Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 121793 |
| ensemblid | ENSG00000153495.11 |
| hgncid | 20370 |
| symbol | TEX29 |
| name | testis expressed 29 |
| refseq_nuc | NM_152324.3 |
| refseq_prot | NP_689537.1 |
| ensembl_nuc | ENST00000283547.2 |
| ensembl_prot | ENSP00000283547.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 111320642 |
| end | 111344248 |
| strand | + |
| ver | v1.2 |
| region | chr13:111320642-111344248 |
| region5000 | chr13:111315642-111349248 |
| regionname0 | TEX29_chr13_111320642_111344248 |
| regionname5000 | TEX29_chr13_111315642_111349248 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 151 | 410 | 88 | 78 | 184 | 16 | 42 | 138 | TEX29_chr13_111315642_111349248 | TEX29 | MEYVL others(146): Show |
chr13 | 111315642 | 111349248 |
| a0002 | 0/0 | 151 | 4 | 3 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | MEYVL others(146): Show |
chr13 | 111315642 | 111349248 |
| a0003 | 0/0 | 151 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | MEYVL others(146): Show |
chr13 | 111315642 | 111349248 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 453 | 219 | 21 | 41 | 118 | 9 | 30 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0001c0002 | 1/1 | 453 | 164 | 63 | 30 | 52 | 7 | 10 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0001c0003 | 0/0 | 453 | 21 | 0 | 6 | 13 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0001c0005 | 0/0 | 453 | 3 | 2 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0001c0006 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0001c0008 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0001c0010 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0002c0004 | 0/0 | 453 | 4 | 3 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0003c0007 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 | ||
| a0003c0009 | 0/0 | 453 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | ATGGA others(448): Show |
chr13 | 111315642 | 111349248 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 736 | 74 | 11 | 20 | 17 | 5 | 21 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0002 | 0/0 | 736 | 132 | 1 | 20 | 101 | 4 | 6 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0003 | 0/0 | 736 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0006 | 0/0 | 736 | 3 | 3 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0007 | 0/0 | 736 | 3 | 0 | 1 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0008 | 0/0 | 736 | 3 | 3 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0010 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0001t0011 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0002t0001 | 1/0 | 736 | 102 | 29 | 18 | 41 | 4 | 9 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0002t0002 | 0/0 | 736 | 11 | 0 | 6 | 4 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0002t0003 | 0/1 | 736 | 35 | 18 | 6 | 7 | 2 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0002t0004 | 0/0 | 736 | 9 | 9 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0002t0005 | 0/0 | 733 | 5 | 5 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(728): Show |
chr13 | 111315642 | 111349248 |
| a0001c0002t0009 | 0/0 | 736 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0003t0001 | 0/0 | 736 | 11 | 0 | 6 | 3 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0003t0002 | 0/0 | 736 | 10 | 0 | 0 | 10 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0005t0001 | 0/0 | 736 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0005t0003 | 0/0 | 736 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0006t0002 | 0/0 | 736 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0008t0006 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0001c0010t0001 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0002c0004t0001 | 0/0 | 736 | 4 | 3 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0003c0007t0003 | 0/0 | 736 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| a0003c0009t0001 | 0/0 | 736 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | ATAGT others(731): Show |
chr13 | 111315642 | 111349248 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0001 | 0/0 | 22 | 0 | 4 | 17 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0002 | 0/0 | 11 | 0 | 4 | 5 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0006g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0007g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0010g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0004 | 0/0 | 8 | 0 | 1 | 2 | 2 | 3 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0004g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0002t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0005t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0006t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0008t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0001c0010t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0002c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0002c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0002c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0003c0007t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| a0003c0009t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0100 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | GBR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0052 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0052 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0226 | EUR | FIN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0061 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0025 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0258 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01081 | hp1 | a0001 | c0005 | t0003 | g0137 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0050 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0167 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0165 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0062 | AMR | PUR | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0108 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0285 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0025 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01884 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0139 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02132 | hp1 | a0001 | c0006 | t0002 | g0278 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0053 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0254 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02258 | hp1 | a0002 | c0004 | t0001 | g0030 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0016 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02280 | hp1 | a0001 | c0002 | t0009 | g0275 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0255 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0042 | EAS | KHV | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0161 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0288 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0065 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0051 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0024 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02723 | hp1 | a0003 | c0007 | t0003 | g0256 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0274 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02895 | hp2 | a0002 | c0004 | t0001 | g0164 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0049 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0049 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0021 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0157 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02976 | hp1 | a0001 | c0002 | t0003 | g0044 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0141 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0066 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03130 | hp2 | a0001 | c0002 | t0003 | g0257 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0067 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03209 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0277 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0046 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03516 | hp2 | a0001 | c0008 | t0006 | g0090 | AFR | ESN | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0138 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | GWD | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03579 | hp1 | a0001 | c0002 | t0003 | g0279 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0103 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0267 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0266 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04115 | hp2 | a0003 | c0009 | t0001 | g0242 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | BEB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0076 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18906 | hp1 | a0001 | c0002 | t0009 | g0276 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0193 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18962 | hp1 | a0001 | c0003 | t0002 | g0237 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0039 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0282 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0283 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0281 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18997 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19030 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0280 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0039 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0017 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | YRI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ASW | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | ASW | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0083 | EUR | TSI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0284 | SAS | GIH | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0053 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0253 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02486 | hp2 | a0001 | c0002 | t0003 | g0046 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0140 | AFR | ACB | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG06807 | hp1 | a0001 | c0010 | t0001 | g0126 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | USA | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | LWK | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0060 | REF | REF | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0135 | REF | REF | TEX29_chr13_111315642_111349248 | TEX29 | chr13 | 111315642 | 111349248 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111342757 | G | A | 1 | a0002 | 4 | HG01884.hp1 HG02258.hp1 HG02738.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.241G>A | p.Val81Ile | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 396/736 | 241/456 | 81/151 | chr13 | 111342757 | |||
| chr13:111342802 | G | A | 1 | a0003 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.286G>A | p.Ala96Thr | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 441/736 | 286/456 | 96/151 | chr13 | 111342802 | |||
| chr13:111342803 | C | T | 1 | a0003 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.287C>T | p.Ala96Val | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 442/736 | 287/456 | 96/151 | chr13 | 111342803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111328190 | C | T | 5 | a0001c0001 a0001c0003 a0001c0010 others(2): Show |
246 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(243): Show |
synonymous_variant | LOW | c.66C>T | p.Asp22Asp | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/6 | 221/736 | 66/456 | 22/151 | chr13 | 111328190 | |||
| chr13:111339900 | C | A | 2 | a0001c0003 a0001c0005 |
24 | HG00544.hp2 HG00735.hp1 HG01070.hp2 others(21): Show |
synonymous_variant | LOW | c.207C>A | p.Ile69Ile | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/6 | 362/736 | 207/456 | 69/151 | chr13 | 111339900 | |||
| chr13:111339912 | C | T | 1 | a0001c0008 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.219C>T | p.Phe73Phe | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/6 | 374/736 | 219/456 | 73/151 | chr13 | 111339912 | |||
| chr13:111342822 | C | T | 1 | a0001c0010 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.306C>T | p.Ser102Ser | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 461/736 | 306/456 | 102/151 | chr13 | 111342822 | |||
| chr13:111342903 | G | A | 1 | a0001c0006 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.387G>A | p.Ser129Ser | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/6 | 542/736 | 387/456 | 129/151 | chr13 | 111342903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111320650 | C | T | 1 | a0001c0002t0005 | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-147C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | 241 | chr13 | 111320650 | ||||||
| chr13:111320672 | TTTG | T | 1 | a0001c0002t0005 | 5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-119_-117delGTT | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | 211 | INFO_REALIGN_3_PRIME | chr13 | 111320672 | |||||
| chr13:111320703 | G | A | 7 | a0001c0001t0003 a0001c0001t0010 a0001c0002t0003 others(4): Show |
50 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(47): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | chr13 | 111320703 | |||||||
| chr13:111320751 | T | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(8): Show |
204 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(201): Show |
5_prime_UTR_variant | MODIFIER | c.-46T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/6 | 140 | chr13 | 111320751 | ||||||
| chr13:111344130 | C | T | 1 | a0001c0001t0011 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 7 | chr13 | 111344130 | ||||||
| chr13:111344172 | G | C | 2 | a0001c0001t0007 a0001c0001t0010 |
4 | HG01255.hp2 HG02698.hp2 HG03654.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 49 | chr13 | 111344172 | ||||||
| chr13:111344201 | A | G | 2 | a0001c0001t0008 a0001c0002t0004 |
12 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*78A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 78 | chr13 | 111344201 | ||||||
| chr13:111344221 | G | A | 3 | a0001c0001t0006 a0001c0002t0009 a0001c0008t0006 |
6 | HG02280.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*98G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 6/6 | 98 | chr13 | 111344221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111320850 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.-34-7T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 1/5 | chr13 | 111320850 | |||||||
| chr13:111320974 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0287 a0001c0001t0006g0288 |
4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+26C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111320974 | |||||||
| chr13:111320983 | T | C | 1 | a0001c0002t0001g0056 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.58+35T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111320983 | |||||||
| chr13:111320995 | T | TG | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(157): Show |
235 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.58+56dupG | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111320995 | ||||||
| chr13:111321006 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(179): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.58+58A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321006 | |||||||
| chr13:111321072 | G | A | 1 | a0001c0002t0003g0159 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.58+124G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321072 | |||||||
| chr13:111321107 | G | A | 8 | a0001c0002t0003g0142 a0001c0002t0004g0016 a0001c0002t0004g0034 others(5): Show |
11 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+159G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321107 | |||||||
| chr13:111321115 | G | A | 2 | a0001c0005t0001g0160 a0001c0005t0001g0161 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.58+167G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321115 | |||||||
| chr13:111321198 | A | G | 1 | a0001c0001t0002g0286 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58+250A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321198 | |||||||
| chr13:111321241 | C | T | 28 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0003g0048 others(25): Show |
38 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.58+293C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321241 | |||||||
| chr13:111321242 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.58+294G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321242 | |||||||
| chr13:111321334 | A | C | 81 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0154 others(78): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.58+386A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321334 | |||||||
| chr13:111321365 | C | T | 2 | a0001c0002t0001g0031 a0001c0002t0001g0032 |
4 | NA18950.hp1 NA18957.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+417C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321365 | |||||||
| chr13:111321433 | G | A | 5 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0057 others(2): Show |
11 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+485G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321433 | |||||||
| chr13:111321442 | G | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0166 others(97): Show |
157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.58+494G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321442 | |||||||
