Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7103 |
| ensemblid | ENSG00000127324.9 |
| hgncid | 11855 |
| symbol | TSPAN8 |
| name | tetraspanin 8 |
| refseq_nuc | NM_004616.3 |
| refseq_prot | NP_004607.1 |
| ensembl_nuc | ENST00000247829.8 |
| ensembl_prot | ENSP00000247829.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 71125096 |
| end | 71157999 |
| strand | - |
| ver | v1.2 |
| region | chr12:71125096-71157999 |
| region5000 | chr12:71120096-71162999 |
| regionname0 | TSPAN8_chr12_71125096_71157999 |
| regionname5000 | TSPAN8_chr12_71120096_71162999 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 237 | 274 | 85 | 44 | 104 | 11 | 28 | 74 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0002 | 0/0 | 237 | 89 | 3 | 15 | 53 | 5 | 13 | 42 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0003 | 0/0 | 237 | 36 | 1 | 5 | 28 | 0 | 2 | 23 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0004 | 0/0 | 237 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0005 | 0/0 | 237 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0006 | 0/0 | 237 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0007 | 0/0 | 237 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| a0008 | 0/0 | 237 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | MAGVS others(232): Show |
chr12 | 71120096 | 71162999 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 711 | 178 | 80 | 27 | 41 | 11 | 17 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0001c0003 | 0/0 | 711 | 87 | 5 | 17 | 54 | 0 | 11 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0001c0006 | 0/0 | 711 | 9 | 0 | 0 | 9 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0002c0002 | 0/0 | 711 | 89 | 3 | 15 | 53 | 5 | 13 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0003c0004 | 0/0 | 711 | 36 | 1 | 5 | 28 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0004c0005 | 0/0 | 711 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0005c0008 | 0/0 | 711 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0006c0007 | 0/0 | 711 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0007c0009 | 0/0 | 711 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 | ||
| a0008c0010 | 0/0 | 711 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | ATGGC others(706): Show |
chr12 | 71120096 | 71162999 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1131 | 164 | 71 | 25 | 40 | 9 | 17 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0001c0001t0002 | 0/0 | 1131 | 5 | 2 | 0 | 1 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0001c0001t0003 | 0/0 | 1131 | 7 | 6 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0001c0001t0004 | 0/0 | 1131 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTCC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0001c0003t0001 | 0/0 | 1131 | 86 | 4 | 17 | 54 | 0 | 11 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0001c0003t0003 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0001c0006t0001 | 0/0 | 1131 | 9 | 0 | 0 | 9 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0002c0002t0001 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0002c0002t0002 | 0/0 | 1131 | 87 | 3 | 14 | 52 | 5 | 13 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0002c0002t0006 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0003c0004t0001 | 0/0 | 1131 | 36 | 1 | 5 | 28 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0004c0005t0002 | 0/0 | 1131 | 8 | 8 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0004c0005t0005 | 0/0 | 1131 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0005c0008t0001 | 0/0 | 1131 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0006c0007t0002 | 0/0 | 1131 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0007c0009t0001 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| a0008c0010t0001 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | AGTGC others(1126): Show |
chr12 | 71120096 | 71162999 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 4 | 1 | 5 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0009 | 1/0 | 5 | 0 | 3 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0011 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0221 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0002g0018 | 0/0 | 4 | 1 | 0 | 1 | 2 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0003 | 0/0 | 11 | 1 | 2 | 7 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0014 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0015 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0003t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0001c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0005 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0002c0002t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0001 | 0/0 | 13 | 0 | 0 | 11 | 0 | 2 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0006 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0003c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0004c0005t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0005c0008t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0006c0007t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0006c0007t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0007c0009t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| a0008c0010t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0087 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0110 | EUR | FIN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0192 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0160 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0164 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0093 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0182 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0183 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0208 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0193 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0134 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0209 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01496 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0090 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01934 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0168 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01943 | hp2 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01981 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0171 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02027 | hp2 | a0002 | c0002 | t0006 | g0273 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0210 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02071 | hp1 | a0003 | c0004 | t0001 | g0010 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0189 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0153 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02129 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02145 | hp2 | a0004 | c0005 | t0002 | g0050 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0215 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0140 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0170 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02280 | hp2 | a0004 | c0005 | t0002 | g0020 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0190 | AMR | PEL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0191 | EAS | KHV | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0196 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0082 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0206 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02683 | hp2 | a0006 | c0007 | t0002 | g0128 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02698 | hp1 | a0003 | c0004 | t0001 | g0001 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02896 | hp2 | a0004 | c0005 | t0005 | g0248 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03130 | hp2 | a0005 | c0008 | t0001 | g0049 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03209 | hp2 | a0004 | c0005 | t0002 | g0020 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03225 | hp1 | a0004 | c0005 | t0002 | g0272 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0089 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0088 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0177 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03654 | hp1 | a0003 | c0004 | t0001 | g0001 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0241 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03704 | hp2 | a0007 | c0009 | t0001 | g0256 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0084 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0242 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0274 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0099 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0154 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | BEB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0014 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04204 | hp1 | a0006 | c0007 | t0002 | g0127 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0166 | SAS | STU | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18747 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | CHB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18906 | hp2 | a0004 | c0005 | t0002 | g0050 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18942 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18943 | hp1 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18944 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18947 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18951 | hp1 | a0003 | c0004 | t0001 | g0041 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18957 | hp1 | a0003 | c0004 | t0001 | g0131 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18960 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0173 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18964 | hp1 | a0001 | c0006 | t0001 | g0042 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18966 | hp2 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18970 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18971 | hp1 | a0003 | c0004 | t0001 | g0129 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18977 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18984 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18985 | hp2 | a0001 | c0006 | t0001 | g0042 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18986 | hp1 | a0001 | c0003 | t0001 | g0172 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18990 | hp2 | a0003 | c0004 | t0001 | g0130 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18991 | hp1 | a0001 | c0006 | t0001 | g0152 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18992 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18998 | hp2 | a0003 | c0004 | t0001 | g0010 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19002 | hp2 | a0008 | c0010 | t0001 | g0232 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19009 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19009 | hp2 | a0003 | c0004 | t0001 | g0133 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19010 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19011 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0063 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19030 | hp2 | a0003 | c0004 | t0001 | g0149 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19054 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19055 | hp1 | a0003 | c0004 | t0001 | g0041 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19055 | hp2 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19063 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19068 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19072 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19079 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19080 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0142 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0141 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19088 | hp1 | a0001 | c0006 | t0001 | g0007 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19089 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19091 | hp1 | a0003 | c0004 | t0001 | g0001 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19091 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA19240 | hp2 | a0004 | c0005 | t0002 | g0020 | AFR | YRI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20129 | hp1 | a0004 | c0005 | t0002 | g0067 | AFR | ASW | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0003 | AFR | ASW | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0019 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0122 | EUR | TSI | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | GIH | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | GIH | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02486 | hp2 | a0005 | c0008 | t0001 | g0049 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG02559 | hp2 | a0004 | c0005 | t0002 | g0156 | AFR | ACB | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | MSL | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18955 | hp1 | a0003 | c0004 | t0001 | g0264 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA18955 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | USA | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0221 | REF | REF | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | TSPAN8_chr12_71120096_71162999 | TSPAN8 | chr12 | 71120096 | 71162999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71129354 | A | C | 3 | a0002 a0004 a0006 |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
missense_variant | MODERATE | c.637T>G | p.Ser213Ala | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/9 | 816/1131 | 637/714 | 213/237 | chr12 | 71129354 | |||
| chr12:71132802 | T | C | 1 | a0007 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.467A>G | p.Asn156Ser | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/9 | 646/1131 | 467/714 | 156/237 | chr12 | 71132802 | |||
| chr12:71138054 | G | A | 1 | a0008 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.343C>T | p.Arg115Cys | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/9 | 522/1131 | 343/714 | 115/237 | chr12 | 71138054 | |||
| chr12:71139754 | C | G | 2 | a0002 a0006 |
