Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26136 |
| ensemblid | ENSG00000135269.18 |
| hgncid | 14620 |
| symbol | TES |
| name | testin LIM domain protein |
| refseq_nuc | NM_015641.4 |
| refseq_prot | NP_056456.1 |
| ensembl_nuc | ENST00000358204.9 |
| ensembl_prot | ENSP00000350937.4 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 116210539 |
| end | 116258783 |
| strand | + |
| ver | v1.2 |
| region | chr7:116210539-116258783 |
| region5000 | chr7:116205539-116263783 |
| regionname0 | TES_chr7_116210539_116258783 |
| regionname5000 | TES_chr7_116205539_116263783 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 421 | 372 | 78 | 67 | 174 | 14 | 37 | 134 | TES_chr7_116205539_116263783 | TES | MDLEN others(416): Show |
chr7 | 116205539 | 116263783 |
| a0002 | 0/0 | 421 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | TES_chr7_116205539_116263783 | TES | MDLEN others(416): Show |
chr7 | 116205539 | 116263783 |
| a0003 | 0/0 | 421 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TES_chr7_116205539_116263783 | TES | MDLEN others(416): Show |
chr7 | 116205539 | 116263783 |
| a0004 | 0/0 | 421 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | MDLEN others(416): Show |
chr7 | 116205539 | 116263783 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1263 | 199 | 37 | 43 | 83 | 8 | 26 | TES_chr7_116205539_116263783 | TES | ATGGA others(1258): Show |
chr7 | 116205539 | 116263783 | ||
| a0001c0002 | 0/0 | 1263 | 172 | 40 | 24 | 91 | 6 | 11 | TES_chr7_116205539_116263783 | TES | ATGGA others(1258): Show |
chr7 | 116205539 | 116263783 | ||
| a0001c0006 | 0/0 | 1263 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | ATGGA others(1258): Show |
chr7 | 116205539 | 116263783 | ||
| a0002c0003 | 0/0 | 1263 | 10 | 0 | 0 | 10 | 0 | 0 | TES_chr7_116205539_116263783 | TES | ATGGA others(1258): Show |
chr7 | 116205539 | 116263783 | ||
| a0003c0004 | 0/0 | 1263 | 3 | 0 | 0 | 0 | 0 | 3 | TES_chr7_116205539_116263783 | TES | ATGGA others(1258): Show |
chr7 | 116205539 | 116263783 | ||
| a0004c0005 | 0/0 | 1263 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | ATGGA others(1258): Show |
chr7 | 116205539 | 116263783 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2736 | 71 | 0 | 16 | 48 | 1 | 6 | TES_chr7_116205539_116263783 | TES | GCTGC others(2731): Show |
chr7 | 116205539 | 116263783 |
| a0001c0001t0003 | 0/0 | 2735 | 67 | 10 | 14 | 27 | 5 | 11 | TES_chr7_116205539_116263783 | TES | GCTGC others(2730): Show |
chr7 | 116205539 | 116263783 |
| a0001c0001t0005 | 1/1 | 2736 | 57 | 23 | 13 | 8 | 2 | 9 | TES_chr7_116205539_116263783 | TES | GCTGC others(2731): Show |
chr7 | 116205539 | 116263783 |
| a0001c0001t0007 | 0/0 | 2736 | 4 | 4 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2731): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0001 | 0/0 | 2731 | 88 | 12 | 10 | 58 | 4 | 4 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0004 | 0/0 | 2733 | 61 | 10 | 11 | 31 | 2 | 7 | TES_chr7_116205539_116263783 | TES | GCTGC others(2728): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0006 | 0/0 | 2734 | 15 | 15 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2729): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0008 | 0/0 | 2731 | 4 | 1 | 2 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0009 | 0/0 | 2731 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0010 | 0/0 | 2731 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0001c0002t0011 | 0/0 | 2731 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0001c0006t0001 | 0/0 | 2731 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0002c0003t0001 | 0/0 | 2731 | 10 | 0 | 0 | 10 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2726): Show |
chr7 | 116205539 | 116263783 |
| a0003c0004t0004 | 0/0 | 2733 | 3 | 0 | 0 | 0 | 0 | 3 | TES_chr7_116205539_116263783 | TES | GCTGC others(2728): Show |
chr7 | 116205539 | 116263783 |
| a0004c0005t0005 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | GCTGC others(2731): Show |
chr7 | 116205539 | 116263783 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0052 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0053 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0007g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0008g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0002t0011g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0001c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0003c0004t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0003c0004t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| a0004c0005t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0073 | EUR | GBR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0015 | EUR | GBR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | FIN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0272 | EUR | FIN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00438 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0223 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0217 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00733 | hp1 | a0001 | c0002 | t0011 | g0200 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0270 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00738 | hp1 | a0001 | c0002 | t0004 | g0076 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01070 | hp2 | a0001 | c0002 | t0008 | g0039 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01071 | hp1 | a0001 | c0002 | t0008 | g0039 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0087 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0226 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01168 | hp1 | a0001 | c0002 | t0004 | g0089 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01243 | hp1 | a0004 | c0005 | t0005 | g0259 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0269 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01257 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01358 | hp2 | a0001 | c0002 | t0004 | g0092 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0220 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0162 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0253 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0189 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0013 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01928 | hp2 | a0001 | c0002 | t0004 | g0082 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01943 | hp2 | a0001 | c0002 | t0004 | g0069 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0227 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0091 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02055 | hp1 | a0001 | c0002 | t0006 | g0112 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0086 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02258 | hp2 | a0001 | c0002 | t0006 | g0105 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02280 | hp1 | a0001 | c0002 | t0006 | g0062 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02300 | hp1 | a0001 | c0002 | t0004 | g0072 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0103 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0264 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0214 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0218 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0083 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02738 | hp1 | a0001 | c0002 | t0004 | g0022 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0063 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0074 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02895 | hp1 | a0001 | c0002 | t0009 | g0032 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02896 | hp1 | a0001 | c0002 | t0009 | g0032 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0100 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0020 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0101 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0099 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0029 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0113 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0224 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03453 | hp1 | a0001 | c0002 | t0006 | g0029 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0061 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03491 | hp1 | a0003 | c0004 | t0004 | g0023 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0283 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03492 | hp1 | a0003 | c0004 | t0004 | g0023 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0104 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0266 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0265 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0022 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03942 | hp1 | a0003 | c0004 | t0004 | g0081 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0281 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04199 | hp1 | a0001 | c0002 | t0004 | g0084 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04204 | hp1 | a0001 | c0002 | t0004 | g0071 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0275 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0079 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0030 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0098 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0008 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18747 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18906 | hp1 | a0001 | c0002 | t0006 | g0288 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0095 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0093 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0088 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18957 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18959 | hp1 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0090 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18968 | hp1 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18975 | hp2 | a0001 | c0002 | t0004 | g0025 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0094 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18988 | hp1 | a0001 | c0002 | t0004 | g0080 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18989 | hp2 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18990 | hp1 | a0001 | c0002 | t0008 | g0138 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18997 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18999 | hp1 | a0001 | c0002 | t0004 | g0024 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19006 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19007 | hp1 | a0001 | c0002 | t0010 | g0205 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19058 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19058 | hp2 | a0002 | c0003 | t0001 | g0014 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19063 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19064 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19065 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0025 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0024 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19070 | hp1 | a0001 | c0002 | t0004 | g0008 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19072 | hp2 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19074 | hp1 | a0001 | c0002 | t0004 | g0097 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19075 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19089 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0096 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA19240 | hp2 | a0001 | c0002 | t0006 | g0102 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | ASW | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | ASW | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0067 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0254 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0150 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0213 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | GIH | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0070 | SAS | GIH | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0075 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0020 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0045 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20300 | hp1 | a0001 | c0002 | t0008 | g0131 | AFR | USA | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | USA | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| NA21309 | hp2 | a0001 | c0002 | t0006 | g0106 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0286 | REF | REF | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0263 | REF | REF | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116234536 | G | A | 1 | a0004 | 1 | HG01243.hp1 | missense_variant&splice_region_variant | MODERATE | c.30G>A | p.Met10Ile | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/7 | 199/2736 | 30/1266 | 10/421 | chr7 | 116234536 | |||
| chr7:116250456 | C | T | 1 | a0002 | 10 | NA18953.hp2 NA18957.hp2 NA18989.hp2 others(7): Show |
missense_variant | MODERATE | c.662C>T | p.Ala221Val | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/7 | 831/2736 | 662/1266 | 221/421 | chr7 | 116250456 | |||
| chr7:116257352 | A | G | 1 | a0003 | 3 | HG03491.hp1 HG03492.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.1136A>G | p.Asn379Ser | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1305/2736 | 1136/1266 | 379/421 | chr7 | 116257352 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116257338 | G | C | 3 | a0001c0002 a0002c0003 a0003c0004 |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
synonymous_variant | LOW | c.1122G>C | p.Arg374Arg | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1291/2736 | 1122/1266 | 374/421 | chr7 | 116257338 | |||
| chr7:116257338 | G | T | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1122G>T | p.Arg374Arg | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1291/2736 | 1122/1266 | 374/421 | chr7 | 116257338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116210588 | G | C | 1 | a0001c0002t0009 | 2 | HG02895.hp1 HG02896.hp1 |
5_prime_UTR_variant | MODIFIER | c.-120G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/7 | 120 | chr7 | 116210588 | ||||||
| chr7:116210621 | C | T | 2 | a0001c0001t0002 a0001c0002t0008 |
75 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
5_prime_UTR_variant | MODIFIER | c.-87C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/7 | 87 | chr7 | 116210621 | ||||||
| chr7:116257569 | G | A | 1 | a0001c0002t0010 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 87 | chr7 | 116257569 | ||||||
| chr7:116257638 | AT | A | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*164delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 164 | INFO_REALIGN_3_PRIME | chr7 | 116257638 | |||||
| chr7:116257738 | T | TAG | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*256_*257insAG | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 257 | chr7 | 116257738 | ||||||
| chr7:116257817 | A | G | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*335A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 335 | chr7 | 116257817 | ||||||
| chr7:116257830 | C | T | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*348C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 348 | chr7 | 116257830 | ||||||
| chr7:116257872 | AAAG | A | 7 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0009 others(4): Show |
107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*395delGAA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 393 | INFO_REALIGN_3_PRIME | chr7 | 116257872 | |||||
