(78): Show |
81 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1821-3403dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689249 | C | CAA | 34 | a0001c0001t0001g0132 a0001c0001t0001g0148 a0001c0001t0001g0149 others(31): Show |
34 | HG00423.hp1 HG01109.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.1821-3404_1821-340 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689249 | C | CAAA | 12 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0161 others(9): Show |
12 | HG00673.hp2 HG02055.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1821-3405_1821-340 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689249 | CA | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 others(3): Show |
6 | HG01261.hp1 HG02615.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821-3403delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689249 | CAAAAAAA others(1): Show |
C | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1821-3410_1821-340 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689249 | CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(11): Show |
14 | HG02257.hp2 HG02451.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1821-3411_1821-340 others(13): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689249 | CAAAAAAA others(3): Show |
C | 100 | a0001c0001t0001g0366 a0001c0002t0001g0085 a0001c0002t0001g0097 others(97): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1821-3412_1821-340 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689249 | ||||||
| chr8:94689319 | CTT | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-3353_1821-335 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689319 | ||||||
| chr8:94689321 | TTTTTC | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0166 |
3 | HG01069.hp1 HG02300.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1821-3351_1821-334 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689321 | ||||||
| chr8:94689407 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0213 |
3 | HG02615.hp1 HG02886.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1821-3270T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689407 | |||||||
| chr8:94689599 | A | G | 4 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-3078A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689599 | |||||||
| chr8:94689657 | A | G | 243 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(240): Show |
244 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.1821-3020A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689657 | |||||||
| chr8:94689657 | A | T | 1 | a0001c0002t0002g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1821-3020A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689657 | |||||||
| chr8:94689673 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0163 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1821-3004A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689673 | |||||||
| chr8:94689715 | T | G | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2962T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689715 | |||||||
| chr8:94689788 | C | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1821-2889C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689788 | |||||||
| chr8:94689806 | C | T | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1821-2871C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689806 | |||||||
| chr8:94689811 | C | CT | 25 | a0001c0001t0001g0107 a0001c0001t0001g0112 a0001c0001t0001g0113 others(22): Show |
25 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1821-2841dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0169 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-2850_1821-284 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(2): Show |
5 | HG01261.hp2 HG02055.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821-2851_1821-284 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0186 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1821-2852_1821-284 others(16): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(6): Show |
5 | a0001c0001t0001g0185 a0001c0001t0001g0189 a0001c0003t0001g0333 others(2): Show |
5 | HG02647.hp1 HG02738.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821-2853_1821-284 others(17): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0270 others(5): Show |
8 | HG01069.hp2 HG01099.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1821-2854_1821-284 others(18): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(8): Show |
27 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(24): Show |
27 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1821-2855_1821-284 others(19): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(9): Show |
17 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0144 others(14): Show |
17 | HG00423.hp1 HG01346.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1821-2856_1821-284 others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(10): Show |
9 | a0001c0001t0001g0279 a0001c0001t0001g0285 a0001c0001t0001g0308 others(6): Show |
9 | HG02004.hp1 HG02015.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1821-2857_1821-284 others(21): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(11): Show |
9 | a0001c0001t0001g0139 a0001c0001t0001g0293 a0001c0001t0001g0298 others(6): Show |
9 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1821-2858_1821-284 others(22): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0140 a0001c0001t0001g0180 a0001c0001t0001g0256 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-2859_1821-284 others(23): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0003 a0001c0003t0001g0340 |
2 | HG00733.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1821-2860_1821-284 others(24): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(14): Show |
1 | a0001c0003t0001g0338 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1821-2861_1821-284 others(25): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(15): Show |
3 | a0001c0001t0001g0278 a0001c0001t0001g0296 a0001c0001t0001g0302 |
3 | HG00558.hp1 HG03017.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1821-2862_1821-284 others(26): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | NA18957.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1821-2863_1821-284 others(27): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(20): Show |
1 | a0001c0003t0001g0339 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1821-2841_1821-284 others(31): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1821-2841_1821-284 others(35): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | CT | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0155 a0001c0001t0001g0156 others(21): Show |
25 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1821-2841delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | CTTTT | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG01109.hp1 HG02486.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1821-2844_1821-284 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | CTTTTT | C | 7 | a0001c0001t0001g0276 a0001c0001t0001g0280 a0001c0001t0001g0287 others(4): Show |
7 | HG00673.hp2 HG02602.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1821-2845_1821-284 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689811 | CTTTTTTT others(3): Show |
C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2850_1821-284 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94689811 | ||||||
| chr8:94689851 | C | G | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2826C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689851 | |||||||
| chr8:94689877 | C | T | 1 | a0001c0006t0001g0352 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1821-2800C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689877 | |||||||
| chr8:94689878 | G | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0072 others(95): Show |
