Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 158427 |
| ensemblid | ENSG00000136925.15 |
| hgncid | 30087 |
| symbol | TSTD2 |
| name | thiosulfate sulfurtransferase like domain containing 2 |
| refseq_nuc | NM_139246.5 |
| refseq_prot | NP_640339.4 |
| ensembl_nuc | ENST00000341170.5 |
| ensembl_prot | ENSP00000342499.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 97600080 |
| end | 97633368 |
| strand | - |
| ver | v1.2 |
| region | chr9:97600080-97633368 |
| region5000 | chr9:97595080-97638368 |
| regionname0 | TSTD2_chr9_97600080_97633368 |
| regionname5000 | TSTD2_chr9_97595080_97638368 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 516 | 228 | 71 | 46 | 81 | 9 | 21 | 63 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| a0002 | 1/1 | 516 | 70 | 6 | 11 | 45 | 3 | 3 | 38 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| a0003 | 0/0 | 516 | 69 | 9 | 6 | 36 | 2 | 16 | 27 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| a0004 | 0/0 | 516 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| a0005 | 0/0 | 516 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| a0006 | 0/0 | 516 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| a0007 | 0/0 | 516 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | MPSST others(511): Show |
chr9 | 97595080 | 97638368 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1548 | 138 | 19 | 30 | 60 | 9 | 20 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0001c0004 | 0/0 | 1548 | 46 | 44 | 2 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0001c0005 | 0/0 | 1548 | 34 | 0 | 12 | 21 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0001c0006 | 0/0 | 1548 | 7 | 5 | 2 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0001c0007 | 0/0 | 1548 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0002c0002 | 1/1 | 1548 | 70 | 6 | 11 | 45 | 3 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0003c0003 | 0/0 | 1548 | 68 | 9 | 6 | 35 | 2 | 16 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0003c0012 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0004c0008 | 0/0 | 1548 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0005c0009 | 0/0 | 1548 | 2 | 0 | 1 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0006c0010 | 0/0 | 1548 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 | ||
| a0007c0011 | 0/0 | 1548 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | ATGCC others(1543): Show |
chr9 | 97595080 | 97638368 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4116 | 126 | 16 | 30 | 57 | 8 | 15 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0010 | 0/0 | 4116 | 3 | 0 | 0 | 0 | 1 | 2 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0012 | 0/0 | 4116 | 2 | 0 | 0 | 0 | 0 | 2 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0014 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0016 | 0/0 | 4127 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4122): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0018 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0019 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0021 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0001t0022 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0004 | 0/0 | 4116 | 13 | 12 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0005 | 0/0 | 4116 | 9 | 9 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0006 | 0/0 | 4116 | 11 | 10 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0008 | 0/0 | 4116 | 6 | 6 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0009 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0011 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0017 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0004t0023 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0005t0002 | 0/0 | 4116 | 20 | 0 | 12 | 7 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0005t0003 | 0/0 | 4116 | 14 | 0 | 0 | 14 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0006t0007 | 0/0 | 4116 | 7 | 5 | 2 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0001c0007t0001 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0002c0002t0001 | 1/1 | 4116 | 69 | 5 | 11 | 45 | 3 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0002c0002t0020 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0003c0003t0001 | 0/0 | 4116 | 65 | 7 | 6 | 35 | 2 | 15 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0003c0003t0013 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0003c0003t0015 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0003c0012t0001 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0004c0008t0005 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0005c0009t0001 | 0/0 | 4116 | 2 | 0 | 1 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0006c0010t0007 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| a0007c0011t0001 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | GTCAC others(4111): Show |
chr9 | 97595080 | 97638368 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 28 | 1 | 8 | 15 | 1 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0004 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0005 | 0/0 | 14 | 2 | 6 | 2 | 1 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0012 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0010g0022 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0012g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0012g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0014g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0016g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0018g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0019g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0021g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0001t0022g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0004g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0006g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0008g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0009g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0017g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0004t0023g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0002g0006 | 0/0 | 14 | 0 | 9 | 4 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0005t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0006t0007g0011 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0001c0007t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0001 | 1/1 | 35 | 0 | 11 | 20 | 1 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0002c0002t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0003 | 0/0 | 24 | 2 | 1 | 18 | 0 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0007 | 0/0 | 13 | 4 | 3 | 2 | 1 | 3 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0013g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0003t0015g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0003c0012t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0004c0008t0005g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0005c0009t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0005c0009t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0006c0010t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| a0007c0011t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0007 | EUR | GBR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0138 | EUR | GBR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | FIN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0007 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00597 | hp2 | a0001 | c0005 | t0003 | g0016 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00609 | hp2 | a0001 | c0005 | t0003 | g0013 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | CHS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01099 | hp1 | a0001 | c0005 | t0002 | g0006 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0037 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01109 | hp2 | a0001 | c0006 | t0007 | g0011 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01167 | hp2 | a0001 | c0005 | t0002 | g0006 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01192 | hp2 | a0001 | c0005 | t0002 | g0006 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01243 | hp1 | a0001 | c0006 | t0007 | g0011 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01243 | hp2 | a0001 | c0004 | t0004 | g0058 | AMR | PUR | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0007 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0036 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0022 | EUR | IBS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0080 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01884 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01891 | hp1 | a0001 | c0004 | t0005 | g0057 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01891 | hp2 | a0001 | c0004 | t0006 | g0052 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01934 | hp2 | a0001 | c0005 | t0002 | g0111 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0153 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01952 | hp1 | a0001 | c0004 | t0006 | g0051 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01978 | hp2 | a0001 | c0005 | t0002 | g0006 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01981 | hp2 | a0001 | c0005 | t0002 | g0006 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01993 | hp1 | a0005 | c0009 | t0001 | g0070 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01993 | hp2 | a0001 | c0005 | t0002 | g0006 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02004 | hp2 | a0001 | c0005 | t0002 | g0006 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0007 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0121 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02145 | hp1 | a0002 | c0002 | t0020 | g0133 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02145 | hp2 | a0001 | c0004 | t0005 | g0062 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02148 | hp1 | a0001 | c0005 | t0002 | g0109 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02155 | hp2 | a0001 | c0005 | t0003 | g0016 | EAS | CDX | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02165 | hp1 | a0001 | c0005 | t0003 | g0016 | EAS | CDX | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | CDX | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02257 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02258 | hp1 | a0001 | c0004 | t0023 | g0054 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02258 | hp2 | a0001 | c0004 | t0006 | g0008 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02273 | hp1 | a0001 | c0005 | t0002 | g0006 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02280 | hp2 | a0001 | c0004 | t0008 | g0014 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02451 | hp1 | a0001 | c0004 | t0005 | g0027 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02451 | hp2 | a0006 | c0010 | t0007 | g0091 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02523 | hp1 | a0001 | c0005 | t0003 | g0016 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | KHV | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02572 | hp1 | a0003 | c0003 | t0013 | g0038 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0148 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02622 | hp1 | a0001 | c0004 | t0005 | g0027 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02622 | hp2 | a0001 | c0004 | t0004 | g0059 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02630 | hp2 | a0001 | c0004 | t0011 | g0155 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02717 | hp1 | a0001 | c0004 | t0006 | g0053 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02723 | hp1 | a0001 | c0004 | t0017 | g0050 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02723 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02809 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02818 | hp1 | a0001 | c0006 | t0007 | g0011 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02818 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02886 | hp1 | a0001 | c0004 | t0011 | g0154 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02886 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02895 | hp1 | a0001 | c0004 | t0004 | g0049 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02895 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02896 | hp1 | a0003 | c0003 | t0013 | g0038 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0032 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02897 | hp2 | a0001 | c0006 | t0007 | g0011 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0119 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0108 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02970 | hp1 | a0001 | c0004 | t0004 | g0009 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02970 | hp2 | a0001 | c0004 | t0006 | g0008 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02976 | hp1 | a0004 | c0008 | t0005 | g0025 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02976 | hp2 | a0001 | c0004 | t0005 | g0055 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0037 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03041 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0063 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03098 | hp2 | a0001 | c0004 | t0008 | g0014 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03139 | hp1 | a0001 | c0004 | t0004 | g0009 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03209 | hp1 | a0001 | c0004 | t0004 | g0009 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03209 | hp2 | a0001 | c0007 | t0001 | g0021 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03225 | hp2 | a0001 | c0004 | t0009 | g0060 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03239 | hp1 | a0001 | c0005 | t0002 | g0006 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03486 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03490 | hp2 | a0001 | c0001 | t0021 | g0065 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0128 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03516 | hp1 | a0001 | c0004 | t0005 | g0029 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03516 | hp2 | a0001 | c0004 | t0004 | g0009 | AFR | ESN | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | GWD | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03579 | hp1 | a0004 | c0008 | t0005 | g0025 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0022 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0007 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03704 | hp1 | a0001 | c0001 | t0010 | g0022 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03704 | hp2 | a0003 | c0003 | t0015 | g0043 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0039 | SAS | PJL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03831 | hp2 | a0001 | c0001 | t0012 | g0077 | SAS | BEB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0007 | SAS | BEB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0086 | SAS | BEB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0113 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0039 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0036 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0076 | SAS | STU | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18522 | hp1 | a0001 | c0004 | t0004 | g0009 | AFR | YRI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18906 | hp1 | a0001 | c0004 | t0009 | g0028 | AFR | YRI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18906 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | YRI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18947 | hp2 | a0001 | c0005 | t0002 | g0006 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18954 | hp2 | a0001 | c0001 | t0018 | g0099 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18956 | hp1 | a0001 | c0001 | t0016 | g0100 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18962 | hp1 | a0001 | c0005 | t0003 | g0048 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18966 | hp1 | a0001 | c0005 | t0002 | g0112 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18967 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18968 | hp1 | a0001 | c0005 | t0002 | g0006 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18970 | hp1 | a0001 | c0005 | t0003 | g0013 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18975 | hp1 | a0001 | c0005 | t0003 | g0047 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18977 | hp2 | a0001 | c0005 | t0003 | g0107 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18982 | hp2 | a0003 | c0012 | t0001 | g0123 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0129 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18989 | hp2 | a0001 | c0005 | t0003 | g0110 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19002 | hp1 | a0001 | c0005 | t0002 | g0035 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19004 | hp2 | a0001 | c0005 | t0002 | g0035 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19006 | hp2 | a0001 | c0005 | t0002 | g0006 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19009 | hp1 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19043 | hp1 | a0001 | c0004 | t0009 | g0028 | AFR | LWK | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0061 | AFR | LWK | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0093 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19055 | hp2 | a0001 | c0005 | t0003 | g0013 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19063 | hp2 | a0001 | c0005 | t0003 | g0013 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19066 | hp1 | a0005 | c0009 | t0001 | g0069 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19075 | hp1 | a0001 | c0001 | t0019 | g0104 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19081 | hp1 | a0001 | c0005 | t0002 | g0006 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19083 | hp1 | a0001 | c0005 | t0003 | g0046 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19084 | hp1 | a0001 | c0005 | t0003 | g0013 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19087 | hp1 | a0007 | c0011 | t0001 | g0103 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0120 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19240 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | YRI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA19240 | hp2 | a0001 | c0004 | t0008 | g0014 | AFR | YRI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20129 | hp1 | a0004 | c0008 | t0005 | g0025 | AFR | ASW | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20129 | hp2 | a0001 | c0004 | t0006 | g0008 | AFR | ASW | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0126 | EUR | TSI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0125 | SAS | GIH | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01123 | hp1 | a0001 | c0005 | t0002 | g0006 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02109 | hp1 | a0001 | c0004 | t0006 | g0008 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02109 | hp2 | a0001 | c0004 | t0008 | g0014 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | ACB | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03471 | hp1 | a0001 | c0004 | t0005 | g0029 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG03471 | hp2 | a0001 | c0004 | t0004 | g0056 | AFR | MSL | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | USA | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| HG06807 | hp2 | a0001 | c0004 | t0008 | g0014 | AFR | USA | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA20300 | hp2 | a0001 | c0004 | t0006 | g0008 | AFR | USA | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA21309 | hp1 | a0001 | c0004 | t0005 | g0064 | AFR | LWK | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0001 | REF | REF | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0001 | REF | REF | TSTD2_chr9_97595080_97638368 | TSTD2 | chr9 | 97595080 | 97638368 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97604748 | A | G | 1 | a0006 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1231T>C | p.Tyr411His | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/10 | 1407/4116 | 1231/1551 | 411/516 | chr9 | 97604748 | |||
| chr9:97610420 | T | C | 1 | a0007 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.761A>G | p.Glu254Gly | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/10 | 937/4116 | 761/1551 | 254/516 | chr9 | 97610420 | |||
| chr9:97625804 | C | T | 1 | a0005 | 2 | HG01993.hp1 NA19066.hp1 |
missense_variant | MODERATE | c.359G>A | p.Ser120Asn | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/10 | 535/4116 | 359/1551 | 120/516 | chr9 | 97625804 | |||
| chr9:97625837 | G | T | 1 | a0003 | 69 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(66): Show |
