Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2040 |
| ensemblid | ENSG00000148175.13 |
| hgncid | 3383 |
| symbol | STOM |
| name | stomatin |
| refseq_nuc | NM_004099.6 |
| refseq_prot | NP_004090.4 |
| ensembl_nuc | ENST00000286713.7 |
| ensembl_prot | ENSP00000286713.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 121338987 |
| end | 121370250 |
| strand | - |
| ver | v1.2 |
| region | chr9:121338987-121370250 |
| region5000 | chr9:121333987-121375250 |
| regionname0 | STOM_chr9_121338987_121370250 |
| regionname5000 | STOM_chr9_121333987_121375250 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 288 | 379 | 90 | 72 | 165 | 18 | 32 | 125 | STOM_chr9_121333987_121375250 | STOM | MAEKR others(283): Show |
chr9 | 121333987 | 121375250 |
| a0002 | 0/0 | 288 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | STOM_chr9_121333987_121375250 | STOM | MAEKR others(283): Show |
chr9 | 121333987 | 121375250 |
| a0003 | 0/0 | 288 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | STOM_chr9_121333987_121375250 | STOM | MAEKR others(283): Show |
chr9 | 121333987 | 121375250 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 864 | 377 | 89 | 72 | 164 | 18 | 32 | STOM_chr9_121333987_121375250 | STOM | ATGGC others(859): Show |
chr9 | 121333987 | 121375250 | ||
| a0001c0004 | 0/0 | 864 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | ATGGC others(859): Show |
chr9 | 121333987 | 121375250 | ||
| a0001c0005 | 0/0 | 864 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | ATGGC others(859): Show |
chr9 | 121333987 | 121375250 | ||
| a0002c0002 | 0/0 | 864 | 4 | 0 | 2 | 0 | 0 | 2 | STOM_chr9_121333987_121375250 | STOM | ATGGC others(859): Show |
chr9 | 121333987 | 121375250 | ||
| a0003c0003 | 0/0 | 864 | 3 | 0 | 0 | 3 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | ATGGC others(859): Show |
chr9 | 121333987 | 121375250 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3145 | 198 | 44 | 32 | 91 | 14 | 16 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0002 | 0/0 | 3145 | 52 | 10 | 7 | 33 | 0 | 2 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0003 | 0/0 | 3146 | 51 | 0 | 13 | 29 | 0 | 9 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3141): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0004 | 0/0 | 3146 | 25 | 3 | 12 | 5 | 2 | 3 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3141): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0005 | 1/0 | 3145 | 23 | 10 | 8 | 1 | 1 | 2 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0006 | 0/0 | 3145 | 11 | 11 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0007 | 0/0 | 3146 | 5 | 5 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3141): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0008 | 0/0 | 3146 | 3 | 3 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3141): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0009 | 0/0 | 3145 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0010 | 0/0 | 3146 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3141): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0011 | 0/0 | 3145 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0013 | 0/0 | 3146 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3141): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0015 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0001t0016 | 0/0 | 3145 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0004t0002 | 0/0 | 3145 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0001c0005t0001 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0002c0002t0005 | 0/0 | 3145 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0002c0002t0012 | 0/0 | 3145 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0002c0002t0014 | 0/0 | 3145 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| a0003c0003t0001 | 0/0 | 3145 | 3 | 0 | 0 | 3 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | GCATT others(3140): Show |
chr9 | 121333987 | 121375250 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 10 | 2 | 2 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0006 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0005 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0047 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0002 | 0/0 | 8 | 5 | 1 | 0 | 1 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0008g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0009g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0011g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0001c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0002c0002t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0002c0002t0012g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0002c0002t0014g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0003c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0002 | EUR | GBR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0245 | EUR | GBR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0138 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01069 | hp1 | a0002 | c0002 | t0012 | g0022 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01071 | hp2 | a0002 | c0002 | t0012 | g0022 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0240 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0140 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PUR | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0057 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0251 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CDX | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0139 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02647 | hp1 | a0001 | c0001 | t0010 | g0172 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0135 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0248 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02738 | hp2 | a0002 | c0002 | t0005 | g0196 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0203 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0197 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0276 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0210 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0252 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | STU | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | BEB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | BEB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0131 | SAS | BEB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0171 | SAS | STU | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | STU | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG04199 | hp1 | a0002 | c0002 | t0014 | g0125 | SAS | STU | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | YRI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | YRI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | CHB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | YRI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | YRI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0044 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18962 | hp1 | a0001 | c0001 | t0016 | g0087 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0088 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0020 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19012 | hp2 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | LWK | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | LWK | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | LWK | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0044 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19077 | hp2 | a0001 | c0004 | t0002 | g0272 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | YRI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0127 | AFR | ASW | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0244 | EUR | TSI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA20805 | hp2 | a0001 | c0001 | t0013 | g0075 | EUR | TSI | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0124 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | MSL | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | USA | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0180 | REF | REF | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0237 | REF | REF | STOM_chr9_121333987_121375250 | STOM | chr9 | 121333987 | 121375250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:121341245 | A | G | 1 | a0002 | 4 | HG01069.hp1 HG01071.hp2 HG02738.hp2 others(1): Show |
missense_variant | MODERATE | c.824T>C | p.Met275Thr | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 887/3145 | 824/867 | 275/288 | chr9 | 121341245 | |||
| chr9:121354630 | C | T | 1 | a0003 | 3 | NA18970.hp2 NA18984.hp1 NA19010.hp1 |
missense_variant | MODERATE | c.209G>A | p.Arg70His | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/7 | 272/3145 | 209/867 | 70/288 | chr9 | 121354630 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:121348090 | C | T | 1 | a0001c0005 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.585G>A | p.Lys195Lys | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/7 | 648/3145 | 585/867 | 195/288 | chr9 | 121348090 | |||