| chr13:111321444 | G | A | 1 | a0001c0002t0001g0238 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.58+496G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321444 | |||||||
| chr13:111321469 | T | G | 2 | a0001c0002t0003g0061 a0001c0002t0003g0062 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.58+521T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321469 | |||||||
| chr13:111321625 | C | CAA | 80 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0154 others(77): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+685_58+686dupAA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111321625 | ||||||
| chr13:111321635 | C | A | 2 | a0001c0002t0003g0061 a0001c0002t0003g0062 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.58+687C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321635 | |||||||
| chr13:111321646 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.58+698C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321646 | |||||||
| chr13:111321648 | G | A | 5 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0057 others(2): Show |
11 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+700G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321648 | |||||||
| chr13:111321654 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0166 others(97): Show |
157 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.58+706C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321654 | |||||||
| chr13:111321700 | G | A | 80 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0154 others(77): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+752G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321700 | |||||||
| chr13:111321701 | C | T | 80 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0154 others(77): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+753C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321701 | |||||||
| chr13:111321798 | C | T | 2 | a0001c0005t0001g0160 a0001c0005t0001g0161 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.58+850C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321798 | |||||||
| chr13:111321848 | C | T | 1 | a0001c0003t0002g0237 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.58+900C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321848 | |||||||
| chr13:111321903 | G | A | 2 | a0001c0002t0003g0061 a0001c0002t0003g0062 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.58+955G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321903 | |||||||
| chr13:111321919 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58+971G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321919 | |||||||
| chr13:111321973 | G | C | 18 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0244 others(15): Show |
19 | HG02135.hp1 HG03704.hp2 HG04115.hp2 others(16): Show |
intron_variant | MODIFIER | c.58+1025G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111321973 | |||||||
| chr13:111322049 | GAGCACCT others(9): Show |
G | 2 | a0001c0002t0003g0061 a0001c0002t0003g0062 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.58+1110_58+1125del others(16): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111322049 | ||||||
| chr13:111322084 | T | A | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1136T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322084 | |||||||
| chr13:111322102 | C | T | 84 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0153 others(81): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.58+1154C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322102 | |||||||
| chr13:111322188 | G | T | 17 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0003g0048 others(14): Show |
24 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.58+1240G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322188 | |||||||
| chr13:111322287 | TGGG | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0069 others(18): Show |
27 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.58+1341_58+1343del others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111322287 | ||||||
| chr13:111322308 | C | T | 2 | a0001c0002t0003g0053 a0001c0002t0003g0285 |
3 | HG01261.hp1 HG02109.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.58+1360C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322308 | |||||||
| chr13:111322309 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.58+1361G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322309 | |||||||
| chr13:111322356 | G | GC | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(273): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.58+1410dupC | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111322356 | ||||||
| chr13:111322388 | C | T | 2 | a0001c0002t0001g0252 a0001c0002t0003g0253 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.58+1440C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322388 | |||||||
| chr13:111322459 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.58+1511T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322459 | |||||||
| chr13:111322497 | G | A | 51 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0003g0033 others(48): Show |
73 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+1549G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322497 | |||||||
| chr13:111322543 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.58+1595C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322543 | |||||||
| chr13:111322546 | G | C | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.58+1598G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322546 | |||||||
| chr13:111322860 | T | C | 30 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0003g0048 others(27): Show |
40 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.58+1912T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322860 | |||||||
| chr13:111322883 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.58+1935G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322883 | |||||||
| chr13:111322966 | A | G | 34 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0003g0044 others(31): Show |
45 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.58+2018A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111322966 | |||||||
| chr13:111323054 | T | C | 13 | a0001c0001t0001g0022 a0001c0002t0001g0006 a0001c0002t0001g0011 others(10): Show |
22 | HG00099.hp1 HG01070.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+2106T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323054 | |||||||
| chr13:111323308 | C | A | 1 | a0001c0002t0002g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.58+2360C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323308 | |||||||
| chr13:111323309 | G | A | 31 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0001g0086 others(28): Show |
41 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+2361G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323309 | |||||||
| chr13:111323354 | G | A | 44 | a0001c0001t0001g0047 a0001c0001t0001g0153 a0001c0001t0001g0154 others(41): Show |
56 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.58+2406G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323354 | |||||||
| chr13:111323354 | G | C | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.58+2406G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323354 | |||||||
| chr13:111323441 | G | T | 31 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0001g0086 others(28): Show |
41 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.58+2493G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323441 | |||||||
| chr13:111323453 | T | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(286): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.58+2505T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323453 | |||||||
| chr13:111323562 | C | T | 5 | a0001c0002t0001g0156 a0001c0002t0001g0273 a0001c0002t0003g0277 others(2): Show |
5 | HG00642.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+2614C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323562 | |||||||
| chr13:111323645 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+2697T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323645 | |||||||
| chr13:111323652 | C | A | 2 | a0001c0002t0003g0061 a0001c0002t0003g0062 |
2 | HG00639.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.58+2704C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323652 | |||||||
| chr13:111323670 | G | A | 20 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0092 others(17): Show |
33 | HG00558.hp2 HG02145.hp2 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.58+2722G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323670 | |||||||
| chr13:111323682 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+2734T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323682 | |||||||
| chr13:111323774 | C | T | 19 | a0001c0001t0001g0063 a0001c0001t0001g0091 a0001c0001t0001g0092 others(16): Show |
31 | HG00558.hp2 HG00738.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.58+2826C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323774 | |||||||
| chr13:111323853 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.58+2905A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111323853 | |||||||
| chr13:111324135 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0069 others(90): Show |
148 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.58+3187G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324135 | |||||||
| chr13:111324234 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(186): Show |
274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.58+3286T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324234 | |||||||
| chr13:111324458 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+3510G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324458 | |||||||
| chr13:111324462 | A | G | 1 | a0001c0002t0003g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58+3514A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324462 | |||||||
| chr13:111324547 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58+3599C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324547 | |||||||
| chr13:111324564 | C | A | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.58+3616C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324564 | |||||||
| chr13:111324598 | T | G | 1 | a0001c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.59-3585T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324598 | |||||||
| chr13:111324615 | C | CAG | 28 | a0001c0001t0003g0033 a0001c0001t0010g0284 a0001c0002t0001g0086 others(25): Show |
38 | HG00280.hp2 HG00323.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.59-3561_59-3560dup others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111324615 | ||||||
| chr13:111324719 | A | G | 1 | a0001c0002t0005g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-3464A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324719 | |||||||
| chr13:111324748 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-3435G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324748 | |||||||
| chr13:111324752 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-3431C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324752 | |||||||
| chr13:111324933 | G | T | 67 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(64): Show |
87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.59-3250G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324933 | |||||||
| chr13:111324951 | C | T | 1 | a0001c0002t0003g0044 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.59-3232C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324951 | |||||||
| chr13:111324976 | G | T | 1 | a0001c0001t0002g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.59-3207G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111324976 | |||||||
| chr13:111325001 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.59-3182G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325001 | |||||||
| chr13:111325021 | C | T | 15 | a0001c0001t0002g0043 a0001c0001t0002g0224 a0001c0001t0002g0225 others(12): Show |
19 | HG00438.hp1 HG01081.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-3162C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325021 | |||||||
| chr13:111325147 | G | A | 10 | a0001c0001t0001g0063 a0001c0002t0001g0086 a0001c0002t0003g0142 others(7): Show |
13 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.59-3036G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325147 | |||||||
| chr13:111325225 | C | T | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-2958C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325225 | |||||||
| chr13:111325323 | C | T | 1 | a0001c0002t0001g0020 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.59-2860C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325323 | |||||||
| chr13:111325350 | G | A | 1 | a0001c0003t0001g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.59-2833G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325350 | |||||||
| chr13:111325430 | A | T | 2 | a0001c0002t0002g0223 a0001c0002t0002g0235 |
2 | NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.59-2753A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325430 | |||||||
| chr13:111325640 | C | A | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2543C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325640 | |||||||
| chr13:111325662 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.59-2521G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325662 | |||||||
| chr13:111325863 | T | C | 18 | a0001c0002t0001g0006 a0001c0002t0001g0011 a0001c0002t0001g0021 others(15): Show |
27 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.59-2320T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325863 | |||||||
| chr13:111325868 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02280.hp2 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.59-2315C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325868 | |||||||
| chr13:111325917 | C | T | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2266C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325917 | |||||||
| chr13:111325918 | G | A | 63 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(60): Show |
78 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.59-2265G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111325918 | |||||||
| chr13:111326015 | C | T | 17 | a0001c0002t0001g0083 a0001c0002t0001g0239 a0001c0002t0002g0084 others(14): Show |
23 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.59-2168C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326015 | |||||||
| chr13:111326163 | C | T | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2020C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326163 | |||||||
| chr13:111326206 | C | T | 1 | a0001c0002t0005g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-1977C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326206 | |||||||
| chr13:111326242 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.59-1941C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326242 | |||||||
| chr13:111326251 | C | CGAGCCCG others(123): Show |
2 | a0001c0001t0001g0287 a0001c0001t0006g0288 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-1927_59-1926ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326251 | ||||||
| chr13:111326251 | C | T | 1 | a0001c0002t0003g0044 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.59-1932C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326251 | |||||||
| chr13:111326257 | T | C | 46 | a0001c0001t0001g0054 a0001c0002t0001g0005 a0001c0002t0001g0006 others(43): Show |
76 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.59-1926T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326257 | |||||||
| chr13:111326259 | G | C | 2 | a0001c0001t0001g0287 a0001c0001t0006g0288 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.59-1924G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326259 | |||||||
| chr13:111326259 | G | GCGCTGGT others(123): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-1898_59-1897ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326259 | ||||||
| chr13:111326259 | G | GCGCTGGT others(123): Show |
79 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0026 others(76): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.59-1898_59-1897ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326259 | ||||||
| chr13:111326259 | G | GCGCTGGT others(302): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0080 a0001c0001t0001g0120 |
6 | HG01099.hp2 HG01358.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1898_59-1897ins others(309): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326259 | ||||||
| chr13:111326260 | CGCTGGTG others(81): Show |
C | 53 | a0001c0002t0001g0005 a0001c0002t0001g0006 a0001c0002t0001g0011 others(50): Show |
78 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.59-1897_59-1810del others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326260 | ||||||
| chr13:111326286 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(107): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1897A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326286 | |||||||
| chr13:111326292 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(107): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1891T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326292 | |||||||
| chr13:111326301 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(107): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1882T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326301 | |||||||
| chr13:111326305 | AGCCTGTC others(42): Show |
