Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6932 |
| ensemblid | ENSG00000081059.20 |
| hgncid | 11639 |
| symbol | TCF7 |
| name | transcription factor 7 |
| refseq_nuc | NM_003202.5 |
| refseq_prot | NP_003193.2 |
| ensembl_nuc | ENST00000342854.10 |
| ensembl_prot | ENSP00000340347.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 134114681 |
| end | 134148210 |
| strand | + |
| ver | v1.2 |
| region | chr5:134114681-134148210 |
| region5000 | chr5:134109681-134153210 |
| regionname0 | TCF7_chr5_134114681_134148210 |
| regionname5000 | TCF7_chr5_134109681_134153210 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 384 | 328 | 77 | 57 | 141 | 14 | 37 | 101 | TCF7_chr5_134109681_134153210 | TCF7 | MPQLD others(379): Show |
chr5 | 134109681 | 134153210 |
| a0002 | 0/0 | 384 | 8 | 1 | 5 | 0 | 0 | 2 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | MPQLD others(379): Show |
chr5 | 134109681 | 134153210 |
| a0003 | 0/0 | 384 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | MPQLD others(379): Show |
chr5 | 134109681 | 134153210 |
| a0004 | 0/0 | 384 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | MPQLD others(379): Show |
chr5 | 134109681 | 134153210 |
| a0005 | 0/0 | 384 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | MPQLD others(379): Show |
chr5 | 134109681 | 134153210 |
| a0006 | 0/0 | 384 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | MPQLD others(379): Show |
chr5 | 134109681 | 134153210 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1152 | 312 | 66 | 55 | 141 | 14 | 34 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0001c0002 | 0/0 | 1152 | 11 | 10 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0001c0006 | 0/0 | 1152 | 2 | 0 | 0 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0001c0007 | 0/0 | 1152 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0001c0010 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0002c0003 | 0/0 | 1152 | 7 | 1 | 4 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0002c0011 | 0/0 | 1152 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0003c0004 | 0/0 | 1152 | 4 | 0 | 0 | 0 | 0 | 4 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0004c0005 | 0/0 | 1152 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0005c0008 | 0/0 | 1152 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 | ||
| a0006c0009 | 0/0 | 1152 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ATGCC others(1147): Show |
chr5 | 134109681 | 134153210 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3288 | 70 | 12 | 11 | 40 | 3 | 4 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0002 | 0/0 | 3289 | 68 | 0 | 10 | 53 | 1 | 4 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0003 | 0/0 | 3289 | 32 | 6 | 13 | 9 | 1 | 3 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0004 | 0/1 | 3289 | 28 | 4 | 4 | 6 | 3 | 10 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0005 | 0/0 | 3288 | 19 | 1 | 3 | 7 | 1 | 7 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0007 | 0/0 | 3287 | 9 | 6 | 2 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3282): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0008 | 0/0 | 3290 | 7 | 0 | 0 | 6 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0009 | 0/0 | 3290 | 6 | 1 | 4 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0010 | 0/0 | 3289 | 5 | 4 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0011 | 0/0 | 3289 | 6 | 0 | 3 | 0 | 2 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0012 | 0/0 | 3291 | 6 | 6 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3286): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0013 | 0/0 | 3288 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0014 | 0/0 | 3290 | 5 | 0 | 0 | 5 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0015 | 0/0 | 3286 | 4 | 3 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3281): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0016 | 0/0 | 3289 | 4 | 0 | 1 | 0 | 2 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0017 | 0/0 | 3288 | 3 | 1 | 0 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0018 | 0/0 | 3289 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0019 | 0/0 | 3290 | 2 | 1 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0020 | 0/0 | 3287 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3282): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0022 | 0/0 | 3289 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0023 | 0/0 | 3289 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0024 | 0/0 | 3288 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0025 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0026 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0028 | 0/0 | 3287 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3282): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0029 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0030 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0031 | 0/0 | 3289 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0032 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3281): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0033 | 1/0 | 3288 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0034 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0035 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3286): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0036 | 0/0 | 3288 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0037 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0038 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0039 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0040 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0041 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0042 | 0/0 | 3289 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0044 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0045 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3281): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0046 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0047 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0048 | 0/0 | 3287 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3282): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0049 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0001c0001t0050 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3286): Show |
chr5 | 134109681 | 134153210 |
| a0001c0002t0006 | 0/0 | 3286 | 10 | 9 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3281): Show |
chr5 | 134109681 | 134153210 |
| a0001c0002t0043 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3281): Show |
chr5 | 134109681 | 134153210 |
| a0001c0006t0003 | 0/0 | 3289 | 2 | 0 | 0 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0007t0021 | 0/0 | 3289 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0001c0010t0008 | 0/0 | 3290 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0002c0003t0001 | 0/0 | 3288 | 7 | 1 | 4 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0002c0011t0009 | 0/0 | 3290 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0003c0004t0002 | 0/0 | 3289 | 4 | 0 | 0 | 0 | 0 | 4 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0004c0005t0013 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| a0004c0005t0027 | 0/0 | 3290 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3285): Show |
chr5 | 134109681 | 134153210 |
| a0005c0008t0010 | 0/0 | 3289 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3284): Show |
chr5 | 134109681 | 134153210 |
| a0006c0009t0005 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | ACTCG others(3283): Show |
chr5 | 134109681 | 134153210 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 3 | 4 | 18 | 2 | 3 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0002 | 0/0 | 16 | 0 | 1 | 14 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0004 | 0/0 | 12 | 0 | 0 | 10 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0005 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0143 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0006 | 0/0 | 8 | 0 | 3 | 1 | 0 | 4 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0007g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0007g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0007g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0008g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0009g0003 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0010g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0011g0009 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0012g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0013g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0014g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0014g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0015g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0015g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0016g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0016g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0017g0028 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0017g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0018g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0018g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0019g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0020g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0020g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0022g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0023g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0023g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0024g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0024g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0025g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0026g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0028g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0030g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0031g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0032g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0033g0021 