missense_variant | MODERATE | c.326C>A | p.Ala109Asp | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/10 | 502/4116 | 326/1551 | 109/516 | chr9 | 97625837 | |||
| chr9:97625915 | C | T | 5 | a0001 a0004 a0005 others(2): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
missense_variant | MODERATE | c.248G>A | p.Arg83Gln | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/10 | 424/4116 | 248/1551 | 83/516 | chr9 | 97625915 | |||
| chr9:97627414 | G | A | 1 | a0004 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.149C>T | p.Ser50Leu | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/10 | 325/4116 | 149/1551 | 50/516 | chr9 | 97627414 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97602583 | G | A | 1 | a0003c0012 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.1437C>T | p.Cys479Cys | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1613/4116 | 1437/1551 | 479/516 | chr9 | 97602583 | |||
| chr9:97602640 | T | C | 1 | a0001c0006 | 7 | HG01109.hp2 HG01243.hp1 HG02723.hp2 others(4): Show |
synonymous_variant | LOW | c.1380A>G | p.Gln460Gln | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1556/4116 | 1380/1551 | 460/516 | chr9 | 97602640 | |||
| chr9:97605528 | G | A | 3 | a0001c0004 a0001c0005 a0004c0008 |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
synonymous_variant | LOW | c.1068C>T | p.Thr356Thr | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/10 | 1244/4116 | 1068/1551 | 356/516 | chr9 | 97605528 | |||
| chr9:97605531 | A | G | 3 | a0001c0004 a0001c0005 a0004c0008 |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
synonymous_variant | LOW | c.1065T>C | p.Cys355Cys | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/10 | 1241/4116 | 1065/1551 | 355/516 | chr9 | 97605531 | |||
| chr9:97617811 | T | C | 1 | a0001c0005 | 34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
synonymous_variant | LOW | c.549A>G | p.Gln183Gln | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/10 | 725/4116 | 549/1551 | 183/516 | chr9 | 97617811 | |||
| chr9:97625875 | C | A | 1 | a0001c0007 | 3 | HG02809.hp2 HG03209.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.288G>T | p.Val96Val | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/10 | 464/4116 | 288/1551 | 96/516 | chr9 | 97625875 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97600086 | T | C | 1 | a0002c0002t0020 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2383A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 2383 | chr9 | 97600086 | ||||||
| chr9:97600300 | T | C | 1 | a0001c0001t0010 | 3 | HG01516.hp1 HG03669.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2169A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 2169 | chr9 | 97600300 | ||||||
| chr9:97600317 | T | C | 12 | a0001c0001t0022 a0001c0004t0004 a0001c0004t0005 others(9): Show |
84 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2152A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 2152 | chr9 | 97600317 | ||||||
| chr9:97600375 | C | G | 3 | a0001c0001t0014 a0001c0006t0007 a0006c0010t0007 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2094G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 2094 | chr9 | 97600375 | ||||||
| chr9:97600441 | T | G | 1 | a0001c0004t0009 | 3 | HG03225.hp2 NA18906.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2028A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 2028 | chr9 | 97600441 | ||||||
| chr9:97600609 | G | A | 1 | a0001c0001t0021 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1860C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1860 | chr9 | 97600609 | ||||||
| chr9:97600792 | A | G | 1 | a0001c0001t0022 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1677 | chr9 | 97600792 | ||||||
| chr9:97600793 | T | G | 1 | a0003c0003t0015 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1676A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1676 | chr9 | 97600793 | ||||||
| chr9:97600886 | T | C | 1 | a0001c0004t0008 | 6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1583A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1583 | chr9 | 97600886 | ||||||
| chr9:97601035 | C | T | 2 | a0001c0004t0006 a0001c0004t0017 |
12 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1434G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1434 | chr9 | 97601035 | ||||||
| chr9:97601171 | T | C | 1 | a0001c0001t0012 | 2 | HG03831.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1298A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1298 | chr9 | 97601171 | ||||||
| chr9:97601294 | C | T | 11 | a0001c0004t0004 a0001c0004t0005 a0001c0004t0006 others(8): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1175G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1175 | chr9 | 97601294 | ||||||
| chr9:97601396 | T | G | 1 | a0001c0004t0011 | 2 | HG02630.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1073A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 1073 | chr9 | 97601396 | ||||||
| chr9:97601622 | A | G | 1 | a0001c0001t0019 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 847 | chr9 | 97601622 | ||||||
| chr9:97601630 | A | T | 11 | a0001c0004t0004 a0001c0004t0005 a0001c0004t0006 others(8): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*839T>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 839 | chr9 | 97601630 | ||||||
| chr9:97601652 | A | G | 1 | a0001c0004t0004 | 13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*817T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 817 | chr9 | 97601652 | ||||||
| chr9:97601739 | T | C | 1 | a0001c0005t0002 | 20 | HG01099.hp1 HG01123.hp1 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*730A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 730 | chr9 | 97601739 | ||||||
| chr9:97601755 | T | C | 1 | a0003c0003t0013 | 2 | HG02572.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*714A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 714 | chr9 | 97601755 | ||||||
| chr9:97601817 | T | C | 12 | a0001c0001t0022 a0001c0004t0004 a0001c0004t0005 others(9): Show |
84 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*652A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 652 | chr9 | 97601817 | ||||||
| chr9:97602020 | C | T | 1 | a0001c0001t0018 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 449 | chr9 | 97602020 | ||||||
| chr9:97602094 | G | C | 3 | a0001c0004t0008 a0001c0005t0002 a0001c0005t0003 |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*375C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 375 | chr9 | 97602094 | ||||||
| chr9:97602148 | C | T | 1 | a0001c0004t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*321G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 321 | chr9 | 97602148 | ||||||
| chr9:97602169 | A | C | 11 | a0001c0004t0004 a0001c0004t0005 a0001c0004t0006 others(8): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*300T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 300 | chr9 | 97602169 | ||||||
| chr9:97602212 | C | A | 1 | a0001c0004t0023 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*257G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 257 | chr9 | 97602212 | ||||||
| chr9:97602426 | A | ACCTACTT others(4): Show |
1 | a0001c0001t0016 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32_*42dupGTAAAAGT others(3): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 10/10 | 42 | chr9 | 97602426 | ||||||
| chr9:97627572 | T | C | 1 | a0001c0001t0014 | 2 | HG02896.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-10A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/10 | 10 | chr9 | 97627572 | ||||||
| chr9:97633334 | C | G | 1 | a0003c0003t0015 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/10 | 5772 | chr9 | 97633334 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:97602803 | T | C | 1 | a0001c0004t0005g0027 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1253-36A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97602803 | |||||||
| chr9:97602804 | A | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1253-37T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97602804 | |||||||
| chr9:97603128 | TTTGA | T | 9 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(6): Show |
17 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1253-365_1253-362d others(6): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603128 | |||||||
| chr9:97603149 | G | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1253-382C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603149 | |||||||
| chr9:97603191 | T | G | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1253-424A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603191 | |||||||
| chr9:97603210 | C | T | 2 | a0003c0003t0001g0024 a0003c0003t0001g0124 |
4 | NA18971.hp2 NA18998.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1253-443G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603210 | |||||||
| chr9:97603228 | G | T | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1253-461C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603228 | |||||||
| chr9:97603332 | C | T | 1 | a0004c0008t0005g0025 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1253-565G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603332 | |||||||
| chr9:97603512 | A | G | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1253-745T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603512 | |||||||
| chr9:97603734 | G | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1253-967C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603734 | |||||||
| chr9:97603879 | A | G | 1 | a0003c0003t0001g0122 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1252+848T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603879 | |||||||
| chr9:97603881 | A | C | 1 | a0002c0002t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1252+846T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97603881 | |||||||
| chr9:97604082 | C | G | 1 | a0003c0003t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1252+645G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604082 | |||||||
| chr9:97604123 | A | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1252+604T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604123 | |||||||
| chr9:97604212 | A | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1252+515T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604212 | |||||||
| chr9:97604376 | G | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1252+351C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604376 | |||||||