| chr9:121356137 | A | G | 1 | a0001c0004 | 1 | NA19077.hp2 | synonymous_variant | LOW | c.81T>C | p.Leu27Leu | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/7 | 144/3145 | 81/867 | 27/288 | chr9 | 121356137 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:121339188 | A | G | 1 | a0002c0002t0014 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2014T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 2014 | chr9 | 121339188 | ||||||
| chr9:121339285 | C | T | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(5): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1917G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 1917 | chr9 | 121339285 | ||||||
| chr9:121339691 | T | C | 1 | a0001c0001t0015 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1511A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 1511 | chr9 | 121339691 | ||||||
| chr9:121340043 | G | A | 1 | a0001c0001t0016 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1159C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 1159 | chr9 | 121340043 | ||||||
| chr9:121340072 | T | C | 2 | a0001c0001t0003 a0001c0001t0009 |
53 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1130A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 1130 | chr9 | 121340072 | ||||||
| chr9:121340080 | G | A | 1 | a0002c0002t0012 | 2 | HG01069.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 1122 | chr9 | 121340080 | ||||||
| chr9:121340326 | C | G | 1 | a0001c0001t0010 | 2 | HG02647.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*876G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 876 | chr9 | 121340326 | ||||||
| chr9:121340618 | C | T | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0004t0002 |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*584G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 584 | chr9 | 121340618 | ||||||
| chr9:121340752 | G | GA | 6 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(3): Show |
87 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*449dupT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 449 | chr9 | 121340752 | ||||||
| chr9:121340753 | A | G | 1 | a0001c0001t0006 | 11 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*449T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 449 | chr9 | 121340753 | ||||||
| chr9:121340892 | C | G | 1 | a0001c0001t0013 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*310G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 310 | chr9 | 121340892 | ||||||
| chr9:121340904 | C | T | 4 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(1): Show |
58 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*298G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 298 | chr9 | 121340904 | ||||||
| chr9:121340962 | A | G | 1 | a0001c0001t0011 | 2 | NA18993.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*240T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 240 | chr9 | 121340962 | ||||||
| chr9:121341007 | G | T | 4 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(1): Show |
58 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*195C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 7/7 | 195 | chr9 | 121341007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:121341481 | G | A | 52 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0018 others(49): Show |
64 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.661-73C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121341481 | |||||||
| chr9:121341765 | T | C | 9 | a0001c0001t0006g0017 a0001c0001t0006g0046 a0001c0001t0006g0053 others(6): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.661-357A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121341765 | |||||||
| chr9:121341870 | C | T | 1 | a0001c0001t0002g0283 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.661-462G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121341870 | |||||||
| chr9:121341872 | G | C | 43 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(40): Show |
58 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.661-464C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121341872 | |||||||
| chr9:121341980 | C | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0092 |
2 | NA19009.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.661-572G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121341980 | |||||||
| chr9:121342140 | C | T | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.661-732G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342140 | |||||||
| chr9:121342141 | G | A | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.661-733C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342141 | |||||||
| chr9:121342161 | G | A | 1 | a0001c0001t0005g0138 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.661-753C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342161 | |||||||
| chr9:121342313 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.661-905C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342313 | |||||||
| chr9:121342366 | CA | C | 61 | a0001c0001t0001g0085 a0001c0001t0001g0170 a0001c0001t0001g0235 others(58): Show |
79 | HG00099.hp1 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.661-959delT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342366 | |||||||
| chr9:121342366 | CAA | C | 37 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0037 others(34): Show |
46 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.661-960_661-959del others(2): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342366 | |||||||
| chr9:121342667 | T | C | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.661-1259A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342667 | |||||||
| chr9:121342786 | C | T | 1 | a0003c0003t0001g0088 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.661-1378G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342786 | |||||||
| chr9:121342852 | A | G | 1 | a0001c0001t0003g0221 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.661-1444T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121342852 | |||||||
| chr9:121343201 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.661-1793T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121343201 | |||||||
| chr9:121343462 | A | G | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.661-2054T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121343462 | |||||||
| chr9:121343686 | C | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0201 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.661-2278G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121343686 | |||||||
| chr9:121343918 | G | A | 1 | a0002c0002t0014g0125 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.661-2510C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121343918 | |||||||
| chr9:121343931 | G | A | 39 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(36): Show |
48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.661-2523C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121343931 | |||||||
| chr9:121343999 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0187 |
2 | HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.661-2591C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121343999 | |||||||
| chr9:121344256 | A | G | 43 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(40): Show |
58 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.661-2848T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344256 | |||||||
| chr9:121344287 | C | T | 1 | a0001c0005t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.661-2879G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344287 | |||||||
| chr9:121344288 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.661-2880G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344288 | |||||||
| chr9:121344329 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0161 a0001c0001t0001g0163 others(6): Show |
10 | HG01243.hp1 HG02809.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.661-2921A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344329 | |||||||
| chr9:121344330 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.661-2922G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344330 | |||||||
| chr9:121344342 | A | G | 7 | a0001c0001t0001g0123 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | HG02055.hp2 HG02056.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.661-2934T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344342 | |||||||
| chr9:121344442 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.661-3034C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344442 | |||||||
| chr9:121344837 | A | T | 1 | a0001c0001t0002g0018 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.660+3178T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344837 | |||||||
| chr9:121344977 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.660+3038G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121344977 | |||||||