| chr7:116257915 | T | G | 1 | a0001c0002t0011 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*433T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 433 | chr7 | 116257915 | ||||||
| chr7:116258123 | G | C | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 641 | chr7 | 116258123 | ||||||
| chr7:116258190 | AT | A | 1 | a0001c0001t0003 | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*721delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 721 | INFO_REALIGN_3_PRIME | chr7 | 116258190 | |||||
| chr7:116258190 | ATT | A | 8 | a0001c0002t0001 a0001c0002t0006 a0001c0002t0008 others(5): Show |
122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*721delTT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 720 | INFO_REALIGN_3_PRIME | chr7 | 116258190 | |||||
| chr7:116258190 | ATTT | A | 2 | a0001c0002t0004 a0003c0004t0004 |
64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*721delTTT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 719 | INFO_REALIGN_3_PRIME | chr7 | 116258190 | |||||
| chr7:116258388 | G | C | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*906G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 906 | chr7 | 116258388 | ||||||
| chr7:116258514 | G | T | 1 | a0001c0001t0007 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1032G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1032 | chr7 | 116258514 | ||||||
| chr7:116258561 | AT | A | 10 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0006 others(7): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1087delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1087 | INFO_REALIGN_3_PRIME | chr7 | 116258561 | |||||
| chr7:116258656 | A | G | 1 | a0001c0001t0003 | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1174 | chr7 | 116258656 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:116210756 | G | A | 1 | a0001c0002t0001g0018 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.27+22G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210756 | |||||||
| chr7:116210764 | T | C | 1 | a0001c0001t0003g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.27+30T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210764 | |||||||
| chr7:116210779 | G | C | 1 | a0001c0002t0001g0059 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.27+45G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210779 | |||||||
| chr7:116210861 | C | T | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+127C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210861 | |||||||
| chr7:116210883 | T | A | 1 | a0001c0002t0001g0060 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.27+149T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210883 | |||||||
| chr7:116210883 | T | C | 191 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(188): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+149T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210883 | |||||||
| chr7:116210983 | C | G | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+249C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210983 | |||||||
| chr7:116211123 | G | A | 1 | a0001c0001t0002g0019 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.27+389G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211123 | |||||||
| chr7:116211433 | T | C | 191 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(188): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+699T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211433 | |||||||
| chr7:116211437 | C | A | 3 | a0001c0002t0006g0020 a0001c0002t0006g0061 a0001c0002t0006g0062 |
4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+703C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211437 | |||||||
| chr7:116211649 | G | C | 5 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(2): Show |
6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+915G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211649 | |||||||
| chr7:116211809 | GA | G | 139 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(136): Show |
192 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+1079delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116211809 | ||||||
| chr7:116211927 | G | A | 258 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(255): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.27+1193G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211927 | |||||||
| chr7:116212077 | C | T | 129 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(126): Show |
180 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.27+1343C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212077 | |||||||
| chr7:116212106 | C | G | 191 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(188): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+1372C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212106 | |||||||
| chr7:116212459 | A | T | 1 | a0001c0001t0005g0287 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.27+1725A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212459 | |||||||
| chr7:116212727 | T | C | 1 | a0001c0002t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.27+1993T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212727 | |||||||
| chr7:116212792 | A | G | 115 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(112): Show |
164 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.27+2058A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212792 | |||||||
| chr7:116212915 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.27+2181T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212915 | |||||||
| chr7:116212971 | A | G | 1 | a0001c0002t0010g0205 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.27+2237A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212971 | |||||||
| chr7:116213012 | C | T | 139 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(136): Show |
192 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+2278C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213012 | |||||||
| chr7:116213046 | T | C | 52 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(49): Show |
71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.27+2312T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213046 | |||||||
| chr7:116213055 | T | A | 1 | a0001c0002t0001g0118 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.27+2321T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213055 | |||||||
| chr7:116213214 | C | T | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+2480C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213214 | |||||||
| chr7:116213449 | A | C | 191 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(188): Show |
263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+2715A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213449 | |||||||
| chr7:116213537 | A | C | 1 | a0001c0002t0001g0204 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.27+2803A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213537 | |||||||
| chr7:116213565 | C | T | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+2831C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213565 | |||||||
| chr7:116213916 | T | A | 1 | a0001c0002t0001g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.27+3182T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213916 | |||||||
| chr7:116214261 | A | G | 1 | a0001c0001t0005g0287 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.27+3527A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214261 | |||||||
| chr7:116214418 | A | T | 3 | a0001c0002t0006g0020 a0001c0002t0006g0061 a0001c0002t0006g0062 |
4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3684A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214418 | |||||||
| chr7:116214635 | A | C | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3901A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214635 | |||||||
| chr7:116214667 | A | G | 1 | a0001c0001t0003g0258 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.27+3933A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214667 | |||||||
| chr7:116214802 | C | G | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+4068C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214802 | |||||||
| chr7:116214969 | C | T | 86 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(83): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.27+4235C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214969 | |||||||
| chr7:116215155 | G | A | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+4421G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215155 | |||||||
| chr7:116215226 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.27+4492G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215226 | |||||||
| chr7:116215737 | C | T | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.27+5003C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215737 | |||||||
| chr7:116215798 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.27+5064G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215798 | |||||||
| chr7:116215964 | C | G | 1 | a0001c0001t0003g0257 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+5230C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215964 | |||||||
| chr7:116216403 | C | T | 1 | a0001c0002t0006g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+5669C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216403 | |||||||
| chr7:116216482 | G | A | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+5748G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216482 | |||||||
| chr7:116216548 | T | C | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.27+5814T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216548 | |||||||
| chr7:116216627 | T | C | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+5893T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216627 | |||||||
| chr7:116216970 | G | C | 1 | a0001c0001t0003g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.27+6236G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216970 | |||||||
| chr7:116217039 | C | G | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.27+6305C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217039 | |||||||
| chr7:116217113 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.27+6379T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217113 | |||||||
| chr7:116217116 | A | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+6382A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217116 | |||||||
| chr7:116217155 | C | T | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.27+6421C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217155 | |||||||
| chr7:116217321 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+6587A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217321 | |||||||
| chr7:116217516 | T | C | 1 | a0001c0001t0002g0121 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.27+6782T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217516 | |||||||
| chr7:116217516 | T | G | 1 | a0001c0002t0004g0066 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.27+6782T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217516 | |||||||
| chr7:116217689 | T | G | 1 | a0001c0001t0002g0019 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.27+6955T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217689 | |||||||
| chr7:116217800 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.27+7066C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217800 | |||||||
| chr7:116218061 | A | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+7327A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218061 | |||||||
| chr7:116218236 | T | C | 1 | a0001c0002t0001g0147 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.27+7502T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218236 | |||||||
| chr7:116218310 | A | T | 1 | a0001c0001t0003g0258 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.27+7576A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218310 | |||||||
| chr7:116218593 | G | A | 4 | a0001c0001t0003g0046 a0001c0001t0003g0211 a0001c0001t0003g0212 others(1): Show |
5 | HG02257.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+7859G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218593 | |||||||
| chr7:116218681 | AT | A | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+7948delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218681 | |||||||
| chr7:116218689 | T | A | 6 | a0001c0001t0003g0068 a0001c0002t0004g0007 a0001c0002t0004g0067 others(3): Show |
9 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+7955T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218689 | |||||||
| chr7:116218715 | A | G | 1 | a0001c0001t0005g0285 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.27+7981A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218715 | |||||||
| chr7:116219011 | C | G | 283 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(280): Show |
378 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.27+8277C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219011 | |||||||
| chr7:116219022 | G | A | 1 | a0001c0002t0001g0148 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.27+8288G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219022 | |||||||
| chr7:116219103 | G | T | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+8369G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219103 | |||||||
| chr7:116219108 | G | T | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+8374G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219108 | |||||||
| chr7:116219113 | C | G | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.27+8379C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219113 | |||||||
| chr7:116219347 | GAGCTAGT others(3): Show |
G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+8616_27+8625del others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116219347 | ||||||
| chr7:116219540 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+8806A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219540 | |||||||
| chr7:116220225 | G | A | 1 | a0002c0003t0001g0149 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.27+9491G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220225 | |||||||
| chr7:116220516 | G | A | 1 | a0001c0001t0005g0213 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.27+9782G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220516 | |||||||
| chr7:116220719 | C | A | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+9985C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220719 | |||||||
| chr7:116220729 | A | T | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+9995A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220729 | |||||||
| chr7:116220771 | G | A | 3 | a0001c0001t0005g0264 a0001c0001t0005g0265 a0001c0001t0005g0266 |
3 | HG02683.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.27+10037G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220771 | |||||||
| chr7:116220880 | A | G | 52 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(49): Show |
71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.27+10146A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220880 | |||||||
| chr7:116220910 | A | G | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.27+10176A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220910 | |||||||
| chr7:116220933 | C | T | 6 | a0001c0001t0003g0068 a0001c0002t0004g0007 a0001c0002t0004g0067 others(3): Show |
9 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+10199C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220933 | |||||||