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0034g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0035g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0036g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0037g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0038g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0039g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0040g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0041g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0042g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0044g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0045g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0046g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0047g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0048g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0049g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0001t0050g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0002t0006g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0002t0006g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0002t0043g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0006t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0007t0021g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0001c0010t0008g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0002c0003t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0002c0003t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0002c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0002c0011t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0003c0004t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0003c0004t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0004c0005t0013g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0004c0005t0027g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0005c0008t0010g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| a0006c0009t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0114 | EUR | GBR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0136 | EUR | GBR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0003 | EUR | FIN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0156 | EUR | FIN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0056 | EUR | FIN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00423 | hp2 | a0001 | c0001 | t0042 | g0005 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00673 | hp1 | a0001 | c0001 | t0037 | g0082 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00741 | hp1 | a0001 | c0001 | t0031 | g0154 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG00741 | hp2 | a0001 | c0007 | t0021 | g0023 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01099 | hp2 | a0001 | c0002 | t0006 | g0010 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01109 | hp1 | a0002 | c0011 | t0009 | g0159 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01109 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0088 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01358 | hp2 | a0001 | c0001 | t0039 | g0097 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01433 | hp1 | a0001 | c0001 | t0048 | g0046 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0024 | AMR | CLM | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01515 | hp1 | a0001 | c0001 | t0016 | g0059 | EUR | IBS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0009 | EUR | IBS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01517 | hp1 | a0001 | c0001 | t0016 | g0022 | EUR | IBS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01517 | hp2 | a0001 | c0001 | t0011 | g0009 | EUR | IBS | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01943 | hp1 | a0001 | c0001 | t0011 | g0140 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01952 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01978 | hp2 | a0001 | c0001 | t0016 | g0022 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01981 | hp1 | a0001 | c0001 | t0011 | g0009 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02004 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0051 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02071 | hp1 | a0001 | c0001 | t0008 | g0137 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02129 | hp2 | a0001 | c0001 | t0023 | g0086 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02148 | hp2 | a0001 | c0001 | t0009 | g0003 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02257 | hp2 | a0001 | c0001 | t0017 | g0028 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0011 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02258 | hp2 | a0001 | c0001 | t0019 | g0070 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02280 | hp2 | a0001 | c0001 | t0045 | g0049 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PEL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02451 | hp1 | a0001 | c0001 | t0046 | g0050 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02451 | hp2 | a0001 | c0001 | t0015 | g0067 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | KHV | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02572 | hp1 | a0001 | c0001 | t0010 | g0160 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0020 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0073 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02602 | hp2 | a0003 | c0004 | t0002 | g0018 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02615 | hp1 | a0001 | c0001 | t0049 | g0045 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02615 | hp2 | a0001 | c0001 | t0041 | g0171 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0069 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02647 | hp2 | a0001 | c0002 | t0006 | g0010 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02683 | hp2 | a0001 | c0001 | t0016 | g0060 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0064 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0074 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0142 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02738 | hp2 | a0001 | c0001 | t0017 | g0079 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02809 | hp1 | a0004 | c0005 | t0013 | g0149 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02809 | hp2 | a0001 | c0007 | t0021 | g0023 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0169 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0065 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02922 | hp1 | a0001 | c0001 | t0047 | g0047 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02922 | hp2 | a0004 | c0005 | t0027 | g0147 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02965 | hp1 | a0001 | c0001 | t0029 | g0163 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02970 | hp2 | a0001 | c0001 | t0032 | g0062 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0153 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03017 | hp1 | a0003 | c0004 | t0002 | g0018 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03017 | hp2 | a0001 | c0006 | t0003 | g0003 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0020 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | GWD | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03098 | hp1 | a0001 | c0001 | t0028 | g0162 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03098 | hp2 | a0001 | c0001 | t0015 | g0066 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0010 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03209 | hp1 | a0001 | c0002 | t0006 | g0010 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0146 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0016 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03486 | hp1 | a0001 | c0001 | t0012 | g0011 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03516 | hp1 | a0001 | c0001 | t0034 | g0063 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0113 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0010 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03654 | hp1 | a0001 | c0001 | t0017 | g0028 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0139 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03688 | hp2 | a0001 | c0001 | t0036 | g0001 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0009 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03710 | hp2 | a0003 | c0004 | t0002 | g0018 | SAS | PJL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03831 | hp2 | a0001 | c0006 | t0003 | g0003 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03834 | hp1 | a0001 | c0010 | t0008 | g0035 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0150 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0108 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04184 | hp1 | a0005 | c0008 | t0010 | g0006 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0152 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04204 | hp2 | a0003 | c0004 | t0002 | g0116 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | STU | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0148 | AFR | YRI | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18522 | hp2 | a0001 | c0001 | t0035 | g0112 | AFR | YRI | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18612 | hp2 | a0001 | c0001 | t0026 | g0003 | EAS | CHB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0002 | EAS | CHB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18747 | hp2 | a0001 | c0001 | t0014 | g0131 | EAS | CHB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | YRI | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | YRI | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18945 | hp2 | a0001 | c0001 | t0023 | g0128 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18948 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18964 | hp1 | a0001 | c0001 | t0022 | g0033 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18975 | hp2 | a0001 | c0001 | t0024 | g0100 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18978 | hp2 | a0001 | c0001 | t0019 | g0054 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18980 | hp1 | a0006 | c0009 | t0005 | g0057 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18986 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0157 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18995 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18998 | hp2 | a0001 | c0001 | t0025 | g0012 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19012 | hp1 | a0001 | c0001 | t0038 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19012 | hp2 | a0001 | c0001 | t0014 | g0124 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | LWK | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19030 | hp2 | a0001 | c0001 | t0020 | g0161 | AFR | LWK | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19043 | hp1 | a0001 | c0001 | t0050 | g0061 | AFR | LWK | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19065 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19065 | hp2 | a0001 | c0001 | t0040 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19070 | hp2 | a0001 | c0001 | t0024 | g0098 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19082 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19082 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0008 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA19091 | hp2 | a0001 | c0001 | t0022 | g0033 | EAS | JPT | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0135 | EUR | TSI | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | GIH | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02486 | hp1 | a0001 | c0002 | t0043 | g0168 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02559 | hp1 | a0001 | c0002 | t0006 | g0170 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0048 | AFR | ACB | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03471 | hp1 | a0001 | c0001 | t0030 | g0044 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG06807 | hp1 | a0001 | c0001 | t0044 | g0115 | AFR | USA | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | USA | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA20300 | hp1 | a0001 | c0002 | t0006 | g0020 | AFR | USA | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | USA | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | LWK | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0024 | AFR | LWK | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0143 | REF | REF | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0033 | g0021 | REF | REF | TCF7_chr5_134109681_134153210 | TCF7 | chr5 | 134109681 | 134153210 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:134115096 | G | A | 1 | a0003 | 4 | HG02602.hp2 HG03017.hp1 HG03710.hp2 others(1): Show |
missense_variant | MODERATE | c.190G>A | p.Gly64Ser | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 416/3288 | 190/1155 | 64/384 | chr5 | 134115096 | |||
| chr5:134115117 | G | A | 1 | a0001 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.211G>A | p.Val71Ile | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 437/3288 | 211/1155 | 71/384 | chr5 | 134115117 | |||
| chr5:134115135 | G | A | 1 | a0004 | 2 | HG02809.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.229G>A | p.Gly77Arg | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 455/3288 | 229/1155 | 77/384 | chr5 | 134115135 | |||
| chr5:134115992 | C | A | 1 | a0002 | 7 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(4): Show |
missense_variant | MODERATE | c.400C>A | p.Pro134Thr | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/10 | 626/3288 | 400/1155 | 134/384 | chr5 | 134115992 | |||
| chr5:134115992 | C | G | 1 | a0002 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.400C>G | p.Pro134Ala | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/10 | 626/3288 | 400/1155 | 134/384 | chr5 | 134115992 | |||
| chr5:134138075 | C | T | 1 | a0006 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.458C>T | p.Pro153Leu | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/10 | 684/3288 | 458/1155 | 153/384 | chr5 | 134138075 | |||
| chr5:134139028 | A | G | 1 | a0005 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.625A>G | p.Thr209Ala | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/10 | 851/3288 | 625/1155 | 209/384 | chr5 | 134139028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:134115098 | C | T | 1 | a0001c0002 | 11 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
synonymous_variant | LOW | c.192C>T | p.Gly64Gly | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 418/3288 | 192/1155 | 64/384 | chr5 | 134115098 | |||
| chr5:134115113 | G | C | 1 | a0001c0001 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.207G>C | p.Pro69Pro | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 433/3288 | 207/1155 | 69/384 | chr5 | 134115113 | |||
| chr5:134115961 | C | T | 1 | a0002c0011 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.369C>T | p.Ser123Ser | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/10 | 595/3288 | 369/1155 | 123/384 | chr5 | 134115961 | |||
| chr5:134115976 | C | T | 1 | a0001c0010 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.384C>T | p.Leu128Leu | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/10 | 610/3288 | 384/1155 | 128/384 | chr5 | 134115976 | |||
| chr5:134142263 | C | T | 1 | a0001c0007 | 2 | HG00741.hp2 HG02809.hp2 |
synonymous_variant | LOW | c.714C>T | p.Pro238Pro | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 6/10 | 940/3288 | 714/1155 | 238/384 | chr5 | 134142263 | |||
| chr5:134142784 | C | T | 1 | a0001c0006 | 2 | HG03017.hp2 HG03831.hp2 |
synonymous_variant | LOW | c.819C>T | p.Leu273Leu | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 7/10 | 1045/3288 | 819/1155 | 273/384 | chr5 | 134142784 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:134114700 | T | C | 1 | a0001c0001t0025 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 207 | chr5 | 134114700 | ||||||
| chr5:134114708 | C | T | 1 | a0001c0001t0050 | 1 | NA19043.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | chr5 | 134114708 | |||||||
| chr5:134114806 | A | G | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(30): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-101A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 101 | chr5 | 134114806 | ||||||
| chr5:134114860 | G | A | 1 | a0001c0001t0026 | 1 | NA18612.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 47 | chr5 | 134114860 | ||||||
| chr5:134114887 | C | T | 6 | a0001c0001t0012 a0001c0001t0045 a0001c0001t0046 others(3): Show |
11 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-20C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/10 | 20 | chr5 | 134114887 | ||||||
| chr5:134146373 | T | C | 1 | a0001c0001t0018 | 2 | HG02723.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*70T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 70 | chr5 | 134146373 | ||||||
| chr5:134146524 | G | C | 2 | a0001c0001t0035 a0001c0001t0050 |
2 | NA18522.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*221G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 221 | chr5 | 134146524 | ||||||
| chr5:134146536 | C | G | 1 | a0001c0001t0034 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*233C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 233 | chr5 | 134146536 | ||||||
| chr5:134146657 | G | A | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*354G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 354 | chr5 | 134146657 | ||||||
| chr5:134146752 | G | C | 1 | a0001c0001t0045 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 449 | chr5 | 134146752 | ||||||
| chr5:134146884 | C | A | 2 | a0001c0001t0046 a0004c0005t0027 |
2 | HG02451.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 581 | chr5 | 134146884 | ||||||
| chr5:134146890 | C | G | 1 | a0001c0001t0044 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 587 | chr5 | 134146890 | ||||||
| chr5:134146958 | T | C | 1 | a0001c0001t0028 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 655 | chr5 | 134146958 | ||||||
| chr5:134146968 | G | A | 1 | a0001c0001t0036 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 665 | chr5 | 134146968 | ||||||
| chr5:134147007 | A | T | 1 | a0001c0001t0024 | 2 | NA18975.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*704A>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 704 | chr5 | 134147007 | ||||||
| chr5:134147057 | A | T | 1 | a0001c0001t0023 | 2 | HG02129.hp2 NA18945.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754A>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 754 | chr5 | 134147057 | ||||||
| chr5:134147125 | A | G | 1 | a0001c0002t0043 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 822 | chr5 | 134147125 | ||||||
| chr5:134147235 | G | A | 9 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(6): Show |
49 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*932G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 932 | chr5 | 134147235 | ||||||
| chr5:134147260 | G | T | 1 | a0001c0001t0022 | 2 | NA18964.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*957G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 957 | chr5 | 134147260 | ||||||
| chr5:134147275 | GC | G | 2 | a0001c0001t0015 a0001c0001t0045 |
5 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*976delC | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 976 | INFO_REALIGN_3_PRIME | chr5 | 134147275 | |||||
| chr5:134147691 | C | T | 34 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(31): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1388C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1388 | chr5 | 134147691 | ||||||
| chr5:134147693 | G | A | 4 | a0001c0001t0020 a0001c0001t0028 a0001c0001t0047 others(1): Show |
5 | HG01433.hp1 HG02922.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1390G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1390 | chr5 | 134147693 | ||||||