A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0168 |
5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1876_59-1828del others(49): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326305 | ||||||
| chr13:111326306 | G | A | 1 | a0001c0001t0002g0001 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.59-1877G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326306 | |||||||
| chr13:111326307 | C | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1876C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326307 | |||||||
| chr13:111326321 | T | TGGAGGAG others(35): Show |
107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(104): Show |
168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.59-1858_59-1857ins others(42): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326321 | ||||||
| chr13:111326330 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0063 others(106): Show |
170 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.59-1853C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326330 | |||||||
| chr13:111326336 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1847A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326336 | |||||||
| chr13:111326337 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1846C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326337 | |||||||
| chr13:111326339 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1844C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326339 | |||||||
| chr13:111326347 | G | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1836G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326347 | |||||||
| chr13:111326348 | G | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(109): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1835G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326348 | |||||||
| chr13:111326354 | T | C | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-1829T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326354 | |||||||
| chr13:111326357 | G | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0168 |
5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1826G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326357 | |||||||
| chr13:111326374 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1809G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326374 | |||||||
| chr13:111326380 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(109): Show |
173 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.59-1803C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326380 | |||||||
| chr13:111326389 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1794C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326389 | |||||||
| chr13:111326391 | T | C | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.59-1792T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326391 | |||||||
| chr13:111326395 | G | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1788G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326395 | |||||||
| chr13:111326409 | TGGA | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1769_59-1767del others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326409 | ||||||
| chr13:111326419 | G | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0262 others(1): Show |
5 | HG01255.hp1 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1764G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326419 | |||||||
| chr13:111326419 | G | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(107): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1764G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326419 | |||||||
| chr13:111326421 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(109): Show |
174 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.59-1762T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326421 | |||||||
| chr13:111326427 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1756G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326427 | |||||||
| chr13:111326428 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0168 |
5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1755C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326428 | |||||||
| chr13:111326430 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(105): Show |
169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.59-1753T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326430 | |||||||
| chr13:111326430 | T | TGAGGCTG others(120): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0001g0262 others(1): Show |
5 | HG01255.hp1 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1750_59-1749ins others(127): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326430 | ||||||
| chr13:111326431 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.59-1752G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326431 | |||||||
| chr13:111326432 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-1751A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326432 | |||||||
| chr13:111326438 | G | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0168 |
5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1745G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326438 | |||||||
| chr13:111326482 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0168 |
5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1701C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326482 | |||||||
| chr13:111326486 | CCTGTCTG others(32): Show |
C | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1678_59-1640del others(39): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326486 | ||||||
| chr13:111326500 | TGGA | T | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1678_59-1676del others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326500 | ||||||
| chr13:111326510 | C | T | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1673C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326510 | |||||||
| chr13:111326511 | A | G | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1672A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326511 | |||||||
| chr13:111326518 | G | A | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1665G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326518 | |||||||
| chr13:111326523 | A | AGCCTGGC others(6): Show |
1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1659_59-1658ins others(13): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326523 | ||||||
| chr13:111326526 | C | G | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1657C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326526 | |||||||
| chr13:111326540 | G | GGAA | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1641_59-1640ins others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326540 | ||||||
| chr13:111326548 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.59-1635C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326548 | |||||||
| chr13:111326553 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.59-1630A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326553 | |||||||
| chr13:111326554 | A | G | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1629A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326554 | |||||||
| chr13:111326555 | C | T | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1628C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326555 | |||||||
| chr13:111326558 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0002g0169 |
2 | HG02004.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.59-1625G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326558 | |||||||
| chr13:111326562 | CTGGTGCT others(6): Show |
C | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1618_59-1606del others(13): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326562 | ||||||
| chr13:111326566 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1617T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326566 | |||||||
| chr13:111326566 | TGCTGGCG others(120): Show |
T | 1 | a0001c0002t0003g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.59-1599_59-1473del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326566 | ||||||
| chr13:111326572 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1611C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326572 | |||||||
| chr13:111326573 | G | A | 59 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(56): Show |
74 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.59-1610G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326573 | |||||||
| chr13:111326584 | C | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0168 |
5 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1599C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326584 | |||||||
| chr13:111326592 | A | G | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1591A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326592 | |||||||
| chr13:111326598 | T | C | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1585T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326598 | |||||||
| chr13:111326599 | G | A | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1584G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326599 | |||||||
| chr13:111326623 | G | A | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1560G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326623 | |||||||
| chr13:111326623 | G | GGGGTGGA others(32): Show |
4 | a0001c0002t0001g0045 a0001c0002t0001g0259 a0001c0002t0001g0260 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1522_59-1521ins others(39): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326623 | ||||||
| chr13:111326637 | C | T | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1546C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326637 | |||||||
| chr13:111326638 | A | G | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1545A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326638 | |||||||
| chr13:111326646 | T | C | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1537T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326646 | |||||||
| chr13:111326647 | G | A | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1536G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326647 | |||||||
| chr13:111326648 | C | CGAGCCTG others(32): Show |
222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(219): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.59-1522_59-1521ins others(39): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326648 | ||||||
| chr13:111326648 | C | T | 1 | a0001c0001t0002g0013 | 4 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1535C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326648 | |||||||
| chr13:111326651 | G | T | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1532G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326651 | |||||||
| chr13:111326652 | C | G | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1531C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326652 | |||||||
| chr13:111326682 | CGTGAGCC others(45): Show |
C | 1 | a0001c0001t0002g0168 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.59-1499_59-1448del others(52): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr13 | 111326682 | ||||||
| chr13:111326739 | T | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(230): Show |
340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.59-1444T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326739 | |||||||
| chr13:111326745 | C | G | 1 | a0001c0002t0001g0270 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.59-1438C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326745 | |||||||
| chr13:111326745 | C | T | 3 | a0001c0001t0001g0054 a0001c0001t0002g0168 a0001c0001t0006g0288 |
4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-1438C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326745 | |||||||
| chr13:111326823 | T | C | 1 | a0001c0002t0003g0048 | 2 | NA19066.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.59-1360T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326823 | |||||||
| chr13:111326924 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.59-1259C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326924 | |||||||
| chr13:111326945 | C | T | 1 | a0001c0002t0001g0032 | 2 | NA18950.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.59-1238C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111326945 | |||||||
| chr13:111327056 | G | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(42): Show |
58 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.59-1127G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327056 | |||||||
| chr13:111327066 | G | A | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-1117G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327066 | |||||||
| chr13:111327073 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.59-1110C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327073 | |||||||
| chr13:111327175 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.59-1008G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327175 | |||||||
| chr13:111327344 | G | A | 6 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(3): Show |
6 | HG00673.hp1 HG02056.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-839G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327344 | |||||||
| chr13:111327348 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.59-835A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327348 | |||||||
| chr13:111327593 | G | A | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-590G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327593 | |||||||
| chr13:111327599 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.59-584G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327599 | |||||||
| chr13:111327643 | C | T | 1 | a0002c0004t0001g0030 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.59-540C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327643 | |||||||
| chr13:111327689 | G | A | 5 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0020 others(2): Show |
12 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-494G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327689 | |||||||
| chr13:111327749 | C | T | 1 | a0001c0002t0005g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.59-434C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327749 | |||||||
| chr13:111327803 | T | C | 60 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(57): Show |
75 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.59-380T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327803 | |||||||
| chr13:111327882 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.59-301G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327882 | |||||||
| chr13:111327924 | G | A | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-259G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111327924 | |||||||
| chr13:111328131 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(231): Show |
341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.59-52A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 2/5 | chr13 | 111328131 | |||||||
| chr13:111328437 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+144C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328437 | |||||||
| chr13:111328473 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+180G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328473 | |||||||
| chr13:111328497 | C | T | 5 | a0001c0002t0001g0239 a0001c0002t0003g0052 a0001c0002t0003g0159 others(2): Show |
6 | HG00280.hp2 HG00323.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.169+204C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328497 | |||||||
| chr13:111328647 | C | T | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+354C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328647 | |||||||
| chr13:111328649 | G | T | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
12 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+356G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328649 | |||||||
| chr13:111328676 | G | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(211): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.169+383G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328676 | |||||||
| chr13:111328686 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.169+393C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328686 | |||||||
| chr13:111328740 | T | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0287 others(1): Show |
5 | HG01891.hp1 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+447T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328740 | |||||||
| chr13:111328750 | G | C | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+457G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328750 | |||||||
| chr13:111328846 | A | C | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+553A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328846 | |||||||
| chr13:111328868 | C | G | 6 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0020 others(3): Show |
13 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+575C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328868 | |||||||
| chr13:111328875 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(207): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.169+582G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328875 | |||||||
| chr13:111328893 | C | T | 2 | a0001c0005t0001g0160 a0001c0005t0001g0161 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.169+600C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328893 | |||||||