| chr9:121345208 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.660+2807T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345208 | |||||||
| chr9:121345230 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.660+2785T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345230 | |||||||
| chr9:121345241 | T | TTGCCAGA others(3): Show |
1 | a0001c0001t0002g0195 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.660+2764_660+2773d others(12): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345241 | |||||||
| chr9:121345260 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.660+2755T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345260 | |||||||
| chr9:121345261 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.660+2754C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345261 | |||||||
| chr9:121345382 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.660+2633C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345382 | |||||||
| chr9:121345444 | T | C | 1 | a0001c0001t0002g0195 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.660+2571A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345444 | |||||||
| chr9:121345445 | C | G | 1 | a0001c0001t0002g0195 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.660+2570G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345445 | |||||||
| chr9:121345517 | C | T | 51 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(48): Show |
63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.660+2498G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345517 | |||||||
| chr9:121345567 | G | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.660+2448C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345567 | |||||||
| chr9:121345598 | A | T | 1 | a0001c0001t0002g0195 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.660+2417T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345598 | |||||||
| chr9:121345671 | A | G | 4 | a0001c0001t0008g0039 a0001c0001t0008g0210 a0001c0001t0010g0172 others(1): Show |
5 | HG02572.hp1 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.660+2344T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345671 | |||||||
| chr9:121345792 | G | C | 1 | a0001c0005t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.660+2223C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345792 | |||||||
| chr9:121345867 | T | C | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.660+2148A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345867 | |||||||
| chr9:121345894 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.660+2121G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345894 | |||||||
| chr9:121345984 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(38): Show |
74 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.660+2031T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121345984 | |||||||
| chr9:121346116 | A | G | 7 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0001g0151 others(4): Show |
7 | HG02074.hp2 HG02523.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+1899T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346116 | |||||||
| chr9:121346254 | T | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0254 |
2 | HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.660+1761A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346254 | |||||||
| chr9:121346339 | C | T | 1 | a0001c0001t0003g0226 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.660+1676G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346339 | |||||||
| chr9:121346340 | A | G | 45 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(42): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.660+1675T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346340 | |||||||
| chr9:121346462 | A | G | 1 | a0002c0002t0012g0022 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.660+1553T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346462 | |||||||
| chr9:121346681 | A | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
362 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.660+1334T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346681 | |||||||
| chr9:121346744 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
362 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.660+1271T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121346744 | |||||||
| chr9:121347389 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.660+626G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347389 | |||||||
| chr9:121347643 | C | T | 105 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(102): Show |
133 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.660+372G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347643 | |||||||
| chr9:121347716 | A | G | 1 | a0001c0001t0005g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.660+299T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347716 | |||||||
| chr9:121347855 | T | A | 1 | a0001c0001t0003g0212 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.660+160A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347855 | |||||||
| chr9:121347901 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.660+114A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347901 | |||||||
| chr9:121347984 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.660+31C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347984 | |||||||
| chr9:121347991 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.660+24T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 6/6 | chr9 | 121347991 | |||||||
| chr9:121348173 | C | G | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.526-24G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348173 | |||||||
| chr9:121348419 | C | T | 1 | a0001c0001t0002g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.526-270G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348419 | |||||||
| chr9:121348496 | A | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0080 others(4): Show |
8 | HG01175.hp1 HG01255.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-347T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348496 | |||||||
| chr9:121348518 | A | C | 18 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(15): Show |
24 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.526-369T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348518 | |||||||
| chr9:121348590 | T | G | 1 | a0001c0001t0002g0018 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.526-441A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348590 | |||||||
| chr9:121348857 | A | G | 51 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(48): Show |
63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.525+263T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348857 | |||||||
| chr9:121348911 | A | T | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.525+209T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121348911 | |||||||
| chr9:121349001 | G | GA | 9 | a0001c0001t0001g0070 a0001c0001t0001g0160 a0001c0001t0001g0181 others(6): Show |
9 | HG00621.hp2 HG01433.hp1 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+118dupT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121349001 | |||||||
| chr9:121349046 | G | A | 2 | a0001c0001t0004g0197 a0001c0001t0004g0244 |
2 | HG03239.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.525+74C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121349046 | |||||||
| chr9:121349092 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0148 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.525+28C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 5/6 | chr9 | 121349092 | |||||||
| chr9:121349350 | A | C | 45 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(42): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.322-27T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121349350 | |||||||
| chr9:121349419 | C | A | 1 | a0001c0001t0001g0029 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.322-96G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121349419 | |||||||
| chr9:121349914 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.322-591G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121349914 | |||||||
| chr9:121350043 | T | G | 1 | a0001c0001t0003g0213 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.322-720A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350043 | |||||||
| chr9:121350059 | T | C | 5 | a0001c0001t0007g0248 a0001c0001t0007g0249 a0002c0002t0005g0196 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-736A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350059 | |||||||
| chr9:121350061 | G | A | 39 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(36): Show |
48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.322-738C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350061 | |||||||
| chr9:121350090 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.322-767A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350090 | |||||||