| chr7:116221156 | A | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+10422A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221156 | |||||||
| chr7:116221348 | G | A | 1 | a0001c0002t0004g0072 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.27+10614G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221348 | |||||||
| chr7:116221592 | T | C | 5 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(2): Show |
6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+10858T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221592 | |||||||
| chr7:116221606 | T | C | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+10872T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221606 | |||||||
| chr7:116221631 | A | T | 1 | a0001c0001t0003g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.27+10897A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221631 | |||||||
| chr7:116221718 | C | T | 1 | a0001c0001t0005g0284 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.27+10984C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221718 | |||||||
| chr7:116221792 | G | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0011 others(6): Show |
21 | HG00438.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.27+11058G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221792 | |||||||
| chr7:116222238 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.27+11504G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222238 | |||||||
| chr7:116222242 | A | T | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+11508A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222242 | |||||||
| chr7:116222281 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.27+11547C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222281 | |||||||
| chr7:116222286 | T | C | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+11552T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222286 | |||||||
| chr7:116222350 | C | T | 1 | a0001c0002t0004g0028 | 2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.27+11616C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222350 | |||||||
| chr7:116222848 | A | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-11686A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222848 | |||||||
| chr7:116222917 | C | T | 1 | a0001c0002t0001g0203 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.28-11617C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222917 | |||||||
| chr7:116222920 | A | G | 3 | a0001c0001t0003g0058 a0001c0001t0003g0255 a0001c0001t0003g0256 |
3 | HG02027.hp1 NA18747.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.28-11614A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222920 | |||||||
| chr7:116222981 | G | A | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-11553G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222981 | |||||||
| chr7:116223260 | T | C | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.28-11274T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223260 | |||||||
| chr7:116223340 | C | T | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-11194C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223340 | |||||||
| chr7:116223387 | A | G | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.28-11147A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223387 | |||||||
| chr7:116223392 | G | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-11142G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223392 | |||||||
| chr7:116223416 | T | C | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-11118T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223416 | |||||||
| chr7:116223569 | G | A | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.28-10965G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223569 | |||||||
| chr7:116223571 | G | A | 1 | a0001c0001t0003g0046 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.28-10963G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223571 | |||||||
| chr7:116223949 | T | C | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-10585T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223949 | |||||||
| chr7:116224156 | G | A | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-10378G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224156 | |||||||
| chr7:116224158 | G | A | 35 | a0001c0002t0004g0003 a0001c0002t0004g0008 a0001c0002t0004g0021 others(32): Show |
48 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.28-10376G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224158 | |||||||
| chr7:116224278 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-10256A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224278 | |||||||
| chr7:116224331 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0253 a0001c0001t0003g0254 |
6 | HG01175.hp2 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-10203A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224331 | |||||||
| chr7:116224342 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-10192A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224342 | |||||||
| chr7:116224469 | G | A | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.28-10065G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224469 | |||||||
| chr7:116224692 | G | A | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(90): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.28-9842G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224692 | |||||||
| chr7:116224696 | T | C | 1 | a0001c0002t0004g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.28-9838T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224696 | |||||||
| chr7:116224828 | C | T | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-9706C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224828 | |||||||
| chr7:116224835 | C | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-9699C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224835 | |||||||
| chr7:116224869 | G | A | 2 | a0001c0001t0005g0267 a0001c0001t0005g0268 |
2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.28-9665G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224869 | |||||||
| chr7:116224870 | GA | G | 197 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(194): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.28-9655delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116224870 | ||||||
| chr7:116224987 | A | G | 1 | a0001c0001t0003g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.28-9547A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224987 | |||||||
| chr7:116225121 | A | T | 4 | a0001c0002t0001g0114 a0001c0002t0001g0115 a0001c0002t0001g0116 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-9413A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225121 | |||||||
| chr7:116225172 | T | TAAAAACA others(313): Show |
1 | a0001c0002t0001g0153 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(302): Show |
1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(309): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(311): Show |
1 | a0001c0002t0006g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(318): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(310): Show |
2 | a0001c0002t0006g0105 a0001c0002t0006g0106 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(317): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(314): Show |
17 | a0001c0002t0001g0108 a0001c0002t0001g0118 a0001c0002t0001g0154 others(14): Show |
17 | HG00408.hp1 HG00609.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(321): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(313): Show |
65 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(62): Show |
84 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(312): Show |
5 | a0001c0002t0001g0201 a0001c0002t0006g0020 a0001c0002t0006g0029 others(2): Show |
7 | HG02280.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(319): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(314): Show |
1 | a0001c0002t0001g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(321): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(313): Show |
1 | a0001c0002t0001g0152 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(313): Show |
1 | a0001c0002t0001g0202 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225172 | T | TAAAAACA others(314): Show |
1 | a0001c0002t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(321): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | ||||||
| chr7:116225196 | C | A | 3 | a0001c0001t0003g0209 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG01255.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28-9338C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225196 | |||||||
| chr7:116225458 | G | C | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.28-9076G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225458 | |||||||
| chr7:116225537 | A | G | 1 | a0001c0002t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.28-8997A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225537 | |||||||
| chr7:116225569 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.28-8965C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225569 | |||||||
| chr7:116225684 | A | G | 1 | a0001c0002t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-8850A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225684 | |||||||
| chr7:116225794 | G | A | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-8740G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225794 | |||||||
| chr7:116226300 | A | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-8234A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226300 | |||||||
| chr7:116226480 | A | G | 2 | a0001c0001t0002g0040 a0001c0002t0008g0138 |
3 | HG02165.hp2 NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.28-8054A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226480 | |||||||
| chr7:116226502 | G | A | 1 | a0001c0001t0002g0019 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.28-8032G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226502 | |||||||
| chr7:116226517 | C | T | 1 | a0001c0001t0003g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.28-8017C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226517 | |||||||
| chr7:116226518 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.28-8016G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226518 | |||||||
| chr7:116226734 | G | A | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-7800G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226734 | |||||||
| chr7:116226768 | C | A | 1 | a0001c0001t0002g0033 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.28-7766C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226768 | |||||||
| chr7:116226820 | G | T | 1 | a0001c0001t0003g0250 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.28-7714G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226820 | |||||||
| chr7:116226826 | A | G | 72 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(69): Show |
89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.28-7708A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226826 | |||||||
| chr7:116226944 | G | A | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.28-7590G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226944 | |||||||
| chr7:116227088 | T | TTTTA | 7 | a0001c0001t0005g0049 a0001c0001t0005g0222 a0001c0001t0005g0223 others(4): Show |
8 | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-7403_28-7400dup others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | ||||||
| chr7:116227088 | TTTTA | T | 66 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(63): Show |
100 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.28-7403_28-7400del others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | ||||||
| chr7:116227088 | TTTTATTT others(1): Show |
T | 10 | a0001c0001t0002g0123 a0001c0001t0003g0258 a0001c0002t0001g0060 others(7): Show |
11 | HG00423.hp1 HG00733.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-7407_28-7400del others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | ||||||
| chr7:116227088 | TTTTATTT others(5): Show |
T | 186 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(183): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.28-7411_28-7400del others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | ||||||
| chr7:116227088 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0003g0228 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-7415_28-7400del others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | ||||||
| chr7:116227088 | TTTTATTT others(13): Show |
T | 2 | a0001c0001t0003g0209 a0001c0002t0001g0170 |
2 | HG01255.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.28-7419_28-7400del others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | ||||||
| chr7:116227241 | C | T | 95 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(92): Show |
116 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.28-7293C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227241 | |||||||
| chr7:116227272 | G | A | 2 | a0001c0002t0004g0074 a0001c0002t0004g0075 |
2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.28-7262G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227272 | |||||||
| chr7:116227318 | T | G | 1 | a0001c0001t0002g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-7216T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227318 | |||||||
| chr7:116227446 | A | G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-7088A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227446 | |||||||
| chr7:116227485 | C | T | 6 | a0001c0002t0004g0003 a0001c0002t0004g0093 a0001c0002t0004g0094 others(3): Show |
10 | HG00408.hp2 HG00438.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-7049C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227485 | |||||||
| chr7:116227486 | G | A | 1 | a0001c0002t0004g0076 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-7048G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227486 | |||||||
| chr7:116227693 | A | G | 2 | a0001c0002t0004g0070 a0001c0002t0004g0071 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.28-6841A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227693 | |||||||
| chr7:116227703 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-6831A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227703 | |||||||
| chr7:116227728 | A | G | 3 | a0001c0002t0006g0029 a0001c0002t0006g0102 a0001c0002t0006g0103 |
4 | HG02622.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6806A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227728 | |||||||
| chr7:116227839 | G | A | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-6695G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227839 | |||||||
| chr7:116227999 | C | CT | 47 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0002t0004g0003 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-6527dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227999 | ||||||
| chr7:116227999 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.28-6516_28-6503del others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227999 | ||||||
| chr7:116228008 | G | GT | 20 | a0001c0001t0003g0055 a0001c0001t0005g0047 a0001c0001t0005g0048 others(17): Show |
24 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.28-6513dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228008 | ||||||
| chr7:116228008 | G | T | 5 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 others(2): Show |