91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
missense_variant | MODERATE | c.218G>C | p.Gly73Ala | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 397/1131 | 218/714 | 73/237 | chr12 | 71139754 | |||
| chr12:71139812 | C | T | 1 | a0005 | 2 | HG02486.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.160G>A | p.Val54Ile | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 339/1131 | 160/714 | 54/237 | chr12 | 71139812 | |||
| chr12:71139842 | C | T | 1 | a0003 | 36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
missense_variant | MODERATE | c.130G>A | p.Gly44Ser | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 309/1131 | 130/714 | 44/237 | chr12 | 71139842 | |||
| chr12:71144171 | C | T | 1 | a0006 | 2 | HG02683.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.103G>A | p.Val35Ile | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/9 | 282/1131 | 103/714 | 35/237 | chr12 | 71144171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71132813 | G | A | 1 | a0001c0003 | 87 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(84): Show |
synonymous_variant | LOW | c.456C>T | p.Cys152Cys | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/9 | 635/1131 | 456/714 | 152/237 | chr12 | 71132813 | |||
| chr12:71139714 | C | T | 1 | a0001c0006 | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
synonymous_variant | LOW | c.258G>A | p.Leu86Leu | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 437/1131 | 258/714 | 86/237 | chr12 | 71139714 | |||
| chr12:71139801 | G | A | 1 | a0001c0006 | 9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
synonymous_variant | LOW | c.171C>T | p.Asp57Asp | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/9 | 350/1131 | 171/714 | 57/237 | chr12 | 71139801 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71125220 | A | G | 1 | a0004c0005t0005 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 9/9 | 114 | chr12 | 71125220 | ||||||
| chr12:71125316 | G | C | 6 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0006 others(3): Show |
104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*18C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 9/9 | 18 | chr12 | 71125316 | ||||||
| chr12:71157681 | C | T | 2 | a0001c0001t0003 a0001c0003t0003 |
8 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-3G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/9 | 3 | chr12 | 71157681 | ||||||
| chr12:71157769 | G | A | 1 | a0002c0002t0006 | 1 | HG02027.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/9 | chr12 | 71157769 | |||||||
| chr12:71157996 | C | G | 1 | a0001c0001t0004 | 2 | HG01496.hp2 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-176G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/9 | 318 | chr12 | 71157996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:71125393 | G | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.661-6C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125393 | |||||||
| chr12:71125614 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.661-227T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125614 | |||||||
| chr12:71125710 | G | A | 1 | a0002c0002t0002g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.661-323C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125710 | |||||||
| chr12:71125713 | C | T | 76 | a0001c0001t0002g0018 a0001c0001t0002g0203 a0002c0002t0002g0005 others(73): Show |
104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-326G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125713 | |||||||
| chr12:71125766 | A | C | 222 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(219): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.661-379T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125766 | |||||||
| chr12:71125768 | G | A | 76 | a0001c0001t0002g0018 a0001c0001t0002g0203 a0002c0002t0002g0005 others(73): Show |
104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-381C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125768 | |||||||
| chr12:71125820 | A | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(128): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.661-433T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125820 | |||||||
| chr12:71125870 | T | TA | 76 | a0001c0001t0002g0018 a0001c0001t0002g0203 a0002c0002t0002g0005 others(73): Show |
104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-484dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125870 | |||||||
| chr12:71125887 | C | CT | 76 | a0001c0001t0002g0018 a0001c0001t0002g0203 a0002c0002t0002g0005 others(73): Show |
104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-501dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125887 | |||||||
| chr12:71125978 | A | C | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.661-591T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71125978 | |||||||
| chr12:71126139 | T | C | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.661-752A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126139 | |||||||
| chr12:71126157 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(218): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.661-770T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126157 | |||||||
| chr12:71126173 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.661-786T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126173 | |||||||
| chr12:71126272 | C | A | 1 | a0001c0001t0003g0064 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661-885G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126272 | |||||||
| chr12:71126487 | G | C | 76 | a0001c0001t0002g0018 a0001c0001t0002g0203 a0002c0002t0002g0005 others(73): Show |
104 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.661-1100C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126487 | |||||||
| chr12:71126488 | T | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(218): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.661-1101A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126488 | |||||||
| chr12:71126561 | G | C | 75 | a0001c0001t0002g0203 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.661-1174C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126561 | |||||||
| chr12:71126647 | T | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-1260A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126647 | |||||||
| chr12:71126697 | A | C | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.661-1310T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126697 | |||||||
| chr12:71126761 | CT | C | 77 | a0001c0001t0001g0113 a0001c0001t0002g0203 a0001c0003t0001g0172 others(74): Show |
102 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.661-1375delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126761 | |||||||
| chr12:71126820 | T | C | 76 | a0001c0001t0002g0203 a0002c0002t0001g0223 a0002c0002t0002g0005 others(73): Show |
101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-1433A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126820 | |||||||
| chr12:71126866 | G | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-1479C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126866 | |||||||
| chr12:71126970 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661-1583A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126970 | |||||||
| chr12:71126981 | T | G | 81 | a0001c0001t0002g0203 a0001c0001t0003g0027 a0001c0001t0003g0066 others(78): Show |
113 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.661-1594A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71126981 | |||||||
| chr12:71127057 | G | A | 76 | a0001c0001t0002g0203 a0002c0002t0001g0223 a0002c0002t0002g0005 others(73): Show |
101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.661-1670C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127057 | |||||||
| chr12:71127092 | T | A | 1 | a0001c0001t0001g0051 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.661-1705A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127092 | |||||||
| chr12:71127284 | C | CT | 216 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(213): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.661-1898dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127284 | |||||||
| chr12:71127288 | G | T | 219 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(216): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.661-1901C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127288 | |||||||
| chr12:71127465 | A | G | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.660+1866T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127465 | |||||||
| chr12:71127618 | G | A | 1 | a0004c0005t0002g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.660+1713C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127618 | |||||||
| chr12:71127656 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.660+1675A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71127656 | |||||||
| chr12:71128003 | A | C | 1 | a0003c0004t0001g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.660+1328T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128003 | |||||||
| chr12:71128051 | T | C | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.660+1280A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128051 | |||||||
| chr12:71128176 | T | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0199 others(4): Show |
11 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+1155A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128176 | |||||||
| chr12:71128247 | C | G | 3 | a0001c0003t0001g0171 a0001c0003t0001g0175 a0001c0003t0001g0195 |
3 | HG02015.hp2 NA18955.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.660+1084G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128247 | |||||||
| chr12:71128270 | A | T | 3 | a0001c0003t0001g0171 a0001c0003t0001g0175 a0001c0003t0001g0195 |
3 | HG02015.hp2 NA18955.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.660+1061T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128270 | |||||||
| chr12:71128279 | A | T | 1 | a0002c0002t0002g0091 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.660+1052T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128279 | |||||||
| chr12:71128342 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.660+989G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128342 | |||||||
| chr12:71128377 | C | A | 1 | a0001c0003t0001g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.660+954G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128377 | |||||||
| chr12:71128555 | G | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0199 others(4): Show |
11 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.660+776C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128555 | |||||||
| chr12:71128617 | G | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(21): Show |
45 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.660+714C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128617 | |||||||
| chr12:71128641 | G | GT | 66 | a0001c0003t0001g0107 a0001c0003t0001g0191 a0002c0002t0001g0223 others(63): Show |
88 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.660+689dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128641 | |||||||
| chr12:71128641 | G | GTT | 5 | a0002c0002t0002g0019 a0002c0002t0002g0079 a0002c0002t0002g0116 others(2): Show |
7 | HG01106.hp2 HG01952.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.660+688_660+689dup others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128641 | |||||||
| chr12:71128655 | T | A | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
9 | HG01109.hp2 HG01123.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+676A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128655 | |||||||
| chr12:71128655 | TA | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0150 a0001c0006t0001g0007 others(15): Show |
39 | HG01069.hp1 HG01257.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.660+675delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128655 | |||||||
| chr12:71128656 | A | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(60): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.660+675T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128656 | |||||||
| chr12:71128657 | A | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0051 others(15): Show |
37 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.660+674T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128657 | |||||||
| chr12:71128658 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.660+673T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128658 | |||||||
| chr12:71128772 | T | C | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.660+559A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71128772 | |||||||
| chr12:71129008 | CT | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(45): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.660+322delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129008 | |||||||
| chr12:71129027 | G | C | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.660+304C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129027 | |||||||
| chr12:71129068 | C | A | 6 | a0001c0003t0001g0015 a0001c0003t0001g0164 a0001c0003t0001g0189 others(3): Show |
9 | HG00558.hp1 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+263G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129068 | |||||||
| chr12:71129080 | C | G | 1 | a0001c0003t0001g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.660+251G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129080 | |||||||
| chr12:71129107 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(208): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.660+224T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129107 | |||||||
| chr12:71129173 | G | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(104): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.660+158C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129173 | |||||||
| chr12:71129232 | GT | G | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.660+98delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129232 | |||||||
| chr12:71129263 | C | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(127): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.660+68G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129263 | |||||||
