Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10100 |
| ensemblid | ENSG00000134198.10 |
| hgncid | 20659 |
| symbol | TSPAN2 |
| name | tetraspanin 2 |
| refseq_nuc | NM_005725.6 |
| refseq_prot | NP_005716.2 |
| ensembl_nuc | ENST00000369516.7 |
| ensembl_prot | ENSP00000358529.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 115048011 |
| end | 115089503 |
| strand | - |
| ver | v1.2 |
| region | chr1:115048011-115089503 |
| region5000 | chr1:115043011-115094503 |
| regionname0 | TSPAN2_chr1_115048011_115089503 |
| regionname5000 | TSPAN2_chr1_115043011_115094503 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 221 | 361 | 95 | 62 | 150 | 16 | 36 | 120 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | MGRFR others(216): Show |
chr1 | 115043011 | 115094503 |
| a0002 | 0/0 | 221 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | MGRFR others(216): Show |
chr1 | 115043011 | 115094503 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 663 | 221 | 61 | 39 | 80 | 15 | 24 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 | ||
| a0001c0002 | 0/0 | 663 | 107 | 11 | 19 | 68 | 1 | 8 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 | ||
| a0001c0003 | 0/0 | 663 | 30 | 20 | 4 | 2 | 0 | 4 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 | ||
| a0001c0004 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 | ||
| a0001c0005 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 | ||
| a0001c0006 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 | ||
| a0002c0007 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ATGGG others(658): Show |
chr1 | 115043011 | 115094503 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3222 | 122 | 13 | 19 | 66 | 8 | 16 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0002 | 0/0 | 3220 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0003 | 0/1 | 3218 | 30 | 4 | 15 | 0 | 3 | 7 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3213): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0004 | 0/0 | 3222 | 14 | 14 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0006 | 0/0 | 3222 | 8 | 8 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0007 | 0/0 | 3224 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3219): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0008 | 1/0 | 3216 | 6 | 4 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3211): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0009 | 0/0 | 3220 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0010 | 0/0 | 3217 | 5 | 0 | 2 | 3 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3212): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0011 | 0/0 | 3220 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0012 | 0/0 | 3218 | 4 | 0 | 1 | 0 | 3 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3213): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0015 | 0/0 | 3224 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3219): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0017 | 0/0 | 3217 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3212): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0019 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0022 | 0/0 | 3218 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | ACCGG others(3213): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0023 | 0/0 | 3209 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GAAGG others(3204): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0024 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0025 | 0/0 | 3220 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0027 | 0/0 | 3220 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0028 | 0/0 | 3220 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0030 | 0/0 | 3222 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0031 | 0/0 | 3222 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0001t0032 | 0/0 | 3218 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3213): Show |
chr1 | 115043011 | 115094503 |
| a0001c0002t0002 | 0/0 | 3220 | 95 | 5 | 17 | 64 | 1 | 8 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0002t0004 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0002t0009 | 0/0 | 3220 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0002t0014 | 0/0 | 3220 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0002t0016 | 0/0 | 3220 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| a0001c0002t0018 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3211): Show |
chr1 | 115043011 | 115094503 |
| a0001c0003t0004 | 0/0 | 3222 | 11 | 4 | 3 | 0 | 0 | 4 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0003t0005 | 0/0 | 3222 | 11 | 10 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0003t0013 | 0/0 | 3222 | 4 | 4 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0003t0020 | 0/0 | 3222 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0003t0021 | 0/0 | 3222 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0004t0029 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0005t0001 | 0/0 | 3222 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3217): Show |
chr1 | 115043011 | 115094503 |
| a0001c0006t0003 | 0/0 | 3218 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3213): Show |
chr1 | 115043011 | 115094503 |
| a0002c0007t0026 | 0/0 | 3220 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | GCCGG others(3215): Show |
chr1 | 115043011 | 115094503 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 1 | 4 | 3 | 2 | 2 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0005 | 0/0 | 7 | 0 | 6 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0007 | 0/0 | 6 | 3 | 2 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0006g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0007g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0008g0244 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0010g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0010g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0012g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0012g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0015g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0017g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0019g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0022g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0024g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0025g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0027g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0028g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0030g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0031g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0001t0032g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0001 | 0/0 | 22 | 0 | 8 | 12 | 1 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0009g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0014g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0014g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0014g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0016g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0016g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0018g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0002t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0005g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0013g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0013g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0020g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0021g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0003t0021g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0004t0029g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0001c0006t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| a0002c0007t0026g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0212 | EUR | GBR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00280 | hp2 | a0001 | c0001 | t0012 | g0216 | EUR | FIN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0245 | EUR | FIN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0066 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | CHS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00735 | hp1 | a0001 | c0002 | t0016 | g0183 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00741 | hp1 | a0001 | c0003 | t0004 | g0098 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01167 | hp1 | a0001 | c0003 | t0004 | g0203 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01168 | hp2 | a0001 | c0003 | t0004 | g0040 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0226 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01192 | hp1 | a0001 | c0001 | t0031 | g0067 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01257 | hp2 | a0001 | c0002 | t0016 | g0182 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01358 | hp2 | a0001 | c0001 | t0010 | g0225 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01433 | hp2 | a0001 | c0003 | t0005 | g0159 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01515 | hp1 | a0001 | c0001 | t0012 | g0046 | EUR | IBS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01517 | hp1 | a0001 | c0001 | t0012 | g0046 | EUR | IBS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01891 | hp1 | a0001 | c0002 | t0009 | g0048 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01934 | hp1 | a0001 | c0001 | t0012 | g0227 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0210 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02055 | hp1 | a0001 | c0001 | t0027 | g0246 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02135 | hp2 | a0001 | c0003 | t0021 | g0205 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02145 | hp1 | a0002 | c0007 | t0026 | g0207 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02257 | hp1 | a0001 | c0003 | t0020 | g0020 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02257 | hp2 | a0001 | c0003 | t0005 | g0034 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0209 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02280 | hp2 | a0001 | c0001 | t0025 | g0061 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0138 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0112 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02572 | hp1 | a0001 | c0002 | t0009 | g0048 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0164 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0191 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0139 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0243 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02630 | hp1 | a0001 | c0003 | t0013 | g0021 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0052 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02647 | hp2 | a0001 | c0003 | t0013 | g0021 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0154 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0100 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0133 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02809 | hp1 | a0001 | c0002 | t0018 | g0152 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02818 | hp1 | a0001 | c0001 | t0024 | g0141 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02886 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02895 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0137 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02896 | hp2 | a0001 | c0003 | t0013 | g0232 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02897 | hp1 | a0001 | c0003 | t0013 | g0211 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02897 | hp2 | a0001 | c0003 | t0005 | g0009 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0157 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0140 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03041 | hp1 | a0001 | c0001 | t0019 | g0051 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03041 | hp2 | a0001 | c0002 | t0018 | g0111 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03098 | hp1 | a0001 | c0003 | t0005 | g0034 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0231 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0023 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0063 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03225 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0176 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03453 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0166 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03486 | hp2 | a0001 | c0001 | t0022 | g0242 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03540 | hp2 | a0001 | c0006 | t0003 | g0217 | AFR | GWD | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0103 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03704 | hp1 | a0001 | c0003 | t0004 | g0200 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03834 | hp1 | a0001 | c0003 | t0004 | g0057 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0192 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0035 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0142 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | STU | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG04115 | hp2 | a0001 | c0001 | t0030 | g0086 | SAS | STU | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG04184 | hp2 | a0001 | c0003 | t0004 | g0040 | SAS | BEB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18522 | hp1 | a0001 | c0004 | t0029 | g0199 | AFR | YRI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | YRI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | CHB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18612 | hp2 | a0001 | c0001 | t0010 | g0234 | EAS | CHB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0235 | AFR | YRI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18942 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18954 | hp2 | a0001 | c0002 | t0014 | g0180 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18965 | hp1 | a0001 | c0002 | t0014 | g0198 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18967 | hp2 | a0001 | c0003 | t0021 | g0202 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18974 | hp2 | a0001 | c0001 | t0028 | g0146 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18978 | hp2 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18986 | hp2 | a0001 | c0001 | t0010 | g0213 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18989 | hp2 | a0001 | c0002 | t0014 | g0088 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18993 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19006 | hp2 | a0001 | c0002 | t0014 | g0089 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19007 | hp1 | a0001 | c0001 | t0017 | g0045 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | LWK | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | LWK | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | LWK | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0008 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19080 | hp2 | a0001 | c0001 | t0017 | g0045 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19081 | hp2 | a0001 | c0001 | t0010 | g0222 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | YRI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20129 | hp2 | a0001 | c0003 | t0004 | g0204 | AFR | ASW | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0223 | EUR | TSI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | GIH | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20905 | hp2 | a0001 | c0003 | t0004 | g0201 | SAS | GIH | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG01123 | hp2 | a0001 | c0001 | t0032 | g0054 | AMR | CLM | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0241 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02486 | hp2 | a0001 | c0001 | t0023 | g0049 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0163 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0158 | AFR | MSL | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG06807 | hp1 | a0001 | c0003 | t0004 | g0102 | AFR | USA | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | USA | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | USA | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0024 | AFR | USA | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | LWK | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| NA21309 | hp2 | a0001 | c0003 | t0020 | g0020 | AFR | LWK | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0215 | REF | REF | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0244 | REF | REF | TSPAN2_chr1_115043011_115094503 | TSPAN2 | chr1 | 115043011 | 115094503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115058974 | C | A | 1 | a0002 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.353G>T | p.Arg118Leu | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/8 | 424/3216 | 353/666 | 118/221 | chr1 | 115058974 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115057582 | G | A | 1 | a0001c0005 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.471C>T | p.Ser157Ser | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/8 | 542/3216 | 471/666 | 157/221 | chr1 | 115057582 | |||