6 | HG01358.hp2 HG02559.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-6526G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228008 | |||||||
| chr7:116228019 | T | G | 1 | a0001c0002t0004g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.28-6515T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228019 | |||||||
| chr7:116228021 | T | G | 1 | a0001c0002t0001g0171 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.28-6513T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228021 | |||||||
| chr7:116228022 | G | GT | 95 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(92): Show |
116 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.28-6503dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228022 | ||||||
| chr7:116228022 | G | T | 1 | a0001c0002t0001g0171 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.28-6512G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228022 | |||||||
| chr7:116228255 | A | G | 10 | a0001c0001t0005g0049 a0001c0001t0005g0213 a0001c0001t0005g0219 others(7): Show |
11 | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-6279A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228255 | |||||||
| chr7:116228318 | A | G | 1 | a0001c0001t0005g0280 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.28-6216A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228318 | |||||||
| chr7:116228663 | T | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-5871T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228663 | |||||||
| chr7:116228744 | T | C | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-5790T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228744 | |||||||
| chr7:116228779 | T | G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-5755T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228779 | |||||||
| chr7:116228861 | C | A | 5 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(2): Show |
6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5673C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228861 | |||||||
| chr7:116228885 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-5649A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228885 | |||||||
| chr7:116228917 | C | T | 1 | a0001c0001t0005g0279 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.28-5617C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228917 | |||||||
| chr7:116228998 | C | CTATATAT others(3): Show |
1 | a0001c0001t0007g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28-5509_28-5500dup others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | C | CTATATAT others(9): Show |
1 | a0002c0003t0001g0014 | 3 | NA18989.hp2 NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.28-5515_28-5500dup others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | C | CTATATAT others(11): Show |
5 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0002t0001g0044 others(2): Show |
6 | HG00423.hp2 HG02559.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5517_28-5500dup others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | C | CTATATAT others(13): Show |
1 | a0001c0001t0007g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-5519_28-5500dup others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | C | CTATATAT others(15): Show |
1 | a0002c0003t0001g0197 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.28-5521_28-5500dup others(22): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | C | CTATATAT others(19): Show |
4 | a0001c0002t0006g0113 a0002c0003t0001g0149 a0002c0003t0001g0166 others(1): Show |
4 | HG03209.hp2 NA18999.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-5525_28-5500dup others(26): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | C | CTATATAT others(21): Show |
1 | a0002c0003t0001g0199 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.28-5527_28-5500dup others(28): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | CTA | C | 8 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0135 others(5): Show |
12 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-5501_28-5500del others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | CTATA | C | 21 | a0001c0001t0002g0038 a0001c0001t0002g0121 a0001c0001t0002g0134 others(18): Show |
27 | HG00280.hp2 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.28-5503_28-5500del others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | CTATATA | C | 73 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(70): Show |
107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.28-5505_28-5500del others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | CTATATAT others(1): Show |
C | 67 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(64): Show |
94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.28-5507_28-5500del others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | CTATATAT others(3): Show |
C | 20 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(17): Show |
23 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.28-5509_28-5500del others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116228998 | CTATATAT others(13): Show |
C | 1 | a0001c0002t0001g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.28-5519_28-5500del others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | ||||||
| chr7:116229025 | TATATATA others(3): Show |
T | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-5508_28-5499del others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229025 | |||||||
| chr7:116229033 | T | A | 10 | a0001c0001t0005g0056 a0001c0002t0001g0001 a0001c0002t0001g0060 others(7): Show |
11 | HG00408.hp1 HG02155.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.28-5501T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229033 | |||||||
| chr7:116229033 | T | TAA | 5 | a0001c0002t0006g0029 a0001c0002t0006g0102 a0001c0002t0006g0104 others(2): Show |
6 | HG02258.hp2 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-5500_28-5499dup others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(1): Show |
12 | a0001c0002t0001g0001 a0001c0002t0001g0107 a0001c0002t0001g0156 others(9): Show |
16 | HG00544.hp1 HG02015.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(3): Show |
4 | a0001c0002t0001g0059 a0001c0002t0001g0175 a0001c0002t0001g0202 others(1): Show |
4 | HG02071.hp1 NA18906.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(5): Show |
7 | a0001c0002t0001g0006 a0001c0002t0001g0030 a0001c0002t0001g0163 others(4): Show |
7 | HG00544.hp2 HG00609.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(7): Show |
6 | a0001c0002t0001g0006 a0001c0002t0001g0148 a0001c0002t0001g0170 others(3): Show |
6 | HG00558.hp1 HG02074.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(9): Show |
1 | a0001c0002t0001g0006 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(11): Show |
5 | a0001c0002t0001g0110 a0001c0002t0001g0114 a0001c0002t0001g0186 others(2): Show |
5 | HG01433.hp2 HG02129.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(13): Show |
5 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0183 others(2): Show |
7 | HG00733.hp1 HG01099.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(15): Show |
6 | a0001c0002t0001g0031 a0001c0002t0001g0109 a0001c0002t0001g0151 others(3): Show |
7 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(22): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(17): Show |
5 | a0001c0002t0001g0108 a0001c0002t0001g0150 a0001c0002t0001g0165 others(2): Show |
5 | HG02055.hp1 HG02647.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(24): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(18): Show |
1 | a0001c0002t0001g0001 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(25): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(19): Show |
8 | a0001c0002t0001g0115 a0001c0002t0001g0116 a0001c0002t0001g0119 others(5): Show |
8 | HG00639.hp1 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(26): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(21): Show |
7 | a0001c0002t0001g0042 a0001c0002t0001g0043 a0001c0002t0001g0117 others(4): Show |
8 | HG01256.hp1 HG01934.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(28): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(23): Show |
5 | a0001c0002t0001g0153 a0001c0002t0001g0158 a0001c0002t0001g0167 others(2): Show |
5 | HG00280.hp1 HG03098.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(30): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(25): Show |
3 | a0001c0002t0001g0018 a0001c0002t0001g0152 a0001c0002t0001g0193 |
4 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(32): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(27): Show |
2 | a0001c0002t0001g0043 a0001c0002t0010g0205 |
2 | HG01952.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(34): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(29): Show |
1 | a0001c0002t0001g0164 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(36): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229033 | T | TATATATA others(31): Show |
1 | a0001c0002t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(38): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | ||||||
| chr7:116229034 | A | ATATATAT others(28): Show |
2 | a0001c0002t0001g0006 a0001c0002t0001g0185 |
2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(35): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229034 | |||||||
| chr7:116229145 | T | G | 1 | a0001c0002t0006g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-5389T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229145 | |||||||
| chr7:116229155 | T | C | 1 | a0001c0001t0005g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28-5379T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229155 | |||||||
| chr7:116229179 | C | A | 1 | a0001c0001t0003g0230 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.28-5355C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229179 | |||||||
| chr7:116229205 | G | A | 1 | a0001c0001t0002g0033 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.28-5329G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229205 | |||||||
| chr7:116229274 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-5260A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229274 | |||||||
| chr7:116229323 | C | G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-5211C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229323 | |||||||
| chr7:116229374 | G | C | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-5160G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229374 | |||||||
| chr7:116229589 | T | C | 35 | a0001c0002t0004g0003 a0001c0002t0004g0008 a0001c0002t0004g0021 others(32): Show |
48 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.28-4945T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229589 | |||||||
| chr7:116229806 | A | G | 2 | a0001c0002t0006g0112 a0001c0002t0006g0113 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28-4728A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229806 | |||||||
| chr7:116229948 | T | C | 4 | a0001c0002t0001g0156 a0001c0002t0001g0175 a0001c0002t0001g0176 others(1): Show |
4 | NA18941.hp1 NA18944.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-4586T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229948 | |||||||
| chr7:116229956 | A | C | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-4578A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229956 | |||||||
| chr7:116230002 | A | G | 5 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4532A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230002 | |||||||
| chr7:116230074 | T | C | 1 | a0001c0002t0001g0178 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.28-4460T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230074 | |||||||
| chr7:116230079 | C | G | 1 | a0001c0001t0002g0124 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-4455C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230079 | |||||||
| chr7:116230083 | A | G | 1 | a0002c0003t0001g0166 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.28-4451A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230083 | |||||||
| chr7:116230211 | C | T | 18 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(15): Show |
21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.28-4323C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230211 | |||||||
| chr7:116230788 | TC | T | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-3744delC | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116230788 | ||||||
| chr7:116230904 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.28-3630C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230904 | |||||||
| chr7:116230907 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-3627C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230907 | |||||||
| chr7:116231355 | A | T | 1 | a0001c0002t0009g0032 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.28-3179A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231355 | |||||||
| chr7:116231480 | A | T | 1 | a0001c0002t0001g0173 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.28-3054A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231480 | |||||||
| chr7:116231490 | C | CAGAGATG others(2): Show |
148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-3041_28-3040ins others(9): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116231490 | ||||||
| chr7:116231498 | C | T | 1 | a0001c0002t0001g0043 | 2 | HG01256.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.28-3036C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231498 | |||||||
| chr7:116231821 | A | G | 1 | a0001c0002t0004g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.28-2713A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231821 | |||||||
| chr7:116232027 | C | T | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-2507C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232027 | |||||||
| chr7:116232351 | T | C | 18 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(15): Show |
21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.28-2183T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232351 | |||||||
| chr7:116232354 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.28-2180A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232354 | |||||||
| chr7:116232556 | A | AAC | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-1977_28-1976dup others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116232556 | ||||||
| chr7:116232666 | C | G | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.28-1868C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232666 | |||||||
| chr7:116232715 | CAATTT | C | 3 | a0001c0001t0005g0269 a0001c0001t0005g0270 a0001c0001t0005g0283 |
3 | HG00735.hp1 HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.28-1814_28-1810del others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116232715 | ||||||
| chr7:116232816 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.28-1718G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232816 | |||||||
| chr7:116233066 | A | G | 1 | a0001c0001t0005g0275 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.28-1468A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233066 | |||||||
| chr7:116233098 | G | A | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-1436G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233098 | |||||||
| chr7:116233116 | T | A | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-1418T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233116 | |||||||
| chr7:116233228 | T | C | 3 | a0001c0001t0003g0209 a0001c0001t0003g0228 a0001c0001t0003g0229 |
3 | HG01255.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28-1306T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233228 | |||||||