99 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1821-2799G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689878 | |||||||
| chr8:94689892 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1821-2785C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689892 | |||||||
| chr8:94689912 | G | A | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-2765G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94689912 | |||||||
| chr8:94690020 | G | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-2657G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690020 | |||||||
| chr8:94690107 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 |
3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1821-2570C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690107 | |||||||
| chr8:94690120 | A | AT | 115 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(112): Show |
115 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1821-2549dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690120 | ||||||
| chr8:94690152 | GTTTTTTA | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0155 a0001c0001t0001g0156 others(18): Show |
21 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1821-2524_1821-251 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690152 | |||||||
| chr8:94690267 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0171 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1821-2410G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690267 | |||||||
| chr8:94690276 | A | AT | 63 | a0001c0001t0001g0115 a0001c0001t0001g0148 a0001c0001t0001g0149 others(60): Show |
63 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.1821-2373dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | ||||||
| chr8:94690276 | A | ATT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0123 others(45): Show |
49 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.1821-2374_1821-237 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | ||||||
| chr8:94690276 | A | ATTT | 26 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0143 others(23): Show |
26 | HG00642.hp1 HG00735.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.1821-2375_1821-237 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | ||||||
| chr8:94690276 | A | ATTTT | 9 | a0001c0001t0001g0258 a0001c0001t0001g0360 a0001c0003t0001g0153 others(6): Show |
9 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1821-2376_1821-237 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | ||||||
| chr8:94690276 | A | ATTTTT | 11 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0169 others(8): Show |
11 | HG01261.hp2 HG01517.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1821-2377_1821-237 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | ||||||
| chr8:94690276 | AT | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0001g0190 others(9): Show |
13 | HG01168.hp1 HG01169.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1821-2373delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr8 | 94690276 | ||||||
| chr8:94690294 | TTTTTTTT others(4): Show |
T | 1 | a0001c0003t0001g0348 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1821-2382_1821-237 others(15): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690294 | |||||||
| chr8:94690295 | TTTTTTTT others(3): Show |
T | 8 | a0001c0003t0001g0319 a0001c0003t0001g0347 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1821-2381_1821-237 others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690295 | |||||||
| chr8:94690298 | TTTTTTTG | T | 9 | a0001c0002t0002g0029 a0001c0002t0002g0037 a0001c0002t0002g0065 others(6): Show |
9 | HG01070.hp1 HG01256.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1821-2378_1821-237 others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690298 | |||||||
| chr8:94690299 | TTTTTTG | T | 92 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0002g0006 others(89): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1821-2377_1821-237 others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690299 | |||||||
| chr8:94690623 | G | A | 8 | a0001c0003t0001g0347 a0001c0003t0001g0348 a0001c0003t0001g0349 others(5): Show |
8 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1821-2054G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690623 | |||||||
| chr8:94690707 | C | T | 4 | a0001c0004t0002g0090 a0001c0004t0002g0091 a0001c0004t0002g0099 others(1): Show |
4 | HG00323.hp1 HG01243.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-1970C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690707 | |||||||
| chr8:94690741 | T | C | 282 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0125 others(279): Show |
283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.1821-1936T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690741 | |||||||
| chr8:94690895 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-1782T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690895 | |||||||
| chr8:94690920 | A | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1821-1757A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690920 | |||||||
| chr8:94690932 | T | C | 116 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(113): Show |
116 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1821-1745T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94690932 | |||||||
| chr8:94691034 | C | T | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-1643C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691034 | |||||||
| chr8:94691096 | T | G | 1 | a0001c0001t0004g0254 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1821-1581T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691096 | |||||||
| chr8:94691129 | C | G | 1 | a0001c0004t0002g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1821-1548C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691129 | |||||||
| chr8:94691170 | G | A | 1 | a0001c0002t0002g0008 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1821-1507G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691170 | |||||||
| chr8:94691360 | G | A | 150 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(147): Show |
150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1821-1317G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691360 | |||||||
| chr8:94691369 | T | A | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-1308T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691369 | |||||||
| chr8:94691390 | G | A | 5 | a0001c0001t0001g0256 a0001c0001t0006g0151 a0001c0001t0006g0152 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1821-1287G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691390 | |||||||
| chr8:94691395 | C | T | 1 | a0001c0002t0002g0022 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1821-1282C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691395 | |||||||
| chr8:94691517 | T | C | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1821-1160T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691517 | |||||||
| chr8:94691582 | G | T | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-1095G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691582 | |||||||
| chr8:94691692 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1821-985G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691692 | |||||||
| chr8:94691833 | C | T | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0206 others(1): Show |
4 | NA18971.hp1 NA19062.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-844C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691833 | |||||||
| chr8:94691869 | T | G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0276 a0001c0001t0001g0280 others(1): Show |
4 | NA18962.hp1 NA18972.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821-808T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691869 | |||||||