| chr12:71129307 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.660+24G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 8/8 | chr12 | 71129307 | |||||||
| chr12:71129419 | TA | T | 17 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0200 others(14): Show |
19 | HG00423.hp2 HG01884.hp2 HG02040.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.577-6delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129419 | |||||||
| chr12:71129419 | TAA | T | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
splice_region_variant&intron_variant | LOW | c.577-7_577-6delTT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129419 | |||||||
| chr12:71129429 | A | C | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.577-15T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129429 | |||||||
| chr12:71129692 | T | C | 1 | a0001c0003t0001g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.577-278A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129692 | |||||||
| chr12:71129746 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0224 a0001c0001t0001g0229 others(1): Show |
5 | HG00621.hp1 NA18612.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-332A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129746 | |||||||
| chr12:71129761 | T | C | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.577-347A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129761 | |||||||
| chr12:71129783 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.577-369A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129783 | |||||||
| chr12:71129854 | T | A | 74 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(71): Show |
99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.577-440A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129854 | |||||||
| chr12:71129951 | C | CT | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(8): Show |
12 | HG01109.hp2 HG01167.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.577-538dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | |||||||
| chr12:71129951 | CT | C | 4 | a0001c0003t0001g0173 a0004c0005t0002g0020 a0004c0005t0002g0156 others(1): Show |
6 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-538delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | |||||||
| chr12:71129951 | CTT | C | 67 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(64): Show |
88 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.577-539_577-538del others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | |||||||
| chr12:71129951 | CTTT | C | 5 | a0002c0002t0002g0019 a0002c0002t0002g0079 a0002c0002t0002g0116 others(2): Show |
7 | HG01106.hp2 HG01952.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-540_577-538del others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129951 | |||||||
| chr12:71129991 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577-577G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71129991 | |||||||
| chr12:71130008 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.577-594T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130008 | |||||||
| chr12:71130161 | C | T | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.577-747G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130161 | |||||||
| chr12:71130262 | C | G | 80 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(77): Show |
112 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.577-848G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130262 | |||||||
| chr12:71130511 | G | A | 143 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0001t0004g0056 others(140): Show |
200 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.577-1097C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130511 | |||||||
| chr12:71130556 | T | C | 1 | a0004c0005t0002g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.577-1142A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130556 | |||||||
| chr12:71130639 | C | CT | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.577-1226dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130639 | |||||||
| chr12:71130693 | G | A | 69 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(66): Show |
91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.577-1279C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130693 | |||||||
| chr12:71130802 | T | C | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.577-1388A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130802 | |||||||
| chr12:71130873 | T | C | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-1459A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71130873 | |||||||
| chr12:71131030 | A | G | 143 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0001t0004g0056 others(140): Show |
200 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.577-1616T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131030 | |||||||
| chr12:71131078 | C | G | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1615G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131078 | |||||||
| chr12:71131157 | T | C | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1536A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131157 | |||||||
| chr12:71131190 | T | C | 1 | a0001c0003t0001g0174 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.576+1503A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131190 | |||||||
| chr12:71131351 | G | A | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1342C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131351 | |||||||
| chr12:71131490 | T | A | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+1203A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131490 | |||||||
| chr12:71131685 | G | GAAGAATA others(329): Show |
1 | a0002c0002t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(338): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(314): Show |
1 | a0002c0002t0002g0101 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(323): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(313): Show |
2 | a0002c0002t0002g0031 a0002c0002t0002g0076 |
3 | NA18942.hp2 NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.576+1007_576+1008i others(322): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(314): Show |
49 | a0002c0002t0002g0005 a0002c0002t0002g0012 a0002c0002t0002g0030 others(46): Show |
66 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(323): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(315): Show |
7 | a0002c0002t0001g0223 a0002c0002t0002g0043 a0002c0002t0002g0093 others(4): Show |
8 | HG00738.hp2 HG01175.hp2 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(324): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(325): Show |
1 | a0004c0005t0002g0020 | 3 | HG02280.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.576+1007_576+1008i others(334): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(326): Show |
4 | a0001c0001t0004g0056 a0004c0005t0002g0067 a0004c0005t0002g0156 others(1): Show |
4 | HG02559.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(335): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(327): Show |
1 | a0004c0005t0002g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(336): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(328): Show |
1 | a0002c0002t0002g0082 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.576+1007_576+1008i others(337): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(329): Show |
4 | a0002c0002t0002g0019 a0002c0002t0002g0116 a0002c0002t0002g0122 others(1): Show |
7 | HG01106.hp2 HG02145.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(338): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(330): Show |
2 | a0002c0002t0002g0083 a0002c0002t0002g0123 |
2 | HG01884.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.576+1007_576+1008i others(339): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131685 | G | GAAGAATA others(314): Show |
3 | a0002c0002t0002g0032 a0002c0002t0002g0103 a0002c0002t0002g0126 |
4 | NA18968.hp1 NA18974.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1007_576+1008i others(323): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131685 | |||||||
| chr12:71131687 | A | AGAATAAC others(327): Show |
1 | a0001c0003t0001g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.576+1005_576+1006i others(336): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | |||||||
| chr12:71131687 | A | AGAATAAC others(326): Show |
8 | a0001c0003t0001g0137 a0001c0003t0001g0143 a0001c0003t0001g0151 others(5): Show |
8 | HG00423.hp2 HG00558.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+1005_576+1006i others(335): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | |||||||
| chr12:71131687 | A | AGAATAAC others(325): Show |
27 | a0001c0003t0001g0014 a0001c0003t0001g0015 a0001c0003t0001g0021 others(24): Show |
37 | HG01175.hp1 HG01192.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.576+1005_576+1006i others(334): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | |||||||
| chr12:71131687 | A | AGAATAAC others(324): Show |
23 | a0001c0003t0001g0003 a0001c0003t0001g0013 a0001c0003t0001g0022 others(20): Show |
38 | HG00544.hp1 HG00639.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.576+1005_576+1006i others(333): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | |||||||
| chr12:71131687 | A | AGAATAAC others(323): Show |
3 | a0001c0003t0001g0170 a0001c0003t0001g0177 a0001c0003t0001g0183 |
3 | HG01169.hp2 HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.576+1005_576+1006i others(332): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131687 | |||||||
| chr12:71131943 | C | T | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+750G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131943 | |||||||
| chr12:71131978 | G | A | 1 | a0001c0003t0001g0153 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.576+715C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131978 | |||||||
| chr12:71131998 | G | T | 4 | a0001c0001t0001g0225 a0001c0001t0003g0026 a0001c0001t0003g0064 others(1): Show |
5 | HG01069.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+695C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71131998 | |||||||
| chr12:71132167 | G | A | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+526C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132167 | |||||||
| chr12:71132284 | T | C | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+409A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132284 | |||||||
| chr12:71132288 | G | A | 3 | a0004c0005t0002g0020 a0004c0005t0002g0156 a0004c0005t0005g0248 |
5 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+405C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132288 | |||||||
| chr12:71132328 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.576+365A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132328 | |||||||
| chr12:71132507 | C | A | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+186G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132507 | |||||||
| chr12:71132531 | C | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.576+162G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132531 | |||||||
| chr12:71132634 | T | C | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.576+59A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 7/8 | chr12 | 71132634 | |||||||
| chr12:71132845 | T | G | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-21A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71132845 | |||||||
| chr12:71132897 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(64): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.445-73T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71132897 | |||||||
| chr12:71132929 | C | T | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-105G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71132929 | |||||||
| chr12:71133137 | G | T | 1 | a0002c0002t0002g0090 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.445-313C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133137 | |||||||
| chr12:71133144 | C | T | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.445-320G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133144 | |||||||
| chr12:71133147 | G | A | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-323C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133147 | |||||||
| chr12:71133152 | C | T | 1 | a0002c0002t0002g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.445-328G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133152 | |||||||
| chr12:71133259 | G | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0199 others(4): Show |
11 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.445-435C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133259 | |||||||
| chr12:71133276 | C | T | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445-452G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133276 | |||||||
| chr12:71133277 | G | A | 2 | a0001c0003t0001g0177 a0001c0003t0003g0063 |
2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.445-453C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133277 | |||||||
| chr12:71133285 | C | A | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-461G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133285 | |||||||
| chr12:71133430 | T | C | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-606A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133430 | |||||||
| chr12:71133458 | G | T | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445-634C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133458 | |||||||
| chr12:71133541 | C | T | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-717G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133541 | |||||||
| chr12:71133771 | A | G | 1 | a0001c0003t0001g0194 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.445-947T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133771 | |||||||
| chr12:71133866 | T | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(64): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.445-1042A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133866 | |||||||
| chr12:71133927 | A | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(64): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.445-1103T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71133927 | |||||||