| chr7:116233231 | A | G | 2 | a0001c0002t0004g0028 a0001c0002t0004g0091 |
3 | HG02040.hp1 NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.28-1303A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233231 | |||||||
| chr7:116233347 | A | G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-1187A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233347 | |||||||
| chr7:116233614 | A | G | 1 | a0001c0002t0001g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.28-920A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233614 | |||||||
| chr7:116233644 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0122 a0001c0001t0002g0134 others(1): Show |
5 | HG02165.hp2 NA18960.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-890G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233644 | |||||||
| chr7:116234037 | A | T | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-497A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234037 | |||||||
| chr7:116234261 | T | A | 3 | a0001c0002t0006g0020 a0001c0002t0006g0061 a0001c0002t0006g0062 |
4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-273T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234261 | |||||||
| chr7:116234356 | G | A | 1 | a0001c0001t0005g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-178G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234356 | |||||||
| chr7:116234381 | T | C | 2 | a0001c0002t0006g0029 a0001c0002t0006g0102 |
3 | HG03195.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28-153T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234381 | |||||||
| chr7:116234412 | T | C | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-122T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234412 | |||||||
| chr7:116234506 | C | T | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-28C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234506 | |||||||
| chr7:116234668 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.113+49A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116234668 | |||||||
| chr7:116234675 | C | T | 1 | a0001c0002t0010g0205 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.113+56C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116234675 | |||||||
| chr7:116234755 | A | C | 1 | a0001c0001t0002g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.113+136A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116234755 | |||||||
| chr7:116234763 | TAA | T | 215 | a0001c0001t0002g0133 a0001c0001t0003g0012 a0001c0001t0003g0013 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.113+148_113+149del others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116234763 | ||||||
| chr7:116234953 | C | CT | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+343dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116234953 | ||||||
| chr7:116235046 | C | T | 1 | a0001c0001t0003g0240 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.113+427C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235046 | |||||||
| chr7:116235098 | G | A | 2 | a0001c0001t0007g0065 a0001c0002t0006g0288 |
2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.113+479G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235098 | |||||||
| chr7:116235107 | C | CTAAT | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.113+490_113+493dup others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116235107 | ||||||
| chr7:116235305 | G | C | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+686G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235305 | |||||||
| chr7:116235317 | C | T | 2 | a0001c0002t0001g0192 a0001c0002t0001g0193 |
2 | HG01934.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.113+698C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235317 | |||||||
| chr7:116235578 | T | G | 1 | a0001c0001t0007g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113+959T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235578 | |||||||
| chr7:116235637 | A | ATAGTGGT others(11): Show |
1 | a0001c0002t0004g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.113+1019_113+1036d others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116235637 | ||||||
| chr7:116235678 | G | C | 1 | a0001c0001t0005g0269 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.113+1059G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235678 | |||||||
| chr7:116235714 | TGGCAGCT others(9): Show |
T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0141 |
3 | NA18981.hp1 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.113+1098_113+1113d others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116235714 | ||||||
| chr7:116235887 | T | C | 15 | a0001c0001t0005g0017 a0001c0001t0005g0264 a0001c0001t0005g0265 others(12): Show |
17 | HG00280.hp2 HG00735.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.113+1268T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235887 | |||||||
| chr7:116236050 | G | T | 1 | a0001c0002t0006g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113+1431G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236050 | |||||||
| chr7:116236084 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+1465A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236084 | |||||||
| chr7:116236283 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.113+1664C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236283 | |||||||
| chr7:116236311 | C | T | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+1692C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236311 | |||||||
| chr7:116236381 | T | C | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+1762T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236381 | |||||||
| chr7:116236425 | A | G | 1 | a0001c0001t0005g0218 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.113+1806A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236425 | |||||||
| chr7:116236501 | T | G | 1 | a0001c0001t0003g0046 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.113+1882T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236501 | |||||||
| chr7:116236580 | A | G | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.113+1961A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236580 | |||||||
| chr7:116236627 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+2008A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236627 | |||||||
| chr7:116236648 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113+2029C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236648 | |||||||
| chr7:116236649 | G | A | 1 | a0001c0002t0001g0179 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.113+2030G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236649 | |||||||
| chr7:116236665 | C | T | 18 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(15): Show |
21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.113+2046C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236665 | |||||||
| chr7:116237231 | G | T | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+2612G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237231 | |||||||
| chr7:116237379 | C | A | 1 | a0001c0002t0004g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.113+2760C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237379 | |||||||
| chr7:116237524 | T | G | 1 | a0001c0001t0002g0034 | 2 | NA18949.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.113+2905T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237524 | |||||||
| chr7:116237606 | A | G | 86 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(83): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.113+2987A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237606 | |||||||
| chr7:116237747 | GCCAACAT others(53): Show |
G | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3132_113+3191d others(62): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116237747 | ||||||
| chr7:116237750 | A | G | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3131A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237750 | |||||||
| chr7:116237812 | G | T | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3193G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237812 | |||||||
| chr7:116237813 | T | A | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3194T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237813 | |||||||
| chr7:116237815 | C | A | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3196C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237815 | |||||||
| chr7:116237816 | T | A | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3197T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237816 | |||||||
| chr7:116237819 | C | T | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3200C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237819 | |||||||
| chr7:116237820 | A | G | 46 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(43): Show |
64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.113+3201A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237820 | |||||||
| chr7:116237824 | C | T | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3205C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237824 | |||||||
| chr7:116237825 | C | T | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3206C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237825 | |||||||
| chr7:116237826 | T | A | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3207T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237826 | |||||||
| chr7:116237830 | C | CAACCTTT others(53): Show |
1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3211_113+3212i others(62): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237830 | |||||||
| chr7:116237831 | T | G | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3212T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237831 | |||||||
| chr7:116237833 | G | A | 1 | a0001c0002t0004g0088 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3214G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237833 | |||||||
| chr7:116237843 | G | GGT | 147 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(144): Show |
187 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.113+3239_113+3240d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116237843 | ||||||
| chr7:116238066 | C | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113+3447C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238066 | |||||||
| chr7:116238177 | C | G | 1 | a0001c0002t0004g0083 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.113+3558C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238177 | |||||||
| chr7:116238268 | A | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0137 |
6 | HG01346.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+3649A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238268 | |||||||
| chr7:116238438 | T | G | 1 | a0001c0001t0003g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+3819T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238438 | |||||||
| chr7:116238458 | A | G | 86 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(83): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.113+3839A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238458 | |||||||
| chr7:116238468 | G | A | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.113+3849G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238468 | |||||||
| chr7:116238479 | CTA | C | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+3862_113+3863d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238479 | ||||||
| chr7:116238585 | C | CATCATTA others(5): Show |
3 | a0001c0002t0006g0020 a0001c0002t0006g0061 a0001c0002t0006g0062 |
4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3968_113+3969i others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATT | 5 | a0001c0001t0002g0126 a0001c0001t0003g0209 a0001c0001t0003g0228 others(2): Show |
5 | HG00609.hp1 HG01255.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+3994_113+3996d others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATTATT | 40 | a0001c0001t0003g0068 a0001c0001t0003g0246 a0001c0001t0005g0273 others(37): Show |
55 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.113+3991_113+3996d others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATTATTA others(2): Show |
40 | a0001c0001t0003g0013 a0001c0001t0003g0015 a0001c0001t0003g0016 others(37): Show |
54 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.113+3988_113+3996d others(11): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATTATTA others(5): Show |
36 | a0001c0001t0003g0210 a0001c0001t0003g0242 a0001c0001t0003g0258 others(33): Show |
42 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.113+3985_113+3996d others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATTATTA others(8): Show |
53 | a0001c0001t0003g0232 a0001c0002t0001g0001 a0001c0002t0001g0006 others(50): Show |
67 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+3982_113+3996d others(17): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATTATTA others(11): Show |
3 | a0001c0002t0001g0042 a0001c0002t0001g0181 a0001c0002t0001g0203 |
4 | HG02165.hp1 NA18977.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3979_113+3996d others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238585 | C | CATTATTA others(14): Show |
2 | a0001c0002t0001g0180 a0001c0002t0001g0195 |
2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.113+3976_113+3996d others(23): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | ||||||
| chr7:116238588 | T | C | 6 | a0001c0002t0004g0026 a0001c0002t0004g0027 a0001c0002t0004g0098 others(3): Show |
8 | HG02809.hp1 HG02970.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+3969T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238588 | |||||||
| chr7:116238596 | T | TTATTATT others(7): Show |
1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113+3979_113+3992d others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238596 | ||||||
| chr7:116238616 | T | A | 50 | a0001c0001t0003g0068 a0001c0001t0007g0045 a0001c0001t0007g0207 others(47): Show |
69 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.113+3997T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238616 | |||||||
| chr7:116238756 | C | T | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+4137C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238756 | |||||||
| chr7:116238775 | A | C | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+4156A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238775 | |||||||
| chr7:116239113 | T | C | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.113+4494T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239113 | |||||||
| chr7:116239386 | A | G | 2 | a0001c0002t0001g0162 a0001c0002t0001g0189 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.113+4767A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239386 | |||||||
| chr7:116239478 | G | A | 1 | a0001c0002t0001g0173 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.113+4859G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239478 | |||||||
| chr7:116239511 | C | G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113+4892C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239511 | |||||||
| chr7:116239648 | G | A | 1 | a0001c0001t0005g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.113+5029G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239648 | |||||||
| chr7:116239754 | G | A | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113+5135G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239754 | |||||||