| chr8:94691975 | C | G | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 |
3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1821-702C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94691975 | |||||||
| chr8:94692054 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1821-623C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692054 | |||||||
| chr8:94692126 | C | T | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821-551C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692126 | |||||||
| chr8:94692187 | G | A | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1821-490G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692187 | |||||||
| chr8:94692390 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0170 |
2 | NA18947.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1821-287G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692390 | |||||||
| chr8:94692478 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0163 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1821-199T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692478 | |||||||
| chr8:94692496 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1821-181T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 13/15 | chr8 | 94692496 | |||||||
| chr8:94693007 | C | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 |
3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1971+180C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693007 | |||||||
| chr8:94693008 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+181C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693008 | |||||||
| chr8:94693026 | CT | C | 150 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(147): Show |
150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1971+204delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94693026 | ||||||
| chr8:94693100 | G | A | 4 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 others(1): Show |
4 | HG02109.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971+273G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693100 | |||||||
| chr8:94693182 | A | G | 104 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0001g0124 others(101): Show |
104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1971+355A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693182 | |||||||
| chr8:94693313 | G | GT | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971+487dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94693313 | ||||||
| chr8:94693545 | A | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+718A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693545 | |||||||
| chr8:94693681 | A | G | 1 | a0001c0002t0002g0075 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1971+854A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693681 | |||||||
| chr8:94693904 | A | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1077A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94693904 | |||||||
| chr8:94694027 | C | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1200C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694027 | |||||||
| chr8:94694042 | A | G | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1971+1215A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694042 | |||||||
| chr8:94694106 | T | C | 10 | a0001c0001t0001g0256 a0001c0002t0012g0141 a0001c0003t0001g0347 others(7): Show |
10 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1971+1279T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694106 | |||||||
| chr8:94694132 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1305T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694132 | |||||||
| chr8:94694182 | G | T | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971+1355G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694182 | |||||||
| chr8:94694344 | C | A | 1 | a0001c0003t0001g0353 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1971+1517C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694344 | |||||||
| chr8:94694349 | G | C | 2 | a0001c0002t0002g0065 a0001c0002t0002g0076 |
2 | NA18994.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1971+1522G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694349 | |||||||
| chr8:94694433 | G | A | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1971+1606G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694433 | |||||||
| chr8:94694561 | T | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1734T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694561 | |||||||
| chr8:94694598 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1771T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694598 | |||||||
| chr8:94694651 | A | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+1824A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694651 | |||||||
| chr8:94694662 | G | A | 1 | a0001c0007t0001g0346 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1971+1835G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94694662 | |||||||
| chr8:94695005 | T | C | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1972-1847T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695005 | |||||||
| chr8:94695039 | A | T | 1 | a0001c0001t0001g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1972-1813A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695039 | |||||||
| chr8:94695055 | G | A | 103 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0002g0006 others(100): Show |
103 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1972-1797G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695055 | |||||||
| chr8:94695106 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1746T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695106 | |||||||
| chr8:94695128 | T | A | 3 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0312 |
3 | NA18994.hp1 NA19002.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1972-1724T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695128 | |||||||
| chr8:94695240 | G | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0072 others(44): Show |
47 | HG00140.hp2 HG00423.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.1972-1612G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695240 | |||||||
| chr8:94695348 | C | CT | 92 | a0001c0002t0001g0085 a0001c0002t0001g0097 a0001c0002t0002g0006 others(89): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1972-1480dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | ||||||
| chr8:94695348 | C | CTT | 8 | a0001c0001t0010g0005 a0001c0002t0002g0012 a0001c0002t0002g0046 others(5): Show |
8 | HG00597.hp1 HG02080.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972-1481_1972-148 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | ||||||
| chr8:94695348 | CT | C | 14 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(11): Show |
14 | HG01167.hp2 HG01261.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1972-1480delT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | ||||||
| chr8:94695348 | CTT | C | 8 | a0001c0001t0001g0169 a0001c0001t0001g0247 a0001c0001t0001g0257 others(5): Show |
8 | HG02559.hp2 HG02622.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1972-1481_1972-148 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | ||||||
| chr8:94695348 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1487_1972-148 others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695348 | ||||||
| chr8:94695371 | T | C | 4 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1972-1481T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695371 | |||||||
| chr8:94695371 | T | TTC | 9 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
9 | HG00558.hp1 HG01891.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | ||||||
| chr8:94695371 | T | TTTC | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(7): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | ||||||