| chr9:121350282 | G | T | 1 | a0001c0005t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.322-959C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350282 | |||||||
| chr9:121350490 | G | A | 1 | a0001c0001t0007g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.322-1167C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350490 | |||||||
| chr9:121350550 | T | C | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.322-1227A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350550 | |||||||
| chr9:121350943 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0084 |
2 | HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.322-1620G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350943 | |||||||
| chr9:121350974 | C | T | 1 | a0001c0005t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.322-1651G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121350974 | |||||||
| chr9:121351005 | C | A | 1 | a0001c0001t0002g0268 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.322-1682G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351005 | |||||||
| chr9:121351047 | C | T | 1 | a0001c0001t0001g0003 | 8 | HG01074.hp1 HG02148.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.322-1724G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351047 | |||||||
| chr9:121351085 | G | C | 1 | a0001c0001t0002g0275 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.322-1762C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351085 | |||||||
| chr9:121351276 | G | A | 3 | a0002c0002t0005g0196 a0002c0002t0012g0022 a0002c0002t0014g0125 |
4 | HG01069.hp1 HG01071.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1944C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351276 | |||||||
| chr9:121351279 | G | A | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.321+1941C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351279 | |||||||
| chr9:121351335 | G | A | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01261.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1885C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351335 | |||||||
| chr9:121351338 | G | A | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.321+1882C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351338 | |||||||
| chr9:121351455 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.321+1765C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351455 | |||||||
| chr9:121351619 | A | G | 1 | a0001c0001t0001g0033 | 2 | NA18953.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.321+1601T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351619 | |||||||
| chr9:121351927 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.321+1293T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121351927 | |||||||
| chr9:121352027 | A | G | 39 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(36): Show |
48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.321+1193T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352027 | |||||||
| chr9:121352077 | T | A | 1 | a0001c0001t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.321+1143A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352077 | |||||||
| chr9:121352095 | G | T | 53 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(50): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.321+1125C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352095 | |||||||
| chr9:121352424 | T | C | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.321+796A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352424 | |||||||
| chr9:121352440 | T | G | 1 | a0001c0001t0003g0219 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.321+780A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352440 | |||||||
| chr9:121352450 | G | C | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.321+770C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352450 | |||||||
| chr9:121352587 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.321+633T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352587 | |||||||
| chr9:121352734 | C | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0236 |
3 | HG02965.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.321+486G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352734 | |||||||
| chr9:121352822 | C | G | 42 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(39): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.321+398G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352822 | |||||||
| chr9:121352823 | G | T | 1 | a0001c0001t0002g0016 | 3 | HG00408.hp2 HG02040.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.321+397C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352823 | |||||||
| chr9:121352917 | C | T | 1 | a0001c0001t0002g0018 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.321+303G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121352917 | |||||||
| chr9:121353021 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.321+199G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121353021 | |||||||
| chr9:121353074 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(41): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.321+146G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121353074 | |||||||
| chr9:121353154 | C | G | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01261.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+66G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 4/6 | chr9 | 121353154 | |||||||
| chr9:121353315 | T | C | 1 | a0001c0001t0005g0024 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.239-13A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121353315 | |||||||
| chr9:121353633 | C | T | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.239-331G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121353633 | |||||||
| chr9:121353756 | T | G | 2 | a0001c0001t0002g0231 a0001c0001t0002g0232 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.239-454A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121353756 | |||||||
| chr9:121354064 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.238+537T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354064 | |||||||
| chr9:121354367 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.238+234T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354367 | |||||||
| chr9:121354382 | C | T | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.238+219G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354382 | |||||||
| chr9:121354417 | A | G | 69 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(66): Show |
90 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.238+184T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354417 | |||||||
| chr9:121354449 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0010g0172 a0001c0001t0015g0139 |
3 | HG02451.hp2 HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.238+152C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354449 | |||||||
| chr9:121354498 | C | A | 53 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(50): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.238+103G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354498 | |||||||
| chr9:121354515 | G | A | 51 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(48): Show |
63 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.238+86C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354515 | |||||||
| chr9:121354574 | TA | T | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.238+26delT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 3/6 | chr9 | 121354574 | |||||||
| chr9:121354910 | T | C | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.166-237A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121354910 | |||||||
| chr9:121355016 | T | C | 1 | a0001c0001t0005g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-343A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355016 | |||||||
| chr9:121355231 | C | CAAT | 6 | a0001c0001t0002g0018 a0001c0001t0002g0195 a0001c0001t0002g0260 others(3): Show |
7 | HG00639.hp1 HG00735.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-559_166-558ins others(3): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355231 | |||||||
| chr9:121355231 | C | CAATA | 46 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(43): Show |
57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.166-559_166-558ins others(4): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355231 | |||||||
| chr9:121355231 | CA | C | 8 | a0001c0001t0001g0083 a0001c0001t0001g0123 a0001c0001t0001g0166 others(5): Show |
9 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-559delT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355231 | |||||||
| chr9:121355245 | A | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.166-572T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355245 | |||||||
| chr9:121355248 | A | T | 21 | a0001c0001t0001g0126 a0001c0001t0001g0161 a0001c0001t0001g0165 others(18): Show |