| chr12:71134005 | A | T | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-1181T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134005 | |||||||
| chr12:71134148 | C | A | 1 | a0003c0004t0001g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.445-1324G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134148 | |||||||
| chr12:71134423 | T | C | 1 | a0004c0005t0005g0248 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.445-1599A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134423 | |||||||
| chr12:71134657 | A | T | 1 | a0001c0003t0001g0214 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.445-1833T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134657 | |||||||
| chr12:71134713 | TC | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-1890delG | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134713 | |||||||
| chr12:71134720 | T | C | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445-1896A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134720 | |||||||
| chr12:71134721 | A | G | 14 | a0003c0004t0001g0001 a0003c0004t0001g0006 a0003c0004t0001g0010 others(11): Show |
36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.445-1897T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134721 | |||||||
| chr12:71134747 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(207): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.445-1923C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134747 | |||||||
| chr12:71134808 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(207): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.445-1984A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134808 | |||||||
| chr12:71134848 | C | T | 1 | a0001c0003t0001g0169 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.445-2024G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134848 | |||||||
| chr12:71134957 | A | G | 1 | a0002c0002t0002g0090 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.445-2133T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71134957 | |||||||
| chr12:71135036 | C | T | 1 | a0003c0004t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.445-2212G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135036 | |||||||
| chr12:71135067 | A | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2243T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135067 | |||||||
| chr12:71135116 | C | T | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.445-2292G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135116 | |||||||
| chr12:71135216 | GAGGAGGA others(52): Show |
G | 135 | a0001c0003t0001g0003 a0001c0003t0001g0013 a0001c0003t0001g0014 others(132): Show |
185 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.445-2451_445-2393d others(61): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135216 | |||||||
| chr12:71135218 | GGAGGAAG others(55): Show |
G | 2 | a0001c0001t0004g0056 a0001c0003t0001g0084 |
2 | HG03540.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.445-2456_445-2395d others(64): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135218 | |||||||
| chr12:71135219 | GAGGAAGA others(49): Show |
G | 1 | a0001c0003t0001g0161 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.445-2451_445-2396d others(58): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135219 | |||||||
| chr12:71135224 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2400T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135224 | |||||||
| chr12:71135229 | AAGG | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 others(20): Show |
47 | HG00423.hp1 HG01109.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.445-2408_445-2406d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135229 | |||||||
| chr12:71135232 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(48): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.445-2408C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135232 | |||||||
| chr12:71135234 | G | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(45): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.445-2410C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135234 | |||||||
| chr12:71135235 | G | A | 21 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(18): Show |
44 | HG01109.hp2 HG01167.hp2 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.445-2411C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135235 | |||||||
| chr12:71135237 | G | A | 14 | a0003c0004t0001g0001 a0003c0004t0001g0006 a0003c0004t0001g0010 others(11): Show |
36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.445-2413C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135237 | |||||||
| chr12:71135238 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2414C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135238 | |||||||
| chr12:71135272 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2448C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135272 | |||||||
| chr12:71135275 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2451T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135275 | |||||||
| chr12:71135277 | G | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
6 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-2453C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135277 | |||||||
| chr12:71135291 | A | G | 19 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(16): Show |
41 | HG01109.hp2 HG01257.hp1 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.445-2467T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135291 | |||||||
| chr12:71135294 | G | A | 2 | a0002c0002t0002g0100 a0002c0002t0002g0101 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.445-2470C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135294 | |||||||
| chr12:71135295 | A | AGGG | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-2472_445-2471i others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135295 | |||||||
| chr12:71135297 | GA | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445-2474delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135297 | |||||||
| chr12:71135340 | G | A | 1 | a0001c0003t0001g0208 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.445-2516C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135340 | |||||||
| chr12:71135356 | AAAG | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.445-2535_445-2533d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135356 | |||||||
| chr12:71135369 | A | AAGG | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-2548_445-2546d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135369 | |||||||
| chr12:71135379 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(45): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.445-2555T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135379 | |||||||
| chr12:71135425 | AGAG | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0068 |
3 | HG00735.hp1 HG01952.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.444+2525_444+2527d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135425 | |||||||
| chr12:71135524 | A | AGAAGGG | 206 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(203): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.444+2423_444+2428d others(8): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135524 | |||||||
| chr12:71135529 | G | GGGAAGA | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+2423_444+2424i others(8): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135529 | |||||||
| chr12:71135566 | G | A | 138 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(135): Show |
188 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.444+2387C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135566 | |||||||
| chr12:71135607 | G | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(207): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.444+2346C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135607 | |||||||
| chr12:71135711 | G | A | 76 | a0001c0001t0004g0056 a0002c0002t0001g0223 a0002c0002t0002g0005 others(73): Show |
101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.444+2242C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135711 | |||||||
| chr12:71135762 | A | G | 1 | a0001c0003t0001g0210 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.444+2191T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135762 | |||||||
| chr12:71135782 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0250 a0001c0001t0001g0252 |
6 | HG01361.hp1 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+2171A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135782 | |||||||
| chr12:71135874 | T | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(207): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.444+2079A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135874 | |||||||
| chr12:71135918 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG00639.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.444+2035G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135918 | |||||||
| chr12:71135948 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(66): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.444+2005G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135948 | |||||||
| chr12:71135969 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.444+1984T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71135969 | |||||||
| chr12:71136005 | A | G | 1 | a0001c0003t0001g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.444+1948T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136005 | |||||||
| chr12:71136093 | G | GAA | 137 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(134): Show |
187 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.444+1858_444+1859d others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136093 | |||||||
| chr12:71136099 | A | AAG | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1853_444+1854i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136099 | |||||||
| chr12:71136170 | GAAC | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1780_444+1782d others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136170 | |||||||
| chr12:71136310 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.444+1643A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136310 | |||||||
| chr12:71136379 | C | T | 62 | a0001c0003t0001g0003 a0001c0003t0001g0013 a0001c0003t0001g0014 others(59): Show |
87 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.444+1574G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136379 | |||||||
| chr12:71136441 | A | T | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+1512T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136441 | |||||||
| chr12:71136851 | T | C | 14 | a0003c0004t0001g0001 a0003c0004t0001g0006 a0003c0004t0001g0010 others(11): Show |
36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.444+1102A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136851 | |||||||
| chr12:71136856 | C | T | 63 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(60): Show |
88 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.444+1097G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136856 | |||||||
| chr12:71136978 | G | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+975C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136978 | |||||||
| chr12:71136996 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+957A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71136996 | |||||||
| chr12:71137008 | C | T | 1 | a0004c0005t0005g0248 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.444+945G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137008 | |||||||
| chr12:71137009 | G | A | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.444+944C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137009 | |||||||
| chr12:71137025 | A | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+928T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137025 | |||||||
| chr12:71137166 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+787T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137166 | |||||||
| chr12:71137194 | C | G | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
14 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+759G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137194 | |||||||
| chr12:71137213 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+740T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137213 | |||||||
| chr12:71137235 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+718T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137235 | |||||||
| chr12:71137309 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(46): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.444+644C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137309 | |||||||
| chr12:71137358 | G | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+595C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137358 | |||||||
| chr12:71137387 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.444+566A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137387 | |||||||
| chr12:71137400 | A | G | 1 | a0002c0002t0002g0184 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.444+553T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137400 | |||||||
| chr12:71137436 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0230 a0001c0001t0001g0253 others(3): Show |
9 | HG01361.hp2 HG01433.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.444+517A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137436 | |||||||
| chr12:71137443 | AC | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+509delG | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137443 | |||||||
| chr12:71137457 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.444+496C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137457 | |||||||
| chr12:71137477 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+476C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137477 | |||||||
| chr12:71137494 | G | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+459C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137494 | |||||||