| chr7:116239884 | A | T | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+5265A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239884 | |||||||
| chr7:116239885 | G | GT | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+5268dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116239885 | ||||||
| chr7:116239920 | C | T | 2 | a0001c0002t0001g0161 a0001c0002t0001g0188 |
2 | NA18978.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.113+5301C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239920 | |||||||
| chr7:116240223 | G | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+5604G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240223 | |||||||
| chr7:116240315 | G | A | 1 | a0001c0002t0006g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113+5696G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240315 | |||||||
| chr7:116240386 | T | C | 6 | a0001c0002t0006g0020 a0001c0002t0006g0029 a0001c0002t0006g0061 others(3): Show |
8 | HG02280.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+5767T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240386 | |||||||
| chr7:116240434 | G | T | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.113+5815G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240434 | |||||||
| chr7:116240465 | C | A | 1 | a0001c0001t0003g0050 | 2 | NA18970.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.113+5846C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240465 | |||||||
| chr7:116240484 | G | A | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+5865G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240484 | |||||||
| chr7:116240723 | C | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0037 a0001c0001t0002g0139 others(1): Show |
9 | NA18944.hp1 NA18946.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.113+6104C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240723 | |||||||
| chr7:116241105 | G | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+6486G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241105 | |||||||
| chr7:116241218 | G | A | 1 | a0001c0001t0005g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113+6599G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241218 | |||||||
| chr7:116241351 | T | C | 3 | a0001c0001t0003g0012 a0001c0001t0003g0230 a0001c0001t0003g0239 |
6 | HG00621.hp1 NA18946.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+6732T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241351 | |||||||
| chr7:116241386 | T | A | 1 | a0001c0001t0005g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113+6767T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241386 | |||||||
| chr7:116241404 | A | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+6785A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241404 | |||||||
| chr7:116241482 | G | A | 3 | a0001c0002t0006g0020 a0001c0002t0006g0061 a0001c0002t0006g0062 |
4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+6863G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241482 | |||||||
| chr7:116241625 | A | G | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.113+7006A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241625 | |||||||
| chr7:116241653 | G | A | 1 | a0001c0002t0006g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113+7034G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241653 | |||||||
| chr7:116241686 | T | A | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7067T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241686 | |||||||
| chr7:116241689 | G | GTA | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7070_113+7071i others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241689 | |||||||
| chr7:116241690 | G | T | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7071G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241690 | |||||||
| chr7:116241691 | T | G | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7072T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241691 | |||||||
| chr7:116241881 | T | C | 1 | a0001c0001t0005g0222 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114-7139T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241881 | |||||||
| chr7:116242269 | G | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-6751G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242269 | |||||||
| chr7:116242469 | A | G | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.114-6551A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242469 | |||||||
| chr7:116242507 | A | ATC | 15 | a0001c0001t0002g0035 a0001c0001t0002g0040 a0001c0001t0002g0120 others(12): Show |
17 | HG00423.hp1 HG00639.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.114-6483_114-6482d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242507 | ||||||
| chr7:116242507 | ATCTC | A | 63 | a0001c0001t0003g0068 a0001c0001t0005g0047 a0001c0001t0005g0048 others(60): Show |
84 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.114-6485_114-6482d others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242507 | ||||||
| chr7:116242507 | ATCTCTC | A | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-6487_114-6482d others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242507 | ||||||
| chr7:116242525 | CTCTCTCT others(13): Show |
C | 92 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(89): Show |
112 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.114-6490_114-6471d others(22): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242525 | ||||||
| chr7:116242527 | C | G | 1 | a0001c0001t0003g0249 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.114-6493C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242527 | |||||||
| chr7:116242527 | CTCTCTCT others(11): Show |
C | 4 | a0001c0002t0001g0031 a0001c0002t0001g0108 a0001c0002t0001g0109 others(1): Show |
5 | HG02615.hp1 HG02647.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-6488_114-6471d others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242527 | ||||||
| chr7:116242529 | CTCTCTCT others(3): Show |
C | 41 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(38): Show |
54 | HG00558.hp2 HG00621.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.114-6485_114-6476d others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242529 | ||||||
| chr7:116242531 | CTCTCTCT others(7): Show |
C | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114-6484_114-6471d others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242531 | ||||||
| chr7:116242533 | CTCTCTG | C | 9 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0054 others(6): Show |
12 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-6476_114-6471d others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242533 | ||||||
| chr7:116242542 | T | C | 1 | a0001c0001t0002g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.114-6478T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242542 | |||||||
| chr7:116242545 | G | C | 51 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(48): Show |
70 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.114-6475G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242545 | |||||||
| chr7:116243399 | T | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-5621T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243399 | |||||||
| chr7:116243477 | T | C | 1 | a0001c0002t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.114-5543T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243477 | |||||||
| chr7:116243531 | C | T | 18 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(15): Show |
21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.114-5489C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243531 | |||||||
| chr7:116243753 | A | G | 3 | a0001c0002t0006g0104 a0001c0002t0006g0105 a0001c0002t0006g0106 |
3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.114-5267A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243753 | |||||||
| chr7:116243878 | A | C | 1 | a0001c0001t0005g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.114-5142A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243878 | |||||||
| chr7:116244024 | G | C | 214 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(211): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.114-4996G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244024 | |||||||
| chr7:116244255 | C | T | 1 | a0001c0002t0001g0203 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.114-4765C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244255 | |||||||
| chr7:116244265 | C | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-4755C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244265 | |||||||
| chr7:116244427 | A | G | 1 | a0001c0002t0001g0187 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.114-4593A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244427 | |||||||
| chr7:116244544 | G | C | 49 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(46): Show |
66 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.114-4476G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244544 | |||||||
| chr7:116244575 | C | T | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-4445C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244575 | |||||||
| chr7:116244728 | A | T | 35 | a0001c0002t0004g0003 a0001c0002t0004g0008 a0001c0002t0004g0021 others(32): Show |
48 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.114-4292A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244728 | |||||||
| chr7:116244747 | A | T | 1 | a0001c0002t0004g0101 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.114-4273A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244747 | |||||||
| chr7:116244873 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114-4147C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244873 | |||||||
| chr7:116245031 | C | T | 1 | a0001c0002t0004g0083 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.114-3989C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245031 | |||||||
| chr7:116245038 | A | G | 1 | a0001c0001t0005g0227 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.114-3982A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245038 | |||||||
| chr7:116245142 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-3878G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245142 | |||||||
| chr7:116245251 | T | C | 2 | a0002c0003t0001g0196 a0002c0003t0001g0197 |
2 | NA18957.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.114-3769T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245251 | |||||||
| chr7:116245256 | C | T | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-3764C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245256 | |||||||
| chr7:116245270 | T | C | 2 | a0001c0002t0001g0151 a0001c0002t0001g0152 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.114-3750T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245270 | |||||||
| chr7:116245298 | C | A | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-3722C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245298 | |||||||
| chr7:116245380 | C | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0137 |
6 | HG01346.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-3640C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245380 | |||||||
| chr7:116245566 | C | T | 2 | a0001c0002t0004g0072 a0001c0002t0004g0082 |
2 | HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.114-3454C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245566 | |||||||
| chr7:116245622 | C | G | 1 | a0001c0002t0001g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.114-3398C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245622 | |||||||
| chr7:116245656 | T | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0137 |
6 | HG01346.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-3364T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245656 | |||||||
| chr7:116245953 | A | C | 215 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(212): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.114-3067A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245953 | |||||||
| chr7:116245955 | C | G | 92 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(89): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.114-3065C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245955 | |||||||
| chr7:116246025 | A | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-2995A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246025 | |||||||
| chr7:116246053 | TC | T | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-2966delC | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246053 | |||||||
| chr7:116246340 | T | C | 1 | a0001c0002t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.114-2680T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246340 | |||||||
| chr7:116246497 | C | G | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-2523C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246497 | |||||||
| chr7:116246511 | A | G | 1 | a0001c0002t0001g0160 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.114-2509A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246511 | |||||||
| chr7:116246553 | C | A | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2467C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246553 | |||||||
| chr7:116246748 | G | A | 6 | a0001c0001t0003g0068 a0001c0002t0004g0007 a0001c0002t0004g0067 others(3): Show |
9 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.114-2272G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246748 | |||||||
| chr7:116246766 | A | C | 1 | a0001c0001t0002g0132 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.114-2254A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246766 | |||||||
| chr7:116246779 | A | G | 1 | a0001c0001t0002g0139 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.114-2241A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246779 | |||||||
| chr7:116246797 | G | C | 1 | a0001c0002t0011g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.114-2223G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246797 | |||||||
| chr7:116246805 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.114-2215A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246805 | |||||||
| chr7:116246868 | C | CTGTG | 144 | a0001c0001t0003g0068 a0001c0002t0001g0001 a0001c0002t0001g0006 others(141): Show |
183 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.114-2150_114-2147d others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246868 | ||||||
| chr7:116246872 | G | GTGTGTA | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-2147_114-2146i others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246872 | ||||||
| chr7:116246874 | A | G | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2146A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246874 | |||||||
| chr7:116246874 | A | T | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-2146A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246874 | |||||||
| chr7:116246877 | T | G | 2 | a0001c0002t0006g0112 a0001c0002t0006g0113 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.114-2143T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246877 | |||||||
| chr7:116246911 | C | T | 1 | a0001c0001t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114-2109C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246911 | |||||||
| chr7:116246913 | A | C | 1 | a0001c0001t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114-2107A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246913 | |||||||