| chr1:115058883 | T | C | 1 | a0001c0006 | 1 | HG03540.hp2 | splice_region_variant&synonymous_variant | LOW | c.444A>G | p.Thr148Thr | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/8 | 515/3216 | 444/666 | 148/221 | chr1 | 115058883 | |||
| chr1:115058907 | C | G | 2 | a0001c0003 a0001c0004 |
31 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(28): Show |
synonymous_variant | LOW | c.420G>C | p.Gly140Gly | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/8 | 491/3216 | 420/666 | 140/221 | chr1 | 115058907 | |||
| chr1:115062177 | C | T | 2 | a0001c0002 a0001c0003 |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
synonymous_variant | LOW | c.228G>A | p.Gly76Gly | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/8 | 299/3216 | 228/666 | 76/221 | chr1 | 115062177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115048173 | G | GTA | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(10): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*2315_*2316dupTA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2316 | chr1 | 115048173 | ||||||
| chr1:115048173 | G | GTATA | 1 | a0001c0001t0015 | 3 | HG03098.hp2 HG03453.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2313_*2316dupTATA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2316 | chr1 | 115048173 | ||||||
| chr1:115048235 | T | C | 1 | a0001c0004t0029 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2255A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2255 | chr1 | 115048235 | ||||||
| chr1:115048237 | T | C | 2 | a0001c0001t0006 a0001c0001t0024 |
9 | HG02647.hp1 HG02818.hp1 HG03195.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2253A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2253 | chr1 | 115048237 | ||||||
| chr1:115048284 | A | C | 1 | a0001c0001t0025 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2206T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2206 | chr1 | 115048284 | ||||||
| chr1:115048297 | G | A | 1 | a0001c0001t0030 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2193C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2193 | chr1 | 115048297 | ||||||
| chr1:115048299 | C | CTATT | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*2190_*2191insAATA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2190 | chr1 | 115048299 | ||||||
| chr1:115048301 | A | ATT | 3 | a0001c0001t0009 a0001c0001t0032 a0001c0002t0009 |
7 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2188_*2189insAA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2188 | chr1 | 115048301 | ||||||
| chr1:115048304 | C | T | 3 | a0001c0001t0009 a0001c0001t0032 a0001c0002t0009 |
7 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2186G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2186 | chr1 | 115048304 | ||||||
| chr1:115048306 | G | C | 3 | a0001c0001t0009 a0001c0001t0032 a0001c0002t0009 |
7 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2184C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2184 | chr1 | 115048306 | ||||||
| chr1:115048306 | G | GAT | 7 | a0001c0001t0004 a0001c0001t0007 a0001c0002t0004 others(4): Show |
51 | HG00621.hp1 HG00741.hp1 HG01167.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2182_*2183dupAT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2183 | chr1 | 115048306 | ||||||
| chr1:115048308 | T | G | 3 | a0001c0001t0009 a0001c0001t0032 a0001c0002t0009 |
7 | HG01123.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2182A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2182 | chr1 | 115048308 | ||||||
| chr1:115048377 | T | C | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(9): Show |
146 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*2113A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2113 | chr1 | 115048377 | ||||||
| chr1:115048432 | T | G | 3 | a0001c0001t0003 a0001c0001t0012 a0001c0006t0003 |
34 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2058A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2058 | chr1 | 115048432 | ||||||
| chr1:115048437 | T | C | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(14): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*2053A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 2053 | chr1 | 115048437 | ||||||
| chr1:115048542 | A | G | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(22): Show |
209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*1948T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1948 | chr1 | 115048542 | ||||||
| chr1:115048559 | T | C | 1 | a0001c0003t0020 | 2 | HG02257.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1931 | chr1 | 115048559 | ||||||
| chr1:115048996 | CT | C | 2 | a0001c0001t0010 a0001c0001t0017 |
7 | HG01175.hp1 HG01358.hp2 NA18612.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1493delA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1493 | chr1 | 115048996 | ||||||
| chr1:115049002 | G | A | 2 | a0001c0001t0010 a0001c0001t0017 |
7 | HG01175.hp1 HG01358.hp2 NA18612.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1488C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1488 | chr1 | 115049002 | ||||||
| chr1:115049114 | T | C | 1 | a0001c0002t0014 | 4 | NA18954.hp2 NA18965.hp1 NA18989.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1376A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1376 | chr1 | 115049114 | ||||||
| chr1:115049213 | C | G | 1 | a0001c0001t0019 | 2 | HG02630.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1277G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1277 | chr1 | 115049213 | ||||||
| chr1:115049414 | T | A | 1 | a0002c0007t0026 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1076 | chr1 | 115049414 | ||||||
| chr1:115049456 | T | C | 1 | a0001c0002t0018 | 2 | HG02809.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1034A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 1034 | chr1 | 115049456 | ||||||
| chr1:115049524 | T | C | 1 | a0001c0001t0012 | 4 | HG00280.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*966A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 966 | chr1 | 115049524 | ||||||
| chr1:115049672 | G | C | 1 | a0001c0003t0013 | 4 | HG02630.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*818C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 818 | chr1 | 115049672 | ||||||
| chr1:115049745 | T | C | 1 | a0001c0003t0020 | 2 | HG02257.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*745A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 745 | chr1 | 115049745 | ||||||
| chr1:115049777 | A | C | 7 | a0001c0001t0004 a0001c0001t0025 a0001c0002t0004 others(4): Show |
45 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*713T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 713 | chr1 | 115049777 | ||||||
| chr1:115049797 | T | A | 1 | a0001c0001t0031 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*693A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 693 | chr1 | 115049797 | ||||||
| chr1:115049884 | C | T | 1 | a0001c0003t0005 | 11 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*606G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 606 | chr1 | 115049884 | ||||||
| chr1:115049968 | G | A | 1 | a0001c0001t0027 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*522C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 522 | chr1 | 115049968 | ||||||
| chr1:115049989 | GAC | G | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0012 others(3): Show |
42 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*499_*500delGT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 499 | chr1 | 115049989 | ||||||
| chr1:115050049 | T | C | 1 | a0001c0001t0032 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*441A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 441 | chr1 | 115050049 | ||||||
| chr1:115050199 | T | C | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(14): Show |
162 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*291A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 291 | chr1 | 115050199 | ||||||
| chr1:115050346 | A | G | 1 | a0001c0002t0016 | 2 | HG00735.hp1 HG01257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 144 | chr1 | 115050346 | ||||||
| chr1:115050351 | C | T | 2 | a0001c0001t0011 a0001c0001t0024 |
5 | HG02145.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*139G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 139 | chr1 | 115050351 | ||||||
| chr1:115050389 | T | C | 1 | a0001c0003t0021 | 2 | HG02135.hp2 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*101A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 8/8 | 101 | chr1 | 115050389 | ||||||
| chr1:115089449 | G | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-17C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 17 | chr1 | 115089449 | ||||||
| chr1:115089452 | A | C | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 20 | chr1 | 115089452 | ||||||
| chr1:115089453 | T | A | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 21 | chr1 | 115089453 | ||||||
| chr1:115089454 | C | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 22 | chr1 | 115089454 | ||||||
| chr1:115089457 | C | A | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | chr1 | 115089457 | |||||||
| chr1:115089461 | C | A | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 29 | chr1 | 115089461 | ||||||
| chr1:115089465 | A | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 33 | chr1 | 115089465 | ||||||
| chr1:115089469 | C | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 37 | chr1 | 115089469 | ||||||
| chr1:115089470 | C | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 38 | chr1 | 115089470 | ||||||
| chr1:115089476 | A | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 44 | chr1 | 115089476 | ||||||
| chr1:115089478 | G | A | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | chr1 | 115089478 | |||||||
| chr1:115089479 | AGCGCGGG others(6): Show |
A | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60_-48delCCGCTCCC others(5): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 48 | chr1 | 115089479 | ||||||
| chr1:115089494 | A | C | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 62 | chr1 | 115089494 | ||||||
| chr1:115089495 | G | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | chr1 | 115089495 | |||||||
| chr1:115089501 | G | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 69 | chr1 | 115089501 | ||||||
| chr1:115089502 | G | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 70 | chr1 | 115089502 | ||||||
| chr1:115089503 | C | T | 1 | a0001c0001t0022 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/8 | 71 | chr1 | 115089503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:115050592 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.601-37G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115050592 | |||||||
| chr1:115050793 | C | G | 56 | a0001c0001t0002g0121 a0001c0002t0002g0001 a0001c0002t0002g0004 others(53): Show |
97 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.601-238G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115050793 | |||||||
| chr1:115050942 | A | G | 1 | a0001c0003t0004g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.601-387T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115050942 | |||||||
| chr1:115051117 | C | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
7 | HG01884.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-562G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051117 | |||||||
| chr1:115051136 | C | A | 11 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0047 others(8): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.601-581G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051136 | |||||||
| chr1:115051215 | C | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(21): Show |
34 | HG00099.hp2 HG00558.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.601-660G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051215 | |||||||
| chr1:115051323 | G | A | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.601-768C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051323 | |||||||
| chr1:115051383 | A | G | 1 | a0001c0001t0004g0022 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.601-828T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051383 | |||||||
| chr1:115051417 | A | T | 2 | a0001c0002t0018g0111 a0001c0002t0018g0152 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.601-862T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051417 | |||||||
| chr1:115051506 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.601-951A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051506 | |||||||
| chr1:115051627 | G | C | 1 | a0001c0002t0002g0221 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.601-1072C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051627 | |||||||
| chr1:115051747 | G | C | 90 | a0001c0001t0002g0121 a0001c0001t0003g0005 a0001c0001t0003g0007 others(87): Show |