| chr8:94695371 | T | TTTTC | 101 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0087 others(98): Show |
103 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | ||||||
| chr8:94695371 | T | TTTTTC | 15 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0118 others(12): Show |
15 | HG00438.hp2 HG01175.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1972-1480_1972-147 others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695371 | ||||||
| chr8:94695395 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1972-1457C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695395 | |||||||
| chr8:94695416 | G | A | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1972-1436G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695416 | |||||||
| chr8:94695424 | G | A | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1972-1428G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695424 | |||||||
| chr8:94695497 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1355C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695497 | |||||||
| chr8:94695499 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(264): Show |
269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1972-1353T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695499 | |||||||
| chr8:94695520 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1332T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695520 | |||||||
| chr8:94695599 | G | A | 1 | a0001c0003t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1972-1253G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695599 | |||||||
| chr8:94695606 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1972-1246G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695606 | |||||||
| chr8:94695612 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1972-1240G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695612 | |||||||
| chr8:94695633 | G | A | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1972-1219G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695633 | |||||||
| chr8:94695642 | C | A | 1 | a0001c0003t0001g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1972-1210C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695642 | |||||||
| chr8:94695713 | A | ATTCTGTC others(56): Show |
9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1138_1972-113 others(67): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94695713 | ||||||
| chr8:94695715 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1137C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695715 | |||||||
| chr8:94695776 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1076C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695776 | |||||||
| chr8:94695783 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1069C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695783 | |||||||
| chr8:94695789 | A | G | 13 | a0001c0001t0001g0256 a0001c0003t0001g0319 a0001c0003t0001g0347 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1972-1063A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695789 | |||||||
| chr8:94695796 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-1056T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695796 | |||||||
| chr8:94695882 | G | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG01109.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1972-970G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695882 | |||||||
| chr8:94695905 | A | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-947A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695905 | |||||||
| chr8:94695921 | C | T | 1 | a0001c0004t0002g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1972-931C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695921 | |||||||
| chr8:94695928 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-924T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695928 | |||||||
| chr8:94695961 | G | A | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1972-891G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94695961 | |||||||
| chr8:94696063 | AAAAC | A | 30 | a0001c0001t0001g0137 a0001c0001t0001g0198 a0001c0001t0001g0212 others(27): Show |
30 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1972-777_1972-774d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr8 | 94696063 | ||||||
| chr8:94696087 | C | G | 10 | a0001c0001t0001g0358 a0001c0001t0001g0359 a0001c0001t0001g0360 others(7): Show |
10 | HG02257.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1972-765C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696087 | |||||||
| chr8:94696092 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-760T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696092 | |||||||
| chr8:94696269 | A | G | 1 | a0001c0001t0003g0323 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1972-583A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696269 | |||||||
| chr8:94696330 | C | G | 13 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(10): Show |
13 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1972-522C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696330 | |||||||
| chr8:94696423 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | NA19064.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1972-429T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696423 | |||||||
| chr8:94696495 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-357T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696495 | |||||||
| chr8:94696496 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-356G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696496 | |||||||
| chr8:94696532 | A | G | 3 | a0001c0001t0004g0194 a0001c0001t0004g0195 a0001c0001t0004g0196 |
3 | HG02109.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1972-320A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696532 | |||||||
| chr8:94696704 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1972-148A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696704 | |||||||
| chr8:94696708 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1972-144G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696708 | |||||||
| chr8:94696774 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1972-78G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 14/15 | chr8 | 94696774 | |||||||
| chr8:94696977 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+16G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94696977 | |||||||
| chr8:94697079 | C | A | 2 | a0001c0001t0003g0214 a0001c0001t0003g0217 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.*35+118C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697079 | |||||||
| chr8:94697189 | C | T | 5 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.*35+228C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697189 | |||||||
| chr8:94697219 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.*35+258C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697219 | |||||||
| chr8:94697272 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 |
3 | HG01261.hp2 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*35+311A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697272 | |||||||
| chr8:94697337 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | HG01175.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.*35+376C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697337 | |||||||
| chr8:94697607 | T | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+646T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697607 | |||||||
| chr8:94697746 | G | A | 1 | a0001c0003t0001g0319 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*35+785G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697746 | |||||||
| chr8:94697860 | C | A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00741.hp1 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.*35+899C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697860 | |||||||