24 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-575T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355248 | |||||||
| chr9:121355249 | AAT | A | 34 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(31): Show |
49 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.166-578_166-577del others(2): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355249 | |||||||
| chr9:121355250 | AT | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0173 a0001c0001t0001g0182 others(6): Show |
9 | HG01081.hp2 HG01106.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-578delA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355250 | |||||||
| chr9:121355251 | T | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.166-578A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355251 | |||||||
| chr9:121355254 | T | A | 70 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0063 others(67): Show |
89 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.166-581A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355254 | |||||||
| chr9:121355257 | T | A | 38 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(35): Show |
52 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.166-584A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355257 | |||||||
| chr9:121355281 | G | A | 1 | a0001c0001t0005g0251 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.166-608C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355281 | |||||||
| chr9:121355345 | G | A | 42 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(39): Show |
57 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.166-672C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355345 | |||||||
| chr9:121355387 | C | CA | 20 | a0001c0001t0001g0095 a0001c0001t0001g0126 a0001c0001t0001g0253 others(17): Show |
26 | HG00140.hp1 HG00423.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.165+665dupT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355387 | |||||||
| chr9:121355387 | CA | C | 91 | a0001c0001t0001g0102 a0001c0001t0001g0256 a0001c0001t0002g0008 others(88): Show |
118 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.165+665delT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355387 | |||||||
| chr9:121355442 | G | C | 18 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(15): Show |
24 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+611C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355442 | |||||||
| chr9:121355448 | T | A | 3 | a0001c0001t0001g0256 a0001c0001t0002g0262 a0001c0001t0002g0265 |
3 | HG00438.hp1 HG02135.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.165+605A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355448 | |||||||
| chr9:121355448 | T | G | 1 | a0001c0005t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.165+605A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355448 | |||||||
| chr9:121355454 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165+599C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355454 | |||||||
| chr9:121355469 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.165+584G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355469 | |||||||
| chr9:121355564 | T | C | 3 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 |
3 | HG02976.hp2 HG03130.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.165+489A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355564 | |||||||
| chr9:121355598 | G | C | 10 | a0001c0001t0002g0018 a0001c0001t0006g0017 a0001c0001t0006g0046 others(7): Show |
13 | HG00639.hp1 HG00735.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+455C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355598 | |||||||
| chr9:121355651 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.165+402G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355651 | |||||||
| chr9:121355975 | T | C | 53 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(50): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.165+78A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121355975 | |||||||
| chr9:121356009 | G | T | 1 | a0001c0001t0005g0251 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.165+44C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 2/6 | chr9 | 121356009 | |||||||
| chr9:121356244 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.62-88A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356244 | |||||||
| chr9:121356318 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.62-162G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356318 | |||||||
| chr9:121356498 | A | G | 59 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(56): Show |
72 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.62-342T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356498 | |||||||
| chr9:121356507 | C | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0195 |
2 | NA19059.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.62-351G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356507 | |||||||
| chr9:121356531 | G | A | 6 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-375C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356531 | |||||||
| chr9:121356683 | C | T | 1 | a0001c0001t0008g0039 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.62-527G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356683 | |||||||
| chr9:121356686 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.62-530G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356686 | |||||||
| chr9:121356788 | G | A | 2 | a0001c0001t0002g0267 a0001c0001t0002g0268 |
2 | NA18966.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.62-632C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356788 | |||||||
| chr9:121356881 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.62-725C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121356881 | |||||||
| chr9:121357152 | A | G | 4 | a0001c0001t0002g0037 a0001c0001t0002g0255 a0001c0001t0002g0263 others(1): Show |
5 | HG02965.hp1 HG02970.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.62-996T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357152 | |||||||
| chr9:121357233 | C | T | 41 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(38): Show |
56 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.62-1077G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357233 | |||||||
| chr9:121357234 | G | A | 6 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-1078C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357234 | |||||||
| chr9:121357343 | A | G | 6 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.62-1187T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357343 | |||||||
| chr9:121357416 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.62-1260A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357416 | |||||||
| chr9:121357424 | G | GATATATA others(1): Show |
3 | a0001c0001t0003g0218 a0001c0001t0003g0219 a0001c0001t0003g0226 |
3 | NA18945.hp2 NA18948.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.62-1276_62-1269dup others(8): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(3): Show |
1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62-1278_62-1269dup others(10): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(7): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0104 a0001c0001t0001g0109 |
3 | HG02273.hp1 HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.62-1282_62-1269dup others(14): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(9): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0096 others(3): Show |
12 | HG00642.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-1284_62-1269dup others(16): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(11): Show |
11 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0095 others(8): Show |
17 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(18): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(13): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0102 others(3): Show |
14 | HG02027.hp2 HG02135.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(20): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(15): Show |
14 | a0001c0001t0001g0058 a0001c0001t0001g0071 a0001c0001t0001g0092 others(11): Show |
16 | HG01070.hp1 HG01261.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(22): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(17): Show |
13 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0061 others(10): Show |
16 | HG00673.hp1 HG01346.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(24): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(19): Show |
14 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(11): Show |
17 | HG00280.hp1 HG01106.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(26): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(21): Show |
10 | a0001c0001t0001g0027 a0001c0001t0001g0067 a0001c0001t0001g0082 others(7): Show |
15 | HG00438.hp2 HG00597.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(28): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(23): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0065 others(11): Show |