148 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.601-1192C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051747 | |||||||
| chr1:115051790 | C | T | 2 | a0001c0002t0002g0179 a0001c0002t0002g0191 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.601-1235G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051790 | |||||||
| chr1:115051802 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.601-1247G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051802 | |||||||
| chr1:115051825 | C | G | 6 | a0001c0003t0005g0009 a0001c0003t0005g0034 a0001c0003t0005g0154 others(3): Show |
11 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.601-1270G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051825 | |||||||
| chr1:115051888 | C | T | 4 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 others(1): Show |
6 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1333G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051888 | |||||||
| chr1:115051898 | T | C | 3 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-1343A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115051898 | |||||||
| chr1:115052024 | C | A | 2 | a0001c0002t0018g0111 a0001c0002t0018g0152 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.600+1355G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052024 | |||||||
| chr1:115052274 | G | A | 3 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+1105C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052274 | |||||||
| chr1:115052289 | C | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(100): Show |
144 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.600+1090G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052289 | |||||||
| chr1:115052343 | G | T | 1 | a0001c0003t0020g0020 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.600+1036C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052343 | |||||||
| chr1:115052464 | C | A | 5 | a0001c0001t0011g0135 a0001c0001t0011g0139 a0001c0001t0011g0140 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+915G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052464 | |||||||
| chr1:115052469 | C | A | 1 | a0001c0002t0002g0173 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.600+910G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052469 | |||||||
| chr1:115052638 | A | G | 1 | a0001c0002t0002g0178 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.600+741T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052638 | |||||||
| chr1:115052855 | T | A | 2 | a0001c0001t0006g0160 a0001c0001t0006g0161 |
2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.600+524A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052855 | |||||||
| chr1:115052863 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(202): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.600+516C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052863 | |||||||
| chr1:115052984 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.600+395G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115052984 | |||||||
| chr1:115053132 | A | C | 1 | a0001c0001t0001g0026 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.600+247T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115053132 | |||||||
| chr1:115053321 | A | T | 6 | a0001c0002t0002g0010 a0001c0002t0002g0039 a0001c0002t0002g0053 others(3): Show |
10 | HG00438.hp1 HG00558.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.600+58T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 7/7 | chr1 | 115053321 | |||||||
| chr1:115053631 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(107): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.517-169A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115053631 | |||||||
| chr1:115054152 | T | C | 3 | a0001c0001t0012g0046 a0001c0001t0012g0216 a0001c0001t0012g0227 |
4 | HG00280.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-690A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054152 | |||||||
| chr1:115054165 | A | G | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.517-703T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054165 | |||||||
| chr1:115054170 | C | T | 1 | a0001c0003t0004g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.517-708G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054170 | |||||||
| chr1:115054305 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.517-843C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054305 | |||||||
| chr1:115054645 | GA | G | 4 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 others(1): Show |
6 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-1184delT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054645 | |||||||
| chr1:115054785 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.517-1323C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054785 | |||||||
| chr1:115054843 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.517-1381G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054843 | |||||||
| chr1:115054958 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.517-1496C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115054958 | |||||||
| chr1:115055179 | A | G | 11 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0047 others(8): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.517-1717T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055179 | |||||||
| chr1:115055194 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.517-1732G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055194 | |||||||
| chr1:115055215 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(99): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.517-1753C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055215 | |||||||
| chr1:115055297 | T | C | 1 | a0001c0001t0003g0041 | 2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.517-1835A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055297 | |||||||
| chr1:115055328 | A | AT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(217): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.517-1867dupA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055328 | |||||||
| chr1:115055328 | A | ATT | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0079 others(4): Show |
11 | HG00544.hp1 HG01123.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.517-1868_517-1867d others(4): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055328 | |||||||
| chr1:115055352 | G | A | 89 | a0001c0001t0002g0121 a0001c0001t0003g0005 a0001c0001t0003g0007 others(86): Show |
147 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.517-1890C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055352 | |||||||
| chr1:115055405 | C | CA | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(99): Show |
142 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.517-1944dupT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055405 | |||||||
| chr1:115055417 | C | T | 1 | a0001c0002t0002g0177 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.517-1955G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055417 | |||||||
| chr1:115055421 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.517-1959G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055421 | |||||||
| chr1:115055482 | T | A | 1 | a0001c0003t0020g0020 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.517-2020A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055482 | |||||||
| chr1:115055710 | C | T | 1 | a0001c0002t0002g0035 | 2 | HG01109.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.516+1827G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055710 | |||||||
| chr1:115055860 | T | C | 56 | a0001c0001t0002g0121 a0001c0002t0002g0001 a0001c0002t0002g0004 others(53): Show |
97 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.516+1677A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055860 | |||||||
| chr1:115055930 | G | A | 1 | a0001c0001t0019g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.516+1607C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055930 | |||||||
| chr1:115055943 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.516+1594T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055943 | |||||||
| chr1:115055971 | C | T | 31 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0047 others(28): Show |
45 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.516+1566G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055971 | |||||||
| chr1:115055999 | T | C | 1 | a0001c0001t0022g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+1538A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115055999 | |||||||
| chr1:115056097 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.516+1440A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056097 | |||||||
| chr1:115056125 | T | A | 6 | a0001c0001t0010g0213 a0001c0001t0010g0222 a0001c0001t0010g0225 others(3): Show |
7 | HG01175.hp1 HG01358.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+1412A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056125 | |||||||
| chr1:115056239 | T | G | 1 | a0002c0007t0026g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516+1298A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056239 | |||||||
| chr1:115056268 | G | A | 11 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0047 others(8): Show |
18 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.516+1269C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056268 | |||||||
| chr1:115056319 | A | C | 3 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0241 |
3 | HG02109.hp1 HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.516+1218T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056319 | |||||||
| chr1:115056329 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516+1208G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056329 | |||||||
| chr1:115056365 | C | G | 6 | a0001c0001t0010g0213 a0001c0001t0010g0222 a0001c0001t0010g0225 others(3): Show |
7 | HG01175.hp1 HG01358.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+1172G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056365 | |||||||
| chr1:115056635 | A | C | 1 | a0001c0001t0022g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+902T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056635 | |||||||
| chr1:115056724 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0119 others(7): Show |
17 | HG01255.hp1 HG01993.hp1 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.516+813G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056724 | |||||||
| chr1:115056819 | G | C | 1 | a0001c0002t0002g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.516+718C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056819 | |||||||
| chr1:115056920 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.516+617C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056920 | |||||||
| chr1:115056996 | C | T | 7 | a0001c0003t0004g0158 a0001c0003t0005g0009 a0001c0003t0005g0034 others(4): Show |
12 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.516+541G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115056996 | |||||||
| chr1:115057027 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.516+510G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057027 | |||||||
| chr1:115057288 | C | T | 3 | a0001c0001t0011g0135 a0001c0001t0011g0139 a0001c0001t0011g0150 |
3 | HG02145.hp2 HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.516+249G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057288 | |||||||
| chr1:115057395 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.516+142T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057395 | |||||||
| chr1:115057420 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.516+117G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057420 | |||||||
| chr1:115057450 | G | A | 1 | a0001c0003t0020g0020 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.516+87C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057450 | |||||||
| chr1:115057460 | G | C | 23 | a0001c0003t0004g0040 a0001c0003t0004g0057 a0001c0003t0004g0098 others(20): Show |
31 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.516+77C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057460 | |||||||
| chr1:115057516 | A | G | 25 | a0001c0001t0001g0026 a0001c0001t0008g0112 a0001c0003t0004g0040 others(22): Show |
34 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.516+21T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 6/7 | chr1 | 115057516 | |||||||
| chr1:115057722 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.445-114A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115057722 | |||||||
| chr1:115057803 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(98): Show |
141 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.445-195G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115057803 | |||||||
| chr1:115057957 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0195 |
2 | NA18999.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.445-349C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115057957 | |||||||
| chr1:115058124 | C | A | 1 | a0001c0001t0027g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.445-516G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058124 | |||||||
| chr1:115058133 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.445-525C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058133 | |||||||
| chr1:115058134 | C | A | 1 | a0001c0001t0003g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.445-526G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058134 | |||||||
| chr1:115058445 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.444+438G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058445 | |||||||
| chr1:115058627 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0125 |
2 | HG00597.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.444+256A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058627 | |||||||
| chr1:115058718 | G | T | 1 | a0001c0002t0002g0036 | 2 | HG01346.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.444+165C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058718 | |||||||
| chr1:115058832 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.444+51T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 5/7 | chr1 | 115058832 | |||||||
| chr1:115058994 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(237): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.346-13T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115058994 | |||||||
| chr1:115059031 | A | T | 1 | a0001c0001t0001g0019 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.346-50T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059031 | |||||||
| chr1:115059114 | T | C | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.346-133A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059114 | |||||||
| chr1:115059167 | T | C | 5 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 others(2): Show |