| chr9:97604561 | T | C | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.1252+166A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604561 | |||||||
| chr9:97604671 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1252+56T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604671 | |||||||
| chr9:97604691 | C | T | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.1252+36G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 9/9 | chr9 | 97604691 | |||||||
| chr9:97604927 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1114-62C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97604927 | |||||||
| chr9:97605024 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0045 others(9): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1114-159A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605024 | |||||||
| chr9:97605121 | G | A | 1 | a0001c0001t0016g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1114-256C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605121 | |||||||
| chr9:97605123 | A | G | 1 | a0001c0001t0016g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1114-258T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605123 | |||||||
| chr9:97605124 | G | C | 1 | a0001c0001t0016g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1114-259C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605124 | |||||||
| chr9:97605209 | A | C | 1 | a0002c0002t0001g0041 | 2 | NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1113+274T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605209 | |||||||
| chr9:97605352 | C | A | 1 | a0001c0001t0016g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1113+131G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605352 | |||||||
| chr9:97605352 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.1113+131G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605352 | |||||||
| chr9:97605387 | G | T | 1 | a0002c0002t0001g0139 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1113+96C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605387 | |||||||
| chr9:97605389 | G | C | 1 | a0005c0009t0001g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1113+94C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605389 | |||||||
| chr9:97605418 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1113+65C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 8/9 | chr9 | 97605418 | |||||||
| chr9:97605652 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.955-11C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 7/9 | chr9 | 97605652 | |||||||
| chr9:97605805 | C | A | 1 | a0001c0001t0016g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.955-164G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 7/9 | chr9 | 97605805 | |||||||
| chr9:97605892 | C | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.954+251G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 7/9 | chr9 | 97605892 | |||||||
| chr9:97606062 | A | G | 1 | a0003c0003t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.954+81T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 7/9 | chr9 | 97606062 | |||||||
| chr9:97606064 | G | A | 1 | a0004c0008t0005g0025 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.954+79C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 7/9 | chr9 | 97606064 | |||||||
| chr9:97606899 | GAGAA | G | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.836-642_836-639del others(4): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97606899 | |||||||
| chr9:97606961 | C | T | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-700G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97606961 | |||||||
| chr9:97607043 | G | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.836-782C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607043 | |||||||
| chr9:97607092 | A | G | 2 | a0001c0004t0005g0029 a0001c0004t0005g0057 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.836-831T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607092 | |||||||
| chr9:97607224 | G | C | 1 | a0001c0004t0006g0051 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.836-963C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607224 | |||||||
| chr9:97607473 | G | A | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.836-1212C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607473 | |||||||
| chr9:97607630 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.836-1369A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607630 | |||||||
| chr9:97607645 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.836-1384T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607645 | |||||||
| chr9:97607678 | G | A | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.836-1417C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607678 | |||||||
| chr9:97607752 | A | C | 2 | a0001c0004t0011g0154 a0001c0004t0011g0155 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.836-1491T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607752 | |||||||
| chr9:97607839 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.836-1578C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97607839 | |||||||
| chr9:97608044 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.836-1783C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608044 | |||||||
| chr9:97608052 | G | A | 1 | a0001c0005t0003g0047 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.836-1791C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608052 | |||||||
| chr9:97608139 | C | T | 1 | a0001c0004t0005g0027 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.836-1878G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608139 | |||||||
| chr9:97608294 | G | A | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.836-2033C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608294 | |||||||
| chr9:97608559 | C | T | 1 | a0001c0004t0009g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835+1787G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608559 | |||||||
| chr9:97608570 | A | T | 1 | a0001c0001t0001g0033 | 2 | NA18947.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.835+1776T>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608570 | |||||||
| chr9:97608641 | G | T | 1 | a0003c0003t0001g0121 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.835+1705C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608641 | |||||||
| chr9:97608798 | T | C | 1 | a0003c0003t0001g0039 | 2 | HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.835+1548A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608798 | |||||||
| chr9:97608860 | C | A | 1 | a0003c0003t0001g0124 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.835+1486G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97608860 | |||||||
| chr9:97609032 | G | GA | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.835+1313_835+1314i others(3): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97609032 | |||||||
| chr9:97609170 | AAAT | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0033 others(3): Show |
25 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.835+1173_835+1175d others(5): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97609170 | |||||||
| chr9:97609189 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.835+1157G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97609189 | |||||||
| chr9:97609565 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.835+781G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97609565 | |||||||
| chr9:97609594 | A | G | 2 | a0003c0003t0001g0125 a0003c0003t0001g0126 |
2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.835+752T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97609594 | |||||||
| chr9:97609886 | C | CA | 15 | a0001c0004t0008g0014 a0001c0004t0008g0108 a0001c0005t0002g0006 others(12): Show |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.835+459dupT | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97609886 | |||||||
| chr9:97610273 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.835+73C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 6/9 | chr9 | 97610273 | |||||||
| chr9:97610557 | G | A | 2 | a0003c0003t0001g0093 a0003c0003t0001g0127 |
2 | NA19054.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.730-106C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97610557 | |||||||
| chr9:97610624 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.730-173G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97610624 | |||||||
| chr9:97610698 | T | C | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.730-247A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97610698 | |||||||
| chr9:97610753 | C | T | 1 | a0001c0004t0004g0058 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.730-302G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97610753 | |||||||
| chr9:97610941 | T | C | 1 | a0001c0001t0014g0032 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.730-490A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97610941 | |||||||
| chr9:97611007 | T | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.730-556A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611007 | |||||||
| chr9:97611026 | A | G | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.729+548T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611026 | |||||||
| chr9:97611076 | GAA | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0072 |
4 | HG01358.hp1 HG01515.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+496_729+497del others(2): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611076 | |||||||
| chr9:97611077 | A | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.729+497T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611077 | |||||||
| chr9:97611089 | C | T | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.729+485G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611089 | |||||||
| chr9:97611196 | G | A | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.729+378C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611196 | |||||||
| chr9:97611236 | T | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.729+338A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611236 | |||||||
| chr9:97611248 | C | T | 15 | a0001c0004t0008g0014 a0001c0004t0008g0108 a0001c0005t0002g0006 others(12): Show |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.729+326G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611248 | |||||||