| chr12:71137536 | G | A | 1 | a0001c0003t0001g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.444+417C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137536 | |||||||
| chr12:71137603 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.444+350G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137603 | |||||||
| chr12:71137604 | C | A | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.444+349G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137604 | |||||||
| chr12:71137604 | CA | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(139): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.444+348delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137604 | |||||||
| chr12:71137605 | A | C | 1 | a0004c0005t0002g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.444+348T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137605 | |||||||
| chr12:71137611 | A | G | 1 | a0002c0002t0002g0104 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.444+342T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137611 | |||||||
| chr12:71137747 | C | G | 1 | a0001c0006t0001g0152 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.444+206G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137747 | |||||||
| chr12:71137859 | G | A | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.444+94C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137859 | |||||||
| chr12:71137883 | A | T | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.444+70T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137883 | |||||||
| chr12:71137910 | A | C | 1 | a0002c0002t0002g0089 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.444+43T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137910 | |||||||
| chr12:71137939 | T | C | 3 | a0004c0005t0002g0020 a0004c0005t0002g0156 a0004c0005t0005g0248 |
5 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+14A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 6/8 | chr12 | 71137939 | |||||||
| chr12:71138102 | T | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-42A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 5/8 | chr12 | 71138102 | |||||||
| chr12:71138109 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(61): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.336+47A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 5/8 | chr12 | 71138109 | |||||||
| chr12:71138319 | G | A | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.262-89C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138319 | |||||||
| chr12:71138392 | G | A | 1 | a0001c0003t0001g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.262-162C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138392 | |||||||
| chr12:71138407 | C | T | 1 | a0003c0004t0001g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.262-177G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138407 | |||||||
| chr12:71138414 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-184A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138414 | |||||||
| chr12:71138458 | T | G | 63 | a0001c0001t0004g0056 a0001c0003t0001g0003 a0001c0003t0001g0013 others(60): Show |
88 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.262-228A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138458 | |||||||
| chr12:71138521 | G | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-291C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138521 | |||||||
| chr12:71138548 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0086 others(2): Show |
10 | HG00558.hp2 HG02132.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-318G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138548 | |||||||
| chr12:71138587 | T | C | 4 | a0001c0001t0001g0225 a0001c0001t0003g0026 a0001c0001t0003g0064 others(1): Show |
5 | HG01069.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-357A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138587 | |||||||
| chr12:71138646 | T | G | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-416A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138646 | |||||||
| chr12:71138660 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.262-430G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138660 | |||||||
| chr12:71138807 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-577C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138807 | |||||||
| chr12:71138853 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.262-623G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138853 | |||||||
| chr12:71138856 | T | C | 1 | a0001c0003t0001g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.262-626A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71138856 | |||||||
| chr12:71139099 | A | G | 14 | a0003c0004t0001g0001 a0003c0004t0001g0006 a0003c0004t0001g0010 others(11): Show |
36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.261+612T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139099 | |||||||
| chr12:71139142 | A | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0240 |
3 | HG02886.hp2 HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.261+569T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139142 | |||||||
| chr12:71139176 | C | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+535G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139176 | |||||||
| chr12:71139192 | C | T | 6 | a0001c0003t0001g0015 a0001c0003t0001g0164 a0001c0003t0001g0189 others(3): Show |
9 | HG00558.hp1 HG01255.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+519G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139192 | |||||||
| chr12:71139208 | C | A | 1 | a0002c0002t0002g0040 | 2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.261+503G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139208 | |||||||
| chr12:71139430 | C | T | 69 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(66): Show |
91 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.261+281G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139430 | |||||||
| chr12:71139458 | G | T | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.261+253C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139458 | |||||||
| chr12:71139568 | A | G | 2 | a0001c0001t0001g0244 a0001c0001t0002g0018 |
5 | HG01516.hp1 HG01517.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+143T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139568 | |||||||
| chr12:71139628 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+83G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 4/8 | chr12 | 71139628 | |||||||
| chr12:71139972 | C | CCTTCATT others(491): Show |
14 | a0003c0004t0001g0001 a0003c0004t0001g0006 a0003c0004t0001g0010 others(11): Show |
36 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.124-125_124-124ins others(498): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | |||||||
| chr12:71139972 | C | CCTTCATT others(491): Show |
49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(46): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.124-125_124-124ins others(498): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | |||||||
| chr12:71139972 | C | CCTTCATT others(495): Show |
1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.124-125_124-124ins others(502): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | |||||||
| chr12:71139972 | C | CCTTCATT others(495): Show |
5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-125_124-124ins others(502): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139972 | |||||||
| chr12:71139974 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124-126C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139974 | |||||||
| chr12:71139974 | G | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(66): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.124-126C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71139974 | |||||||
| chr12:71140015 | C | CA | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-168dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140015 | |||||||
| chr12:71140072 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.124-224T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140072 | |||||||
| chr12:71140083 | G | GT | 8 | a0001c0001t0001g0047 a0001c0001t0001g0224 a0001c0001t0001g0227 others(5): Show |
9 | HG00621.hp1 HG02132.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-236dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140083 | |||||||
| chr12:71140094 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(66): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.124-246G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140094 | |||||||
| chr12:71140196 | T | A | 5 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0001c0006t0001g0007 others(2): Show |
12 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.124-348A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140196 | |||||||
| chr12:71140216 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-368G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140216 | |||||||
| chr12:71140314 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124-466T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140314 | |||||||
| chr12:71140446 | C | A | 1 | a0001c0003t0003g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-598G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140446 | |||||||
| chr12:71140476 | C | T | 1 | a0002c0002t0002g0034 | 2 | HG01192.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.124-628G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140476 | |||||||
| chr12:71140644 | C | T | 1 | a0001c0001t0001g0051 | 2 | HG01346.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.124-796G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140644 | |||||||
| chr12:71140806 | T | C | 1 | a0004c0005t0002g0067 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.124-958A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140806 | |||||||
| chr12:71140819 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-971G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71140819 | |||||||
| chr12:71141083 | T | C | 1 | a0002c0002t0002g0094 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.124-1235A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141083 | |||||||
| chr12:71141105 | A | G | 13 | a0003c0004t0001g0001 a0003c0004t0001g0006 a0003c0004t0001g0010 others(10): Show |
35 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.124-1257T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141105 | |||||||
| chr12:71141108 | A | C | 1 | a0001c0001t0001g0259 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.124-1260T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141108 | |||||||
| chr12:71141122 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1274C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141122 | |||||||
| chr12:71141153 | T | C | 1 | a0002c0002t0002g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124-1305A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141153 | |||||||
| chr12:71141234 | A | T | 1 | a0002c0002t0002g0098 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.124-1386T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141234 | |||||||
| chr12:71141249 | G | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(141): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.124-1401C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141249 | |||||||
| chr12:71141315 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(61): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.124-1467A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141315 | |||||||
| chr12:71141393 | G | A | 4 | a0001c0001t0001g0225 a0001c0001t0003g0026 a0001c0001t0003g0064 others(1): Show |
5 | HG01069.hp2 HG03098.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-1545C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141393 | |||||||
| chr12:71141531 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(61): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.124-1684delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141531 | |||||||
| chr12:71141902 | C | T | 1 | a0003c0004t0001g0140 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.124-2054G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71141902 | |||||||
| chr12:71142087 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+2064A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142087 | |||||||
| chr12:71142091 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.123+2060T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142091 | |||||||
| chr12:71142377 | C | T | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.123+1774G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142377 | |||||||
| chr12:71142411 | A | C | 1 | a0003c0004t0001g0142 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.123+1740T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142411 | |||||||
| chr12:71142517 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1634A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142517 | |||||||
| chr12:71142561 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.123+1590A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142561 | |||||||
| chr12:71142622 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+1529G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142622 | |||||||
| chr12:71142701 | A | C | 3 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 |
9 | NA18964.hp1 NA18966.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+1450T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142701 | |||||||
| chr12:71142756 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+1395C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142756 | |||||||
| chr12:71142847 | C | CA | 96 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0025 others(93): Show |
164 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.123+1303dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142847 | |||||||
| chr12:71142847 | C | CAA | 52 | a0001c0001t0001g0053 a0001c0001t0001g0263 a0001c0001t0001g0268 others(49): Show |
70 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.123+1302_123+1303d others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142847 | |||||||
| chr12:71142848 | A | AAC | 4 | a0002c0002t0002g0034 a0002c0002t0002g0087 a0004c0005t0002g0050 others(1): Show |