| chr5:134147713 | C | T | 3 | a0001c0001t0032 a0001c0002t0006 a0001c0002t0043 |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1410C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1410 | chr5 | 134147713 | ||||||
| chr5:134147741 | C | T | 1 | a0001c0001t0042 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1438C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1438 | chr5 | 134147741 | ||||||
| chr5:134147848 | C | T | 1 | a0001c0001t0039 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1545C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1545 | chr5 | 134147848 | ||||||
| chr5:134147869 | G | A | 1 | a0001c0001t0037 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1566G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1566 | chr5 | 134147869 | ||||||
| chr5:134147891 | A | C | 12 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0016 others(9): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1588A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1588 | chr5 | 134147891 | ||||||
| chr5:134147928 | A | G | 1 | a0001c0001t0031 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1625A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1625 | chr5 | 134147928 | ||||||
| chr5:134147937 | T | C | 2 | a0001c0001t0025 a0001c0001t0038 |
2 | NA18998.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1634T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1634 | chr5 | 134147937 | ||||||
| chr5:134147973 | C | CA | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(16): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*1694dupA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1695 | INFO_REALIGN_3_PRIME | chr5 | 134147973 | |||||
| chr5:134147973 | C | CAA | 10 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0014 others(7): Show |
26 | HG00280.hp1 HG01109.hp1 HG01952.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1693_*1694dupAA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1695 | INFO_REALIGN_3_PRIME | chr5 | 134147973 | |||||
| chr5:134147973 | C | CAAA | 3 | a0001c0001t0012 a0001c0001t0035 a0001c0001t0050 |
8 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1692_*1694dupAAA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1695 | INFO_REALIGN_3_PRIME | chr5 | 134147973 | |||||
| chr5:134147973 | CA | C | 6 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0020 others(3): Show |
18 | HG01361.hp1 HG01433.hp1 HG01496.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1694delA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1694 | INFO_REALIGN_3_PRIME | chr5 | 134147973 | |||||
| chr5:134147973 | CAA | C | 3 | a0001c0001t0032 a0001c0002t0006 a0001c0002t0043 |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1693_*1694delAA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1693 | INFO_REALIGN_3_PRIME | chr5 | 134147973 | |||||
| chr5:134148048 | T | G | 1 | a0001c0001t0011 | 6 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1745T>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1745 | chr5 | 134148048 | ||||||
| chr5:134148050 | T | C | 1 | a0001c0001t0015 | 4 | HG01496.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1747T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1747 | chr5 | 134148050 | ||||||
| chr5:134148081 | C | T | 1 | a0001c0001t0040 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1778C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1778 | chr5 | 134148081 | ||||||
| chr5:134148189 | A | C | 1 | a0001c0001t0029 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 10/10 | 1886 | chr5 | 134148189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:134115265 | C | T | 2 | a0001c0001t0003g0173 a0001c0001t0003g0174 |
2 | HG00642.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.250-56C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 1/9 | chr5 | 134115265 | |||||||
| chr5:134115448 | G | C | 8 | a0001c0001t0012g0011 a0001c0001t0012g0048 a0001c0001t0012g0051 others(5): Show |
11 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.316+61G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115448 | |||||||
| chr5:134115522 | A | G | 15 | a0001c0001t0004g0172 a0001c0001t0012g0011 a0001c0001t0012g0048 others(12): Show |
24 | HG01099.hp2 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.316+135A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115522 | |||||||
| chr5:134115527 | G | C | 1 | a0001c0001t0004g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+140G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115527 | |||||||
| chr5:134115530 | G | C | 1 | a0001c0001t0004g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+143G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115530 | |||||||
| chr5:134115612 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.316+225C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115612 | |||||||
| chr5:134115828 | C | T | 2 | a0001c0001t0012g0051 a0001c0001t0046g0050 |
2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.317-81C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115828 | |||||||
| chr5:134115866 | G | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(30): Show |
52 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.317-43G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115866 | |||||||
| chr5:134115867 | C | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(30): Show |
52 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.317-42C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115867 | |||||||
| chr5:134115873 | G | C | 1 | a0001c0001t0004g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.317-36G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 2/9 | chr5 | 134115873 | |||||||
| chr5:134116150 | C | T | 1 | a0001c0001t0045g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.441+117C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116150 | |||||||
| chr5:134116155 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0004g0015 |
4 | NA18951.hp1 NA18986.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+122C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116155 | |||||||
| chr5:134116215 | G | T | 2 | a0001c0001t0012g0011 a0001c0001t0012g0048 |
5 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+182G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116215 | |||||||
| chr5:134116508 | C | T | 5 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(2): Show |
6 | HG02630.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+475C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116508 | |||||||
| chr5:134116804 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(116): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.441+771C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116804 | |||||||
| chr5:134116844 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(178): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.441+811C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116844 | |||||||
| chr5:134116976 | T | A | 1 | a0001c0001t0049g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.441+943T>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134116976 | |||||||
| chr5:134117126 | T | C | 5 | a0001c0002t0006g0010 a0001c0002t0006g0020 a0001c0002t0006g0169 others(2): Show |
11 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+1093T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117126 | |||||||
| chr5:134117224 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.441+1191C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117224 | |||||||
| chr5:134117355 | C | G | 1 | a0001c0001t0003g0058 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.441+1322C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117355 | |||||||
| chr5:134117425 | C | G | 2 | a0001c0001t0003g0173 a0001c0001t0003g0174 |
2 | HG00642.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.441+1392C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117425 | |||||||
| chr5:134117702 | T | C | 31 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(28): Show |
51 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.441+1669T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117702 | |||||||
| chr5:134117831 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.441+1798C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117831 | |||||||
| chr5:134117918 | C | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0073 |
3 | HG01361.hp2 HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.441+1885C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134117918 | |||||||
| chr5:134118030 | T | C | 38 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(35): Show |
59 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.441+1997T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118030 | |||||||
| chr5:134118172 | G | T | 3 | a0001c0001t0003g0044 a0001c0001t0010g0160 a0001c0001t0030g0044 |
3 | HG02572.hp1 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.441+2139G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118172 | |||||||
| chr5:134118176 | A | G | 1 | a0001c0001t0049g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.441+2143A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118176 | |||||||
| chr5:134118232 | G | A | 1 | a0001c0001t0008g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.441+2199G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118232 | |||||||
| chr5:134118402 | T | C | 1 | a0001c0001t0048g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.441+2369T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118402 | |||||||
| chr5:134118493 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.441+2460G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118493 | |||||||
| chr5:134118619 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441+2586G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118619 | |||||||
| chr5:134118662 | GA | G | 3 | a0001c0001t0010g0071 a0001c0001t0010g0072 a0001c0001t0019g0070 |
3 | HG02257.hp1 HG02258.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.441+2631delA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134118662 | ||||||