7 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.346-186A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059167 | |||||||
| chr1:115059204 | C | T | 1 | a0001c0001t0022g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.346-223G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059204 | |||||||
| chr1:115059281 | T | TA | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(204): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.346-301dupT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059281 | |||||||
| chr1:115059313 | T | C | 7 | a0001c0003t0004g0158 a0001c0003t0005g0009 a0001c0003t0005g0034 others(4): Show |
12 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.346-332A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059313 | |||||||
| chr1:115059375 | G | A | 4 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 others(1): Show |
5 | HG02055.hp1 HG02280.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.346-394C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059375 | |||||||
| chr1:115059412 | A | G | 1 | a0001c0001t0031g0067 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.346-431T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059412 | |||||||
| chr1:115059498 | T | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(230): Show |
349 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.346-517A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059498 | |||||||
| chr1:115059573 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(207): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.346-592G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059573 | |||||||
| chr1:115059877 | C | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(232): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.345+587G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059877 | |||||||
| chr1:115059942 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(107): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.345+522T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059942 | |||||||
| chr1:115059985 | C | G | 16 | a0001c0003t0004g0040 a0001c0003t0004g0057 a0001c0003t0004g0098 others(13): Show |
19 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.345+479G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115059985 | |||||||
| chr1:115060164 | A | AC | 6 | a0001c0001t0001g0081 a0001c0001t0003g0228 a0001c0001t0011g0150 others(3): Show |
6 | HG00738.hp2 HG02055.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.345+299dupG | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115060164 | |||||||
| chr1:115060296 | T | C | 3 | a0001c0002t0002g0011 a0001c0002t0002g0055 a0001c0002t0002g0107 |
5 | HG02486.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.345+168A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115060296 | |||||||
| chr1:115060302 | C | T | 7 | a0001c0003t0004g0158 a0001c0003t0005g0009 a0001c0003t0005g0034 others(4): Show |
12 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.345+162G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115060302 | |||||||
| chr1:115060424 | T | C | 1 | a0001c0001t0004g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.345+40A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115060424 | |||||||
| chr1:115060444 | T | G | 1 | a0001c0002t0002g0037 | 2 | HG02132.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.345+20A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 4/7 | chr1 | 115060444 | |||||||
| chr1:115060547 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.271-9C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115060547 | |||||||
| chr1:115060719 | C | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(228): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.271-181G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115060719 | |||||||
| chr1:115060792 | C | T | 81 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(78): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.271-254G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115060792 | |||||||
| chr1:115060883 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(99): Show |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.271-345G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115060883 | |||||||
| chr1:115060914 | G | A | 81 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(78): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.271-376C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115060914 | |||||||
| chr1:115060971 | C | T | 1 | a0001c0002t0016g0182 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.271-433G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115060971 | |||||||
| chr1:115061012 | G | T | 14 | a0001c0003t0004g0040 a0001c0003t0004g0057 a0001c0003t0004g0098 others(11): Show |
16 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-474C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061012 | |||||||
| chr1:115061071 | T | C | 1 | a0001c0003t0005g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.271-533A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061071 | |||||||
| chr1:115061140 | A | G | 81 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(78): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.271-602T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061140 | |||||||
| chr1:115061223 | T | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(228): Show |
346 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.271-685A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061223 | |||||||
| chr1:115061268 | C | G | 1 | a0001c0001t0011g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.271-730G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061268 | |||||||
| chr1:115061281 | C | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(147): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.271-743G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061281 | |||||||
| chr1:115061309 | C | G | 1 | a0001c0001t0011g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.271-771G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061309 | |||||||
| chr1:115061328 | C | T | 1 | a0001c0002t0002g0016 | 3 | NA18989.hp1 NA19054.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.271-790G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061328 | |||||||
| chr1:115061554 | A | C | 81 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(78): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.270+581T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061554 | |||||||
| chr1:115061620 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(105): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.270+515C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061620 | |||||||
| chr1:115061624 | T | C | 1 | a0001c0001t0004g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.270+511A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061624 | |||||||
| chr1:115061696 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(99): Show |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.270+439T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061696 | |||||||
| chr1:115061833 | C | T | 14 | a0001c0003t0004g0040 a0001c0003t0004g0057 a0001c0003t0004g0098 others(11): Show |
16 | HG00741.hp1 HG01167.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+302G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115061833 | |||||||
| chr1:115062060 | A | G | 85 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(82): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.270+75T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 3/7 | chr1 | 115062060 | |||||||
| chr1:115062560 | C | T | 85 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(82): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.173-328G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115062560 | |||||||
| chr1:115062655 | A | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0095 |
2 | NA18992.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.173-423T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115062655 | |||||||
| chr1:115062941 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.173-709G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115062941 | |||||||
| chr1:115063025 | T | C | 85 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(82): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.173-793A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063025 | |||||||
| chr1:115063111 | T | C | 1 | a0001c0003t0020g0020 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.173-879A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063111 | |||||||
| chr1:115063300 | C | T | 2 | a0001c0002t0018g0111 a0001c0002t0018g0152 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.173-1068G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063300 | |||||||
| chr1:115063515 | C | T | 86 | a0001c0001t0032g0054 a0001c0002t0002g0001 a0001c0002t0002g0004 others(83): Show |
138 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.173-1283G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063515 | |||||||
| chr1:115063547 | C | T | 1 | a0001c0002t0009g0048 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.173-1315G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063547 | |||||||
| chr1:115063638 | A | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(142): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.173-1406T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063638 | |||||||
| chr1:115063716 | T | C | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.173-1484A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063716 | |||||||
| chr1:115063729 | A | G | 1 | a0001c0003t0021g0202 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.173-1497T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063729 | |||||||
| chr1:115063822 | G | A | 1 | a0001c0001t0008g0112 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.173-1590C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063822 | |||||||
| chr1:115063870 | A | G | 30 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(27): Show |
45 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.173-1638T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063870 | |||||||
| chr1:115063931 | C | G | 1 | a0001c0002t0002g0175 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.173-1699G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063931 | |||||||
| chr1:115063945 | A | G | 11 | a0001c0003t0004g0040 a0001c0003t0004g0057 a0001c0003t0004g0200 others(8): Show |
13 | HG01167.hp1 HG01168.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.173-1713T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063945 | |||||||
| chr1:115063976 | C | A | 2 | a0001c0003t0021g0202 a0001c0003t0021g0205 |
2 | HG02135.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.173-1744G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063976 | |||||||
| chr1:115063987 | G | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(105): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.173-1755C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115063987 | |||||||
| chr1:115064053 | A | G | 4 | a0001c0001t0010g0213 a0001c0001t0010g0222 a0001c0001t0010g0234 others(1): Show |
5 | NA18612.hp2 NA18986.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-1821T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064053 | |||||||
| chr1:115064058 | G | GA | 85 | a0001c0001t0032g0054 a0001c0002t0002g0001 a0001c0002t0002g0004 others(82): Show |
137 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.173-1827dupT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064058 | |||||||
| chr1:115064113 | A | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0091 a0001c0001t0001g0095 others(1): Show |
4 | NA18941.hp2 NA18992.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-1881T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064113 | |||||||
| chr1:115064136 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.173-1904G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064136 | |||||||
| chr1:115064137 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.173-1905C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064137 | |||||||
| chr1:115064137 | G | C | 87 | a0001c0001t0032g0054 a0001c0002t0002g0001 a0001c0002t0002g0004 others(84): Show |
139 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.173-1905C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064137 | |||||||
| chr1:115064343 | T | G | 1 | a0001c0003t0020g0020 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.173-2111A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064343 | |||||||
| chr1:115064397 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.173-2165T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064397 | |||||||
| chr1:115064434 | A | G | 2 | a0001c0002t0004g0163 a0001c0002t0004g0164 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.173-2202T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064434 | |||||||
| chr1:115064437 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.173-2205T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064437 | |||||||
| chr1:115064448 | C | A | 2 | a0001c0003t0004g0102 a0001c0003t0004g0103 |
2 | HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.173-2216G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064448 | |||||||
| chr1:115064596 | T | C | 3 | a0001c0003t0013g0021 a0001c0003t0013g0211 a0001c0003t0013g0232 |
4 | HG02630.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.173-2364A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064596 | |||||||
| chr1:115064693 | T | C | 1 | a0001c0003t0020g0020 | 2 | HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.173-2461A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064693 | |||||||
| chr1:115064804 | T | C | 39 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(36): Show |
60 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.173-2572A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064804 | |||||||
| chr1:115064831 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(237): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.173-2599A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115064831 | |||||||
| chr1:115065121 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0218 |
3 | HG00733.hp1 HG02004.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.173-2889C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065121 | |||||||
| chr1:115065148 | T | C | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.173-2916A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065148 | |||||||
| chr1:115065208 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.173-2976C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065208 | |||||||
| chr1:115065234 | G | A | 32 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(29): Show |
47 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.173-3002C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065234 | |||||||