| chr13:111328915 | C | T | 18 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0239 others(15): Show |
24 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.169+622C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328915 | |||||||
| chr13:111328917 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.169+624C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111328917 | |||||||
| chr13:111329009 | T | A | 1 | a0001c0003t0001g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169+716T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329009 | |||||||
| chr13:111329014 | C | G | 1 | a0001c0003t0001g0124 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169+721C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329014 | |||||||
| chr13:111329052 | T | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(222): Show |
329 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.169+759T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329052 | |||||||
| chr13:111329138 | C | G | 1 | a0001c0002t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.169+845C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329138 | |||||||
| chr13:111329254 | C | A | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+961C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329254 | |||||||
| chr13:111329360 | C | G | 141 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(138): Show |
194 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.169+1067C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329360 | |||||||
| chr13:111329397 | G | T | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+1104G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329397 | |||||||
| chr13:111329454 | A | G | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+1161A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329454 | |||||||
| chr13:111329505 | G | A | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+1212G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329505 | |||||||
| chr13:111329699 | A | G | 1 | a0002c0004t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.169+1406A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329699 | |||||||
| chr13:111329763 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.169+1470A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329763 | |||||||
| chr13:111329775 | G | A | 17 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0239 others(14): Show |
23 | HG00280.hp2 HG00323.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.169+1482G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329775 | |||||||
| chr13:111329781 | G | C | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+1488G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329781 | |||||||
| chr13:111329944 | C | T | 61 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(58): Show |
76 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.169+1651C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111329944 | |||||||
| chr13:111330038 | C | CA | 3 | a0001c0001t0001g0054 a0001c0001t0001g0287 a0001c0001t0006g0288 |
4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+1746dupA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111330038 | ||||||
| chr13:111330043 | CA | C | 6 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0020 others(3): Show |
13 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.169+1752delA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111330043 | ||||||
| chr13:111330119 | A | G | 10 | a0001c0001t0001g0063 a0001c0002t0001g0008 a0001c0002t0001g0009 others(7): Show |
17 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.169+1826A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330119 | |||||||
| chr13:111330129 | GA | G | 10 | a0001c0002t0001g0086 a0001c0002t0001g0102 a0001c0002t0003g0142 others(7): Show |
13 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.169+1845delA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111330129 | ||||||
| chr13:111330176 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0070 a0001c0001t0001g0170 others(13): Show |
25 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.169+1883C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330176 | |||||||
| chr13:111330209 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0070 others(91): Show |
148 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.169+1916C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330209 | |||||||
| chr13:111330268 | A | G | 110 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(107): Show |
148 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.169+1975A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330268 | |||||||
| chr13:111330327 | G | A | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+2034G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330327 | |||||||
| chr13:111330497 | A | C | 1 | a0001c0002t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.169+2204A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330497 | |||||||
| chr13:111330525 | C | T | 30 | a0001c0002t0001g0004 a0001c0002t0001g0018 a0001c0002t0001g0035 others(27): Show |
39 | HG00099.hp2 HG00280.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.169+2232C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330525 | |||||||
| chr13:111330551 | C | T | 9 | a0001c0002t0001g0086 a0001c0002t0003g0142 a0001c0002t0004g0016 others(6): Show |
12 | HG01081.hp1 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+2258C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330551 | |||||||
| chr13:111330603 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.169+2310T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330603 | |||||||
| chr13:111330764 | A | G | 2 | a0002c0004t0001g0030 a0002c0004t0001g0164 |
3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.169+2471A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330764 | |||||||
| chr13:111330853 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169+2560C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330853 | |||||||
| chr13:111330865 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0203 |
3 | NA18947.hp1 NA19075.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.169+2572A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330865 | |||||||
| chr13:111330895 | T | C | 1 | a0001c0005t0003g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.169+2602T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330895 | |||||||
| chr13:111330898 | G | A | 9 | a0001c0002t0001g0005 a0001c0002t0001g0015 a0001c0002t0001g0031 others(6): Show |
19 | HG00558.hp2 NA18939.hp2 NA18950.hp1 others(16): Show |
intron_variant | MODIFIER | c.169+2605G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330898 | |||||||
| chr13:111330914 | G | C | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+2621G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330914 | |||||||
| chr13:111330986 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.169+2693A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111330986 | |||||||
| chr13:111331000 | T | A | 5 | a0001c0002t0004g0016 a0001c0002t0004g0034 a0001c0002t0004g0138 others(2): Show |
8 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+2707T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331000 | |||||||
| chr13:111331171 | G | A | 1 | a0001c0002t0001g0005 | 7 | NA18953.hp1 NA18972.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.169+2878G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331171 | |||||||
| chr13:111331202 | C | T | 14 | a0001c0001t0001g0092 a0001c0002t0001g0006 a0001c0002t0001g0011 others(11): Show |
22 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.169+2909C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331202 | |||||||
| chr13:111331263 | T | C | 1 | a0001c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.169+2970T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331263 | |||||||
| chr13:111331312 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169+3019T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331312 | |||||||
| chr13:111331316 | AT | A | 11 | a0001c0002t0001g0009 a0001c0002t0001g0020 a0001c0002t0001g0058 others(8): Show |
18 | HG01106.hp2 HG01109.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.169+3043delT | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | ||||||
| chr13:111331316 | ATT | A | 14 | a0001c0002t0001g0008 a0001c0002t0001g0057 a0001c0002t0001g0082 others(11): Show |
20 | HG00280.hp2 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.169+3042_169+3043d others(4): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | ||||||
| chr13:111331316 | ATTT | A | 9 | a0001c0001t0001g0134 a0001c0001t0002g0200 a0001c0001t0002g0201 others(6): Show |
9 | HG02080.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.169+3041_169+3043d others(5): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | ||||||
| chr13:111331316 | ATTTT | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(184): Show |
275 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.169+3040_169+3043d others(6): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | ||||||
| chr13:111331316 | ATTTTT | A | 30 | a0001c0001t0001g0054 a0001c0001t0001g0092 a0001c0001t0001g0105 others(27): Show |
42 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.169+3039_169+3043d others(7): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111331316 | ||||||
| chr13:111331380 | C | T | 2 | a0001c0002t0003g0254 a0001c0002t0003g0255 |
2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.169+3087C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331380 | |||||||
| chr13:111331420 | T | C | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+3127T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331420 | |||||||
| chr13:111331569 | C | T | 1 | a0001c0002t0003g0257 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.169+3276C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331569 | |||||||
| chr13:111331656 | C | A | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+3363C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331656 | |||||||
| chr13:111331788 | G | T | 1 | a0001c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.169+3495G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331788 | |||||||
| chr13:111331865 | A | C | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+3572A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331865 | |||||||
| chr13:111331890 | C | T | 1 | a0001c0002t0003g0157 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.169+3597C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331890 | |||||||
| chr13:111331897 | A | G | 105 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(102): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.169+3604A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331897 | |||||||
| chr13:111331995 | C | T | 4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+3702C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111331995 | |||||||
| chr13:111332031 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.169+3738T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332031 | |||||||
| chr13:111332032 | G | A | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.169+3739G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332032 | |||||||
| chr13:111332060 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.169+3767A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332060 | |||||||
| chr13:111332396 | C | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0287 a0001c0001t0006g0288 |
4 | HG01891.hp1 HG02630.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.169+4103C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332396 | |||||||
| chr13:111332412 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.169+4119G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332412 | |||||||
| chr13:111332598 | T | G | 2 | a0001c0002t0004g0034 a0001c0002t0004g0138 |
3 | HG01884.hp2 HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.169+4305T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332598 | |||||||
| chr13:111332768 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+4475A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332768 | |||||||
| chr13:111332803 | T | C | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.169+4510T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332803 | |||||||
| chr13:111332858 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0006g0288 |
3 | HG01891.hp1 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169+4565C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332858 | |||||||
| chr13:111332884 | A | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0203 |
3 | NA18947.hp1 NA19075.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.169+4591A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332884 | |||||||
| chr13:111332911 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(104): Show |
165 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.169+4618G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111332911 | |||||||
| chr13:111333006 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.169+4713A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333006 | |||||||
| chr13:111333025 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.169+4732G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333025 | |||||||
| chr13:111333141 | A | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+4848A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333141 | |||||||
| chr13:111333185 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.169+4892G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333185 | |||||||
| chr13:111333527 | A | G | 5 | a0001c0001t0001g0119 a0001c0002t0001g0121 a0001c0002t0002g0167 others(2): Show |
5 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5234A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333527 | |||||||
| chr13:111333573 | A | G | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+5280A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333573 | |||||||
| chr13:111333589 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(223): Show |
325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.169+5296C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333589 | |||||||
| chr13:111333729 | C | G | 1 | a0001c0001t0002g0198 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169+5436C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333729 | |||||||
| chr13:111333731 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.169+5438A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333731 | |||||||
| chr13:111333737 | C | T | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5444C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333737 | |||||||
| chr13:111333738 | A | C | 1 | a0001c0001t0011g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.169+5445A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333738 | |||||||
| chr13:111333738 | A | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5445A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333738 | |||||||
| chr13:111333743 | T | G | 24 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0081 others(21): Show |
26 | HG00673.hp1 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.169+5450T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333743 | |||||||
| chr13:111333746 | A | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5453A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333746 | |||||||
| chr13:111333752 | A | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5459A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333752 | |||||||
| chr13:111333755 | T | C | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5462T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333755 | |||||||
| chr13:111333763 | G | A | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5470G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333763 | |||||||
| chr13:111333766 | G | GTGTCAGG others(5): Show |
5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5473_169+5474i others(14): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333766 | |||||||
| chr13:111333767 | C | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5474C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333767 | |||||||
| chr13:111333776 | T | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5483T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333776 | |||||||
| chr13:111333777 | GTGGGAA | G | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5485_169+5490d others(8): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333777 | |||||||
| chr13:111333792 | C | T | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5499C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333792 | |||||||
| chr13:111333795 | A | C | 5 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(2): Show |
5 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.169+5502A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333795 | |||||||
| chr13:111333809 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0028 others(153): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.169+5516A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333809 | |||||||
| chr13:111333969 | T | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(246): Show |
357 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.169+5676T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111333969 | |||||||