| chr8:94697941 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.*35+980T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94697941 | |||||||
| chr8:94698120 | A | G | 1 | a0004c0010t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*35+1159A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698120 | |||||||
| chr8:94698181 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+1220G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698181 | |||||||
| chr8:94698348 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.*35+1387T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698348 | |||||||
| chr8:94698390 | TTA | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 |
3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*35+1431_*35+1432d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94698390 | ||||||
| chr8:94698398 | T | A | 26 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(23): Show |
26 | HG00438.hp2 HG01361.hp2 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.*35+1437T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698398 | |||||||
| chr8:94698463 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+1502G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698463 | |||||||
| chr8:94698505 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.*35+1544C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698505 | |||||||
| chr8:94698664 | A | G | 1 | a0001c0002t0002g0357 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.*35+1703A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698664 | |||||||
| chr8:94698819 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+1858T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698819 | |||||||
| chr8:94698871 | A | T | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.*35+1910A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94698871 | |||||||
| chr8:94699002 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2041A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699002 | |||||||
| chr8:94699003 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2042C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699003 | |||||||
| chr8:94699004 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2043A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699004 | |||||||
| chr8:94699054 | A | G | 1 | a0001c0002t0002g0100 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.*35+2093A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699054 | |||||||
| chr8:94699190 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2229C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699190 | |||||||
| chr8:94699240 | G | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.*35+2279G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699240 | |||||||
| chr8:94699287 | T | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2326T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699287 | |||||||
| chr8:94699304 | T | C | 3 | a0001c0003t0001g0368 a0001c0003t0001g0369 a0001c0006t0001g0345 |
3 | HG01167.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.*35+2343T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699304 | |||||||
| chr8:94699415 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.*35+2454C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699415 | |||||||
| chr8:94699478 | C | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.*35+2517C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699478 | |||||||
| chr8:94699479 | GA | G | 10 | a0001c0001t0001g0179 a0001c0001t0001g0256 a0001c0003t0001g0347 others(7): Show |
10 | HG01070.hp2 HG01081.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.*35+2526delA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94699479 | ||||||
| chr8:94699487 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0207 |
2 | NA18949.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.*35+2526A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699487 | |||||||
| chr8:94699524 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2563C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699524 | |||||||
| chr8:94699613 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0103 others(72): Show |
76 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.*35+2652C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699613 | |||||||
| chr8:94699658 | A | G | 1 | a0004c0010t0001g0321 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*35+2697A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699658 | |||||||
| chr8:94699755 | A | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2794A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699755 | |||||||
| chr8:94699907 | A | AT | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+2953dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94699907 | ||||||
| chr8:94699908 | T | TA | 260 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
262 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.*35+2947_*35+2948i others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699908 | |||||||
| chr8:94699918 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+2957G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94699918 | |||||||
| chr8:94700005 | A | T | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*35+3044A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700005 | |||||||
| chr8:94700006 | C | T | 4 | a0001c0003t0001g0327 a0001c0003t0001g0328 a0001c0003t0001g0329 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.*35+3045C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700006 | |||||||
| chr8:94700020 | A | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3059A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700020 | |||||||
| chr8:94700024 | G | A | 11 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(8): Show |
11 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.*35+3063G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700024 | |||||||
| chr8:94700033 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*35+3072G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700033 | |||||||
| chr8:94700166 | A | T | 1 | a0001c0001t0005g0299 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.*35+3205A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700166 | |||||||
| chr8:94700208 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3247T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700208 | |||||||
| chr8:94700219 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.*35+3258G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700219 | |||||||
| chr8:94700301 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.*35+3340C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700301 | |||||||
| chr8:94700436 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3475G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700436 | |||||||
| chr8:94700522 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3561T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700522 | |||||||
| chr8:94700741 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+3780A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700741 | |||||||
| chr8:94700757 | G | A | 1 | a0001c0003t0001g0334 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*35+3796G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700757 | |||||||
| chr8:94700796 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3835G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700796 | |||||||
| chr8:94700810 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3849C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700810 | |||||||
| chr8:94700853 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3892C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700853 | |||||||