| chr1:115065258 | G | C | 7 | a0001c0001t0001g0132 a0001c0001t0008g0112 a0001c0001t0009g0023 others(4): Show |
9 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-3026C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065258 | |||||||
| chr1:115065714 | A | T | 3 | a0001c0002t0002g0011 a0001c0002t0002g0055 a0001c0002t0002g0107 |
5 | HG02486.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.173-3482T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065714 | |||||||
| chr1:115065802 | C | T | 48 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(45): Show |
69 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.173-3570G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065802 | |||||||
| chr1:115065823 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(100): Show |
144 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.173-3591A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065823 | |||||||
| chr1:115065951 | C | G | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.173-3719G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115065951 | |||||||
| chr1:115066086 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.173-3854A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066086 | |||||||
| chr1:115066219 | A | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0127 |
2 | NA19058.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.173-3987T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066219 | |||||||
| chr1:115066367 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.173-4135G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066367 | |||||||
| chr1:115066582 | C | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(164): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.173-4350G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066582 | |||||||
| chr1:115066646 | C | T | 3 | a0001c0001t0011g0135 a0001c0001t0011g0139 a0001c0001t0011g0150 |
3 | HG02145.hp2 HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.173-4414G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066646 | |||||||
| chr1:115066679 | A | AT | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(100): Show |
144 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.173-4448dupA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066679 | |||||||
| chr1:115066722 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.173-4490G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066722 | |||||||
| chr1:115066779 | T | G | 2 | a0001c0002t0016g0182 a0001c0002t0016g0183 |
2 | HG00735.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.173-4547A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066779 | |||||||
| chr1:115066793 | G | A | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.173-4561C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115066793 | |||||||
| chr1:115067048 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.173-4816T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067048 | |||||||
| chr1:115067101 | T | G | 2 | a0001c0002t0016g0182 a0001c0002t0016g0183 |
2 | HG00735.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.173-4869A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067101 | |||||||
| chr1:115067179 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.173-4947T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067179 | |||||||
| chr1:115067226 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.173-4994A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067226 | |||||||
| chr1:115067418 | C | T | 6 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0060 others(3): Show |
12 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.173-5186G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067418 | |||||||
| chr1:115067470 | T | C | 48 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(45): Show |
69 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.173-5238A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067470 | |||||||
| chr1:115067471 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0093 |
2 | NA19006.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.173-5239G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067471 | |||||||
| chr1:115067538 | G | A | 1 | a0001c0002t0002g0184 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.173-5306C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067538 | |||||||
| chr1:115067597 | C | G | 1 | a0001c0001t0008g0112 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.172+5308G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067597 | |||||||
| chr1:115067770 | A | T | 48 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(45): Show |
69 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.172+5135T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067770 | |||||||
| chr1:115067869 | T | C | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.172+5036A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115067869 | |||||||
| chr1:115068125 | C | T | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172+4780G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068125 | |||||||
| chr1:115068325 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.172+4580A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068325 | |||||||
| chr1:115068394 | C | T | 9 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0060 others(6): Show |
15 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.172+4511G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068394 | |||||||
| chr1:115068648 | C | T | 1 | a0001c0003t0005g0157 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.172+4257G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068648 | |||||||
| chr1:115068875 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
6 | NA18949.hp2 NA18986.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.172+4030G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068875 | |||||||
| chr1:115068877 | C | A | 49 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(46): Show |
71 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.172+4028G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068877 | |||||||
| chr1:115068918 | C | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(100): Show |
144 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.172+3987G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115068918 | |||||||
| chr1:115069021 | T | G | 1 | a0001c0001t0001g0127 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.172+3884A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069021 | |||||||
| chr1:115069072 | T | C | 1 | a0001c0001t0004g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.172+3833A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069072 | |||||||
| chr1:115069216 | C | T | 3 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0241 |
3 | HG02109.hp1 HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.172+3689G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069216 | |||||||
| chr1:115069272 | G | C | 1 | a0001c0001t0010g0222 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.172+3633C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069272 | |||||||
| chr1:115069301 | T | G | 7 | a0001c0003t0004g0158 a0001c0003t0005g0009 a0001c0003t0005g0034 others(4): Show |
12 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+3604A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069301 | |||||||
| chr1:115069380 | A | T | 1 | a0001c0003t0005g0009 | 5 | HG02886.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+3525T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069380 | |||||||
| chr1:115069399 | C | A | 47 | a0001c0001t0001g0195 a0001c0001t0003g0005 a0001c0001t0003g0007 others(44): Show |
70 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.172+3506G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069399 | |||||||
| chr1:115069433 | G | A | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172+3472C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069433 | |||||||
| chr1:115069601 | T | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(111): Show |
156 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.172+3304A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069601 | |||||||
| chr1:115069718 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.172+3187G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115069718 | |||||||
| chr1:115070081 | C | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(107): Show |
151 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.172+2824G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070081 | |||||||
| chr1:115070100 | G | A | 1 | a0001c0001t0027g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.172+2805C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070100 | |||||||
| chr1:115070278 | A | G | 47 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0010 others(44): Show |
87 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.172+2627T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070278 | |||||||
| chr1:115070326 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(108): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.172+2579G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070326 | |||||||
| chr1:115070350 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172+2555G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070350 | |||||||
| chr1:115070351 | G | A | 7 | a0001c0003t0004g0158 a0001c0003t0005g0009 a0001c0003t0005g0034 others(4): Show |
12 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+2554C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070351 | |||||||
| chr1:115070374 | C | CT | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(149): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.172+2530dupA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070374 | |||||||
| chr1:115070374 | C | CTT | 11 | a0001c0001t0003g0005 a0001c0001t0003g0042 a0001c0001t0003g0214 others(8): Show |
18 | HG00733.hp1 HG00741.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.172+2529_172+2530d others(4): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070374 | |||||||
| chr1:115070452 | A | G | 52 | a0001c0001t0001g0195 a0001c0001t0001g0230 a0001c0001t0003g0005 others(49): Show |
72 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.172+2453T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070452 | |||||||
| chr1:115070550 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172+2355G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070550 | |||||||
| chr1:115070580 | A | G | 2 | a0001c0002t0002g0043 a0001c0002t0002g0220 |
3 | NA18952.hp2 NA19056.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.172+2325T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070580 | |||||||
| chr1:115070748 | C | A | 5 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0060 others(2): Show |
11 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.172+2157G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070748 | |||||||
| chr1:115070888 | A | G | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.172+2017T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115070888 | |||||||
| chr1:115071061 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.172+1844G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071061 | |||||||
| chr1:115071071 | C | T | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.172+1834G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071071 | |||||||
| chr1:115071415 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.172+1490C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071415 | |||||||
| chr1:115071492 | C | T | 1 | a0001c0001t0011g0140 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.172+1413G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071492 | |||||||
| chr1:115071610 | G | A | 1 | a0001c0001t0006g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.172+1295C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071610 | |||||||
| chr1:115071666 | A | G | 1 | a0001c0002t0002g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.172+1239T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071666 | |||||||
| chr1:115071803 | G | A | 2 | a0001c0002t0018g0111 a0001c0002t0018g0152 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.172+1102C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071803 | |||||||
| chr1:115071837 | T | C | 68 | a0001c0001t0001g0132 a0001c0001t0001g0230 a0001c0001t0003g0005 others(65): Show |
95 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.172+1068A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071837 | |||||||
| chr1:115071894 | G | GCT | 8 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0060 others(5): Show |
14 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.172+1009_172+1010d others(4): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071894 | |||||||
| chr1:115071988 | C | G | 3 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+917G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115071988 | |||||||
| chr1:115072055 | T | C | 68 | a0001c0001t0001g0132 a0001c0001t0001g0230 a0001c0001t0003g0005 others(65): Show |
95 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.172+850A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072055 | |||||||
| chr1:115072119 | G | A | 68 | a0001c0001t0001g0132 a0001c0001t0001g0230 a0001c0001t0003g0005 others(65): Show |
95 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.172+786C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072119 | |||||||
| chr1:115072143 | T | G | 68 | a0001c0001t0001g0132 a0001c0001t0001g0230 a0001c0001t0003g0005 others(65): Show |
95 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.172+762A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072143 | |||||||
| chr1:115072200 | C | G | 68 | a0001c0001t0001g0132 a0001c0001t0001g0230 a0001c0001t0003g0005 others(65): Show |
95 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.172+705G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072200 | |||||||
| chr1:115072534 | C | T | 1 | a0001c0001t0023g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.172+371G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072534 | |||||||
| chr1:115072582 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0004g0162 a0001c0001t0008g0112 |
4 | HG01884.hp2 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+323A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072582 | |||||||
| chr1:115072625 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.172+280C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072625 | |||||||
| chr1:115072737 | T | C | 68 | a0001c0001t0001g0132 a0001c0001t0001g0230 a0001c0001t0003g0005 others(65): Show |
95 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.172+168A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072737 | |||||||
| chr1:115072812 | C | A | 3 | a0001c0001t0011g0135 a0001c0001t0011g0139 a0001c0001t0011g0150 |