| chr13:111334031 | A | C | 1 | a0001c0002t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.169+5738A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334031 | |||||||
| chr13:111334034 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(215): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.169+5741G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334034 | |||||||
| chr13:111334121 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.170-5742C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334121 | |||||||
| chr13:111334181 | A | G | 3 | a0001c0001t0001g0128 a0001c0002t0003g0254 a0001c0002t0003g0255 |
3 | HG02257.hp2 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.170-5682A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334181 | |||||||
| chr13:111334189 | T | C | 1 | a0003c0007t0003g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.170-5674T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334189 | |||||||
| chr13:111334211 | G | A | 1 | a0001c0001t0008g0029 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.170-5652G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334211 | |||||||
| chr13:111334415 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0109 |
2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.170-5448G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334415 | |||||||
| chr13:111334483 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.170-5380T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334483 | |||||||
| chr13:111334621 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.170-5242C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334621 | |||||||
| chr13:111334879 | G | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.170-4984G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111334879 | |||||||
| chr13:111335093 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(202): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.170-4770G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335093 | |||||||
| chr13:111335124 | T | A | 1 | a0001c0002t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.170-4739T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335124 | |||||||
| chr13:111335271 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.170-4592G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335271 | |||||||
| chr13:111335340 | T | C | 6 | a0001c0001t0008g0076 a0001c0002t0005g0064 a0001c0002t0005g0065 others(3): Show |
6 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.170-4523T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335340 | |||||||
| chr13:111335442 | A | G | 1 | a0001c0002t0001g0247 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.170-4421A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335442 | |||||||
| chr13:111335507 | T | A | 1 | a0001c0001t0002g0177 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.170-4356T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335507 | |||||||
| chr13:111335598 | CAT | C | 10 | a0001c0001t0001g0130 a0001c0001t0002g0178 a0001c0001t0002g0205 others(7): Show |
21 | HG00558.hp2 HG02895.hp1 HG02896.hp1 others(18): Show |
intron_variant | MODIFIER | c.170-4263_170-4262d others(4): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111335598 | ||||||
| chr13:111335698 | G | A | 40 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0002g0040 others(37): Show |
52 | HG00544.hp2 HG00597.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.170-4165G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335698 | |||||||
| chr13:111335759 | T | A | 2 | a0001c0001t0002g0197 a0001c0002t0001g0265 |
2 | HG01928.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.170-4104T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335759 | |||||||
| chr13:111335825 | C | A | 30 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0105 others(27): Show |
38 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.170-4038C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335825 | |||||||
| chr13:111335840 | C | T | 1 | a0001c0002t0001g0267 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.170-4023C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111335840 | |||||||
| chr13:111336050 | G | C | 1 | a0001c0001t0002g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.170-3813G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336050 | |||||||
| chr13:111336487 | A | T | 1 | a0001c0002t0003g0049 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.170-3376A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336487 | |||||||
| chr13:111336549 | A | G | 2 | a0002c0004t0001g0030 a0002c0004t0001g0164 |
3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.170-3314A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336549 | |||||||
| chr13:111336559 | C | CT | 49 | a0001c0001t0001g0026 a0001c0001t0001g0069 a0001c0001t0001g0085 others(46): Show |
61 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.170-3302dupT | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111336559 | ||||||
| chr13:111336904 | C | T | 1 | a0001c0002t0001g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.170-2959C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336904 | |||||||
| chr13:111336920 | G | A | 3 | a0001c0001t0011g0131 a0001c0002t0003g0049 a0001c0002t0003g0279 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-2943G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336920 | |||||||
| chr13:111336950 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.170-2913G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336950 | |||||||
| chr13:111336962 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.170-2901C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111336962 | |||||||
| chr13:111337043 | G | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(132): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.170-2820G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337043 | |||||||
| chr13:111337123 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(195): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.170-2740G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337123 | |||||||
| chr13:111337319 | C | T | 30 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0105 others(27): Show |
38 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.170-2544C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337319 | |||||||
| chr13:111337377 | A | G | 3 | a0002c0004t0001g0030 a0002c0004t0001g0164 a0002c0004t0001g0274 |
4 | HG01884.hp1 HG02258.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-2486A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337377 | |||||||
| chr13:111337530 | G | T | 1 | a0001c0001t0001g0019 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.170-2333G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337530 | |||||||
| chr13:111337571 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.170-2292G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337571 | |||||||
| chr13:111337618 | G | A | 2 | a0001c0002t0009g0275 a0001c0002t0009g0276 |
2 | HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.170-2245G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337618 | |||||||
| chr13:111337706 | A | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(4): Show |
8 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-2157A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337706 | |||||||
| chr13:111337772 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.170-2091A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337772 | |||||||
| chr13:111337883 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(136): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.170-1980C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337883 | |||||||
| chr13:111337941 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(4): Show |
8 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-1922G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111337941 | |||||||
| chr13:111338022 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(137): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.170-1841C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338022 | |||||||
| chr13:111338025 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.170-1838C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338025 | |||||||
| chr13:111338074 | C | T | 3 | a0001c0001t0011g0131 a0001c0002t0003g0049 a0001c0002t0003g0279 |
4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-1789C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338074 | |||||||
| chr13:111338117 | TGCG | T | 30 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0105 others(27): Show |
38 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.170-1743_170-1741d others(5): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111338117 | ||||||
| chr13:111338118 | G | A | 3 | a0001c0001t0001g0119 a0001c0002t0003g0061 a0001c0002t0003g0062 |
3 | HG00639.hp1 HG01243.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.170-1745G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338118 | |||||||
| chr13:111338120 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.170-1743G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338120 | |||||||
| chr13:111338185 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(137): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.170-1678G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338185 | |||||||
| chr13:111338305 | G | C | 3 | a0001c0002t0009g0275 a0001c0002t0009g0276 a0001c0008t0006g0090 |
3 | HG02280.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.170-1558G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338305 | |||||||
| chr13:111338440 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.170-1423C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338440 | |||||||
| chr13:111338441 | T | A | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.170-1422T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338441 | |||||||
| chr13:111338493 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(160): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.170-1370C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338493 | |||||||
| chr13:111338584 | C | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0117 a0001c0002t0001g0251 others(1): Show |
4 | HG02735.hp2 HG03516.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.170-1279C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338584 | |||||||
| chr13:111338743 | C | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(134): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.170-1120C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338743 | |||||||
| chr13:111338751 | GTGATTAG others(36): Show |
G | 1 | a0001c0002t0002g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.170-1111_170-1069d others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338751 | |||||||
| chr13:111338848 | G | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0218 |
3 | HG00621.hp2 NA18979.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.170-1015G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338848 | |||||||
| chr13:111338937 | G | A | 18 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0106 others(15): Show |
23 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.170-926G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338937 | |||||||
| chr13:111338962 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.170-901G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111338962 | |||||||
| chr13:111339116 | G | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(161): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.170-747G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339116 | |||||||
| chr13:111339414 | A | G | 2 | a0001c0001t0002g0148 a0001c0001t0002g0209 |
2 | NA18946.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.170-449A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339414 | |||||||
| chr13:111339490 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.170-373G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339490 | |||||||
| chr13:111339528 | G | A | 1 | a0001c0002t0003g0044 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.170-335G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339528 | |||||||
| chr13:111339535 | T | TTCCATGC others(31): Show |
1 | a0001c0001t0001g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.170-304_170-267dup others(38): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr13 | 111339535 | ||||||
| chr13:111339545 | T | C | 1 | a0001c0002t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170-318T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339545 | |||||||
| chr13:111339663 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.170-200C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339663 | |||||||
| chr13:111339716 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(4): Show |
8 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.170-147C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339716 | |||||||
| chr13:111339735 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.170-128G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339735 | |||||||
| chr13:111339779 | A | T | 4 | a0001c0002t0001g0045 a0001c0002t0001g0259 a0001c0002t0001g0260 others(1): Show |
5 | HG02630.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.170-84A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 3/5 | chr13 | 111339779 | |||||||
| chr13:111339941 | C | T | 36 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0119 others(33): Show |
53 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.239+9C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111339941 | |||||||
| chr13:111339967 | A | G | 19 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0119 others(16): Show |
30 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.239+35A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111339967 | |||||||
| chr13:111339998 | TCCTGCCT others(32): Show |
T | 1 | a0001c0002t0002g0221 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+67_239+105delC others(38): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111339998 | |||||||
| chr13:111340019 | C | T | 1 | a0001c0001t0002g0002 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.239+87C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340019 | |||||||
| chr13:111340040 | G | A | 11 | a0001c0001t0001g0166 a0001c0001t0001g0213 a0001c0001t0002g0144 others(8): Show |
11 | HG00438.hp1 NA18612.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.239+108G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340040 | |||||||
| chr13:111340064 | C | A | 1 | a0001c0002t0002g0221 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+132C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340064 | |||||||
| chr13:111340088 | C | G | 1 | a0001c0002t0001g0099 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.239+156C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340088 | |||||||
| chr13:111340116 | AGTGCTTG others(79): Show |
A | 7 | a0001c0001t0001g0063 a0001c0001t0011g0131 a0001c0002t0001g0012 others(4): Show |
12 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.239+254_239+339del others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340116 | ||||||
| chr13:111340136 | A | G | 2 | a0001c0001t0001g0287 a0001c0001t0003g0033 |
3 | HG03486.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.239+204A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340136 | |||||||
| chr13:111340143 | A | ATGTTTAG others(122): Show |
1 | a0001c0002t0003g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239+254_239+382dup others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340143 | ||||||
| chr13:111340146 | T | TTAGTGAG others(248): Show |
1 | a0001c0002t0002g0221 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+215_239+216ins others(255): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340146 | ||||||
| chr13:111340171 | T | G | 1 | a0001c0003t0001g0014 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.239+239T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340171 | |||||||
| chr13:111340171 | T | TGAAAATC others(160): Show |
1 | a0001c0002t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+253_239+254ins others(167): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340171 | ||||||
| chr13:111340175 | A | C | 1 | a0001c0002t0002g0221 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+243A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340175 | |||||||
| chr13:111340175 | AATCATAA others(380): Show |
A | 1 | a0001c0002t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.239+254_239+640del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340175 | ||||||
| chr13:111340175 | AATCATAA others(509): Show |
A | 1 | a0001c0002t0001g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239+254_239+769del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340175 | ||||||
| chr13:111340186 | A | ATGTTTAG others(380): Show |
7 | a0001c0001t0008g0029 a0001c0001t0008g0076 a0001c0002t0004g0016 others(4): Show |
11 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+296_239+297ins others(387): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | ||||||
| chr13:111340186 | A | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(8): Show |
13 | HG00639.hp1 HG00733.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.239+254A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340186 | |||||||
| chr13:111340186 | ATGTTTAG others(79): Show |
A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0109 |
2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.239+297_239+382del others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | ||||||