19 | HG00140.hp1 HG00597.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(30): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(25): Show |
17 | a0001c0001t0001g0078 a0001c0001t0001g0148 a0001c0001t0001g0157 others(14): Show |
19 | HG00140.hp2 HG01081.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(32): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(27): Show |
11 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0112 others(8): Show |
11 | HG01255.hp1 HG01256.hp1 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(34): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(29): Show |
8 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG01069.hp2 HG01934.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(36): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(31): Show |
4 | a0001c0001t0001g0062 a0001c0001t0001g0111 a0001c0001t0003g0211 others(1): Show |
4 | HG00741.hp2 HG01123.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(38): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATATA others(37): Show |
1 | a0001c0001t0001g0146 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.62-1269_62-1268ins others(44): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357424 | G | GATATTGA others(21): Show |
2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.62-1269_62-1268ins others(28): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357424 | |||||||
| chr9:121357435 | ATATATT | A | 58 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(55): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.62-1285_62-1280del others(6): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357435 | |||||||
| chr9:121357437 | A | ATATATAT others(29): Show |
3 | a0001c0001t0003g0209 a0001c0001t0003g0220 a0001c0001t0004g0132 |
3 | HG01346.hp1 NA18966.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.62-1282_62-1281ins others(36): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(27): Show |
3 | a0001c0001t0003g0228 a0001c0001t0004g0005 a0001c0001t0009g0044 |
4 | HG01433.hp2 NA18941.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-1282_62-1281ins others(34): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(25): Show |
5 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0003g0206 others(2): Show |
5 | HG00621.hp1 HG01081.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-1282_62-1281ins others(32): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(23): Show |
6 | a0001c0001t0001g0126 a0001c0001t0003g0045 a0001c0001t0003g0119 others(3): Show |
9 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.62-1282_62-1281ins others(30): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(21): Show |
5 | a0001c0001t0001g0181 a0001c0001t0001g0185 a0001c0001t0001g0186 others(2): Show |
5 | HG01255.hp2 HG01993.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-1282_62-1281ins others(28): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0227 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.62-1282_62-1281ins others(32): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.62-1282_62-1281ins others(24): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.62-1282_62-1281ins others(20): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357437 | A | ATATATAT others(9): Show |
1 | a0001c0005t0001g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.62-1282_62-1281ins others(16): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357437 | |||||||
| chr9:121357441 | T | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.62-1285A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357441 | |||||||
| chr9:121357444 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0154 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.62-1289_62-1288ins others(23): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357444 | |||||||
| chr9:121357444 | T | TATATATA others(24): Show |
1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.62-1289_62-1288ins others(31): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357444 | |||||||
| chr9:121357444 | T | TATATATA others(26): Show |
1 | a0001c0001t0001g0106 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.62-1289_62-1288ins others(33): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357444 | |||||||
| chr9:121357445 | T | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | HG02083.hp1 NA18941.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.62-1289A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357445 | |||||||
| chr9:121357449 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.62-1293A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357449 | |||||||
| chr9:121357453 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.62-1297A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357453 | |||||||
| chr9:121357455 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.62-1299A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357455 | |||||||
| chr9:121357496 | G | T | 1 | a0001c0001t0007g0128 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62-1340C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357496 | |||||||
| chr9:121357597 | A | G | 59 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(56): Show |
72 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.62-1441T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357597 | |||||||
| chr9:121357614 | A | G | 14 | a0001c0001t0005g0002 a0001c0001t0005g0023 a0001c0001t0005g0024 others(11): Show |
23 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-1458T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357614 | |||||||
| chr9:121357729 | C | T | 14 | a0001c0001t0005g0002 a0001c0001t0005g0023 a0001c0001t0005g0024 others(11): Show |
23 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.62-1573G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357729 | |||||||
| chr9:121357772 | A | C | 1 | a0001c0001t0002g0037 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.62-1616T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357772 | |||||||
| chr9:121357874 | G | A | 53 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(50): Show |
65 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.62-1718C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357874 | |||||||
| chr9:121357908 | CA | C | 100 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(97): Show |
128 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.62-1753delT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121357908 | |||||||
| chr9:121358095 | G | T | 1 | a0001c0001t0004g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.62-1939C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358095 | |||||||
| chr9:121358140 | TA | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0145 a0001c0001t0001g0164 others(3): Show |
7 | HG02630.hp1 HG03041.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.62-1985delT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358140 | |||||||
| chr9:121358149 | A | AAC | 18 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(15): Show |
24 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.62-1994_62-1993ins others(2): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358149 | |||||||
| chr9:121358149 | A | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0110 a0001c0001t0002g0050 others(1): Show |
4 | HG01934.hp2 HG02922.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-1993T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358149 | |||||||
| chr9:121358152 | A | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(159): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.62-1996T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358152 | |||||||
| chr9:121358154 | AT | A | 3 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0003g0224 |
3 | HG01081.hp2 HG01168.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.62-1999delA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358154 | |||||||
| chr9:121358155 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0105 others(34): Show |
46 | HG00438.hp2 HG00621.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.62-1999A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358155 | |||||||
| chr9:121358191 | T | C | 1 | a0001c0001t0005g0250 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62-2035A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358191 | |||||||
| chr9:121358264 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.62-2108T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358264 | |||||||
| chr9:121358444 | G | GGAAA | 7 | a0001c0001t0007g0128 a0001c0001t0007g0129 a0001c0001t0007g0133 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.62-2292_62-2289dup others(4): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358444 | |||||||
| chr9:121358463 | A | AAAGGAAG others(5): Show |
2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.62-2319_62-2308dup others(12): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358463 | |||||||