| chr8:94700856 | A | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+3895A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700856 | |||||||
| chr8:94700920 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0177 |
3 | NA18961.hp2 NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.*35+3959C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700920 | |||||||
| chr8:94700923 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(64): Show |
67 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.*35+3962C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700923 | |||||||
| chr8:94700924 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.*35+3963G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700924 | |||||||
| chr8:94700937 | ATGTGTGT others(11): Show |
A | 1 | a0001c0002t0002g0043 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*35+3992_*35+4009d others(20): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700937 | ||||||
| chr8:94700937 | ATGTGTGT others(25): Show |
A | 8 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(5): Show |
8 | HG00438.hp2 NA18747.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.*35+3992_*35+4023d others(34): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700937 | ||||||
| chr8:94700951 | GTA | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG01109.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.*35+3992_*35+3993d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700951 | ||||||
| chr8:94700953 | A | ATG | 9 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(6): Show |
9 | HG00642.hp2 HG02015.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.*35+4022_*35+4023d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | ||||||
| chr8:94700953 | A | G | 16 | a0001c0001t0001g0179 a0001c0001t0001g0256 a0001c0003t0001g0319 others(13): Show |
16 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.*35+3992A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700953 | |||||||
| chr8:94700953 | ATG | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(88): Show |
91 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.*35+4022_*35+4023d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | ||||||
| chr8:94700953 | ATGTG | A | 62 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(59): Show |
62 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.*35+4020_*35+4023d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | ||||||
| chr8:94700953 | ATGTGTG | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0103 others(38): Show |
42 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.*35+4018_*35+4023d others(8): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | ||||||
| chr8:94700953 | ATGTGTGT others(1): Show |
A | 19 | a0001c0001t0001g0168 a0001c0001t0001g0185 a0001c0001t0001g0186 others(16): Show |
19 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.*35+4016_*35+4023d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | ||||||
| chr8:94700953 | ATGTGTGT others(5): Show |
A | 1 | a0001c0004t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*35+4012_*35+4023d others(14): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700953 | ||||||
| chr8:94700957 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.*35+3996G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700957 | |||||||
| chr8:94700959 | G | GTGTGTGT others(3): Show |
9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4007_*35+4008i others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94700959 | ||||||
| chr8:94700962 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+4001T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700962 | |||||||
| chr8:94700963 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*35+4002G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700963 | |||||||
| chr8:94700969 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4008G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700969 | |||||||
| chr8:94700979 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4018G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700979 | |||||||
| chr8:94700995 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.*35+4034G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94700995 | |||||||
| chr8:94701089 | G | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4128G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701089 | |||||||
| chr8:94701274 | C | CA | 20 | a0001c0001t0001g0208 a0001c0001t0001g0256 a0001c0001t0001g0304 others(17): Show |
20 | HG01070.hp2 HG01081.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.*35+4328dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94701274 | ||||||
| chr8:94701289 | AG | A | 21 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(18): Show |
21 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.*35+4329delG | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701289 | |||||||
| chr8:94701290 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
251 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.*35+4329G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701290 | |||||||
| chr8:94701301 | T | A | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4340T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701301 | |||||||
| chr8:94701315 | G | A | 30 | a0001c0001t0001g0137 a0001c0001t0001g0198 a0001c0001t0001g0212 others(27): Show |
30 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*35+4354G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701315 | |||||||
| chr8:94701319 | A | G | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 |
3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*35+4358A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701319 | |||||||
| chr8:94701420 | C | T | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 |
3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*35+4459C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701420 | |||||||
| chr8:94701421 | G | A | 9 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(6): Show |
9 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.*35+4460G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701421 | |||||||
| chr8:94701509 | G | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.*36-4416G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701509 | |||||||
| chr8:94701511 | G | T | 2 | a0001c0002t0002g0039 a0001c0002t0002g0079 |
2 | NA18941.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.*36-4414G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701511 | |||||||
| chr8:94701532 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-4393G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701532 | |||||||
| chr8:94701689 | C | G | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-4236C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701689 | |||||||
| chr8:94701690 | T | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-4235T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701690 | |||||||
| chr8:94701735 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*36-4190G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701735 | |||||||
| chr8:94701869 | G | T | 4 | a0001c0005t0001g0181 a0001c0005t0001g0182 a0001c0005t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.*36-4056G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701869 | |||||||
| chr8:94701886 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.*36-4039C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701886 | |||||||
| chr8:94701989 | G | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(3): Show |
6 | HG01175.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.*36-3936G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94701989 | |||||||
| chr8:94702018 | C | T | 2 | a0001c0002t0002g0071 a0001c0002t0002g0084 |
2 | NA18988.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.*36-3907C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702018 | |||||||