| chr13:111340186 | ATGTTTAG others(337): Show |
A | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.239+286_239+629del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | ||||||
| chr13:111340186 | ATGTTTAG others(380): Show |
A | 6 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0002t0001g0008 others(3): Show |
12 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.239+297_239+683del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340186 | ||||||
| chr13:111340218 | A | AATCATAA others(79): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(4): Show |
8 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.239+296_239+297ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340218 | ||||||
| chr13:111340218 | A | C | 1 | a0001c0002t0002g0221 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.239+286A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340218 | |||||||
| chr13:111340229 | A | ATGTTTAG others(36): Show |
3 | a0001c0002t0001g0094 a0001c0002t0003g0051 a0001c0002t0003g0157 |
4 | HG02615.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+458_239+500dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | A | ATGTTTAG others(1283): Show |
1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1290): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | A | ATGTTTAG others(337): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+382_239+383ins others(344): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | A | ATGTTTAG others(1154): Show |
1 | a0001c0002t0001g0020 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.239+501_240-1163du others(1162): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | A | ATGTTTAG others(1369): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0118 |
2 | HG03491.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.239+457_239+458ins others(1376): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | A | ATGTTTAG others(1842): Show |
1 | a0001c0001t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.239+457_239+458ins others(1849): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0069 others(62): Show |
84 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.239+297A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340229 | |||||||
| chr13:111340229 | ATGTTTAG others(36): Show |
A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0194 |
3 | HG02027.hp1 NA19074.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.239+458_239+500del others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340229 | ATGTTTAG others(79): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+415_239+500del others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340229 | ||||||
| chr13:111340260 | A | C | 1 | a0001c0002t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+328A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340260 | |||||||
| chr13:111340261 | A | AATCATAA others(123): Show |
1 | a0001c0001t0002g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.239+363_239+364ins others(130): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1154): Show |
1 | a0001c0002t0002g0084 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1161): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1111): Show |
1 | a0001c0010t0001g0126 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1111): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
5 | HG01934.hp2 HG01952.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(466): Show |
1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(473): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1111): Show |
1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1111): Show |
3 | a0001c0001t0001g0122 a0001c0002t0001g0006 a0001c0002t0002g0006 |
7 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1111): Show |
2 | a0001c0002t0001g0101 a0001c0002t0003g0258 |
2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.239+382_239+383ins others(1118): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1198): Show |
1 | a0001c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1205): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340261 | A | AATCATAA others(1068): Show |
1 | a0001c0001t0001g0136 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1075): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340261 | ||||||
| chr13:111340272 | G | GTGTTTAG others(79): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
9 | HG01192.hp2 HG03239.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+382_239+383ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340272 | ||||||
| chr13:111340272 | G | GTGTTTAG others(79): Show |
2 | a0001c0002t0001g0097 a0001c0002t0001g0099 |
2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+425_239+426ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340272 | ||||||
| chr13:111340272 | G | GTGTTTAG others(79): Show |
1 | a0001c0002t0001g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+371_239+372ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340272 | ||||||
| chr13:111340304 | A | AATCATAA others(1068): Show |
1 | a0001c0002t0001g0100 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(1075): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | ||||||
| chr13:111340304 | A | AATCATAA others(1068): Show |
1 | a0001c0002t0002g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1075): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | ||||||
| chr13:111340304 | A | AATCATAA others(1369): Show |
1 | a0001c0001t0001g0176 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.239+382_239+383ins others(1376): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | ||||||
| chr13:111340304 | A | AATCATAA others(466): Show |
1 | a0001c0002t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.239+382_239+383ins others(473): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | ||||||
| chr13:111340304 | A | AATCATAA others(251): Show |
1 | a0001c0002t0009g0275 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+458_239+715dup others(258): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | ||||||
| chr13:111340304 | A | AATCATAA others(122): Show |
51 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0166 others(48): Show |
87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.239+457_239+458ins others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340304 | ||||||
| chr13:111340304 | A | C | 4 | a0001c0001t0002g0206 a0001c0002t0001g0251 a0001c0002t0002g0221 others(1): Show |
4 | HG02083.hp1 HG03704.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+372A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340304 | |||||||
| chr13:111340315 | G | C | 1 | a0001c0002t0004g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.239+383G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340315 | |||||||
| chr13:111340324 | G | GAGCACCT others(251): Show |
1 | a0001c0008t0006g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.239+649_239+650ins others(258): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340324 | ||||||
| chr13:111340347 | A | AATCATAA others(332): Show |
1 | a0001c0002t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+450_239+451ins others(339): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340347 | ||||||
| chr13:111340347 | A | AATCATAA others(36): Show |
4 | a0001c0001t0002g0215 a0001c0002t0001g0056 a0001c0002t0001g0088 others(1): Show |
4 | HG00558.hp2 HG02027.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+457_239+458ins others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340347 | ||||||
| chr13:111340347 | A | AATCATAA others(79): Show |
1 | a0003c0009t0001g0242 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.239+457_239+458ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340347 | ||||||
| chr13:111340347 | A | C | 5 | a0001c0001t0001g0113 a0001c0001t0001g0176 a0001c0001t0002g0150 others(2): Show |
5 | HG01975.hp2 HG03688.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+415A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340347 | |||||||
| chr13:111340357 | C | T | 2 | a0002c0004t0001g0030 a0002c0004t0001g0164 |
3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239+425C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340357 | |||||||
| chr13:111340358 | G | C | 2 | a0001c0001t0001g0287 a0001c0002t0004g0141 |
2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.239+426G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340358 | |||||||
| chr13:111340358 | GTGTTTAG others(724): Show |
G | 3 | a0001c0002t0001g0012 a0001c0002t0003g0049 a0001c0002t0003g0279 |
7 | HG02895.hp1 HG02896.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+501_239+1231de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340358 | ||||||
| chr13:111340358 | GTGTTTAG others(982): Show |
G | 5 | a0001c0001t0007g0024 a0001c0001t0007g0103 a0001c0001t0010g0284 others(2): Show |
6 | HG01255.hp2 HG02698.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+501_240-1335de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340358 | ||||||
| chr13:111340372 | C | T | 2 | a0001c0002t0001g0097 a0001c0002t0001g0099 |
2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+440C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340372 | |||||||
| chr13:111340389 | A | C | 1 | a0001c0002t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+457A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340389 | |||||||
| chr13:111340390 | A | AATCATAA others(36): Show |
1 | a0001c0001t0001g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239+501_239+543dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340390 | ||||||
| chr13:111340390 | A | AATCATAA others(122): Show |
1 | a0001c0002t0001g0082 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.239+716_239+844dup others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340390 | ||||||
| chr13:111340390 | A | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(137): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.239+458A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340390 | |||||||
| chr13:111340390 | AATCATAA others(294): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.239+501_239+801del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340390 | ||||||
| chr13:111340401 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+469G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340401 | |||||||
| chr13:111340401 | GTGTTTAG others(939): Show |
G | 1 | a0002c0004t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.239+501_240-1378de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340401 | ||||||
| chr13:111340433 | C | A | 44 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0092 others(41): Show |
58 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.239+501C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340433 | |||||||
| chr13:111340433 | C | CATCATAA others(36): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+544_239+586dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340433 | ||||||
| chr13:111340444 | G | C | 7 | a0001c0001t0008g0029 a0001c0001t0008g0076 a0001c0002t0004g0016 others(4): Show |
11 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.239+512G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340444 | |||||||
| chr13:111340465 | T | C | 1 | a0001c0002t0001g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+533T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340465 | |||||||
| chr13:111340476 | A | AATCATAA others(79): Show |
1 | a0001c0002t0001g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+618_239+619ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340476 | ||||||
| chr13:111340476 | A | C | 15 | a0001c0001t0001g0113 a0001c0001t0001g0122 a0001c0001t0002g0190 others(12): Show |
23 | HG01070.hp1 HG01071.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.239+544A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340476 | |||||||
| chr13:111340476 | AATCATAA others(208): Show |
A | 2 | a0002c0004t0001g0030 a0002c0004t0001g0164 |
3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239+587_239+801del | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340476 | ||||||
| chr13:111340487 | G | C | 3 | a0001c0001t0001g0128 a0001c0002t0003g0254 a0001c0002t0003g0255 |
3 | HG02257.hp2 HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.239+555G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340487 | |||||||
| chr13:111340519 | C | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0115 others(18): Show |
28 | HG01168.hp2 HG01192.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.239+587C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340519 | |||||||
| chr13:111340551 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+619T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340551 | |||||||
| chr13:111340562 | C | A | 21 | a0001c0001t0001g0092 a0001c0001t0001g0113 a0001c0001t0001g0114 others(18): Show |
29 | HG01168.hp2 HG01192.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.239+630C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340562 | |||||||
| chr13:111340562 | C | CATCATAA others(36): Show |
1 | a0001c0001t0002g0003 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.239+673_239+715dup others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | ||||||
| chr13:111340562 | C | CATCATAA others(79): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0091 a0001c0001t0001g0166 others(49): Show |
85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.239+715_239+716ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | ||||||
| chr13:111340562 | C | CATCATAA others(208): Show |
8 | a0001c0001t0001g0213 a0001c0001t0002g0036 a0001c0001t0002g0150 others(5): Show |
11 | HG03927.hp2 HG04115.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.239+716_239+930dup others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | ||||||
| chr13:111340562 | C | CATCATAA others(79): Show |
1 | a0001c0001t0002g0001 | 2 | NA18970.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.239+672_239+673ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | ||||||
| chr13:111340562 | C | CATCATAA others(122): Show |
1 | a0001c0001t0002g0190 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.239+672_239+673ins others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340562 | ||||||
| chr13:111340568 | A | AACCCGTG others(36): Show |
1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+672_239+673ins others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340568 | ||||||
| chr13:111340568 | A | T | 2 | a0001c0001t0011g0131 a0001c0002t0001g0251 |
2 | HG02622.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.239+636A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340568 | |||||||
| chr13:111340582 | G | A | 4 | a0001c0001t0006g0023 a0001c0001t0006g0288 a0001c0002t0001g0252 others(1): Show |
5 | HG02559.hp1 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.239+650G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340582 | |||||||
| chr13:111340605 | A | C | 45 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0077 others(42): Show |
59 | HG00099.hp1 HG00323.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.239+673A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340605 | |||||||
| chr13:111340605 | AATCATAA others(595): Show |
A | 1 | a0001c0002t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.239+802_239+1403de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340605 | ||||||
| chr13:111340648 | C | A | 44 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0071 others(41): Show |
58 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.239+716C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340648 | |||||||
| chr13:111340648 | C | CATCATAA others(79): Show |
4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+759_239+844dup others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340648 | ||||||
| chr13:111340648 | CATCATAA others(509): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+802_239+1317de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340648 | ||||||
| chr13:111340648 | CATCATAA others(767): Show |
C | 1 | a0001c0001t0011g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.239+759_240-1292de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340648 | ||||||
| chr13:111340658 | C | CGTGTTTA others(165): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+801_239+802ins others(172): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340658 | ||||||
| chr13:111340659 | G | GTGTTTAG others(79): Show |
1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239+758_239+759ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340659 | ||||||
| chr13:111340691 | C | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0176 a0001c0001t0001g0287 others(5): Show |
9 | HG01167.hp2 HG02027.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+759C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340691 | |||||||
| chr13:111340691 | C | CATCATAA others(1240): Show |
1 | a0001c0001t0001g0114 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.239+801_239+802ins others(1247): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340691 | ||||||
| chr13:111340691 | CATCATAA others(724): Show |
C | 1 | a0001c0002t0001g0152 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.239+956_240-1138de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340691 | ||||||
| chr13:111340702 | GTGTTTAG others(638): Show |
G | 2 | a0002c0004t0001g0030 a0002c0004t0001g0164 |
3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239+956_240-1224de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340702 | ||||||