| chr9:121358476 | A | G | 1 | a0001c0001t0006g0054 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.62-2320T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358476 | |||||||
| chr9:121358656 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.62-2500T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358656 | |||||||
| chr9:121358781 | G | A | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.62-2625C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358781 | |||||||
| chr9:121358880 | C | G | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.62-2724G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358880 | |||||||
| chr9:121358991 | A | C | 136 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0253 others(133): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.62-2835T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121358991 | |||||||
| chr9:121359150 | G | A | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.62-2994C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121359150 | |||||||
| chr9:121359564 | G | C | 38 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(35): Show |
52 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.62-3408C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121359564 | |||||||
| chr9:121360236 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.62-4080A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360236 | |||||||
| chr9:121360417 | A | T | 1 | a0001c0001t0006g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.62-4261T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360417 | |||||||
| chr9:121360456 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62-4300A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360456 | |||||||
| chr9:121360482 | T | C | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.62-4326A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360482 | |||||||
| chr9:121360491 | G | A | 1 | a0001c0001t0002g0269 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.62-4335C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360491 | |||||||
| chr9:121360560 | A | C | 49 | a0001c0001t0001g0143 a0001c0001t0001g0256 a0001c0001t0002g0008 others(46): Show |
61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.62-4404T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360560 | |||||||
| chr9:121360751 | A | G | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG01123.hp2 HG01358.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-4595T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360751 | |||||||
| chr9:121360776 | G | GT | 9 | a0001c0001t0002g0018 a0001c0001t0006g0017 a0001c0001t0006g0046 others(6): Show |
12 | HG00639.hp1 HG00735.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.62-4621dupA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360776 | |||||||
| chr9:121360805 | T | C | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.62-4649A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121360805 | |||||||
| chr9:121361129 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.62-4973C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361129 | |||||||
| chr9:121361380 | CT | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.62-5225delA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361380 | |||||||
| chr9:121361380 | CTT | C | 54 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0109 others(51): Show |
70 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.62-5226_62-5225del others(2): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361380 | |||||||
| chr9:121361380 | CTTT | C | 18 | a0001c0001t0001g0178 a0001c0001t0003g0225 a0001c0001t0003g0226 others(15): Show |
27 | HG00099.hp2 HG00738.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.62-5227_62-5225del others(3): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361380 | |||||||
| chr9:121361380 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.62-5235_62-5225del others(11): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361380 | |||||||
| chr9:121361427 | C | T | 25 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(22): Show |
32 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.62-5271G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361427 | |||||||
| chr9:121361578 | C | T | 25 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(22): Show |
32 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.62-5422G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361578 | |||||||
| chr9:121361631 | T | G | 136 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0253 others(133): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.62-5475A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361631 | |||||||
| chr9:121361727 | T | G | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.62-5571A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361727 | |||||||
| chr9:121361872 | A | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.62-5716T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121361872 | |||||||
| chr9:121362035 | AT | A | 41 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(38): Show |
56 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.62-5880delA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121362035 | |||||||
| chr9:121362121 | C | G | 1 | a0001c0001t0003g0206 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.62-5965G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121362121 | |||||||
| chr9:121362203 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.62-6047A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121362203 | |||||||
| chr9:121362236 | G | T | 55 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0025 others(52): Show |
79 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.62-6080C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121362236 | |||||||
| chr9:121362393 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02486.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.62-6237T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121362393 | |||||||
| chr9:121362690 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.62-6534G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121362690 | |||||||
| chr9:121363046 | C | A | 29 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0002g0231 others(26): Show |
36 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.62-6890G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363046 | |||||||
| chr9:121363242 | A | G | 136 | a0001c0001t0001g0059 a0001c0001t0001g0123 a0001c0001t0001g0126 others(133): Show |
179 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.61+6885T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363242 | |||||||
| chr9:121363410 | A | G | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.61+6717T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363410 | |||||||
| chr9:121363574 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.61+6553T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363574 | |||||||
| chr9:121363580 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.61+6547T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363580 | |||||||
| chr9:121363706 | G | C | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+6421C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363706 | |||||||
| chr9:121363947 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61+6180C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121363947 | |||||||
| chr9:121364340 | G | A | 29 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0002g0231 others(26): Show |
36 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.61+5787C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121364340 | |||||||
| chr9:121364663 | T | C | 25 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(22): Show |
32 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.61+5464A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121364663 | |||||||
| chr9:121364727 | A | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(98): Show |
130 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.61+5400T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121364727 | |||||||
| chr9:121364912 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.61+5215G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121364912 | |||||||
| chr9:121365057 | C | T | 89 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0230 others(86): Show |
120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.61+5070G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365057 | |||||||
| chr9:121365059 | C | T | 1 | a0001c0001t0005g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.61+5068G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365059 | |||||||
| chr9:121365264 | T | A | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+4863A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365264 | |||||||