| chr8:94702048 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.*36-3877A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702048 | |||||||
| chr8:94702160 | G | GT | 9 | a0001c0001t0001g0179 a0001c0001t0001g0267 a0001c0001t0001g0268 others(6): Show |
9 | HG02165.hp2 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3758dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94702160 | ||||||
| chr8:94702226 | C | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3699C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702226 | |||||||
| chr8:94702416 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3509G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702416 | |||||||
| chr8:94702417 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3508T>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702417 | |||||||
| chr8:94702418 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3507C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702418 | |||||||
| chr8:94702441 | A | C | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3484A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702441 | |||||||
| chr8:94702448 | A | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-3477A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702448 | |||||||
| chr8:94702590 | G | A | 4 | a0001c0003t0001g0319 a0001c0003t0001g0368 a0001c0003t0001g0369 others(1): Show |
4 | HG01167.hp2 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.*36-3335G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702590 | |||||||
| chr8:94702770 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3155G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702770 | |||||||
| chr8:94702771 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.*36-3154C>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702771 | |||||||
| chr8:94702955 | T | C | 3 | a0001c0001t0006g0151 a0001c0001t0006g0152 a0001c0001t0006g0215 |
3 | HG02109.hp2 HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*36-2970T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94702955 | |||||||
| chr8:94703105 | A | AT | 5 | a0001c0001t0001g0180 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.*36-2818dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703105 | ||||||
| chr8:94703108 | G | GT | 32 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(29): Show |
32 | HG01070.hp2 HG01081.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.*36-2801dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | ||||||
| chr8:94703108 | G | GTT | 38 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0198 others(35): Show |
38 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.*36-2802_*36-2801d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | ||||||
| chr8:94703108 | G | GTTT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(159): Show |
164 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.*36-2803_*36-2801d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | ||||||
| chr8:94703108 | G | GTTTT | 12 | a0001c0001t0001g0072 a0001c0001t0001g0105 a0001c0001t0001g0119 others(9): Show |
12 | HG01261.hp1 HG01934.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.*36-2804_*36-2801d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703108 | ||||||
| chr8:94703108 | G | T | 7 | a0001c0001t0001g0168 a0001c0001t0001g0180 a0001c0001t0001g0267 others(4): Show |
7 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.*36-2817G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703108 | |||||||
| chr8:94703153 | T | TTTG | 17 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(14): Show |
17 | HG01261.hp2 HG02055.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.*36-2753_*36-2751d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703153 | ||||||
| chr8:94703153 | TTTG | T | 9 | a0001c0001t0001g0256 a0001c0003t0001g0347 a0001c0003t0001g0348 others(6): Show |
9 | HG01070.hp2 HG01081.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.*36-2753_*36-2751d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94703153 | ||||||
| chr8:94703279 | C | T | 30 | a0001c0001t0001g0137 a0001c0001t0001g0198 a0001c0001t0001g0212 others(27): Show |
30 | HG00140.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.*36-2646C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703279 | |||||||
| chr8:94703335 | G | C | 1 | a0003c0012t0002g0122 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*36-2590G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703335 | |||||||
| chr8:94703441 | C | A | 1 | a0001c0002t0002g0120 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.*36-2484C>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703441 | |||||||
| chr8:94703574 | A | G | 1 | a0001c0002t0012g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.*36-2351A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703574 | |||||||
| chr8:94703599 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*36-2326A>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703599 | |||||||
| chr8:94703757 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.*36-2168G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703757 | |||||||
| chr8:94703824 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.*36-2101T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703824 | |||||||
| chr8:94703894 | T | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.*36-2031T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703894 | |||||||
| chr8:94703907 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.*36-2018A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703907 | |||||||
| chr8:94703937 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-1988G>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94703937 | |||||||
| chr8:94704001 | T | C | 1 | a0001c0001t0001g0361 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.*36-1924T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704001 | |||||||
| chr8:94704040 | C | T | 1 | a0001c0004t0002g0086 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.*36-1885C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704040 | |||||||
| chr8:94704064 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-1861A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704064 | |||||||
| chr8:94704175 | C | CTT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0155 others(12): Show |
15 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.*36-1735_*36-1734d others(4): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704175 | ||||||
| chr8:94704175 | C | CTTT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0042 others(183): Show |
188 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.*36-1736_*36-1734d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704175 | ||||||
| chr8:94704175 | C | CTTTT | 56 | a0001c0001t0001g0087 a0001c0001t0001g0108 a0001c0001t0001g0119 others(53): Show |
56 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.*36-1737_*36-1734d others(6): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704175 | ||||||
| chr8:94704263 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-1662T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704263 | |||||||
| chr8:94704359 | C | T | 1 | a0001c0002t0002g0018 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.*36-1566C>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704359 | |||||||
| chr8:94704481 | G | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0103 others(72): Show |
76 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.*36-1444G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704481 | |||||||
| chr8:94704504 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-1421T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704504 | |||||||
| chr8:94704542 | T | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-1383T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704542 | |||||||