| chr13:111340705 | T | TTTAGTGA others(802): Show |
1 | a0001c0002t0001g0098 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.239+801_239+802ins others(809): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340705 | ||||||
| chr13:111340734 | A | AATCATAA others(122): Show |
1 | a0001c0002t0004g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.239+898_239+899ins others(129): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | ||||||
| chr13:111340734 | A | AATCATAA others(638): Show |
1 | a0001c0002t0003g0257 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(647): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | ||||||
| chr13:111340734 | A | AATCATAA others(165): Show |
2 | a0001c0001t0002g0175 a0001c0001t0002g0217 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.239+930_239+931ins others(172): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | ||||||
| chr13:111340734 | A | AATCATAA others(208): Show |
1 | a0001c0001t0002g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.239+930_239+931ins others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | ||||||
| chr13:111340734 | A | AATCATAA others(36): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 |
4 | HG01258.hp1 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+844_239+845ins others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340734 | ||||||
| chr13:111340734 | A | C | 12 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0127 others(9): Show |
15 | HG00099.hp1 HG00323.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.239+802A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340734 | |||||||
| chr13:111340759 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239+827C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340759 | |||||||
| chr13:111340777 | A | AATCATAA others(939): Show |
2 | a0001c0002t0001g0097 a0001c0002t0001g0099 |
2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+930_239+931ins others(946): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340777 | ||||||
| chr13:111340777 | A | AATCATAA others(552): Show |
1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+887_239+888ins others(559): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340777 | ||||||
| chr13:111340777 | A | C | 2 | a0001c0001t0002g0215 a0001c0002t0001g0251 |
2 | HG02027.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.239+845A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340777 | |||||||
| chr13:111340820 | A | AATCATAA others(79): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 |
4 | HG01258.hp1 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+955_239+956ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340820 | ||||||
| chr13:111340820 | A | AATCATAA others(79): Show |
3 | a0001c0001t0001g0070 a0001c0001t0002g0145 a0001c0002t0003g0052 |
4 | HG00280.hp2 HG00323.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+930_239+931ins others(86): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340820 | ||||||
| chr13:111340820 | A | AATCATAA others(208): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0262 others(1): Show |
7 | HG00140.hp2 HG01099.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+930_239+931ins others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340820 | ||||||
| chr13:111340820 | A | C | 2 | a0001c0001t0002g0215 a0001c0001t0003g0033 |
3 | HG02027.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+888A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340820 | |||||||
| chr13:111340823 | CATAACCC others(165): Show |
C | 1 | a0001c0002t0002g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.239+956_239+1127de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340823 | ||||||
| chr13:111340831 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.239+899G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340831 | |||||||
| chr13:111340831 | GTGTTTAG others(509): Show |
G | 1 | a0001c0001t0002g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.239+956_240-1353de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340831 | ||||||
| chr13:111340845 | CCTGTGCT others(36): Show |
C | 1 | a0001c0002t0001g0032 | 2 | NA18950.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.239+956_239+998del others(43): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340845 | ||||||
| chr13:111340863 | A | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0092 a0001c0001t0001g0115 others(10): Show |
17 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.239+931A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340863 | |||||||
| chr13:111340866 | CATAACCC others(122): Show |
C | 6 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0134 others(3): Show |
12 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.239+956_239+1084de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340866 | ||||||
| chr13:111340869 | A | AACCCGTG others(208): Show |
1 | a0001c0001t0001g0127 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.239+955_239+956ins others(215): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340869 | ||||||
| chr13:111340888 | T | C | 60 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0028 others(57): Show |
76 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.239+956T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340888 | |||||||
| chr13:111340888 | TCTGTGCT others(552): Show |
C | 2 | a0001c0001t0001g0063 a0001c0002t0001g0163 |
2 | HG01167.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.239+956_240-1310de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340888 | |||||||
| chr13:111340906 | A | AATCATAA others(79): Show |
1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+1059_239+1060i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340906 | ||||||
| chr13:111340906 | A | AATCATAA others(36): Show |
1 | a0001c0002t0004g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+1016_239+1017i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340906 | ||||||
| chr13:111340906 | A | AATCATAA others(1240): Show |
4 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0002g0191 others(1): Show |
7 | HG03239.hp2 NA18968.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1016_239+1017i others(1249): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340906 | ||||||
| chr13:111340906 | A | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0240 others(4): Show |
7 | HG00609.hp1 HG01071.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+974A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340906 | |||||||
| chr13:111340931 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0217 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.239+999C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340931 | |||||||
| chr13:111340949 | A | AATCATAA others(208): Show |
1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.239+1062_239+1063i others(217): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340949 | ||||||
| chr13:111340949 | A | C | 10 | a0001c0001t0001g0127 a0001c0001t0008g0029 a0001c0001t0008g0076 others(7): Show |
14 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.239+1017A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340949 | |||||||
| chr13:111340952 | C | A | 1 | a0001c0002t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239+1020C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340952 | |||||||
| chr13:111340959 | C | T | 1 | a0001c0001t0002g0205 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.239+1027C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340959 | |||||||
| chr13:111340974 | C | CCTGTGCT others(36): Show |
1 | a0001c0001t0002g0215 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.239+1062_239+1063i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340974 | ||||||
| chr13:111340992 | A | AATCATAA others(1111): Show |
1 | a0001c0002t0001g0251 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.239+1062_239+1063i others(1120): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111340992 | ||||||
| chr13:111340992 | A | C | 8 | a0001c0001t0001g0127 a0001c0001t0008g0029 a0001c0001t0008g0076 others(5): Show |
12 | HG00738.hp2 HG01884.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.239+1060A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340992 | |||||||
| chr13:111340995 | A | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(182): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.239+1063A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111340995 | |||||||
| chr13:111341003 | G | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 |
4 | HG01258.hp1 HG01361.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1071G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341003 | |||||||
| chr13:111341003 | G | GTGTTTAG others(36): Show |
4 | a0001c0002t0001g0121 a0001c0002t0002g0167 a0001c0002t0003g0061 others(1): Show |
4 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+1113_239+1114i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341003 | ||||||
| chr13:111341017 | C | CCTGTGCT others(79): Show |
1 | a0001c0001t0001g0240 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.239+1113_239+1114i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341017 | ||||||
| chr13:111341035 | A | AATCATAA others(595): Show |
1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.239+1145_239+1146i others(604): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341035 | ||||||
| chr13:111341035 | A | C | 3 | a0001c0001t0001g0028 a0001c0001t0001g0127 a0001c0002t0001g0251 |
4 | HG03491.hp1 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1103A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341035 | |||||||
| chr13:111341078 | A | AATCATAA others(79): Show |
1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.239+1156_239+1157i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | ||||||
| chr13:111341078 | A | AATCATAA others(638): Show |
2 | a0001c0002t0001g0096 a0001c0002t0001g0100 |
2 | HG00099.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.239+1156_239+1157i others(647): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | ||||||
| chr13:111341078 | A | AATCATAA others(681): Show |
1 | a0001c0002t0002g0226 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.239+1156_239+1157i others(690): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | ||||||
| chr13:111341078 | A | AATCATAA others(595): Show |
10 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0136 others(7): Show |
15 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.239+1156_239+1157i others(604): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341078 | ||||||
| chr13:111341078 | A | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0127 a0001c0001t0002g0001 others(1): Show |
4 | HG01123.hp1 HG02040.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.239+1146A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341078 | |||||||
| chr13:111341086 | C | A | 1 | a0001c0002t0009g0275 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.239+1154C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341086 | |||||||
| chr13:111341089 | C | CTGTTTAG others(380): Show |
1 | a0001c0002t0001g0004 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.239+1274_239+1275i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341089 | ||||||
| chr13:111341089 | C | G | 64 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0092 others(61): Show |
84 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.239+1157C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341089 | |||||||
| chr13:111341089 | CTGTTTAG others(595): Show |
C | 1 | a0003c0007t0003g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.239+1232_240-991de others(1): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341089 | ||||||
| chr13:111341103 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.239+1171C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341103 | |||||||
| chr13:111341121 | A | AATCATAA others(79): Show |
1 | a0001c0002t0004g0140 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.239+1231_239+1232i others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341121 | ||||||
| chr13:111341121 | A | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0132 others(1): Show |
4 | HG01934.hp2 HG02165.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.239+1189A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341121 | |||||||
| chr13:111341132 | G | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0217 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.239+1200G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341132 | |||||||
| chr13:111341156 | T | G | 1 | a0001c0002t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239+1224T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341156 | |||||||
| chr13:111341164 | A | AATCATAA others(294): Show |
1 | a0001c0001t0001g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(303): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | ||||||
| chr13:111341164 | A | AATCATAA others(337): Show |
1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(346): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | ||||||
| chr13:111341164 | A | AATCATAA others(79): Show |
1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.239+1329_240-1410d others(88): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | ||||||
| chr13:111341164 | A | AATCATAA others(122): Show |
2 | a0001c0001t0001g0111 a0001c0001t0003g0033 |
3 | HG02615.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.239+1286_240-1410d others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | ||||||
| chr13:111341164 | A | C | 10 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0134 others(7): Show |
16 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.239+1232A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341164 | |||||||
| chr13:111341164 | AATCATAA others(36): Show |
A | 1 | a0001c0001t0002g0208 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.239+1372_240-1410d others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341164 | ||||||
| chr13:111341169 | T | C | 1 | a0001c0002t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.239+1237T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341169 | |||||||
| chr13:111341170 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.239+1238A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341170 | |||||||
| chr13:111341175 | G | GTGTTTAG others(36): Show |
1 | a0001c0001t0002g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.239+1274_239+1275i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341175 | ||||||
| chr13:111341207 | C | A | 99 | a0001c0001t0001g0026 a0001c0001t0001g0054 a0001c0001t0001g0069 others(96): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.239+1275C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341207 | |||||||
| chr13:111341207 | C | CATCATAA others(681): Show |
2 | a0001c0002t0001g0097 a0001c0002t0001g0099 |
2 | HG01168.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.239+1317_239+1318i others(690): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341207 | ||||||
| chr13:111341207 | C | CATCATAA others(294): Show |
1 | a0001c0001t0001g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.240-1410_240-1409i others(303): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341207 | ||||||
| chr13:111341207 | C | CATCATAA others(1283): Show |
1 | a0001c0002t0003g0061 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.239+1366_239+1367i others(1292): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341207 | ||||||
| chr13:111341216 | C | G | 1 | a0001c0002t0001g0239 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.239+1284C>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341216 | |||||||
| chr13:111341218 | G | C | 1 | a0001c0001t0001g0240 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.239+1286G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341218 | |||||||
| chr13:111341250 | C | A | 22 | a0001c0001t0001g0116 a0001c0001t0001g0122 a0001c0001t0001g0127 others(19): Show |
26 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.239+1318C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341250 | |||||||
| chr13:111341250 | C | CATCATAA others(509): Show |
5 | a0001c0001t0008g0029 a0001c0001t0008g0076 a0001c0002t0004g0016 others(2): Show |
9 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.239+1360_239+1361i others(518): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341250 | ||||||
| chr13:111341250 | C | CATCATAA others(380): Show |
7 | a0001c0001t0001g0092 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
10 | HG01071.hp2 HG01192.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.240-1410_240-1409i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341250 | ||||||
| chr13:111341250 | C | CATCATAA others(122): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0119 a0001c0002t0001g0121 others(2): Show |
6 | HG00733.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.239+1366_239+1367i others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341250 | ||||||
| chr13:111341261 | G | A | 1 | a0001c0003t0001g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.239+1329G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341261 | |||||||
| chr13:111341293 | C | A | 5 | a0001c0001t0001g0127 a0001c0001t0001g0240 a0001c0001t0001g0287 others(2): Show |
5 | HG00609.hp1 HG02559.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.239+1361C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341293 | |||||||
| chr13:111341293 | C | CATCATAA others(337): Show |