6 | HG00099.hp1 HG01192.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+1302_123+1303i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142848 | |||||||
| chr12:71142849 | A | AAAC | 4 | a0001c0006t0001g0007 a0001c0006t0001g0042 a0001c0006t0001g0152 others(1): Show |
10 | HG03831.hp2 NA18964.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.123+1301_123+1302i others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142849 | |||||||
| chr12:71142849 | A | AAC | 12 | a0001c0001t0001g0016 a0001c0001t0001g0054 a0001c0001t0001g0199 others(9): Show |
17 | HG01361.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.123+1301_123+1302i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142849 | |||||||
| chr12:71142850 | A | AAC | 14 | a0002c0002t0002g0012 a0002c0002t0002g0032 a0002c0002t0002g0033 others(11): Show |
19 | HG00438.hp2 HG02027.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.123+1300_123+1301i others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142850 | |||||||
| chr12:71142850 | A | AC | 22 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
27 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.123+1300_123+1301i others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142850 | |||||||
| chr12:71142851 | A | C | 3 | a0001c0001t0003g0027 a0001c0001t0003g0066 a0002c0002t0002g0087 |
4 | HG00099.hp1 HG01167.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+1300T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71142851 | |||||||
| chr12:71143281 | T | C | 1 | a0002c0002t0002g0115 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.123+870A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143281 | |||||||
| chr12:71143454 | C | T | 1 | a0001c0003t0001g0189 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.123+697G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143454 | |||||||
| chr12:71143476 | G | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+675C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143476 | |||||||
| chr12:71143507 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.123+644C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143507 | |||||||
| chr12:71143531 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+620T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143531 | |||||||
| chr12:71143549 | T | C | 75 | a0002c0002t0001g0223 a0002c0002t0002g0005 a0002c0002t0002g0012 others(72): Show |
100 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.123+602A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71143549 | |||||||
| chr12:71144052 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0066 |
3 | HG01167.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.123+99A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71144052 | |||||||
| chr12:71144089 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.123+62A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 3/8 | chr12 | 71144089 | |||||||
| chr12:71144274 | C | T | 1 | a0005c0008t0001g0049 | 2 | HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.61-61G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144274 | |||||||
| chr12:71144292 | C | T | 4 | a0001c0001t0001g0235 a0001c0006t0001g0007 a0001c0006t0001g0042 others(1): Show |
10 | HG01255.hp2 NA18964.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.61-79G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144292 | |||||||
| chr12:71144416 | A | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0224 others(14): Show |
22 | HG00621.hp1 HG01361.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.61-203T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144416 | |||||||
| chr12:71144530 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(45): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.61-317A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144530 | |||||||
| chr12:71144976 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.61-763A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144976 | |||||||
| chr12:71144982 | C | T | 63 | a0001c0001t0001g0159 a0001c0001t0001g0258 a0001c0003t0001g0003 others(60): Show |
88 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.61-769G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71144982 | |||||||
| chr12:71145044 | C | T | 1 | a0001c0001t0001g0048 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.61-831G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145044 | |||||||
| chr12:71145064 | T | C | 61 | a0001c0001t0001g0159 a0001c0001t0001g0258 a0001c0003t0001g0003 others(58): Show |
86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-851A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145064 | |||||||
| chr12:71145351 | G | A | 1 | a0002c0002t0002g0081 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.61-1138C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145351 | |||||||
| chr12:71145497 | C | T | 3 | a0002c0002t0002g0098 a0002c0002t0002g0099 a0002c0002t0002g0117 |
3 | HG03942.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.61-1284G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145497 | |||||||
| chr12:71145527 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.61-1314A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145527 | |||||||
| chr12:71145866 | C | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0016 others(80): Show |
148 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.61-1653G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145866 | |||||||
| chr12:71145910 | C | A | 1 | a0002c0002t0002g0095 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.61-1697G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145910 | |||||||
| chr12:71145984 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-1771G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145984 | |||||||
| chr12:71145991 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(182): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.61-1778G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71145991 | |||||||
| chr12:71146060 | C | T | 61 | a0001c0001t0001g0159 a0001c0001t0001g0258 a0001c0003t0001g0003 others(58): Show |
86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-1847G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146060 | |||||||
| chr12:71146135 | A | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(257): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.61-1922T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146135 | |||||||
| chr12:71146135 | A | T | 9 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0055 others(6): Show |
13 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.61-1922T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146135 | |||||||
| chr12:71146237 | C | T | 61 | a0001c0001t0001g0159 a0001c0001t0001g0258 a0001c0003t0001g0003 others(58): Show |
86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-2024G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146237 | |||||||
| chr12:71146306 | T | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(185): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.61-2093A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146306 | |||||||
| chr12:71146359 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-2146A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146359 | |||||||
| chr12:71146385 | C | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(57): Show |
91 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.61-2172G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146385 | |||||||
| chr12:71146492 | A | G | 61 | a0001c0001t0001g0159 a0001c0001t0001g0258 a0001c0003t0001g0003 others(58): Show |
86 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.61-2279T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146492 | |||||||
| chr12:71146806 | A | C | 4 | a0001c0001t0001g0238 a0001c0001t0001g0260 a0001c0001t0001g0261 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-2593T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146806 | |||||||
| chr12:71146858 | A | G | 5 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0250 others(2): Show |
5 | HG01361.hp1 HG02055.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.61-2645T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146858 | |||||||
| chr12:71146881 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0155 |
2 | HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.61-2668G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71146881 | |||||||
| chr12:71147041 | C | T | 2 | a0002c0002t0002g0082 a0002c0002t0002g0083 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.61-2828G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147041 | |||||||
| chr12:71147042 | G | A | 1 | a0002c0002t0002g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.61-2829C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147042 | |||||||
| chr12:71147210 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.61-2997T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147210 | |||||||
| chr12:71147336 | G | A | 1 | a0001c0003t0001g0181 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.61-3123C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147336 | |||||||
| chr12:71147415 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.61-3202C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147415 | |||||||
| chr12:71147445 | T | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0238 a0001c0001t0001g0260 others(7): Show |
12 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-3232A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147445 | |||||||
| chr12:71147599 | C | A | 3 | a0002c0002t0002g0098 a0002c0002t0002g0099 a0002c0002t0002g0117 |
3 | HG03942.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.61-3386G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147599 | |||||||
| chr12:71147652 | C | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0155 others(3): Show |
8 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-3439G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147652 | |||||||
| chr12:71147726 | G | C | 1 | a0001c0001t0004g0057 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.61-3513C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147726 | |||||||
| chr12:71147751 | A | G | 1 | a0004c0005t0002g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.61-3538T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147751 | |||||||
| chr12:71147925 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.61-3712T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147925 | |||||||
| chr12:71147934 | T | C | 5 | a0001c0003t0001g0134 a0001c0003t0001g0143 a0001c0003t0001g0144 others(2): Show |
6 | HG00544.hp2 HG01123.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-3721A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71147934 | |||||||
| chr12:71148029 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG00280.hp2 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-3816G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148029 | |||||||
| chr12:71148256 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0155 |
2 | HG02109.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.61-4043T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148256 | |||||||
| chr12:71148301 | T | C | 1 | a0001c0003t0001g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.61-4088A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148301 | |||||||
| chr12:71148366 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-4153G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148366 | |||||||
| chr12:71148368 | C | T | 2 | a0004c0005t0002g0020 a0004c0005t0002g0156 |
4 | HG02280.hp2 HG02559.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-4155G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148368 | |||||||
| chr12:71148561 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0155 others(3): Show |
8 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-4348G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148561 | |||||||
| chr12:71148573 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG01884.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.61-4360T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148573 | |||||||
| chr12:71148789 | C | T | 6 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0003t0001g0154 others(3): Show |
12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-4576G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71148789 | |||||||
| chr12:71149018 | G | T | 6 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0003t0001g0154 others(3): Show |
12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.61-4805C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149018 | |||||||
| chr12:71149072 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.61-4859A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149072 | |||||||
| chr12:71149213 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61-5000T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149213 | |||||||
| chr12:71149238 | C | T | 4 | a0002c0002t0002g0031 a0002c0002t0002g0080 a0002c0002t0002g0081 others(1): Show |
5 | NA18942.hp2 NA18960.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-5025G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149238 | |||||||
| chr12:71149291 | C | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0199 others(10): Show |
20 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.61-5078G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149291 | |||||||
| chr12:71149369 | C | CA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0039 others(37): Show |
76 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.61-5157dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149369 | |||||||
| chr12:71149369 | CA | C | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(8): Show |
11 | HG01934.hp2 HG02055.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.61-5157delT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149369 | |||||||
| chr12:71149385 | A | G | 12 | a0001c0003t0001g0015 a0001c0003t0001g0021 a0001c0003t0001g0164 others(9): Show |
17 | HG00423.hp2 HG00558.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.61-5172T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149385 | |||||||