| chr9:97611250 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.729+324T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611250 | |||||||
| chr9:97611301 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.729+273G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611301 | |||||||
| chr9:97611368 | G | GATC | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.729+203_729+205dup others(3): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611368 | |||||||
| chr9:97611374 | G | A | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.729+200C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611374 | |||||||
| chr9:97611394 | G | A | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.729+180C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611394 | |||||||
| chr9:97611438 | C | T | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.729+136G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611438 | |||||||
| chr9:97611487 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0072 |
4 | HG01358.hp1 HG01515.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+87A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 5/9 | chr9 | 97611487 | |||||||
| chr9:97611714 | G | A | 1 | a0003c0003t0015g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.604-15C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97611714 | |||||||
| chr9:97611750 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.604-51A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97611750 | |||||||
| chr9:97611846 | A | C | 1 | a0004c0008t0005g0025 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.604-147T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97611846 | |||||||
| chr9:97611959 | C | G | 3 | a0001c0001t0014g0032 a0001c0006t0007g0011 a0006c0010t0007g0091 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.604-260G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97611959 | |||||||
| chr9:97611992 | C | CT | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-294dupA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97611992 | |||||||
| chr9:97612117 | G | C | 2 | a0002c0002t0001g0094 a0002c0002t0001g0157 |
2 | NA18956.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.604-418C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612117 | |||||||
| chr9:97612170 | T | C | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-471A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612170 | |||||||
| chr9:97612183 | G | C | 1 | a0001c0004t0005g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.604-484C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612183 | |||||||
| chr9:97612251 | T | C | 2 | a0001c0004t0011g0154 a0001c0004t0011g0155 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.604-552A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612251 | |||||||
| chr9:97612556 | G | C | 2 | a0003c0003t0001g0093 a0003c0003t0001g0127 |
2 | NA19054.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.604-857C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612556 | |||||||
| chr9:97612704 | C | T | 1 | a0001c0004t0005g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.604-1005G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612704 | |||||||
| chr9:97612744 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.604-1045G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612744 | |||||||
| chr9:97612809 | G | A | 1 | a0001c0001t0012g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.604-1110C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612809 | |||||||
| chr9:97612810 | C | A | 1 | a0001c0001t0012g0077 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.604-1111G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612810 | |||||||
| chr9:97612889 | T | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.604-1190A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612889 | |||||||
| chr9:97612922 | C | T | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.604-1223G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612922 | |||||||
| chr9:97612970 | G | C | 10 | a0003c0003t0001g0007 a0003c0003t0001g0036 a0003c0003t0001g0093 others(7): Show |
23 | HG00140.hp1 HG00438.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.604-1271C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97612970 | |||||||
| chr9:97613291 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.604-1592G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613291 | |||||||
| chr9:97613293 | A | C | 15 | a0001c0004t0008g0014 a0001c0004t0008g0108 a0001c0005t0002g0006 others(12): Show |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.604-1594T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613293 | |||||||
| chr9:97613326 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
6 | HG00099.hp1 HG00733.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.604-1627T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613326 | |||||||
| chr9:97613365 | G | C | 4 | a0002c0002t0001g0026 a0002c0002t0001g0044 a0002c0002t0001g0140 others(1): Show |
5 | HG02074.hp2 NA18943.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-1666C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613365 | |||||||
| chr9:97613493 | A | AT | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-1795dupA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613493 | |||||||
| chr9:97613564 | G | A | 1 | a0001c0006t0007g0011 | 7 | HG01109.hp2 HG01243.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.604-1865C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613564 | |||||||
| chr9:97613596 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.604-1897A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613596 | |||||||
| chr9:97613767 | T | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.604-2068A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613767 | |||||||
| chr9:97613827 | C | CT | 8 | a0001c0001t0001g0072 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG00673.hp2 HG00741.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.604-2129dupA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613827 | |||||||
| chr9:97613827 | C | CTTTTTTT others(13071): Show |
1 | a0002c0002t0001g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.604-2129_604-2128i others(13080): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613827 | |||||||
| chr9:97613827 | CT | C | 38 | a0001c0001t0001g0068 a0001c0001t0001g0085 a0001c0004t0004g0009 others(35): Show |
82 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(79): Show |
intron_variant | MODIFIER | c.604-2129delA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613827 | |||||||
| chr9:97613867 | C | T | 1 | a0001c0004t0005g0027 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.604-2168G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613867 | |||||||
| chr9:97613978 | G | A | 1 | a0001c0004t0005g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.604-2279C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613978 | |||||||
| chr9:97613990 | G | A | 1 | a0002c0002t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.604-2291C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613990 | |||||||
| chr9:97613995 | A | T | 1 | a0007c0011t0001g0103 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.604-2296T>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97613995 | |||||||
| chr9:97614265 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.604-2566C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614265 | |||||||
| chr9:97614392 | G | GCATTCAT others(5): Show |
39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.604-2694_604-2693i others(14): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614392 | |||||||
| chr9:97614573 | T | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(20): Show |
74 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-2874A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614573 | |||||||
| chr9:97614574 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(20): Show |
74 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-2875C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614574 | |||||||
| chr9:97614579 | G | GC | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(20): Show |
74 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-2881_604-2880i others(3): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614579 | |||||||
| chr9:97614580 | G | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(20): Show |
74 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-2881C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614580 | |||||||
| chr9:97614581 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(20): Show |
74 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-2882T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614581 | |||||||
| chr9:97614584 | A | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(20): Show |
74 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.604-2885T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614584 | |||||||
| chr9:97614653 | G | A | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.604-2954C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614653 | |||||||
| chr9:97614702 | C | T | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.604-3003G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614702 | |||||||
| chr9:97614733 | T | C | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.603+3024A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614733 | |||||||
| chr9:97614800 | T | A | 5 | a0001c0004t0006g0008 a0001c0004t0006g0051 a0001c0004t0006g0052 others(2): Show |
12 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.603+2957A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614800 | |||||||
| chr9:97614813 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0089 a0001c0001t0019g0104 others(1): Show |
6 | NA18977.hp1 NA18994.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+2944C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614813 | |||||||
| chr9:97614848 | A | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(19): Show |
73 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.603+2909T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614848 | |||||||