1 | a0001c0001t0001g0176 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.240-1410_240-1409i others(346): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341293 | ||||||
| chr13:111341299 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.239+1367A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341299 | |||||||
| chr13:111341336 | C | A | 6 | a0001c0001t0001g0106 a0001c0001t0002g0208 a0001c0001t0002g0212 others(3): Show |
7 | HG00609.hp1 HG01891.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.239+1404C>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341336 | |||||||
| chr13:111341336 | C | CATCATAA others(36): Show |
1 | a0001c0001t0001g0073 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.240-1410_240-1409i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341336 | ||||||
| chr13:111341342 | A | AACCCGTG others(509): Show |
1 | a0001c0002t0004g0138 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.240-1410_240-1409i others(518): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341342 | ||||||
| chr13:111341342 | A | T | 17 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0134 others(14): Show |
31 | HG00639.hp1 HG01109.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.239+1410A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341342 | |||||||
| chr13:111341347 | A | ATGTTTAG others(36): Show |
2 | a0001c0001t0001g0262 a0001c0002t0001g0269 |
2 | HG01993.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.240-1033_240-991du others(44): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341347 | ||||||
| chr13:111341347 | A | G | 112 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0022 others(109): Show |
149 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.240-1409A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341347 | |||||||
| chr13:111341347 | ATGTTTAG others(36): Show |
G | 1 | a0001c0002t0002g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.240-1409_240-1367d others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341347 | |||||||
| chr13:111341347 | ATGTTTAG others(79): Show |
C | 1 | a0001c0001t0002g0208 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.240-1409_240-1323d others(93): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341347 | |||||||
| chr13:111341379 | A | AATCATAA others(1068): Show |
1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-1249_240-1248i others(1077): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341379 | ||||||
| chr13:111341379 | A | C | 26 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0132 others(23): Show |
39 | HG01109.hp2 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.240-1377A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341379 | |||||||
| chr13:111341390 | G | A | 2 | a0001c0001t0002g0175 a0001c0001t0002g0217 |
2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.240-1366G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341390 | |||||||
| chr13:111341390 | G | GTGTTTAG others(36): Show |
1 | a0001c0001t0002g0145 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.240-1335_240-1334i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341390 | ||||||
| chr13:111341422 | A | AATCATAA others(36): Show |
1 | a0001c0001t0002g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.240-1292_240-1291i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341422 | ||||||
| chr13:111341422 | A | C | 7 | a0001c0001t0001g0106 a0001c0001t0001g0240 a0001c0001t0002g0182 others(4): Show |
11 | HG02155.hp2 HG02895.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-1334A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341422 | |||||||
| chr13:111341465 | A | AATCATAA others(122): Show |
1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-1206_240-1205i others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341465 | ||||||
| chr13:111341465 | A | C | 10 | a0001c0001t0001g0106 a0001c0001t0001g0240 a0001c0001t0008g0029 others(7): Show |
14 | HG00639.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.240-1291A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341465 | |||||||
| chr13:111341476 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.240-1280G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341476 | |||||||
| chr13:111341476 | G | GTGTTTAG others(36): Show |
1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240-1238_240-1237i others(45): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341476 | ||||||
| chr13:111341477 | T | TGTTTAGT others(208): Show |
1 | a0001c0001t0001g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.240-1131_240-1130i others(217): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341477 | ||||||
| chr13:111341490 | C | T | 1 | a0001c0002t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240-1266C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341490 | |||||||
| chr13:111341500 | T | C | 1 | a0002c0004t0001g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.240-1256T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341500 | |||||||
| chr13:111341508 | A | AATCATAA others(1070): Show |
1 | a0001c0001t0001g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.240-1076_240-1075i others(1079): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | ||||||
| chr13:111341508 | A | AATCATAA others(380): Show |
2 | a0001c0002t0004g0140 a0001c0002t0004g0141 |
2 | HG02559.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.240-1077_240-1076i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | ||||||
| chr13:111341508 | A | AATCATAA others(380): Show |
1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240-1077_240-1076i others(389): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | ||||||
| chr13:111341508 | A | AATCATAA others(1154): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0119 a0001c0002t0001g0121 others(2): Show |
6 | HG00733.hp1 HG01167.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.240-1163_240-1162i others(1163): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341508 | ||||||
| chr13:111341508 | A | C | 11 | a0001c0001t0007g0024 a0001c0001t0007g0103 a0001c0001t0008g0029 others(8): Show |
16 | HG00639.hp1 HG01255.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.240-1248A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341508 | |||||||
| chr13:111341518 | C | T | 1 | a0001c0001t0002g0041 | 2 | NA18947.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.240-1238C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341518 | |||||||
| chr13:111341530 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0105 a0001c0001t0001g0112 others(3): Show |
7 | HG01346.hp2 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.240-1226G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341530 | |||||||
| chr13:111341530 | G | GCACCTGT others(122): Show |
1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.240-1098_240-1097i others(131): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341530 | ||||||
| chr13:111341530 | G | GCACCTGT others(251): Show |
1 | a0001c0001t0001g0117 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.240-1206_240-1205i others(260): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341530 | ||||||
| chr13:111341551 | A | AATCATAA others(165): Show |
1 | a0001c0001t0002g0214 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.240-1034_240-1033i others(174): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111341551 | ||||||
| chr13:111341551 | A | C | 7 | a0001c0001t0002g0208 a0001c0001t0011g0131 a0001c0002t0001g0012 others(4): Show |
11 | HG00609.hp1 HG01071.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.240-1205A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341551 | |||||||
| chr13:111341562 | G | C | 1 | a0001c0001t0002g0187 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.240-1194G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341562 | |||||||
| chr13:111341594 | A | C | 10 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0134 others(7): Show |
16 | HG00609.hp1 HG01109.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.240-1162A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341594 | |||||||
| chr13:111341605 | G | A | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-1151G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341605 | |||||||
| chr13:111341622 | G | A | 4 | a0001c0002t0005g0064 a0001c0002t0005g0065 a0001c0002t0005g0066 others(1): Show |
4 | HG02647.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-1134G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341622 | |||||||
| chr13:111341637 | A | C | 14 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0134 others(11): Show |
24 | HG00609.hp1 HG01109.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.240-1119A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341637 | |||||||
| chr13:111341691 | G | C | 1 | a0001c0002t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.240-1065G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341691 | |||||||
| chr13:111341723 | A | C | 13 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0106 others(10): Show |
15 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.240-1033A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341723 | |||||||
| chr13:111341777 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240-979G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341777 | |||||||
| chr13:111341868 | G | A | 44 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0105 others(41): Show |
63 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.240-888G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341868 | |||||||
| chr13:111341874 | G | T | 1 | a0001c0001t0002g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.240-882G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111341874 | |||||||
| chr13:111342247 | A | T | 1 | a0001c0002t0001g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240-509A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342247 | |||||||
| chr13:111342289 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.240-467G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342289 | |||||||
| chr13:111342299 | C | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(4): Show |
8 | HG00639.hp1 HG00733.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-457C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342299 | |||||||
| chr13:111342328 | T | C | 4 | a0001c0001t0011g0131 a0001c0002t0001g0012 a0001c0002t0003g0049 others(1): Show |
8 | HG02622.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.240-428T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342328 | |||||||
| chr13:111342334 | C | T | 9 | a0001c0001t0001g0287 a0001c0001t0008g0029 a0001c0001t0008g0076 others(6): Show |
13 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.240-422C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342334 | |||||||
| chr13:111342501 | A | C | 1 | a0001c0002t0001g0264 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.240-255A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342501 | |||||||
| chr13:111342509 | G | A | 2 | a0001c0002t0001g0252 a0003c0007t0003g0256 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.240-247G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342509 | |||||||
| chr13:111342557 | C | CA | 21 | a0001c0001t0001g0074 a0001c0001t0001g0115 a0001c0001t0001g0118 others(18): Show |
25 | HG00621.hp1 HG00642.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.240-179dupA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | ||||||
| chr13:111342557 | C | CAA | 45 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0092 others(42): Show |
59 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.240-180_240-179dup others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | ||||||
| chr13:111342557 | C | CAAA | 21 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0119 others(18): Show |
32 | HG00639.hp1 HG00733.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.240-181_240-179dup others(3): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | ||||||
| chr13:111342557 | CA | C | 15 | a0001c0001t0001g0069 a0001c0001t0001g0128 a0001c0001t0002g0037 others(12): Show |
16 | HG01243.hp2 HG02083.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.240-179delA | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr13 | 111342557 | ||||||
| chr13:111342576 | A | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0089 |
4 | NA18952.hp2 NA18957.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.240-180A>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342576 | |||||||
| chr13:111342595 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.240-161G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342595 | |||||||
| chr13:111342610 | T | G | 2 | a0001c0001t0002g0179 a0001c0001t0002g0189 |
2 | NA19063.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.240-146T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342610 | |||||||
| chr13:111342741 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.240-15C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342741 | |||||||
| chr13:111342750 | C | T | 1 | a0001c0002t0003g0277 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.240-6C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 4/5 | chr13 | 111342750 | |||||||
| chr13:111342973 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.415+42C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111342973 | |||||||
| chr13:111343032 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.415+101C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343032 | |||||||
| chr13:111343097 | A | C | 1 | a0001c0002t0001g0245 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.415+166A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343097 | |||||||
| chr13:111343103 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.415+172G>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343103 | |||||||
| chr13:111343171 | T | G | 1 | a0001c0003t0001g0027 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.415+240T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343171 | |||||||
| chr13:111343184 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.415+253C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343184 | |||||||
| chr13:111343333 | A | C | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+402A>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343333 | |||||||
| chr13:111343334 | CGTGGTGG | C | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+404_415+410del others(7): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343334 | |||||||
| chr13:111343335 | G | A | 3 | a0001c0002t0001g0094 a0001c0002t0003g0051 a0001c0002t0003g0157 |
4 | HG02615.hp1 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+404G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343335 | |||||||
| chr13:111343342 | T | A | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+411T>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343342 | |||||||
| chr13:111343345 | TG | T | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+416delG | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr13 | 111343345 | ||||||
| chr13:111343347 | G | C | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+416G>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343347 | |||||||
| chr13:111343348 | T | C | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+417T>C | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343348 | |||||||
| chr13:111343352 | GCA | G | 6 | a0001c0003t0001g0025 a0001c0003t0001g0027 a0001c0003t0001g0104 others(3): Show |
8 | HG00735.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+422_415+423del others(2): Show |
TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343352 | |||||||
| chr13:111343401 | G | A | 53 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0063 others(50): Show |
68 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.415+470G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343401 | |||||||
| chr13:111343499 | A | T | 1 | a0001c0001t0002g0183 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.415+568A>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343499 | |||||||
| chr13:111343577 | G | A | 1 | a0001c0002t0001g0045 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.416-506G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343577 | |||||||
| chr13:111343582 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0109 |
2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.416-501C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343582 | |||||||
| chr13:111343593 | C | T | 1 | a0001c0001t0007g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.416-490C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343593 | |||||||
| chr13:111343685 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.416-398G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343685 | |||||||
| chr13:111343687 | C | T | 9 | a0001c0001t0001g0287 a0001c0001t0008g0029 a0001c0001t0008g0076 others(6): Show |
13 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.416-396C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343687 | |||||||
| chr13:111343809 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.416-274G>A | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111343809 | |||||||
| chr13:111344028 | C | T | 1 | a0001c0002t0001g0263 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.416-55C>T | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111344028 | |||||||
| chr13:111344070 | T | G | 1 | a0001c0002t0001g0264 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.416-13T>G | TEX29 | ENSG00000153495.11 | transcript | ENST00000283547.2 | protein_coding | 5/5 | chr13 | 111344070 |