| chr12:71149451 | C | T | 7 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0003t0001g0154 others(4): Show |
13 | HG02080.hp2 HG02155.hp1 HG04115.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-5238G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149451 | |||||||
| chr12:71149590 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.61-5377A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149590 | |||||||
| chr12:71149727 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.61-5514C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149727 | |||||||
| chr12:71149730 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.61-5517G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149730 | |||||||
| chr12:71149731 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.61-5518C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149731 | |||||||
| chr12:71149777 | T | C | 5 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0006t0001g0007 others(2): Show |
11 | HG02080.hp2 NA18964.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-5564A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149777 | |||||||
| chr12:71149795 | G | T | 5 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0006t0001g0007 others(2): Show |
11 | HG02080.hp2 NA18964.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.61-5582C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149795 | |||||||
| chr12:71149856 | G | A | 1 | a0003c0004t0001g0041 | 2 | NA18951.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.61-5643C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149856 | |||||||
| chr12:71149880 | T | A | 1 | a0002c0002t0001g0223 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.61-5667A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149880 | |||||||
| chr12:71149916 | T | C | 2 | a0002c0002t0002g0100 a0002c0002t0002g0101 |
2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.61-5703A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71149916 | |||||||
| chr12:71150051 | C | T | 6 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0064 others(3): Show |
8 | HG01167.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.61-5838G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150051 | |||||||
| chr12:71150094 | G | A | 1 | a0004c0005t0005g0248 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.61-5881C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150094 | |||||||
| chr12:71150141 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(50): Show |
82 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.61-5928G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150141 | |||||||
| chr12:71150186 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(50): Show |
82 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.61-5973G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150186 | |||||||
| chr12:71150344 | C | T | 1 | a0002c0002t0002g0030 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.61-6131G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150344 | |||||||
| chr12:71150353 | C | G | 4 | a0002c0002t0002g0019 a0002c0002t0002g0079 a0002c0002t0002g0122 others(1): Show |
6 | HG01952.hp2 HG02300.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.61-6140G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150353 | |||||||
| chr12:71150374 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02723.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.61-6161C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150374 | |||||||
| chr12:71150501 | GTCCTACT others(3): Show |
G | 1 | a0006c0007t0002g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.61-6298_61-6289del others(10): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150501 | |||||||
| chr12:71150509 | GAT | G | 74 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0016 others(71): Show |
123 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.61-6298_61-6297del others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150509 | |||||||
| chr12:71150527 | C | T | 17 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0199 others(14): Show |
24 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.61-6314G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150527 | |||||||
| chr12:71150528 | G | A | 3 | a0001c0003t0001g0167 a0001c0003t0001g0182 a0001c0003t0001g0183 |
3 | HG01167.hp1 HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.61-6315C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150528 | |||||||
| chr12:71150612 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.61-6399C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150612 | |||||||
| chr12:71150627 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01361.hp1 HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.61-6414C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150627 | |||||||
| chr12:71150692 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.61-6479A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150692 | |||||||
| chr12:71150748 | C | T | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(10): Show |
19 | HG01109.hp2 HG01496.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.61-6535G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150748 | |||||||
| chr12:71150758 | C | T | 1 | a0003c0004t0001g0131 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.61-6545G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150758 | |||||||
| chr12:71150894 | C | G | 37 | a0001c0001t0001g0159 a0001c0001t0001g0179 a0001c0003t0001g0003 others(34): Show |
55 | HG00544.hp1 HG00639.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.61-6681G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150894 | |||||||
| chr12:71150928 | A | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02723.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+6691T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71150928 | |||||||
| chr12:71151056 | C | T | 3 | a0001c0003t0001g0013 a0001c0003t0001g0073 a0001c0003t0001g0135 |
6 | NA18974.hp2 NA18975.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+6563G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151056 | |||||||
| chr12:71151066 | A | AT | 73 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(70): Show |
103 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.60+6552dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151066 | |||||||
| chr12:71151066 | AT | A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0155 others(5): Show |
10 | HG02109.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.60+6552delA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151066 | |||||||
| chr12:71151069 | T | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
7 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+6550A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151069 | |||||||
| chr12:71151221 | G | A | 4 | a0002c0002t0002g0035 a0002c0002t0002g0118 a0002c0002t0002g0119 others(1): Show |
5 | NA18949.hp1 NA18957.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+6398C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151221 | |||||||
| chr12:71151257 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(51): Show |
83 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.60+6362C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151257 | |||||||
| chr12:71151274 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.60+6345C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151274 | |||||||
| chr12:71151354 | C | T | 1 | a0001c0003t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.60+6265G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151354 | |||||||
| chr12:71151391 | T | C | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG01109.hp2 HG01496.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+6228A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151391 | |||||||
| chr12:71151450 | C | A | 1 | a0003c0004t0001g0149 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.60+6169G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151450 | |||||||
| chr12:71151493 | A | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0162 others(16): Show |
26 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.60+6126T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151493 | |||||||
| chr12:71151778 | T | A | 19 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0162 others(16): Show |
26 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.60+5841A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151778 | |||||||
| chr12:71151810 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0053 others(37): Show |
78 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.60+5809T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151810 | |||||||
| chr12:71151879 | G | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
7 | HG01109.hp2 HG01496.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+5740C>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71151879 | |||||||
| chr12:71152006 | T | C | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+5613A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152006 | |||||||
| chr12:71152042 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.60+5577C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152042 | |||||||
| chr12:71152158 | T | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+5461A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152158 | |||||||
| chr12:71152223 | G | A | 1 | a0002c0002t0002g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.60+5396C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152223 | |||||||
| chr12:71152227 | G | C | 1 | a0001c0003t0001g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.60+5392C>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152227 | |||||||
| chr12:71152304 | T | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0230 others(4): Show |
11 | HG01361.hp2 HG01433.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.60+5315A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152304 | |||||||
| chr12:71152482 | A | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(49): Show |
81 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.60+5137T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152482 | |||||||
| chr12:71152778 | A | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0068 |
5 | HG00735.hp1 HG01952.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+4841T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152778 | |||||||
| chr12:71152928 | T | C | 10 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+4691A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152928 | |||||||
| chr12:71152979 | C | T | 1 | a0002c0002t0002g0132 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.60+4640G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152979 | |||||||
| chr12:71152999 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.60+4620T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71152999 | |||||||
| chr12:71153060 | C | G | 1 | a0001c0001t0002g0018 | 4 | HG01516.hp1 HG01517.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+4559G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153060 | |||||||
| chr12:71153152 | T | C | 2 | a0002c0002t0002g0103 a0002c0002t0002g0126 |
2 | NA18974.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.60+4467A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153152 | |||||||
| chr12:71153230 | A | T | 6 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0003t0001g0154 others(3): Show |
12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+4389T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153230 | |||||||
| chr12:71153491 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.60+4128G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153491 | |||||||
| chr12:71153510 | C | T | 1 | a0002c0002t0002g0078 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.60+4109G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153510 | |||||||
| chr12:71153560 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0258 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.60+4059G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153560 | |||||||
| chr12:71153640 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.60+3979A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153640 | |||||||
| chr12:71153678 | G | A | 5 | a0001c0003t0001g0107 a0002c0002t0002g0076 a0002c0002t0002g0104 others(2): Show |
5 | NA18969.hp1 NA18982.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+3941C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153678 | |||||||
| chr12:71153715 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.60+3904G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153715 | |||||||
| chr12:71153739 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(193): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.60+3880A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153739 | |||||||
| chr12:71153837 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0266 a0001c0001t0001g0267 others(2): Show |
7 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+3782G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153837 | |||||||
| chr12:71153878 | A | T | 1 | a0002c0002t0002g0077 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.60+3741T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153878 | |||||||
| chr12:71153936 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60+3683T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153936 | |||||||
| chr12:71153950 | A | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(193): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.60+3669T>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71153950 | |||||||
| chr12:71154035 | G | A | 1 | a0003c0004t0001g0006 | 6 | HG01257.hp1 HG01496.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+3584C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154035 | |||||||
| chr12:71154058 | C | T | 2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.60+3561G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154058 | |||||||
| chr12:71154067 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(164): Show |
265 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.60+3552T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154067 | |||||||