| chr9:97614858 | A | T | 5 | a0001c0004t0006g0008 a0001c0004t0006g0051 a0001c0004t0006g0053 others(2): Show |
14 | HG01952.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.603+2899T>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614858 | |||||||
| chr9:97614864 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.603+2893A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614864 | |||||||
| chr9:97614940 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG00438.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.603+2817A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97614940 | |||||||
| chr9:97615001 | A | G | 1 | a0001c0006t0007g0011 | 7 | HG01109.hp2 HG01243.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.603+2756T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615001 | |||||||
| chr9:97615168 | C | T | 1 | a0003c0003t0001g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.603+2589G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615168 | |||||||
| chr9:97615290 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.603+2467T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615290 | |||||||
| chr9:97615299 | A | G | 1 | a0001c0004t0005g0027 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.603+2458T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615299 | |||||||
| chr9:97615431 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.603+2326G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615431 | |||||||
| chr9:97615740 | G | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.603+2017C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615740 | |||||||
| chr9:97615979 | A | C | 3 | a0001c0001t0014g0032 a0001c0006t0007g0011 a0006c0010t0007g0091 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.603+1778T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97615979 | |||||||
| chr9:97616268 | C | T | 1 | a0003c0003t0001g0118 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.603+1489G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97616268 | |||||||
| chr9:97616688 | T | C | 1 | a0006c0010t0007g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.603+1069A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97616688 | |||||||
| chr9:97616763 | G | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.603+994C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97616763 | |||||||
| chr9:97616794 | T | C | 6 | a0001c0004t0006g0008 a0001c0004t0006g0051 a0001c0004t0006g0052 others(3): Show |
15 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.603+963A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97616794 | |||||||
| chr9:97616814 | A | G | 1 | a0001c0004t0004g0056 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.603+943T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97616814 | |||||||
| chr9:97617325 | A | G | 1 | a0003c0003t0001g0037 | 2 | HG01106.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.603+432T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97617325 | |||||||
| chr9:97617457 | T | C | 1 | a0001c0001t0022g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.603+300A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 4/9 | chr9 | 97617457 | |||||||
| chr9:97617922 | A | G | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.483-45T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97617922 | |||||||
| chr9:97617945 | A | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.483-68T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97617945 | |||||||
| chr9:97618005 | G | T | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-128C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618005 | |||||||
| chr9:97618399 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.483-522T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618399 | |||||||
| chr9:97618400 | T | C | 1 | a0002c0002t0001g0141 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.483-523A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618400 | |||||||
| chr9:97618557 | A | G | 1 | a0001c0005t0002g0112 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.483-680T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618557 | |||||||
| chr9:97618752 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.483-875G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618752 | |||||||
| chr9:97618813 | T | G | 3 | a0001c0001t0014g0032 a0001c0006t0007g0011 a0006c0010t0007g0091 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.483-936A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618813 | |||||||
| chr9:97618829 | T | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.483-952A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618829 | |||||||
| chr9:97618893 | C | G | 1 | a0001c0004t0005g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.483-1016G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618893 | |||||||
| chr9:97618903 | A | G | 2 | a0002c0002t0001g0087 a0002c0002t0001g0136 |
2 | NA18995.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.483-1026T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618903 | |||||||
| chr9:97618910 | G | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.483-1033C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618910 | |||||||
| chr9:97618935 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.483-1058T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618935 | |||||||
| chr9:97618960 | A | G | 9 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(6): Show |
17 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.483-1083T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618960 | |||||||
| chr9:97618987 | T | C | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.483-1110A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97618987 | |||||||
| chr9:97619056 | T | C | 1 | a0002c0002t0001g0142 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.483-1179A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619056 | |||||||
| chr9:97619182 | C | T | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.483-1305G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619182 | |||||||
| chr9:97619280 | T | C | 3 | a0002c0002t0001g0017 a0002c0002t0001g0135 a0002c0002t0020g0133 |
6 | HG02145.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.483-1403A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619280 | |||||||
| chr9:97619316 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0045 others(9): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.483-1439G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619316 | |||||||
| chr9:97619325 | C | A | 1 | a0003c0003t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.483-1448G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619325 | |||||||
| chr9:97619345 | G | C | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-1468C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619345 | |||||||
| chr9:97619346 | T | G | 1 | a0004c0008t0005g0025 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.483-1469A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619346 | |||||||
| chr9:97619480 | A | G | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.483-1603T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619480 | |||||||
| chr9:97619713 | TAGAA | T | 6 | a0001c0004t0005g0029 a0001c0004t0005g0055 a0001c0004t0005g0057 others(3): Show |
8 | HG01891.hp1 HG02976.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.483-1840_483-1837d others(6): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619713 | |||||||
| chr9:97619800 | G | A | 2 | a0001c0004t0005g0029 a0001c0004t0005g0057 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.483-1923C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97619800 | |||||||
| chr9:97620122 | G | A | 1 | a0003c0003t0001g0129 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.483-2245C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620122 | |||||||
| chr9:97620148 | C | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.483-2271G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620148 | |||||||
| chr9:97620195 | C | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.483-2318G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620195 | |||||||
| chr9:97620294 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.483-2417G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620294 | |||||||
| chr9:97620380 | G | A | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-2503C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620380 | |||||||
| chr9:97620381 | C | A | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-2504G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620381 | |||||||
| chr9:97620551 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0081 |
3 | HG00099.hp2 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.483-2674T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620551 | |||||||
| chr9:97620654 | T | C | 1 | a0001c0004t0006g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.483-2777A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620654 | |||||||
| chr9:97620687 | A | G | 1 | a0003c0003t0001g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.483-2810T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620687 | |||||||
| chr9:97620750 | T | A | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-2873A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620750 | |||||||
| chr9:97620785 | G | C | 2 | a0001c0004t0005g0029 a0001c0004t0005g0057 |
3 | HG01891.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.483-2908C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97620785 | |||||||
| chr9:97621131 | A | G | 1 | a0002c0002t0001g0134 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.483-3254T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621131 | |||||||
| chr9:97621185 | A | G | 3 | a0001c0004t0005g0027 a0001c0004t0005g0062 a0001c0004t0005g0064 |
4 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-3308T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621185 | |||||||
| chr9:97621209 | T | C | 1 | a0001c0004t0005g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.483-3332A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621209 | |||||||
| chr9:97621283 | G | A | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.483-3406C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621283 | |||||||