| chr7:116246914 | G | C | 1 | a0001c0001t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114-2106G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246914 | |||||||
| chr7:116246939 | C | G | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.114-2081C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246939 | |||||||
| chr7:116246946 | C | CT | 74 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(71): Show |
93 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.114-2074_114-2073i others(3): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246946 | |||||||
| chr7:116246946 | C | CTT | 19 | a0001c0001t0005g0064 a0001c0002t0001g0155 a0001c0002t0001g0156 others(16): Show |
20 | HG00140.hp1 HG00408.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-2074_114-2073i others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246946 | |||||||
| chr7:116246946 | C | CTTT | 42 | a0001c0002t0001g0172 a0001c0002t0004g0003 a0001c0002t0004g0007 others(39): Show |
60 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.114-2074_114-2073i others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246946 | |||||||
| chr7:116246947 | C | CT | 15 | a0001c0001t0002g0136 a0001c0001t0005g0048 a0001c0001t0005g0213 others(12): Show |
16 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.114-2053dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246947 | ||||||
| chr7:116246947 | C | T | 143 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0002t0001g0001 others(140): Show |
181 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.114-2073C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246947 | |||||||
| chr7:116246947 | CT | C | 49 | a0001c0001t0002g0019 a0001c0001t0002g0128 a0001c0001t0003g0012 others(46): Show |
67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.114-2053delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246947 | ||||||
| chr7:116246970 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.114-2050G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246970 | |||||||
| chr7:116247016 | G | A | 52 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(49): Show |
71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.114-2004G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247016 | |||||||
| chr7:116247144 | A | C | 2 | a0001c0001t0003g0235 a0001c0001t0003g0258 |
2 | HG02083.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.114-1876A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247144 | |||||||
| chr7:116247172 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.114-1848G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247172 | |||||||
| chr7:116247173 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-1847A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247173 | |||||||
| chr7:116247268 | A | T | 1 | a0001c0002t0001g0191 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.114-1752A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247268 | |||||||
| chr7:116247415 | T | C | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114-1605T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247415 | |||||||
| chr7:116247416 | ATTAT | A | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-1597_114-1594d others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116247416 | ||||||
| chr7:116247532 | T | C | 2 | a0001c0002t0004g0022 a0001c0002t0004g0079 |
3 | HG02738.hp1 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.114-1488T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247532 | |||||||
| chr7:116247756 | G | T | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-1264G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247756 | |||||||
| chr7:116247777 | T | G | 1 | a0001c0001t0005g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.114-1243T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247777 | |||||||
| chr7:116247864 | A | G | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-1156A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247864 | |||||||
| chr7:116248014 | G | T | 96 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(93): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.114-1006G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248014 | |||||||
| chr7:116248041 | C | G | 4 | a0001c0002t0004g0093 a0001c0002t0004g0094 a0001c0002t0004g0096 others(1): Show |
4 | NA18942.hp1 NA18978.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-979C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248041 | |||||||
| chr7:116248061 | T | G | 1 | a0001c0002t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.114-959T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248061 | |||||||
| chr7:116248108 | A | G | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-912A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248108 | |||||||
| chr7:116248145 | T | A | 47 | a0001c0001t0003g0068 a0001c0002t0004g0003 a0001c0002t0004g0007 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-875T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248145 | |||||||
| chr7:116248264 | T | G | 2 | a0001c0002t0006g0104 a0001c0002t0006g0105 |
2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114-756T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248264 | |||||||
| chr7:116248285 | G | A | 148 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-735G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248285 | |||||||
| chr7:116248491 | GA | G | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-527delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116248491 | ||||||
| chr7:116248510 | C | T | 1 | a0001c0001t0002g0002 | 6 | HG00438.hp1 NA18940.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-510C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248510 | |||||||
| chr7:116248602 | G | T | 1 | a0001c0001t0005g0265 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.114-418G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248602 | |||||||
| chr7:116248665 | A | T | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-355A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248665 | |||||||
| chr7:116249315 | G | T | 3 | a0001c0002t0001g0155 a0001c0002t0001g0172 a0001c0002t0001g0173 |
3 | HG00408.hp1 NA18940.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.366+43G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249315 | |||||||
| chr7:116249382 | T | A | 1 | a0001c0001t0003g0051 | 2 | NA18953.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.366+110T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249382 | |||||||
| chr7:116249859 | A | G | 52 | a0001c0001t0003g0068 a0001c0001t0005g0064 a0001c0001t0007g0045 others(49): Show |
71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.367-302A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249859 | |||||||
| chr7:116249945 | T | C | 4 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(1): Show |
5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-216T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249945 | |||||||
| chr7:116250002 | C | T | 5 | a0002c0003t0001g0149 a0002c0003t0001g0166 a0002c0003t0001g0196 others(2): Show |
5 | NA18957.hp2 NA18999.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-159C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250002 | |||||||
| chr7:116250056 | A | G | 1 | a0001c0002t0001g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.367-105A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250056 | |||||||
| chr7:116250086 | C | T | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.367-75C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250086 | |||||||
| chr7:116250103 | G | A | 60 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(57): Show |
81 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.367-58G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250103 | |||||||
| chr7:116250133 | A | G | 55 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(52): Show |
72 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.367-28A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250133 | |||||||
| chr7:116250780 | A | G | 184 | a0001c0001t0002g0035 a0001c0001t0003g0012 a0001c0001t0003g0013 others(181): Show |
233 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.702+284A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116250780 | |||||||
| chr7:116251067 | T | C | 1 | a0001c0002t0004g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.702+571T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251067 | |||||||
| chr7:116251091 | G | T | 1 | a0001c0002t0001g0174 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.702+595G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251091 | |||||||
| chr7:116251274 | C | T | 11 | a0001c0002t0004g0007 a0001c0002t0004g0026 a0001c0002t0004g0027 others(8): Show |
16 | HG01109.hp2 HG01256.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-486C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251274 | |||||||
| chr7:116251421 | G | A | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(90): Show |
115 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.703-339G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251421 | |||||||
| chr7:116251459 | A | G | 114 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(111): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.703-301A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251459 | |||||||
| chr7:116251552 | A | G | 1 | a0001c0001t0002g0033 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.703-208A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251552 | |||||||
| chr7:116251573 | C | G | 1 | a0001c0002t0004g0089 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.703-187C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251573 | |||||||
| chr7:116251587 | G | A | 114 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(111): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.703-173G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251587 | |||||||
| chr7:116251593 | G | A | 1 | a0001c0001t0003g0055 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.703-167G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251593 | |||||||
| chr7:116251632 | G | A | 114 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(111): Show |
142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.703-128G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251632 | |||||||
| chr7:116251692 | AAAAG | A | 98 | a0001c0001t0003g0243 a0001c0002t0001g0001 a0001c0002t0001g0006 others(95): Show |
120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.703-56_703-53delGA others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 116251692 | ||||||
| chr7:116251723 | C | T | 1 | a0001c0002t0001g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703-37C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251723 | |||||||
| chr7:116252106 | A | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.918+131A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252106 | |||||||
| chr7:116252224 | C | T | 9 | a0001c0002t0004g0003 a0001c0002t0004g0024 a0001c0002t0004g0066 others(6): Show |
14 | HG00408.hp2 HG00438.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.919-94C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252224 | |||||||
| chr7:116252241 | C | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(95): Show |
120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.919-77C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252241 | |||||||
| chr7:116252291 | C | A | 1 | a0001c0001t0005g0284 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.919-27C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252291 | |||||||
| chr7:116252541 | T | C | 3 | a0001c0002t0004g0008 a0001c0002t0004g0021 a0001c0002t0004g0080 |
7 | NA18612.hp2 NA18959.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+65T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252541 | |||||||
| chr7:116252596 | T | G | 149 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(146): Show |
190 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1077+120T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252596 | |||||||
| chr7:116252641 | A | G | 1 | a0001c0001t0003g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1077+165A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252641 | |||||||
| chr7:116252675 | A | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077+199A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252675 | |||||||
| chr7:116252684 | A | G | 149 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(146): Show |
190 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1077+208A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252684 | |||||||
| chr7:116252703 | G | A | 97 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(94): Show |
119 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1077+227G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252703 | |||||||
| chr7:116252872 | C | A | 2 | a0001c0002t0006g0112 a0001c0002t0006g0113 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1077+396C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252872 | |||||||
| chr7:116252969 | A | G | 1 | a0001c0002t0001g0043 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1077+493A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252969 | |||||||
| chr7:116252991 | A | G | 98 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(95): Show |
120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1077+515A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252991 | |||||||
| chr7:116253039 | A | C | 2 | a0001c0001t0007g0045 a0001c0001t0007g0207 |
3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+563A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253039 | |||||||
| chr7:116253143 | A | G | 1 | a0001c0001t0007g0065 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1077+667A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253143 | |||||||
| chr7:116253308 | A | G | 102 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(99): Show |
125 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1077+832A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253308 | |||||||
| chr7:116253353 | A | T | 145 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(142): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+877A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253353 | |||||||
| chr7:116253428 | T | G | 1 | a0001c0002t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1077+952T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253428 | |||||||
| chr7:116253593 | A | G | 149 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(146): Show |
190 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1077+1117A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253593 | |||||||
| chr7:116253697 | G | A | 1 | a0001c0001t0002g0037 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1077+1221G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253697 | |||||||
| chr7:116253791 | A | C | 145 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(142): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1315A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253791 | |||||||
| chr7:116253822 | C | A | 1 | a0001c0001t0005g0269 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077+1346C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253822 | |||||||
| chr7:116253837 | A | G | 1 | a0001c0002t0006g0112 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1077+1361A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253837 | |||||||