| chr5:134118808 | G | T | 19 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0019 others(16): Show |
31 | HG00140.hp2 HG00642.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.441+2775G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134118808 | |||||||
| chr5:134119172 | A | G | 46 | a0001c0001t0001g0034 a0001c0001t0001g0068 a0001c0001t0002g0002 others(43): Show |
102 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.441+3139A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119172 | |||||||
| chr5:134119329 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+3296C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119329 | |||||||
| chr5:134119354 | G | C | 1 | a0001c0001t0004g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.441+3321G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119354 | |||||||
| chr5:134119367 | G | A | 1 | a0001c0001t0044g0115 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.441+3334G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119367 | |||||||
| chr5:134119425 | A | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.441+3392A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119425 | |||||||
| chr5:134119448 | C | T | 5 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0173 others(2): Show |
7 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+3415C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119448 | |||||||
| chr5:134119449 | ACTGAATT others(7): Show |
A | 1 | a0001c0001t0004g0114 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.441+3419_441+3432d others(16): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134119449 | ||||||
| chr5:134119455 | T | C | 1 | a0001c0001t0002g0005 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.441+3422T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119455 | |||||||
| chr5:134119462 | A | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(182): Show |
320 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(317): Show |
intron_variant | MODIFIER | c.441+3429A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119462 | |||||||
| chr5:134119682 | C | T | 7 | a0001c0001t0012g0011 a0001c0001t0012g0048 a0001c0001t0012g0051 others(4): Show |
10 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.441+3649C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119682 | |||||||
| chr5:134119866 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0075 |
5 | NA18948.hp2 NA18956.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+3833G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119866 | |||||||
| chr5:134119948 | A | G | 13 | a0001c0001t0012g0011 a0001c0001t0012g0048 a0001c0001t0012g0051 others(10): Show |
17 | HG01433.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+3915A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134119948 | |||||||
| chr5:134120035 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.441+4002G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120035 | |||||||
| chr5:134120043 | C | T | 1 | a0001c0001t0014g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.441+4010C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120043 | |||||||
| chr5:134120240 | G | A | 1 | a0001c0001t0013g0146 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.441+4207G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120240 | |||||||
| chr5:134120270 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(78): Show |
135 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.441+4237G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120270 | |||||||
| chr5:134120329 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+4296G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120329 | |||||||
| chr5:134120366 | T | G | 42 | a0001c0001t0001g0034 a0001c0001t0002g0002 a0001c0001t0002g0004 others(39): Show |
97 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.441+4333T>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120366 | |||||||
| chr5:134120392 | G | T | 1 | a0001c0001t0003g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.441+4359G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120392 | |||||||
| chr5:134120709 | C | T | 3 | a0001c0001t0004g0052 a0001c0001t0004g0111 a0001c0001t0004g0172 |
3 | HG02630.hp2 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.441+4676C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134120709 | |||||||
| chr5:134121283 | C | CA | 11 | a0001c0001t0002g0077 a0001c0001t0003g0042 a0001c0001t0003g0151 others(8): Show |
12 | HG01099.hp1 HG01168.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+5264dupA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134121283 | ||||||
| chr5:134121309 | T | C | 101 | a0001c0001t0001g0034 a0001c0001t0002g0002 a0001c0001t0002g0004 others(98): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.441+5276T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121309 | |||||||
| chr5:134121441 | G | A | 1 | a0001c0001t0041g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.441+5408G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121441 | |||||||
| chr5:134121487 | G | A | 1 | a0001c0001t0049g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.441+5454G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121487 | |||||||
| chr5:134121488 | C | T | 1 | a0001c0001t0049g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.441+5455C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121488 | |||||||
| chr5:134121585 | C | CA | 8 | a0001c0001t0004g0078 a0001c0001t0019g0054 a0001c0001t0046g0050 others(5): Show |
14 | HG01099.hp2 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+5569dupA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134121585 | ||||||
| chr5:134121585 | CA | C | 14 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0110 others(11): Show |
16 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+5569delA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134121585 | ||||||
| chr5:134121585 | CAA | C | 42 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(39): Show |
64 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.441+5568_441+5569d others(4): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134121585 | ||||||
| chr5:134121632 | G | A | 1 | a0001c0001t0034g0063 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.441+5599G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121632 | |||||||
| chr5:134121654 | G | A | 1 | a0002c0011t0009g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+5621G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121654 | |||||||
| chr5:134121736 | G | A | 1 | a0001c0001t0004g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.441+5703G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121736 | |||||||
| chr5:134121762 | G | C | 1 | a0001c0001t0013g0148 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.441+5729G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121762 | |||||||
| chr5:134121822 | C | T | 1 | a0001c0001t0041g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.441+5789C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121822 | |||||||
| chr5:134121968 | C | T | 1 | a0001c0001t0003g0041 | 2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.441+5935C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134121968 | |||||||
| chr5:134122118 | C | T | 1 | a0001c0001t0045g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.441+6085C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122118 | |||||||
| chr5:134122211 | C | T | 1 | a0002c0003t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.441+6178C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122211 | |||||||
| chr5:134122223 | G | C | 1 | a0001c0001t0002g0030 | 2 | NA18947.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.441+6190G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122223 | |||||||
| chr5:134122242 | G | T | 1 | a0001c0001t0003g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.441+6209G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122242 | |||||||
| chr5:134122255 | G | A | 4 | a0001c0001t0035g0112 a0001c0001t0041g0171 a0001c0001t0050g0061 others(1): Show |
5 | HG00741.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+6222G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122255 | |||||||
| chr5:134122372 | TC | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(53): Show |
85 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.441+6345delC | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134122372 | ||||||
| chr5:134122381 | G | A | 8 | a0001c0001t0010g0071 a0001c0001t0010g0072 a0001c0001t0018g0064 others(5): Show |
8 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.441+6348G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122381 | |||||||
| chr5:134122439 | G | A | 2 | a0001c0002t0006g0020 a0001c0002t0006g0169 |
4 | HG02572.hp2 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+6406G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122439 | |||||||
| chr5:134122653 | G | T | 40 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(37): Show |
62 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.441+6620G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134122653 | |||||||
| chr5:134123023 | T | C | 100 | a0001c0001t0001g0034 a0001c0001t0002g0002 a0001c0001t0002g0004 others(97): Show |
181 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.441+6990T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123023 | |||||||
| chr5:134123136 | G | A | 1 | a0001c0001t0017g0079 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.441+7103G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123136 | |||||||
| chr5:134123248 | C | T | 56 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(53): Show |
85 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.441+7215C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123248 | |||||||