| chr12:71154145 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+3474G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154145 | |||||||
| chr12:71154177 | G | A | 1 | a0002c0002t0002g0108 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.60+3442C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154177 | |||||||
| chr12:71154210 | T | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0136 others(28): Show |
67 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+3409A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154210 | |||||||
| chr12:71154311 | A | AAAT | 125 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0017 others(122): Show |
184 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.60+3305_60+3307dup others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | |||||||
| chr12:71154311 | A | AAATAAT | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0003t0001g0158 others(4): Show |
7 | HG00558.hp1 HG02074.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+3302_60+3307dup others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | |||||||
| chr12:71154311 | AAAT | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0028 others(24): Show |
39 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.60+3305_60+3307del others(3): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | |||||||
| chr12:71154311 | AAATAAT | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0239 others(14): Show |
32 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.60+3302_60+3307del others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | |||||||
| chr12:71154311 | AAATAATA others(2): Show |
A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0053 others(37): Show |
78 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.60+3299_60+3307del others(9): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154311 | |||||||
| chr12:71154354 | A | AATAATC | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0265 |
5 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+3264_60+3265ins others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154354 | |||||||
| chr12:71154354 | A | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
6 | HG02258.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.60+3265T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154354 | |||||||
| chr12:71154442 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.60+3177C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71154442 | |||||||
| chr12:71155110 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(48): Show |
80 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.60+2509G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155110 | |||||||
| chr12:71155192 | T | C | 2 | a0002c0002t0002g0122 a0002c0002t0002g0123 |
2 | HG01952.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.60+2427A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155192 | |||||||
| chr12:71155316 | C | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(200): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.60+2303G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155316 | |||||||
| chr12:71155332 | T | A | 2 | a0001c0003t0001g0022 a0001c0003t0001g0046 |
5 | NA18947.hp1 NA18978.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.60+2287A>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155332 | |||||||
| chr12:71155545 | A | G | 1 | a0003c0004t0001g0129 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.60+2074T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155545 | |||||||
| chr12:71155613 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.60+2006C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155613 | |||||||
| chr12:71155627 | T | C | 6 | a0001c0003t0001g0151 a0001c0003t0001g0153 a0001c0003t0001g0154 others(3): Show |
12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+1992A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155627 | |||||||
| chr12:71155736 | A | AT | 7 | a0001c0001t0001g0053 a0001c0001t0001g0162 a0001c0001t0001g0163 others(4): Show |
8 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+1882dupA | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155736 | |||||||
| chr12:71155736 | A | ATT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0136 others(28): Show |
67 | HG00423.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.60+1881_60+1882dup others(2): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155736 | |||||||
| chr12:71155878 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0074 |
2 | HG03139.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.60+1741G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155878 | |||||||
| chr12:71155891 | C | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0065 |
3 | HG03471.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.60+1728G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155891 | |||||||
| chr12:71155892 | C | T | 2 | a0006c0007t0002g0127 a0006c0007t0002g0128 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.60+1727G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71155892 | |||||||
| chr12:71156022 | C | T | 4 | a0001c0001t0001g0159 a0001c0003t0001g0158 a0001c0003t0001g0160 others(1): Show |
4 | HG00544.hp1 HG02165.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+1597G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156022 | |||||||
| chr12:71156083 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.60+1536G>A | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156083 | |||||||
| chr12:71156223 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60+1396G>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156223 | |||||||
| chr12:71156250 | C | CA | 6 | a0001c0001t0001g0155 a0002c0002t0002g0124 a0002c0002t0002g0125 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+1368dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA | 6 | a0001c0001t0001g0053 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
7 | HG02257.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+1362_60+1368dup others(7): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(2): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0252 others(3): Show |
7 | HG01167.hp2 HG01361.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+1360_60+1368dup others(9): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG03017.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.60+1359_60+1368dup others(10): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0255 a0007c0009t0001g0256 |
2 | HG03704.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.60+1358_60+1368dup others(11): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0004g0056 a0004c0005t0002g0067 |
2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.60+1357_60+1368dup others(12): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0068 |
3 | HG01993.hp2 NA20300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.60+1356_60+1368dup others(13): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
5 | HG00735.hp1 HG01952.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+1355_60+1368dup others(14): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0218 others(3): Show |
7 | HG01109.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.60+1354_60+1368dup others(15): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.60+1353_60+1368dup others(16): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0257 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.60+1351_60+1368dup others(18): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156250 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0157 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.60+1368_60+1369ins others(23): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156250 | |||||||
| chr12:71156255 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.60+1346_60+1363del others(18): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156255 | |||||||
| chr12:71156257 | AAAAAAAA others(9): Show |
A | 1 | a0004c0005t0002g0050 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60+1346_60+1361del others(16): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156257 | |||||||
| chr12:71156258 | AAAAAAAA others(8): Show |
A | 1 | a0004c0005t0002g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.60+1346_60+1360del others(15): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156258 | |||||||
| chr12:71156260 | AAAAAAAA others(6): Show |
A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0162 others(12): Show |
22 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.60+1346_60+1358del others(13): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156260 | |||||||
| chr12:71156261 | AAAAAAAA others(5): Show |
A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0047 others(22): Show |
43 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.60+1346_60+1357del others(12): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156261 | |||||||
| chr12:71156262 | AAAAAAAC others(4): Show |
A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0243 a0001c0001t0002g0018 others(1): Show |
4 | HG01123.hp2 HG01891.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.60+1346_60+1356del others(11): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156262 | |||||||
| chr12:71156265 | AAAAC | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(19): Show |
24 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.60+1350_60+1353del others(4): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156265 | |||||||
| chr12:71156266 | AAACAAAC | A | 6 | a0001c0003t0001g0013 a0001c0003t0001g0151 a0001c0003t0001g0153 others(3): Show |
12 | HG02080.hp2 HG04115.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.60+1346_60+1352del others(7): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156266 | |||||||
| chr12:71156267 | AACAAAC | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0039 others(31): Show |
61 | HG00544.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.60+1346_60+1351del others(6): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156267 | |||||||
| chr12:71156268 | ACAAAC | A | 60 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(57): Show |
87 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.60+1346_60+1350del others(5): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156268 | |||||||
| chr12:71156269 | C | A | 38 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0052 others(35): Show |
44 | HG00735.hp1 HG01109.hp2 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.60+1350G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156269 | |||||||
| chr12:71156270 | A | C | 1 | a0004c0005t0002g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.60+1349T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156270 | |||||||
| chr12:71156273 | C | A | 71 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0025 others(68): Show |
82 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.60+1346G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156273 | |||||||
| chr12:71156435 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.60+1184A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156435 | |||||||
| chr12:71156441 | AAGCAGCC others(20): Show |
A | 85 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0025 others(82): Show |
120 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.60+1151_60+1177del others(27): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156441 | |||||||
| chr12:71156643 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.60+976A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156643 | |||||||
| chr12:71156649 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0023 others(53): Show |
85 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.60+970A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156649 | |||||||
| chr12:71156901 | T | C | 5 | a0001c0001t0001g0053 a0001c0001t0001g0260 a0001c0001t0001g0261 others(2): Show |
6 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.60+718A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156901 | |||||||
| chr12:71156917 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(201): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.60+702A>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71156917 | |||||||
| chr12:71157021 | T | G | 1 | a0003c0004t0001g0264 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.60+598A>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157021 | |||||||
| chr12:71157060 | A | C | 1 | a0001c0003t0001g0073 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.60+559T>G | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157060 | |||||||
| chr12:71157210 | C | CA | 10 | a0001c0001t0001g0025 a0001c0001t0001g0054 a0001c0001t0001g0055 others(7): Show |
14 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.60+408dupT | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157210 | |||||||
| chr12:71157217 | A | G | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02723.hp1 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.60+402T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157217 | |||||||
| chr12:71157342 | G | A | 1 | a0004c0005t0002g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.60+277C>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157342 | |||||||
| chr12:71157412 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0068 others(2): Show |
7 | HG00735.hp1 HG01952.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+207T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 2/8 | chr12 | 71157412 | |||||||
| chr12:71157866 | A | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(2): Show |
5 | HG01109.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-110+64T>C | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/8 | chr12 | 71157866 | |||||||
| chr12:71157879 | GCAAAGGC others(25): Show |
G | 1 | a0002c0002t0002g0274 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-110+19_-110+50del others(32): Show |
TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/8 | chr12 | 71157879 | |||||||
| chr12:71157897 | C | A | 1 | a0003c0004t0001g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-110+33G>T | TSPAN8 | ENSG00000127324.9 | transcript | ENST00000247829.8 | protein_coding | 1/8 | chr12 | 71157897 |