3 | HG02145.hp2 HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.172+93G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072812 | |||||||
| chr1:115072813 | C | T | 1 | a0001c0003t0004g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.172+92G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072813 | |||||||
| chr1:115072855 | C | G | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172+50G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 2/7 | chr1 | 115072855 | |||||||
| chr1:115073076 | C | T | 2 | a0001c0001t0019g0051 a0001c0001t0019g0052 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.70-69G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073076 | |||||||
| chr1:115073131 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.70-124G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073131 | |||||||
| chr1:115073199 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.70-192A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073199 | |||||||
| chr1:115073265 | C | T | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-258G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073265 | |||||||
| chr1:115073389 | T | C | 1 | a0001c0003t0004g0200 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.70-382A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073389 | |||||||
| chr1:115073398 | C | T | 1 | a0001c0001t0011g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.70-391G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073398 | |||||||
| chr1:115073526 | C | CACCTCGT others(1): Show |
112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.70-527_70-520dupCA others(6): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073526 | |||||||
| chr1:115073687 | A | G | 3 | a0001c0001t0011g0135 a0001c0001t0011g0139 a0001c0001t0011g0150 |
3 | HG02145.hp2 HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.70-680T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073687 | |||||||
| chr1:115073793 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70-786C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073793 | |||||||
| chr1:115073925 | C | T | 3 | a0001c0001t0009g0023 a0001c0001t0009g0063 a0001c0001t0009g0133 |
4 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-918G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073925 | |||||||
| chr1:115073954 | C | T | 1 | a0001c0002t0002g0035 | 2 | HG01109.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.70-947G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115073954 | |||||||
| chr1:115074078 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.70-1071C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074078 | |||||||
| chr1:115074155 | C | T | 49 | a0001c0001t0001g0195 a0001c0001t0015g0166 a0001c0002t0002g0001 others(46): Show |
89 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.70-1148G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074155 | |||||||
| chr1:115074156 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.70-1149C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074156 | |||||||
| chr1:115074157 | C | G | 1 | a0001c0001t0023g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-1150G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074157 | |||||||
| chr1:115074198 | GGTCTAA | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0151 a0001c0001t0028g0146 |
3 | NA18974.hp2 NA18991.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.70-1197_70-1192del others(6): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074198 | |||||||
| chr1:115074250 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.70-1243C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074250 | |||||||
| chr1:115074255 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.70-1248G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074255 | |||||||
| chr1:115074260 | T | C | 1 | a0001c0001t0004g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.70-1253A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074260 | |||||||
| chr1:115074317 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.70-1310A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074317 | |||||||
| chr1:115074335 | C | A | 47 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(44): Show |
66 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.70-1328G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074335 | |||||||
| chr1:115074513 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.70-1506C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074513 | |||||||
| chr1:115074514 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(109): Show |
153 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.70-1507G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074514 | |||||||
| chr1:115074528 | G | A | 1 | a0001c0003t0004g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.70-1521C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074528 | |||||||
| chr1:115074569 | G | A | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70-1562C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074569 | |||||||
| chr1:115074574 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0134 |
3 | HG02717.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.70-1567C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074574 | |||||||
| chr1:115074579 | T | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(183): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.70-1572A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074579 | |||||||
| chr1:115074785 | A | G | 67 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(64): Show |
94 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.70-1778T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074785 | |||||||
| chr1:115074815 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.70-1808T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074815 | |||||||
| chr1:115074941 | A | C | 1 | a0001c0001t0025g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.70-1934T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115074941 | |||||||
| chr1:115075199 | T | C | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-2192A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075199 | |||||||
| chr1:115075206 | T | C | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.70-2199A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075206 | |||||||
| chr1:115075235 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(179): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.70-2228A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075235 | |||||||
| chr1:115075266 | T | C | 1 | a0001c0002t0009g0048 | 2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.70-2259A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075266 | |||||||
| chr1:115075299 | C | T | 1 | a0001c0001t0028g0146 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.70-2292G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075299 | |||||||
| chr1:115075432 | C | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(83): Show |
121 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.70-2425G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075432 | |||||||
| chr1:115075444 | C | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(38): Show |
53 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.70-2437G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075444 | |||||||
| chr1:115075465 | G | A | 1 | a0001c0002t0002g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.70-2458C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075465 | |||||||
| chr1:115075617 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(33): Show |
47 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.70-2610C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075617 | |||||||
| chr1:115075620 | C | T | 4 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0241 others(1): Show |
4 | HG02109.hp1 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2613G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075620 | |||||||
| chr1:115075710 | C | G | 5 | a0001c0001t0001g0092 a0001c0002t0002g0101 a0001c0003t0004g0098 others(2): Show |
5 | HG00741.hp1 HG01978.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-2703G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075710 | |||||||
| chr1:115075858 | AT | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0136 a0001c0001t0011g0135 others(5): Show |
8 | HG00741.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-2852delA | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075858 | |||||||
| chr1:115075926 | T | C | 50 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(47): Show |
88 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.70-2919A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075926 | |||||||
| chr1:115075983 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.70-2976G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115075983 | |||||||
| chr1:115076007 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.70-3000A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076007 | |||||||
| chr1:115076027 | TC | T | 41 | a0001c0001t0001g0033 a0001c0001t0001g0058 a0001c0001t0001g0108 others(38): Show |
59 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.70-3021delG | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076027 | |||||||
| chr1:115076106 | C | A | 1 | a0001c0001t0006g0017 | 2 | HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.70-3099G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076106 | |||||||
| chr1:115076160 | G | T | 18 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0041 others(15): Show |
32 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.70-3153C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076160 | |||||||
| chr1:115076192 | C | T | 71 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0189 others(68): Show |
116 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.70-3185G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076192 | |||||||
| chr1:115076255 | G | C | 72 | a0001c0001t0001g0038 a0001c0001t0001g0186 a0001c0001t0001g0187 others(69): Show |
119 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.70-3248C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076255 | |||||||
| chr1:115076267 | G | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(29): Show |
43 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.70-3260C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076267 | |||||||
| chr1:115076281 | G | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(29): Show |
43 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.70-3274C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076281 | |||||||
| chr1:115076525 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70-3518C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076525 | |||||||
| chr1:115076545 | C | T | 1 | a0001c0002t0002g0197 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.70-3538G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076545 | |||||||
| chr1:115076603 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.70-3596G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076603 | |||||||
| chr1:115076801 | C | T | 71 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(68): Show |
118 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.70-3794G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076801 | |||||||
| chr1:115076808 | C | A | 3 | a0001c0002t0002g0011 a0001c0002t0002g0055 a0001c0002t0002g0107 |
5 | HG02486.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-3801G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115076808 | |||||||
| chr1:115077013 | C | T | 34 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(31): Show |
51 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.70-4006G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077013 | |||||||
| chr1:115077031 | C | T | 1 | a0001c0001t0023g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-4024G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077031 | |||||||
| chr1:115077132 | T | C | 12 | a0001c0001t0001g0230 a0001c0001t0010g0213 a0001c0001t0010g0222 others(9): Show |
15 | HG01175.hp1 HG01358.hp2 NA18612.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-4125A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077132 | |||||||
| chr1:115077139 | G | A | 1 | a0001c0001t0003g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.70-4132C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077139 | |||||||
| chr1:115077164 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(240): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.70-4157A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077164 | |||||||
| chr1:115077210 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(63): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.70-4203A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077210 | |||||||
| chr1:115077301 | C | A | 2 | a0001c0002t0002g0191 a0001c0002t0002g0192 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.70-4294G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077301 | |||||||
| chr1:115077332 | TA | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(140): Show |
192 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.70-4326delT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077332 | |||||||
| chr1:115077332 | TAA | T | 34 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(31): Show |
51 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.70-4327_70-4326del others(2): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077332 | |||||||
| chr1:115077338 | A | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0134 a0001c0001t0004g0047 others(2): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-4331T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077338 | |||||||
| chr1:115077613 | G | A | 2 | a0001c0002t0002g0101 a0001c0003t0004g0098 |
2 | HG00741.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.70-4606C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077613 | |||||||
| chr1:115077812 | G | A | 2 | a0001c0002t0004g0163 a0001c0002t0004g0164 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.70-4805C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077812 | |||||||
| chr1:115077864 | T | C | 66 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(63): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.70-4857A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115077864 | |||||||
| chr1:115078052 | A | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(238): Show |
356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.70-5045T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078052 | |||||||
| chr1:115078062 | T | C | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-5055A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078062 | |||||||
| chr1:115078065 | C | T | 1 | a0001c0001t0008g0112 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.70-5058G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078065 | |||||||