| chr9:97621292 | A | C | 1 | a0001c0004t0005g0027 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.483-3415T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621292 | |||||||
| chr9:97621362 | CAT | C | 10 | a0001c0001t0001g0031 a0001c0004t0004g0009 a0001c0004t0004g0049 others(7): Show |
19 | HG01243.hp2 HG01884.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.483-3487_483-3486d others(4): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621362 | |||||||
| chr9:97621540 | C | T | 9 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(6): Show |
17 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.483-3663G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621540 | |||||||
| chr9:97621567 | T | G | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-3690A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621567 | |||||||
| chr9:97621602 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.483-3725C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621602 | |||||||
| chr9:97621690 | T | C | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.483-3813A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621690 | |||||||
| chr9:97621844 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(69): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.482+3837A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621844 | |||||||
| chr9:97621854 | A | G | 1 | a0002c0002t0020g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.482+3827T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621854 | |||||||
| chr9:97621985 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
6 | HG00099.hp1 HG00733.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+3696T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97621985 | |||||||
| chr9:97622028 | G | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.482+3653C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622028 | |||||||
| chr9:97622033 | G | T | 1 | a0001c0001t0022g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.482+3648C>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622033 | |||||||
| chr9:97622237 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.482+3444G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622237 | |||||||
| chr9:97622287 | T | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.482+3394A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622287 | |||||||
| chr9:97622408 | G | C | 1 | a0005c0009t0001g0070 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.482+3273C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622408 | |||||||
| chr9:97622512 | T | C | 15 | a0001c0004t0008g0014 a0001c0004t0008g0108 a0001c0005t0002g0006 others(12): Show |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.482+3169A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622512 | |||||||
| chr9:97622587 | G | A | 1 | a0002c0002t0001g0151 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.482+3094C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622587 | |||||||
| chr9:97622675 | G | A | 1 | a0002c0002t0001g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.482+3006C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97622675 | |||||||
| chr9:97623128 | CATGGGAG others(7): Show |
C | 2 | a0001c0001t0012g0076 a0001c0001t0012g0077 |
2 | HG03831.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.482+2539_482+2552d others(16): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623128 | |||||||
| chr9:97623298 | C | T | 6 | a0001c0004t0005g0029 a0001c0004t0005g0055 a0001c0004t0005g0057 others(3): Show |
8 | HG01891.hp1 HG02976.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.482+2383G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623298 | |||||||
| chr9:97623335 | T | G | 1 | a0002c0002t0001g0044 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.482+2346A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623335 | |||||||
| chr9:97623575 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.482+2106T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623575 | |||||||
| chr9:97623614 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.482+2067G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623614 | |||||||
| chr9:97623661 | C | A | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+2020G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623661 | |||||||
| chr9:97623741 | C | T | 6 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(3): Show |
13 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+1940G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623741 | |||||||
| chr9:97623904 | T | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0018 others(19): Show |
49 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.482+1777A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623904 | |||||||
| chr9:97623916 | C | T | 1 | a0001c0004t0005g0027 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.482+1765G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97623916 | |||||||
| chr9:97624117 | G | A | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.482+1564C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624117 | |||||||
| chr9:97624136 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.482+1545T>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624136 | |||||||
| chr9:97624151 | T | C | 1 | a0003c0003t0001g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.482+1530A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624151 | |||||||
| chr9:97624164 | G | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.482+1517C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624164 | |||||||
| chr9:97624259 | C | A | 1 | a0002c0002t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.482+1422G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624259 | |||||||
| chr9:97624328 | A | AC | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.482+1352dupG | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624328 | |||||||
| chr9:97624421 | C | T | 1 | a0001c0004t0005g0057 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.482+1260G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624421 | |||||||
| chr9:97624482 | C | A | 1 | a0001c0001t0001g0034 | 2 | HG01978.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.482+1199G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624482 | |||||||
| chr9:97624673 | A | G | 1 | a0001c0004t0005g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.482+1008T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624673 | |||||||
| chr9:97624706 | T | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.482+975A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624706 | |||||||
| chr9:97624811 | T | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.482+870A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624811 | |||||||
| chr9:97624851 | C | T | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.482+830G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97624851 | |||||||
| chr9:97625149 | A | G | 1 | a0003c0003t0001g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.482+532T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625149 | |||||||
| chr9:97625384 | G | C | 3 | a0001c0001t0014g0032 a0001c0006t0007g0011 a0006c0010t0007g0091 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.482+297C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625384 | |||||||
| chr9:97625394 | A | G | 1 | a0001c0005t0003g0046 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.482+287T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625394 | |||||||
| chr9:97625486 | A | G | 3 | a0001c0004t0005g0027 a0002c0002t0001g0131 a0002c0002t0001g0132 |
4 | HG00673.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+195T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625486 | |||||||
| chr9:97625541 | C | G | 15 | a0001c0004t0008g0014 a0001c0004t0008g0108 a0001c0005t0002g0006 others(12): Show |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.482+140G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625541 | |||||||
| chr9:97625566 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.482+115G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625566 | |||||||
| chr9:97625678 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0012g0076 a0001c0001t0012g0077 |
5 | HG03490.hp1 HG03710.hp1 HG03831.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.482+3A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 3/9 | chr9 | 97625678 | |||||||
| chr9:97626226 | AG | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.166-230delC | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626226 | |||||||
| chr9:97626248 | G | A | 1 | a0001c0001t0001g0015 | 4 | NA18949.hp2 NA18955.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-251C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626248 | |||||||
| chr9:97626856 | T | C | 1 | a0001c0004t0004g0063 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165+542A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626856 | |||||||
| chr9:97626900 | A | G | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.165+498T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626900 | |||||||
| chr9:97626924 | AT | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.165+473delA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626924 | |||||||
| chr9:97626924 | ATT | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+472_165+473del others(2): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626924 | |||||||
| chr9:97626935 | T | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.165+463A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97626935 | |||||||
| chr9:97627029 | T | A | 2 | a0001c0005t0002g0035 a0001c0005t0002g0112 |
3 | NA18966.hp1 NA19002.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.165+369A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97627029 | |||||||
| chr9:97627053 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.165+345G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97627053 | |||||||
| chr9:97627086 | A | G | 2 | a0001c0004t0011g0154 a0001c0004t0011g0155 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.165+312T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 2/9 | chr9 | 97627086 | |||||||
| chr9:97627686 | A | G | 1 | a0001c0005t0002g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-50-74T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97627686 | |||||||