| chr7:116253843 | T | C | 145 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(142): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1367T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253843 | |||||||
| chr7:116253965 | T | C | 5 | a0001c0002t0004g0007 a0001c0002t0004g0067 a0001c0002t0004g0069 others(2): Show |
8 | HG01109.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+1489T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253965 | |||||||
| chr7:116254055 | ACAAGACG others(1): Show |
A | 50 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(47): Show |
67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1077+1583_1077+159 others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254055 | ||||||
| chr7:116254322 | T | C | 145 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(142): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1846T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254322 | |||||||
| chr7:116254324 | C | CT | 145 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(142): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1855dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254324 | ||||||
| chr7:116254349 | C | G | 145 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(142): Show |
185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1873C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254349 | |||||||
| chr7:116254462 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1077+1986A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254462 | |||||||
| chr7:116254473 | C | T | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(96): Show |
121 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1077+1997C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254473 | |||||||
| chr7:116254474 | G | A | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(96): Show |
121 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1077+1998G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254474 | |||||||
| chr7:116254504 | G | A | 18 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(15): Show |
21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1077+2028G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254504 | |||||||
| chr7:116254510 | C | T | 1 | a0001c0001t0003g0055 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1077+2034C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254510 | |||||||
| chr7:116254511 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1077+2035G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254511 | |||||||
| chr7:116254529 | T | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077+2053T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254529 | |||||||
| chr7:116254535 | A | T | 148 | a0001c0001t0005g0264 a0001c0001t0007g0065 a0001c0002t0001g0001 others(145): Show |
188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1077+2059A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254535 | |||||||
| chr7:116254546 | C | T | 1 | a0001c0001t0005g0277 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1077+2070C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254546 | |||||||
| chr7:116254585 | A | C | 1 | a0001c0002t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1077+2109A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254585 | |||||||
| chr7:116254611 | C | G | 1 | a0001c0001t0003g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1077+2135C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254611 | |||||||
| chr7:116254735 | C | T | 1 | a0001c0001t0005g0269 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077+2259C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254735 | |||||||
| chr7:116254740 | CA | C | 8 | a0001c0002t0004g0025 a0001c0002t0004g0027 a0001c0002t0004g0067 others(5): Show |
10 | HG02040.hp1 HG02809.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+2272delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254740 | ||||||
| chr7:116254746 | AAAT | A | 99 | a0001c0002t0001g0006 a0001c0002t0001g0018 a0001c0002t0001g0030 others(96): Show |
124 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1077+2272_1077+227 others(7): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254746 | ||||||
| chr7:116254746 | AAATAT | A | 17 | a0001c0002t0001g0001 a0001c0002t0001g0115 a0001c0002t0001g0155 others(14): Show |
27 | HG00408.hp1 HG00609.hp2 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.1077+2272_1077+227 others(9): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254746 | ||||||
| chr7:116254747 | A | AT | 15 | a0001c0002t0004g0022 a0001c0002t0004g0028 a0001c0002t0004g0070 others(12): Show |
17 | HG00140.hp1 HG00738.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077+2271_1077+227 others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254747 | |||||||
| chr7:116254747 | A | ATAT | 6 | a0001c0002t0001g0165 a0001c0002t0004g0075 a0001c0002t0004g0083 others(3): Show |
7 | HG01081.hp1 HG02486.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077+2271_1077+227 others(7): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254747 | |||||||
| chr7:116254747 | A | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0038 |
2 | NA18951.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1077+2271A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254747 | |||||||
| chr7:116254747 | AAT | A | 9 | a0001c0001t0002g0120 a0001c0001t0002g0135 a0001c0001t0003g0051 others(6): Show |
10 | HG00741.hp1 HG01255.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+2282_1077+228 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254747 | ||||||
| chr7:116254749 | T | A | 1 | a0001c0001t0005g0260 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1077+2273T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254749 | |||||||
| chr7:116254752 | A | G | 5 | a0001c0002t0004g0075 a0001c0002t0004g0083 a0001c0002t0004g0087 others(2): Show |
6 | HG01081.hp1 HG02486.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+2276A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254752 | |||||||
| chr7:116254754 | A | G | 20 | a0001c0002t0001g0165 a0001c0002t0004g0022 a0001c0002t0004g0028 others(17): Show |
23 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1077+2278A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254754 | |||||||
| chr7:116254756 | A | ATG | 21 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0053 others(18): Show |
30 | HG00621.hp1 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1077+2281_1077+228 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | ||||||
| chr7:116254756 | A | ATGTG | 13 | a0001c0001t0003g0015 a0001c0001t0003g0068 a0001c0001t0003g0212 others(10): Show |
16 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+2281_1077+228 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | ||||||
| chr7:116254756 | A | ATGTGTG | 4 | a0001c0001t0003g0055 a0001c0001t0003g0234 a0001c0001t0005g0221 others(1): Show |
5 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+2281_1077+228 others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | ||||||
| chr7:116254756 | A | G | 34 | a0001c0001t0003g0239 a0001c0001t0003g0245 a0001c0001t0003g0258 others(31): Show |
39 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1077+2280A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254756 | |||||||
| chr7:116254756 | ATATGTGT others(7): Show |
A | 1 | a0001c0001t0003g0237 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1077+2282_1077+229 others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | ||||||
| chr7:116254758 | A | ATG | 11 | a0001c0001t0002g0036 a0001c0001t0002g0038 a0001c0001t0002g0124 others(8): Show |
13 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077+2320_1077+232 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | ||||||
| chr7:116254758 | A | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0143 others(109): Show |
157 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1077+2282A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254758 | |||||||
| chr7:116254758 | ATG | A | 4 | a0001c0001t0002g0130 a0001c0001t0005g0064 a0001c0001t0005g0283 others(1): Show |
4 | HG03491.hp2 HG03579.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+2320_1077+232 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | ||||||
| chr7:116254758 | ATGTG | A | 65 | a0001c0001t0005g0265 a0001c0002t0001g0006 a0001c0002t0001g0018 others(62): Show |
75 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1077+2318_1077+232 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | ||||||
| chr7:116254758 | ATGTGTG | A | 6 | a0001c0002t0001g0030 a0001c0002t0001g0116 a0001c0002t0001g0118 others(3): Show |
6 | HG02622.hp1 HG03453.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+2316_1077+232 others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | ||||||
| chr7:116254758 | ATGTGTGT others(1): Show |
A | 11 | a0001c0002t0001g0031 a0001c0002t0001g0108 a0001c0002t0006g0020 others(8): Show |
14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1077+2314_1077+232 others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | ||||||
| chr7:116254758 | ATGTGTGT others(3): Show |
A | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1077+2312_1077+232 others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | ||||||
| chr7:116254760 | G | A | 16 | a0001c0001t0007g0045 a0001c0001t0007g0207 a0001c0002t0001g0001 others(13): Show |
26 | HG00408.hp1 HG00609.hp2 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.1077+2284G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254760 | |||||||
| chr7:116254762 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+2286G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254762 | |||||||
| chr7:116254764 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+2288G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254764 | |||||||
| chr7:116254932 | T | C | 1 | a0001c0002t0001g0159 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1078-2362T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254932 | |||||||
| chr7:116254956 | G | T | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-2338G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254956 | |||||||
| chr7:116254974 | T | A | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1078-2320T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254974 | |||||||
| chr7:116255001 | A | AAGAG | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-2289_1078-228 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116255001 | ||||||
| chr7:116255181 | T | C | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-2113T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255181 | |||||||
| chr7:116255379 | T | C | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1915T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255379 | |||||||
| chr7:116255382 | C | T | 50 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(47): Show |
67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-1912C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255382 | |||||||
| chr7:116255461 | T | C | 46 | a0001c0002t0004g0003 a0001c0002t0004g0007 a0001c0002t0004g0008 others(43): Show |
64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1078-1833T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255461 | |||||||
| chr7:116255538 | C | T | 1 | a0001c0001t0005g0218 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1078-1756C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255538 | |||||||
| chr7:116255664 | A | G | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1630A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255664 | |||||||
| chr7:116255697 | A | G | 50 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0015 others(47): Show |
67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-1597A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255697 | |||||||
| chr7:116255768 | T | C | 1 | a0001c0001t0003g0239 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1078-1526T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255768 | |||||||
| chr7:116255834 | A | G | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1078-1460A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255834 | |||||||
| chr7:116255941 | G | GACA | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1352_1078-135 others(7): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116255941 | ||||||
| chr7:116255995 | G | A | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1299G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255995 | |||||||
| chr7:116256037 | C | T | 47 | a0001c0002t0004g0003 a0001c0002t0004g0007 a0001c0002t0004g0008 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078-1257C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256037 | |||||||
| chr7:116256074 | C | CAAAG | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1217_1078-121 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116256074 | ||||||
| chr7:116256139 | A | G | 1 | a0001c0001t0003g0058 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1078-1155A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256139 | |||||||
| chr7:116256198 | C | A | 1 | a0001c0002t0006g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1078-1096C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256198 | |||||||
| chr7:116256312 | CT | C | 99 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(96): Show |
121 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1078-980delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116256312 | ||||||
| chr7:116256353 | A | G | 1 | a0001c0001t0005g0223 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1078-941A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256353 | |||||||
| chr7:116256399 | T | A | 1 | a0001c0002t0006g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1078-895T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256399 | |||||||
| chr7:116256652 | AAC | A | 5 | a0001c0001t0005g0064 a0001c0001t0007g0045 a0001c0001t0007g0065 others(2): Show |
6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-638_1078-637d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116256652 | ||||||
| chr7:116256662 | G | A | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-632G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256662 | |||||||
| chr7:116256690 | G | A | 2 | a0001c0001t0005g0269 a0001c0001t0005g0270 |
2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1078-604G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256690 | |||||||
| chr7:116257042 | T | C | 146 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0018 others(143): Show |
186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-252T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257042 | |||||||
| chr7:116257168 | A | G | 164 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(161): Show |
207 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1078-126A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257168 | |||||||
| chr7:116257181 | G | A | 3 | a0001c0001t0007g0045 a0001c0001t0007g0065 a0001c0001t0007g0207 |
4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-113G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257181 | |||||||
| chr7:116257188 | T | G | 164 | a0001c0001t0005g0047 a0001c0001t0005g0048 a0001c0001t0005g0049 others(161): Show |
207 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1078-106T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257188 | |||||||
| chr7:116257233 | T | G | 47 | a0001c0002t0004g0003 a0001c0002t0004g0007 a0001c0002t0004g0008 others(44): Show |
65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078-61T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257233 |