| chr5:134123427 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA19057.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.441+7394T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123427 | |||||||
| chr5:134123429 | A | T | 1 | a0001c0001t0018g0065 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.441+7396A>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123429 | |||||||
| chr5:134123442 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(192): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.441+7409A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123442 | |||||||
| chr5:134123656 | A | G | 59 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(56): Show |
88 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.441+7623A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123656 | |||||||
| chr5:134123701 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.441+7668G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123701 | |||||||
| chr5:134123731 | G | A | 14 | a0001c0001t0010g0160 a0001c0001t0013g0036 a0001c0001t0013g0146 others(11): Show |
17 | HG00741.hp2 HG01433.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+7698G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123731 | |||||||
| chr5:134123882 | A | G | 37 | a0001c0001t0001g0107 a0001c0001t0002g0014 a0001c0001t0002g0126 others(34): Show |
60 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.441+7849A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134123882 | |||||||
| chr5:134124104 | C | T | 47 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(44): Show |
74 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.441+8071C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124104 | |||||||
| chr5:134124159 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.441+8126G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124159 | |||||||
| chr5:134124256 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.441+8223C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124256 | |||||||
| chr5:134124261 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0005g0166 |
2 | HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.441+8228C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124261 | |||||||
| chr5:134124286 | G | A | 1 | a0001c0001t0037g0082 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.441+8253G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124286 | |||||||
| chr5:134124424 | C | G | 49 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(46): Show |
77 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.441+8391C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124424 | |||||||
| chr5:134124475 | T | A | 1 | a0001c0001t0008g0137 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.441+8442T>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124475 | |||||||
| chr5:134124587 | C | T | 48 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(45): Show |
76 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.441+8554C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124587 | |||||||
| chr5:134124682 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.441+8649C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124682 | |||||||
| chr5:134124892 | G | A | 4 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(1): Show |
5 | HG02630.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+8859G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134124892 | |||||||
| chr5:134125040 | T | A | 3 | a0001c0001t0012g0011 a0001c0001t0012g0048 a0001c0001t0012g0051 |
6 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+9007T>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134125040 | |||||||
| chr5:134125244 | C | T | 29 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(26): Show |
49 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.441+9211C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134125244 | |||||||
| chr5:134125543 | G | C | 1 | a0001c0001t0015g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.441+9510G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134125543 | |||||||
| chr5:134125575 | G | A | 2 | a0001c0001t0035g0112 a0001c0001t0050g0061 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.441+9542G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134125575 | |||||||
| chr5:134125741 | A | G | 3 | a0001c0001t0035g0112 a0001c0001t0050g0061 a0001c0007t0021g0023 |
4 | HG00741.hp2 HG02809.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+9708A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134125741 | |||||||
| chr5:134125895 | G | A | 2 | a0001c0001t0017g0028 a0001c0001t0017g0079 |
3 | HG02257.hp2 HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.441+9862G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134125895 | |||||||
| chr5:134126000 | A | G | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.441+9967A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126000 | |||||||
| chr5:134126011 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.441+9978G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126011 | |||||||
| chr5:134126301 | T | G | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.441+10268T>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126301 | |||||||
| chr5:134126329 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.441+10296T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126329 | |||||||
| chr5:134126413 | C | T | 1 | a0001c0001t0028g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.441+10380C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126413 | |||||||
| chr5:134126440 | C | T | 5 | a0001c0001t0004g0009 a0001c0001t0004g0135 a0001c0001t0008g0074 others(2): Show |
9 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+10407C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126440 | |||||||
| chr5:134126566 | A | G | 10 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(7): Show |
11 | HG01433.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.441+10533A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126566 | |||||||
| chr5:134126586 | G | A | 9 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(6): Show |
10 | HG01433.hp1 HG02630.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+10553G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126586 | |||||||
| chr5:134126673 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.441+10640C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126673 | |||||||
| chr5:134126896 | C | CA | 5 | a0001c0001t0001g0084 a0001c0001t0003g0173 a0001c0001t0016g0059 others(2): Show |
7 | HG00642.hp2 HG01261.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+10878dupA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134126896 | ||||||
| chr5:134126896 | CA | C | 13 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0002g0125 others(10): Show |
14 | HG01433.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.441+10878delA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134126896 | ||||||
| chr5:134126916 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.441+10883G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126916 | |||||||
| chr5:134126966 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.441+10933G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126966 | |||||||
| chr5:134126987 | A | C | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.441+10954A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134126987 | |||||||
| chr5:134127006 | C | G | 1 | a0001c0001t0005g0152 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.441+10973C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127006 | |||||||
| chr5:134127132 | C | T | 1 | a0006c0009t0005g0057 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.442-10927C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127132 | |||||||
| chr5:134127368 | A | G | 1 | a0004c0005t0013g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.442-10691A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127368 | |||||||
| chr5:134127454 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442-10605C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127454 | |||||||
| chr5:134127477 | T | C | 1 | a0001c0001t0010g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.442-10582T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127477 | |||||||
| chr5:134127503 | C | G | 1 | a0001c0001t0003g0040 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.442-10556C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127503 | |||||||
| chr5:134127530 | A | G | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-10529A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127530 | |||||||
| chr5:134127557 | A | T | 35 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(32): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.442-10502A>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127557 | |||||||
| chr5:134127578 | G | A | 8 | a0001c0001t0002g0004 a0001c0001t0002g0031 a0001c0001t0002g0129 others(5): Show |
21 | HG00438.hp2 HG00558.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.442-10481G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127578 | |||||||
| chr5:134127619 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-10440C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127619 | |||||||
| chr5:134127623 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-10436C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127623 | |||||||
| chr5:134127641 | G | A | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-10418G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127641 | |||||||
| chr5:134127755 | C | T | 5 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0173 others(2): Show |
7 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-10304C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134127755 | |||||||
| chr5:134128006 | A | G | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-10053A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128006 | |||||||