| chr1:115078118 | C | T | 66 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(63): Show |
112 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.70-5111G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078118 | |||||||
| chr1:115078141 | G | A | 1 | a0001c0003t0004g0203 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.70-5134C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078141 | |||||||
| chr1:115078387 | G | A | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70-5380C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078387 | |||||||
| chr1:115078435 | T | C | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.70-5428A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078435 | |||||||
| chr1:115078754 | G | A | 1 | a0001c0002t0002g0196 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.70-5747C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115078754 | |||||||
| chr1:115079137 | C | CCA | 6 | a0001c0001t0001g0026 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
7 | HG01175.hp1 HG01358.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-6132_70-6131dup others(2): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | C | CCACA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0018 others(36): Show |
62 | HG00544.hp1 HG00597.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.70-6134_70-6131dup others(4): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | C | CCACACA | 27 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0065 others(24): Show |
30 | HG00621.hp1 HG00741.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.70-6136_70-6131dup others(6): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | C | CCACACAC others(1): Show |
16 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0099 others(13): Show |
20 | HG01891.hp1 HG01978.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.70-6138_70-6131dup others(8): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | C | CCACACAC others(3): Show |
2 | a0001c0001t0001g0012 a0001c0001t0031g0067 |
4 | HG00323.hp2 HG01192.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-6140_70-6131dup others(10): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | C | CCACACAC others(7): Show |
4 | a0001c0001t0011g0140 a0001c0001t0024g0141 a0001c0003t0004g0102 others(1): Show |
4 | HG02818.hp1 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-6144_70-6131dup others(14): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | CCA | C | 30 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(27): Show |
51 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.70-6132_70-6131del others(2): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | CCACA | C | 15 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0060 others(12): Show |
23 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.70-6134_70-6131del others(4): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | CCACACA | C | 14 | a0001c0001t0003g0228 a0001c0001t0006g0160 a0001c0001t0006g0161 others(11): Show |
15 | HG00558.hp1 HG00673.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-6136_70-6131del others(6): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | CCACACAC others(1): Show |
C | 49 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(46): Show |
90 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.70-6138_70-6131del others(8): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079137 | CCACACAC others(3): Show |
C | 1 | a0001c0002t0002g0170 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.70-6140_70-6131del others(10): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079137 | |||||||
| chr1:115079143 | A | C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0022 a0001c0001t0004g0060 others(4): Show |
15 | HG02055.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.70-6136T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079143 | |||||||
| chr1:115079165 | ACACG | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(25): Show |
39 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.70-6162_70-6159del others(4): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079165 | |||||||
| chr1:115079167 | A | G | 1 | a0001c0003t0005g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70-6160T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079167 | |||||||
| chr1:115079167 | ACG | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG03831.hp1 HG03831.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-6162_70-6161del others(2): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079167 | |||||||
| chr1:115079169 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(66): Show |
98 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.70-6162C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079169 | |||||||
| chr1:115079239 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(64): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.70-6232G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079239 | |||||||
| chr1:115079468 | A | G | 2 | a0001c0001t0011g0140 a0001c0001t0024g0141 |
2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.70-6461T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079468 | |||||||
| chr1:115079625 | A | C | 2 | a0001c0001t0019g0051 a0001c0001t0019g0052 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.70-6618T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079625 | |||||||
| chr1:115079651 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0031g0067 |
4 | HG00323.hp2 HG01192.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-6644G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079651 | |||||||
| chr1:115079662 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(134): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.70-6655T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079662 | |||||||
| chr1:115079755 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.70-6748T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115079755 | |||||||
| chr1:115080211 | A | G | 2 | a0001c0002t0002g0015 a0001c0002t0002g0169 |
4 | HG00544.hp2 HG02056.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-7204T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080211 | |||||||
| chr1:115080348 | A | G | 2 | a0001c0002t0004g0163 a0001c0002t0004g0164 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.70-7341T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080348 | |||||||
| chr1:115080503 | G | A | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70-7496C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080503 | |||||||
| chr1:115080508 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(29): Show |
43 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.70-7501G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080508 | |||||||
| chr1:115080535 | A | G | 8 | a0001c0001t0001g0050 a0001c0001t0001g0136 a0001c0001t0008g0137 others(5): Show |
8 | HG02145.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-7528T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080535 | |||||||
| chr1:115080650 | G | T | 3 | a0001c0001t0006g0017 a0001c0001t0006g0024 a0001c0001t0006g0056 |
5 | HG02647.hp1 HG03540.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-7643C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080650 | |||||||
| chr1:115080795 | C | T | 9 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0003t0004g0158 others(6): Show |
14 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-7788G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115080795 | |||||||
| chr1:115081159 | A | G | 1 | a0001c0002t0002g0168 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.70-8152T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081159 | |||||||
| chr1:115081240 | A | G | 32 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(29): Show |
43 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.69+8124T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081240 | |||||||
| chr1:115081446 | T | C | 1 | a0001c0001t0027g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.69+7918A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081446 | |||||||
| chr1:115081481 | A | G | 1 | a0001c0002t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.69+7883T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081481 | |||||||
| chr1:115081524 | G | A | 4 | a0001c0001t0001g0195 a0001c0002t0002g0004 a0001c0002t0002g0196 others(1): Show |
10 | HG02083.hp1 NA18959.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+7840C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081524 | |||||||
| chr1:115081574 | G | A | 1 | a0001c0001t0012g0227 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.69+7790C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081574 | |||||||
| chr1:115081599 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.69+7765G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081599 | |||||||
| chr1:115081783 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(134): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.69+7581T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081783 | |||||||
| chr1:115081817 | C | T | 1 | a0001c0001t0015g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+7547G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115081817 | |||||||
| chr1:115082010 | G | T | 1 | a0001c0001t0006g0206 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+7354C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082010 | |||||||
| chr1:115082112 | C | T | 1 | a0001c0001t0007g0066 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.69+7252G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082112 | |||||||
| chr1:115082239 | C | T | 1 | a0001c0001t0008g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+7125G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082239 | |||||||
| chr1:115082389 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0134 a0001c0001t0004g0047 others(2): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+6975G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082389 | |||||||
| chr1:115082460 | T | C | 10 | a0001c0001t0006g0206 a0001c0001t0009g0023 a0001c0001t0009g0063 others(7): Show |
12 | HG01167.hp1 HG01168.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.69+6904A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082460 | |||||||
| chr1:115082523 | T | C | 1 | a0001c0003t0005g0209 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.69+6841A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082523 | |||||||
| chr1:115082549 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.69+6815A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082549 | |||||||
| chr1:115082554 | C | T | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.69+6810G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082554 | |||||||
| chr1:115082727 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(28): Show |
42 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.69+6637G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115082727 | |||||||
| chr1:115083075 | T | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(135): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.69+6289A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083075 | |||||||
| chr1:115083113 | A | G | 7 | a0001c0003t0004g0040 a0001c0003t0004g0200 a0001c0003t0004g0201 others(4): Show |
8 | HG01167.hp1 HG01168.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+6251T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083113 | |||||||
| chr1:115083200 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.69+6164A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083200 | |||||||
| chr1:115083218 | C | T | 66 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(63): Show |
108 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.69+6146G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083218 | |||||||
| chr1:115083254 | G | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(29): Show |
43 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.69+6110C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083254 | |||||||
| chr1:115083358 | T | C | 1 | a0001c0001t0008g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+6006A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083358 | |||||||
| chr1:115083449 | C | T | 1 | a0001c0002t0002g0165 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.69+5915G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083449 | |||||||
| chr1:115083450 | A | G | 106 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(103): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.69+5914T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083450 | |||||||
| chr1:115083476 | C | T | 1 | a0001c0002t0002g0015 | 3 | HG00544.hp2 HG02523.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.69+5888G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083476 | |||||||
| chr1:115083612 | C | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.69+5752G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083612 | |||||||
| chr1:115083629 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(135): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.69+5735T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083629 | |||||||
| chr1:115083641 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.69+5723G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083641 | |||||||
| chr1:115083664 | G | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(68): Show |
100 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.69+5700C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083664 | |||||||
| chr1:115083771 | G | C | 35 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(32): Show |
52 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.69+5593C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083771 | |||||||
| chr1:115083868 | C | A | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.69+5496G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115083868 | |||||||
| chr1:115084035 | T | G | 2 | a0001c0002t0004g0163 a0001c0002t0004g0164 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.69+5329A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084035 | |||||||
| chr1:115084205 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.69+5159A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084205 | |||||||
| chr1:115084282 | T | C | 1 | a0001c0002t0002g0240 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.69+5082A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084282 | |||||||
| chr1:115084293 | T | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(29): Show |
43 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.69+5071A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084293 | |||||||
| chr1:115084477 | C | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0030 others(132): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.69+4887G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084477 | |||||||