| chr9:121365296 | C | G | 241 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(238): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.61+4831G>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365296 | |||||||
| chr9:121365477 | G | GT | 23 | a0001c0001t0001g0031 a0001c0001t0001g0123 a0001c0001t0001g0200 others(20): Show |
26 | HG00735.hp2 HG01099.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.61+4649dupA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365477 | |||||||
| chr9:121365477 | GT | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.61+4649delA | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365477 | |||||||
| chr9:121365492 | C | T | 135 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0230 others(132): Show |
178 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.61+4635G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365492 | |||||||
| chr9:121365626 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18984.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.61+4501C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365626 | |||||||
| chr9:121365697 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.61+4430G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365697 | |||||||
| chr9:121365769 | C | T | 89 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0230 others(86): Show |
120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.61+4358G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365769 | |||||||
| chr9:121365845 | G | A | 6 | a0001c0001t0002g0049 a0001c0001t0002g0052 a0001c0001t0002g0279 others(3): Show |
7 | NA18956.hp2 NA18965.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+4282C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121365845 | |||||||
| chr9:121366076 | A | C | 56 | a0001c0001t0001g0230 a0001c0001t0003g0006 a0001c0001t0003g0011 others(53): Show |
80 | HG00099.hp2 HG00438.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.61+4051T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366076 | |||||||
| chr9:121366267 | G | T | 3 | a0002c0002t0005g0196 a0002c0002t0012g0022 a0002c0002t0014g0125 |
4 | HG01069.hp1 HG01071.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.61+3860C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366267 | |||||||
| chr9:121366297 | G | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0116 a0001c0001t0001g0117 |
4 | HG00738.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+3830C>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366297 | |||||||
| chr9:121366330 | T | C | 2 | a0001c0001t0005g0140 a0001c0001t0005g0141 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.61+3797A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366330 | |||||||
| chr9:121366438 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(94): Show |
123 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.61+3689T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366438 | |||||||
| chr9:121366746 | C | T | 38 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(35): Show |
47 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.61+3381G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366746 | |||||||
| chr9:121366761 | C | T | 2 | a0001c0001t0007g0248 a0001c0001t0007g0249 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.61+3366G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366761 | |||||||
| chr9:121366787 | A | G | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+3340T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121366787 | |||||||
| chr9:121367070 | C | T | 1 | a0001c0001t0002g0260 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.61+3057G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367070 | |||||||
| chr9:121367204 | AC | A | 48 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(45): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.61+2922delG | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367204 | |||||||
| chr9:121367310 | C | T | 89 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0230 others(86): Show |
120 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.61+2817G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367310 | |||||||
| chr9:121367406 | G | A | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+2721C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367406 | |||||||
| chr9:121367407 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+2720G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367407 | |||||||
| chr9:121367475 | T | C | 1 | a0001c0001t0007g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.61+2652A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367475 | |||||||
| chr9:121367630 | T | C | 144 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0181 others(141): Show |
187 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.61+2497A>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367630 | |||||||
| chr9:121367631 | C | T | 144 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0181 others(141): Show |
187 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.61+2496G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367631 | |||||||
| chr9:121367652 | T | G | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+2475A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367652 | |||||||
| chr9:121367941 | T | G | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
7 | HG01261.hp1 HG02559.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+2186A>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121367941 | |||||||
| chr9:121368044 | C | T | 25 | a0001c0001t0001g0126 a0001c0001t0001g0253 a0001c0001t0004g0005 others(22): Show |
32 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.61+2083G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368044 | |||||||
| chr9:121368100 | TC | T | 39 | a0001c0001t0001g0256 a0001c0001t0002g0008 a0001c0001t0002g0016 others(36): Show |
48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.61+2026delG | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368100 | |||||||
| chr9:121368421 | A | T | 1 | a0001c0001t0002g0190 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.61+1706T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368421 | |||||||
| chr9:121368445 | C | A | 1 | a0001c0001t0004g0188 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.61+1682G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368445 | |||||||
| chr9:121368608 | T | A | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.61+1519A>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368608 | |||||||
| chr9:121368650 | G | A | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+1477C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368650 | |||||||
| chr9:121368869 | G | GGCGGAGG others(9): Show |
1 | a0001c0001t0003g0239 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.61+1242_61+1257dup others(16): Show |
STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368869 | |||||||
| chr9:121368871 | C | T | 2 | a0001c0001t0001g0123 a0001c0005t0001g0124 |
2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.61+1256G>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368871 | |||||||
| chr9:121368932 | C | CA | 60 | a0001c0001t0001g0038 a0001c0001t0001g0199 a0001c0001t0001g0200 others(57): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.61+1194dupT | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121368932 | |||||||
| chr9:121369026 | A | G | 1 | a0001c0001t0010g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.61+1101T>C | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369026 | |||||||
| chr9:121369234 | A | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.61+893T>G | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369234 | |||||||
| chr9:121369453 | G | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(77): Show |
97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.61+674C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369453 | |||||||
| chr9:121369478 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.61+649C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369478 | |||||||
| chr9:121369502 | G | T | 1 | a0001c0001t0003g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.61+625C>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369502 | |||||||
| chr9:121369561 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.61+566C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369561 | |||||||
| chr9:121369756 | G | A | 32 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(29): Show |
40 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.61+371C>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369756 | |||||||
| chr9:121369769 | A | T | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.61+358T>A | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121369769 | |||||||
| chr9:121370031 | C | A | 2 | a0001c0001t0002g0283 a0001c0001t0002g0284 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.61+96G>T | STOM | ENSG00000148175.13 | transcript | ENST00000286713.7 | protein_coding | 1/6 | chr9 | 121370031 |