| chr5:134128082 | G | A | 1 | a0002c0011t0009g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442-9977G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128082 | |||||||
| chr5:134128121 | T | C | 1 | a0001c0001t0005g0166 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.442-9938T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128121 | |||||||
| chr5:134128161 | C | G | 20 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0019 others(17): Show |
32 | HG00140.hp2 HG00642.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.442-9898C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128161 | |||||||
| chr5:134128163 | C | T | 1 | a0001c0001t0004g0142 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.442-9896C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128163 | |||||||
| chr5:134128378 | G | T | 6 | a0001c0001t0032g0062 a0001c0002t0006g0010 a0001c0002t0006g0020 others(3): Show |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-9681G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128378 | |||||||
| chr5:134128424 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0004g0052 |
2 | HG00738.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.442-9635C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128424 | |||||||
| chr5:134128582 | A | ACT | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-9476_442-9475i others(4): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134128582 | ||||||
| chr5:134128584 | A | G | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-9475A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128584 | |||||||
| chr5:134128688 | C | T | 2 | a0001c0001t0003g0173 a0001c0001t0003g0174 |
2 | HG00642.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.442-9371C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128688 | |||||||
| chr5:134128811 | A | T | 35 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(32): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.442-9248A>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128811 | |||||||
| chr5:134128839 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442-9220G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128839 | |||||||
| chr5:134128856 | C | T | 2 | a0001c0001t0035g0112 a0001c0001t0050g0061 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-9203C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128856 | |||||||
| chr5:134128941 | GT | G | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-9116delT | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134128941 | ||||||
| chr5:134128966 | T | C | 36 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
84 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.442-9093T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134128966 | |||||||
| chr5:134129114 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.442-8945C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129114 | |||||||
| chr5:134129357 | C | T | 3 | a0001c0001t0012g0011 a0001c0001t0012g0048 a0001c0001t0012g0051 |
6 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-8702C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129357 | |||||||
| chr5:134129416 | G | A | 4 | a0001c0001t0035g0112 a0001c0001t0041g0171 a0001c0001t0050g0061 others(1): Show |
5 | HG00741.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8643G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129416 | |||||||
| chr5:134129420 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.442-8639C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129420 | |||||||
| chr5:134129701 | C | T | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442-8358C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129701 | |||||||
| chr5:134129717 | T | C | 4 | a0001c0001t0035g0112 a0001c0001t0041g0171 a0001c0001t0050g0061 others(1): Show |
5 | HG00741.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8342T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129717 | |||||||
| chr5:134129832 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.442-8227G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129832 | |||||||
| chr5:134129852 | G | A | 1 | a0001c0001t0019g0070 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.442-8207G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129852 | |||||||
| chr5:134129911 | A | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0030 a0001c0001t0002g0123 others(3): Show |
17 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-8148A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129911 | |||||||
| chr5:134129949 | C | G | 36 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
84 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.442-8110C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129949 | |||||||
| chr5:134129974 | G | A | 11 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(8): Show |
12 | HG01433.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-8085G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129974 | |||||||
| chr5:134129984 | T | A | 3 | a0001c0001t0004g0019 a0001c0001t0004g0136 a0001c0001t0004g0138 |
5 | HG00140.hp2 HG01106.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-8075T>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134129984 | |||||||
| chr5:134130006 | GGTGGGCG others(25): Show |
G | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-8046_442-8015d others(34): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134130006 | ||||||
| chr5:134130270 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-7789G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130270 | |||||||
| chr5:134130325 | C | CT | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-7734_442-7733i others(3): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130325 | |||||||
| chr5:134130385 | T | A | 1 | a0001c0001t0002g0123 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.442-7674T>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130385 | |||||||
| chr5:134130435 | C | T | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442-7624C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130435 | |||||||
| chr5:134130484 | A | T | 2 | a0001c0001t0012g0011 a0001c0001t0012g0051 |
5 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-7575A>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130484 | |||||||
| chr5:134130505 | C | T | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442-7554C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130505 | |||||||
| chr5:134130640 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.442-7419G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130640 | |||||||
| chr5:134130646 | G | A | 3 | a0002c0003t0001g0016 a0002c0003t0001g0088 a0002c0003t0001g0089 |
5 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-7413G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130646 | |||||||
| chr5:134130699 | C | T | 3 | a0001c0001t0012g0011 a0001c0001t0012g0048 a0001c0001t0012g0051 |
6 | HG01884.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-7360C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130699 | |||||||
| chr5:134130791 | T | C | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-7268T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134130791 | |||||||
| chr5:134131024 | G | A | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442-7035G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131024 | |||||||
| chr5:134131115 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-6944G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131115 | |||||||
| chr5:134131132 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 |
3 | HG02055.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.442-6927T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131132 | |||||||
| chr5:134131347 | G | A | 4 | a0001c0001t0015g0024 a0001c0001t0015g0066 a0001c0001t0015g0067 others(1): Show |
5 | HG01496.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-6712G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131347 | |||||||
| chr5:134131375 | C | G | 4 | a0001c0001t0035g0112 a0001c0001t0041g0171 a0001c0001t0050g0061 others(1): Show |
5 | HG00741.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-6684C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131375 | |||||||
| chr5:134131377 | G | A | 1 | a0001c0001t0034g0063 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.442-6682G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131377 | |||||||
| chr5:134131399 | T | C | 1 | a0001c0001t0031g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.442-6660T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131399 | |||||||
| chr5:134131895 | G | A | 1 | a0001c0001t0041g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.442-6164G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134131895 | |||||||
| chr5:134132234 | A | G | 44 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(41): Show |
66 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-5825A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134132234 | |||||||
| chr5:134132309 | A | G | 21 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0019 others(18): Show |
33 | HG00140.hp2 HG00642.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.442-5750A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134132309 | |||||||
| chr5:134132526 | G | A | 2 | a0001c0001t0035g0112 a0001c0001t0050g0061 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-5533G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134132526 | |||||||
| chr5:134132602 | C | T | 1 | a0001c0001t0003g0039 | 2 | HG01175.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.442-5457C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134132602 | |||||||
| chr5:134132910 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-5149G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134132910 | |||||||