| chr1:115084498 | A | G | 8 | a0001c0001t0006g0160 a0001c0001t0006g0161 a0001c0003t0004g0158 others(5): Show |
9 | HG01433.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+4866T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084498 | |||||||
| chr1:115084789 | A | C | 1 | a0001c0001t0008g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+4575T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084789 | |||||||
| chr1:115084929 | C | G | 1 | a0001c0004t0029g0199 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.69+4435G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084929 | |||||||
| chr1:115084973 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.69+4391G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115084973 | |||||||
| chr1:115085510 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG00642.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.69+3854T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085510 | |||||||
| chr1:115085609 | C | T | 51 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(48): Show |
89 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.69+3755G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085609 | |||||||
| chr1:115085652 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG03831.hp1 HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.69+3712C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085652 | |||||||
| chr1:115085692 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0151 others(1): Show |
4 | NA18965.hp2 NA18974.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+3672C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085692 | |||||||
| chr1:115085762 | T | G | 4 | a0001c0001t0015g0231 a0001c0001t0015g0235 a0001c0003t0013g0211 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+3602A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085762 | |||||||
| chr1:115085835 | T | A | 1 | a0001c0002t0002g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.69+3529A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085835 | |||||||
| chr1:115085846 | G | T | 30 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0003g0005 others(27): Show |
48 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.69+3518C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085846 | |||||||
| chr1:115085859 | T | C | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.69+3505A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115085859 | |||||||
| chr1:115086037 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.69+3327A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086037 | |||||||
| chr1:115086130 | C | T | 2 | a0001c0002t0018g0111 a0001c0002t0018g0152 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.69+3234G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086130 | |||||||
| chr1:115086229 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.69+3135A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086229 | |||||||
| chr1:115086375 | C | T | 2 | a0001c0001t0006g0017 a0001c0001t0006g0056 |
3 | HG02647.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.69+2989G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086375 | |||||||
| chr1:115086449 | A | G | 3 | a0001c0001t0008g0112 a0001c0002t0018g0111 a0001c0002t0018g0152 |
3 | HG02451.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.69+2915T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086449 | |||||||
| chr1:115086472 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.69+2892C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086472 | |||||||
| chr1:115086716 | C | T | 3 | a0001c0001t0004g0047 a0001c0001t0004g0243 a0001c0002t0009g0048 |
5 | HG01891.hp1 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+2648G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086716 | |||||||
| chr1:115086943 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(203): Show |
303 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.69+2421C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115086943 | |||||||
| chr1:115087013 | G | A | 2 | a0001c0002t0002g0028 a0001c0002t0002g0110 |
3 | NA18940.hp2 NA18978.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.69+2351C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087013 | |||||||
| chr1:115087018 | C | A | 2 | a0001c0001t0010g0213 a0001c0001t0010g0234 |
2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.69+2346G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087018 | |||||||
| chr1:115087172 | G | C | 34 | a0001c0001t0001g0230 a0001c0001t0003g0005 a0001c0001t0003g0007 others(31): Show |
51 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.69+2192C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087172 | |||||||
| chr1:115087229 | T | C | 62 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(59): Show |
102 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.69+2135A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087229 | |||||||
| chr1:115087274 | A | ATGGTTCC others(3): Show |
1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2089_69+2090ins others(10): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087274 | |||||||
| chr1:115087275 | A | G | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2089T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087275 | |||||||
| chr1:115087280 | T | G | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2084A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087280 | |||||||
| chr1:115087281 | T | C | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2083A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087281 | |||||||
| chr1:115087282 | T | A | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2082A>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087282 | |||||||
| chr1:115087284 | G | C | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2080C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087284 | |||||||
| chr1:115087287 | A | C | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2077T>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087287 | |||||||
| chr1:115087289 | C | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2075G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087289 | |||||||
| chr1:115087290 | C | A | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2074G>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087290 | |||||||
| chr1:115087291 | A | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2073T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087291 | |||||||
| chr1:115087293 | T | C | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2071A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087293 | |||||||
| chr1:115087294 | G | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2070C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087294 | |||||||
| chr1:115087296 | T | G | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2068A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087296 | |||||||
| chr1:115087297 | T | G | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2067A>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087297 | |||||||
| chr1:115087322 | G | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2042C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087322 | |||||||
| chr1:115087324 | G | C | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2040C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087324 | |||||||
| chr1:115087327 | G | A | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2037C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087327 | |||||||
| chr1:115087328 | G | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2036C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087328 | |||||||
| chr1:115087330 | A | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2034T>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087330 | |||||||
| chr1:115087331 | G | C | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2033C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087331 | |||||||
| chr1:115087332 | G | T | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2032C>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087332 | |||||||
| chr1:115087338 | A | G | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2026T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087338 | |||||||
| chr1:115087344 | G | A | 1 | a0001c0001t0015g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2020C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087344 | |||||||
| chr1:115087467 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(203): Show |
303 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.69+1897G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087467 | |||||||
| chr1:115087481 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(240): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.69+1883G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087481 | |||||||
| chr1:115087534 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.69+1830A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087534 | |||||||
| chr1:115087611 | G | A | 77 | a0001c0001t0001g0038 a0001c0001t0001g0171 a0001c0001t0001g0186 others(74): Show |
122 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.69+1753C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087611 | |||||||
| chr1:115087615 | C | CA | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(115): Show |
171 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.69+1748dupT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087615 | |||||||
| chr1:115087615 | C | CAA | 11 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0147 others(8): Show |
15 | HG00544.hp1 HG02145.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.69+1747_69+1748dup others(2): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087615 | |||||||
| chr1:115087615 | CA | C | 7 | a0001c0001t0003g0041 a0001c0001t0003g0212 a0001c0001t0010g0213 others(4): Show |
8 | HG00099.hp1 HG01123.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+1748delT | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087615 | |||||||
| chr1:115087719 | C | T | 1 | a0001c0003t0005g0154 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.69+1645G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087719 | |||||||
| chr1:115087986 | G | A | 1 | a0001c0002t0018g0152 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.69+1378C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115087986 | |||||||
| chr1:115088135 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69+1229A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088135 | |||||||
| chr1:115088273 | C | G | 2 | a0001c0001t0008g0241 a0001c0001t0023g0049 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.69+1091G>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088273 | |||||||
| chr1:115088303 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(126): Show |
181 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.69+1061T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088303 | |||||||
| chr1:115088346 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(75): Show |
118 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.69+1018G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088346 | |||||||
| chr1:115088360 | C | T | 1 | a0001c0001t0032g0054 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.69+1004G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088360 | |||||||
| chr1:115088473 | A | G | 1 | a0001c0001t0022g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.69+891T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088473 | |||||||
| chr1:115088507 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.69+857C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088507 | |||||||
| chr1:115088549 | C | T | 2 | a0001c0001t0023g0049 a0001c0002t0002g0053 |
2 | HG02486.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.69+815G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088549 | |||||||
| chr1:115088612 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(237): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.69+752A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088612 | |||||||
| chr1:115088779 | G | GGGTA | 35 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0003g0005 others(32): Show |
52 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.69+581_69+584dupTA others(2): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088779 | |||||||
| chr1:115088785 | T | C | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(237): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.69+579A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088785 | |||||||
| chr1:115088936 | T | C | 1 | a0001c0001t0008g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+428A>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088936 | |||||||
| chr1:115088979 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69+385C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115088979 | |||||||
| chr1:115089007 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(237): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.69+357T>C | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089007 | |||||||
| chr1:115089024 | A | ACCGCCAG others(3): Show |
243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(240): Show |
359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.69+339_69+340insGC others(8): Show |
TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089024 | |||||||
| chr1:115089119 | G | C | 1 | a0001c0002t0002g0240 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.69+245C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089119 | |||||||
| chr1:115089236 | C | T | 2 | a0001c0001t0019g0051 a0001c0001t0019g0052 |
2 | HG02630.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.69+128G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089236 | |||||||
| chr1:115089275 | G | C | 1 | a0001c0001t0008g0241 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+89C>G | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089275 | |||||||
| chr1:115089291 | G | A | 1 | a0001c0001t0022g0242 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.69+73C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089291 | |||||||
| chr1:115089300 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.69+64G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089300 | |||||||
| chr1:115089303 | C | T | 240 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(237): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.69+61G>A | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089303 | |||||||
| chr1:115089356 | G | A | 1 | a0001c0001t0027g0246 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.69+8C>T | TSPAN2 | ENSG00000134198.10 | transcript | ENST00000369516.7 | protein_coding | 1/7 | chr1 | 115089356 |