| chr9:97627909 | T | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-50-297A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97627909 | |||||||
| chr9:97628032 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-50-420C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97628032 | |||||||
| chr9:97628345 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0045 others(9): Show |
19 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50-733T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97628345 | |||||||
| chr9:97628423 | C | T | 1 | a0003c0003t0015g0043 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-50-811G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97628423 | |||||||
| chr9:97628744 | C | T | 1 | a0002c0002t0001g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-50-1132G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97628744 | |||||||
| chr9:97628859 | G | A | 1 | a0003c0003t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-50-1247C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97628859 | |||||||
| chr9:97629458 | CT | C | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-1847delA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629458 | |||||||
| chr9:97629497 | A | G | 3 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 |
10 | HG01884.hp2 HG02257.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50-1885T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629497 | |||||||
| chr9:97629625 | T | A | 2 | a0001c0004t0008g0014 a0001c0004t0008g0108 |
6 | HG02109.hp2 HG02280.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50-2013A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629625 | |||||||
| chr9:97629774 | A | G | 3 | a0001c0001t0014g0032 a0001c0006t0007g0011 a0006c0010t0007g0091 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-50-2162T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629774 | |||||||
| chr9:97629826 | T | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-50-2214A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629826 | |||||||
| chr9:97629912 | C | T | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG00099.hp1 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-50-2300G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629912 | |||||||
| chr9:97629930 | A | G | 1 | a0001c0004t0005g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-50-2318T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629930 | |||||||
| chr9:97629996 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-50-2384G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97629996 | |||||||
| chr9:97630203 | C | T | 1 | a0001c0001t0021g0065 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-50-2591G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630203 | |||||||
| chr9:97630211 | G | A | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-50-2599C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630211 | |||||||
| chr9:97630250 | G | A | 2 | a0001c0004t0011g0154 a0001c0004t0011g0155 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-50-2638C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630250 | |||||||
| chr9:97630482 | TAAAC | T | 28 | a0001c0001t0001g0079 a0001c0004t0004g0009 a0001c0004t0004g0049 others(25): Show |
52 | HG01243.hp2 HG01256.hp2 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.-51+2757_-51+2760d others(6): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630482 | |||||||
| chr9:97630510 | T | A | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-51+2733A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630510 | |||||||
| chr9:97630552 | T | C | 24 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(21): Show |
43 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.-51+2691A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630552 | |||||||
| chr9:97630634 | T | A | 3 | a0001c0001t0014g0032 a0001c0006t0007g0011 a0006c0010t0007g0091 |
10 | HG01109.hp2 HG01243.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+2609A>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630634 | |||||||
| chr9:97630646 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-51+2597C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630646 | |||||||
| chr9:97630712 | C | A | 13 | a0001c0005t0002g0006 a0001c0005t0002g0035 a0001c0005t0002g0109 others(10): Show |
34 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.-51+2531G>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630712 | |||||||
| chr9:97630867 | CCATATTT others(14): Show |
C | 1 | a0001c0001t0001g0152 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-51+2355_-51+2375d others(23): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630867 | |||||||
| chr9:97630942 | C | G | 1 | a0003c0003t0001g0114 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-51+2301G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97630942 | |||||||
| chr9:97631173 | G | A | 1 | a0002c0002t0001g0147 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-51+2070C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631173 | |||||||
| chr9:97631265 | C | T | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-51+1978G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631265 | |||||||
| chr9:97631340 | C | G | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-51+1903G>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631340 | |||||||
| chr9:97631472 | T | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-51+1771A>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631472 | |||||||
| chr9:97631713 | G | A | 1 | a0001c0005t0003g0048 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-51+1530C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631713 | |||||||
| chr9:97631799 | G | A | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-51+1444C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631799 | |||||||
| chr9:97631843 | C | CA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(59): Show |
156 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.-51+1399dupT | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631843 | |||||||
| chr9:97631943 | C | T | 15 | a0001c0004t0008g0014 a0001c0004t0008g0108 a0001c0005t0002g0006 others(12): Show |
40 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.-51+1300G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631943 | |||||||
| chr9:97631985 | G | C | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-51+1258C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631985 | |||||||
| chr9:97631999 | G | C | 1 | a0001c0004t0005g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-51+1244C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97631999 | |||||||
| chr9:97632071 | A | ACT | 39 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(36): Show |
83 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(80): Show |
intron_variant | MODIFIER | c.-51+1170_-51+1171d others(4): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632071 | |||||||
| chr9:97632255 | A | G | 1 | a0001c0004t0023g0054 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-51+988T>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632255 | |||||||
| chr9:97632314 | G | A | 1 | a0001c0005t0002g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-51+929C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632314 | |||||||
| chr9:97632381 | CT | C | 38 | a0001c0004t0004g0009 a0001c0004t0004g0049 a0001c0004t0004g0056 others(35): Show |
80 | HG00597.hp2 HG00609.hp2 HG01099.hp1 others(77): Show |
intron_variant | MODIFIER | c.-51+861delA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632381 | |||||||
| chr9:97632451 | A | T | 1 | a0003c0003t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-51+792T>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632451 | |||||||
| chr9:97632496 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-51+747T>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632496 | |||||||
| chr9:97632514 | C | CT | 19 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(16): Show |
41 | HG00099.hp1 HG00438.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.-51+728dupA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632514 | |||||||
| chr9:97632549 | A | AT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-51+693dupA | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632549 | |||||||
| chr9:97632549 | A | ATT | 19 | a0001c0004t0004g0009 a0001c0004t0004g0056 a0001c0004t0004g0058 others(16): Show |
35 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-51+692_-51+693dup others(2): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632549 | |||||||
| chr9:97632549 | A | ATTT | 6 | a0001c0004t0004g0049 a0001c0004t0006g0008 a0001c0004t0006g0051 others(3): Show |
13 | HG01891.hp2 HG01952.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+691_-51+693dup others(3): Show |
TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632549 | |||||||
| chr9:97632773 | G | A | 1 | a0004c0008t0005g0025 | 3 | HG02976.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-51+470C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632773 | |||||||
| chr9:97632815 | T | G | 2 | a0001c0004t0011g0154 a0001c0004t0011g0155 |
2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-51+428A>C | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632815 | |||||||
| chr9:97632905 | C | T | 4 | a0001c0005t0003g0013 a0001c0005t0003g0046 a0001c0005t0003g0047 others(1): Show |
8 | HG00609.hp2 NA18962.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51+338G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632905 | |||||||
| chr9:97632919 | G | C | 1 | a0002c0002t0001g0156 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-51+324C>G | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632919 | |||||||
| chr9:97632953 | G | A | 1 | a0002c0002t0001g0157 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-51+290C>T | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97632953 | |||||||
| chr9:97633076 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-51+167G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97633076 | |||||||
| chr9:97633100 | C | T | 2 | a0002c0002t0001g0026 a0002c0002t0001g0044 |
3 | HG02074.hp2 NA18943.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-51+143G>A | TSTD2 | ENSG00000136925.15 | transcript | ENST00000341170.5 | protein_coding | 1/9 | chr9 | 97633100 |