| chr8:94704551 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*36-1374G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704551 | |||||||
| chr8:94704766 | G | GA | 29 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0019 others(26): Show |
29 | HG00597.hp1 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.*36-1132dupA | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | ||||||
| chr8:94704766 | G | GAAA | 11 | a0001c0004t0002g0007 a0001c0004t0002g0033 a0001c0004t0002g0034 others(8): Show |
11 | HG00323.hp1 HG01070.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.*36-1134_*36-1132d others(5): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | ||||||
| chr8:94704766 | GAAAAAAA | G | 39 | a0001c0001t0001g0110 a0001c0001t0001g0118 a0001c0001t0001g0119 others(36): Show |
39 | HG00741.hp2 HG01069.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.*36-1138_*36-1132d others(9): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | ||||||
| chr8:94704766 | GAAAAAAA others(1): Show |
G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(189): Show |
194 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.*36-1139_*36-1132d others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | ||||||
| chr8:94704766 | GAAAAAAA others(2): Show |
G | 35 | a0001c0001t0001g0139 a0001c0001t0001g0149 a0001c0001t0001g0161 others(32): Show |
35 | HG01109.hp1 HG01167.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.*36-1140_*36-1132d others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94704766 | ||||||
| chr8:94704773 | A | G | 2 | a0001c0003t0001g0333 a0001c0003t0001g0371 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.*36-1152A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704773 | |||||||
| chr8:94704774 | A | G | 5 | a0001c0003t0001g0241 a0001c0003t0001g0326 a0001c0003t0001g0335 others(2): Show |
5 | HG00741.hp2 HG01175.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.*36-1151A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704774 | |||||||
| chr8:94704775 | A | G | 19 | a0001c0003t0001g0001 a0001c0003t0001g0088 a0001c0003t0001g0135 others(16): Show |
20 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.*36-1150A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704775 | |||||||
| chr8:94704937 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.*36-988A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94704937 | |||||||
| chr8:94705022 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*36-903G>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705022 | |||||||
| chr8:94705117 | A | G | 31 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0165 others(28): Show |
31 | HG01109.hp1 HG01261.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.*36-808A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705117 | |||||||
| chr8:94705156 | C | CT | 50 | a0001c0001t0006g0151 a0001c0001t0006g0215 a0001c0002t0002g0006 others(47): Show |
50 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.*36-740dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | C | CTT | 13 | a0001c0001t0001g0358 a0001c0001t0001g0360 a0001c0001t0001g0361 others(10): Show |
13 | HG00323.hp1 HG00735.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.*36-741_*36-740dup others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | C | CTTT | 7 | a0001c0001t0001g0359 a0001c0001t0001g0362 a0001c0001t0001g0363 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.*36-742_*36-740dup others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | CTT | C | 6 | a0001c0001t0001g0161 a0001c0001t0001g0167 a0001c0001t0001g0247 others(3): Show |
6 | HG01167.hp2 HG02055.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.*36-741_*36-740del others(2): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | CTTT | C | 12 | a0001c0001t0001g0165 a0001c0001t0001g0169 a0001c0001t0001g0257 others(9): Show |
12 | HG01261.hp2 HG02559.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.*36-742_*36-740del others(3): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | CTTTTTTT others(3): Show |
C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0132 a0001c0001t0001g0137 others(24): Show |
28 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.*36-749_*36-740del others(10): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | CTTTTTTT others(4): Show |
C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0042 others(186): Show |
190 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.*36-750_*36-740del others(11): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705156 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0164 a0001c0001t0001g0302 others(1): Show |
4 | HG00558.hp1 HG01069.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.*36-751_*36-740del others(12): Show |
ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705156 | ||||||
| chr8:94705245 | G | A | 1 | a0001c0011t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*36-680G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705245 | |||||||
| chr8:94705473 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*36-452T>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705473 | |||||||
| chr8:94705633 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(265): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(267): Show |
intron_variant | MODIFIER | c.*36-292A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705633 | |||||||
| chr8:94705633 | A | T | 1 | a0001c0001t0001g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*36-292A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705633 | |||||||
| chr8:94705637 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.*36-288G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705637 | |||||||
| chr8:94705654 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.*36-271A>T | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705654 | |||||||
| chr8:94705677 | G | A | 7 | a0001c0002t0002g0010 a0001c0002t0002g0024 a0001c0002t0002g0053 others(4): Show |
7 | HG00408.hp2 HG00558.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.*36-248G>A | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705677 | |||||||
| chr8:94705680 | T | C | 27 | a0001c0002t0002g0074 a0001c0003t0001g0001 a0001c0003t0001g0088 others(24): Show |
28 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.*36-245T>C | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705680 | |||||||
| chr8:94705902 | A | G | 2 | a0001c0007t0001g0344 a0001c0007t0001g0346 |
2 | HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.*36-23A>G | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | chr8 | 94705902 | |||||||
| chr8:94705903 | C | CT | 6 | a0001c0002t0002g0039 a0001c0002t0002g0057 a0001c0002t0002g0079 others(3): Show |
6 | HG02451.hp1 HG03942.hp2 NA18941.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.*36-4dupT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 | ||||||
| chr8:94705903 | CTT | C | 22 | a0001c0001t0001g0148 a0001c0001t0001g0159 a0001c0001t0001g0256 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01993.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.*36-5_*36-4delTT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 | ||||||
| chr8:94705903 | CTTT | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
188 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
splice_region_variant&intron_variant | LOW | c.*36-6_*36-4delTTT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 | ||||||
| chr8:94705903 | CTTTT | C | 60 | a0001c0001t0001g0137 a0001c0001t0001g0198 a0001c0001t0001g0212 others(57): Show |
61 | HG00140.hp1 HG00558.hp1 HG00642.hp1 others(58): Show |
splice_region_variant&intron_variant | LOW | c.*36-7_*36-4delTTTT | ESRP1 | ENSG00000104413.18 | transcript | ENST00000433389.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr8 | 94705903 |