| chr5:134133058 | C | T | 6 | a0001c0001t0032g0062 a0001c0002t0006g0010 a0001c0002t0006g0020 others(3): Show |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-5001C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133058 | |||||||
| chr5:134133095 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-4964C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133095 | |||||||
| chr5:134133146 | G | C | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-4913G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133146 | |||||||
| chr5:134133238 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.442-4821C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133238 | |||||||
| chr5:134133322 | A | C | 1 | a0001c0001t0007g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.442-4737A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133322 | |||||||
| chr5:134133367 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.442-4692C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133367 | |||||||
| chr5:134133416 | G | A | 1 | a0001c0001t0049g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.442-4643G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133416 | |||||||
| chr5:134133917 | T | C | 1 | a0001c0001t0031g0154 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.442-4142T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134133917 | |||||||
| chr5:134134124 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.442-3935G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134134124 | |||||||
| chr5:134134145 | C | G | 2 | a0001c0001t0032g0062 a0001c0002t0043g0168 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.442-3914C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134134145 | |||||||
| chr5:134134323 | G | GCCCCCCC others(23): Show |
1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-3734_442-3733i others(32): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134134323 | ||||||
| chr5:134134326 | A | C | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.442-3733A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134134326 | |||||||
| chr5:134134603 | C | T | 2 | a0001c0001t0023g0086 a0001c0001t0023g0128 |
2 | HG02129.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.442-3456C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134134603 | |||||||
| chr5:134134778 | A | C | 1 | a0001c0001t0002g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.442-3281A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134134778 | |||||||
| chr5:134135281 | C | G | 1 | a0001c0001t0010g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.442-2778C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135281 | |||||||
| chr5:134135424 | G | C | 1 | a0001c0001t0002g0118 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.442-2635G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135424 | |||||||
| chr5:134135485 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-2574C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135485 | |||||||
| chr5:134135526 | G | C | 39 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(36): Show |
90 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.442-2533G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135526 | |||||||
| chr5:134135701 | A | G | 2 | a0001c0001t0035g0112 a0001c0001t0050g0061 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.442-2358A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135701 | |||||||
| chr5:134135863 | A | G | 1 | a0001c0001t0014g0131 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.442-2196A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135863 | |||||||
| chr5:134135876 | T | G | 1 | a0001c0001t0029g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.442-2183T>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135876 | |||||||
| chr5:134135929 | A | G | 1 | a0001c0001t0041g0171 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.442-2130A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134135929 | |||||||
| chr5:134136053 | CTGTCTGG others(4): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-2005_442-1995d others(13): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136053 | |||||||
| chr5:134136061 | C | T | 1 | a0001c0001t0003g0042 | 2 | HG01099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.442-1998C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136061 | |||||||
| chr5:134136065 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.442-1994G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136065 | |||||||
| chr5:134136174 | G | A | 1 | a0001c0002t0043g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.442-1885G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136174 | |||||||
| chr5:134136240 | A | C | 1 | a0001c0001t0002g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.442-1819A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136240 | |||||||
| chr5:134136320 | T | C | 1 | a0001c0001t0002g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.442-1739T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136320 | |||||||
| chr5:134136408 | G | T | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442-1651G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136408 | |||||||
| chr5:134136411 | C | T | 35 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(32): Show |
80 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.442-1648C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136411 | |||||||
| chr5:134136517 | G | A | 6 | a0001c0001t0032g0062 a0001c0002t0006g0010 a0001c0002t0006g0020 others(3): Show |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-1542G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136517 | |||||||
| chr5:134136591 | T | C | 1 | a0001c0001t0017g0028 | 2 | HG02257.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.442-1468T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136591 | |||||||
| chr5:134136613 | C | A | 11 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(8): Show |
12 | HG01433.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-1446C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136613 | |||||||
| chr5:134136690 | G | C | 1 | a0001c0001t0032g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.442-1369G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136690 | |||||||
| chr5:134136772 | C | T | 1 | a0002c0003t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.442-1287C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136772 | |||||||
| chr5:134136810 | G | A | 1 | a0001c0001t0049g0045 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.442-1249G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136810 | |||||||
| chr5:134136932 | G | A | 1 | a0001c0001t0015g0067 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442-1127G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134136932 | |||||||
| chr5:134137102 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-957G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137102 | |||||||
| chr5:134137109 | G | A | 4 | a0001c0001t0035g0112 a0001c0001t0041g0171 a0001c0001t0050g0061 others(1): Show |
5 | HG00741.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-950G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137109 | |||||||
| chr5:134137180 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-879C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137180 | |||||||
| chr5:134137190 | G | A | 4 | a0001c0002t0006g0010 a0001c0002t0006g0020 a0001c0002t0006g0169 others(1): Show |
10 | HG01099.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-869G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137190 | |||||||
| chr5:134137306 | T | C | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.442-753T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137306 | |||||||
| chr5:134137425 | C | CA | 27 | a0001c0001t0001g0012 a0001c0001t0001g0075 a0001c0001t0001g0080 others(24): Show |
33 | HG00423.hp1 HG01106.hp2 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.442-612dupA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134137425 | ||||||
| chr5:134137425 | CA | C | 32 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0003g0003 others(29): Show |
52 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-612delA | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134137425 | ||||||
| chr5:134137425 | CAA | C | 11 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(8): Show |
12 | HG01433.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-613_442-612del others(2): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134137425 | ||||||
| chr5:134137441 | A | C | 1 | a0001c0001t0003g0038 | 2 | HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.442-618A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137441 | |||||||
| chr5:134137444 | AAAAC | A | 5 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0120 others(2): Show |
7 | HG00558.hp1 HG02004.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-613_442-610del others(4): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134137444 | ||||||
| chr5:134137445 | AAAC | A | 32 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(29): Show |
77 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.442-612_442-610del others(3): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134137445 | ||||||
| chr5:134137461 | A | G | 1 | a0002c0003t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.442-598A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137461 | |||||||
| chr5:134137664 | T | C | 1 | a0001c0001t0014g0124 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.442-395T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137664 | |||||||
| chr5:134137711 | G | GC | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.442-346dupC | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 134137711 | ||||||
| chr5:134137825 | T | C | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.442-234T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137825 | |||||||
| chr5:134137893 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.442-166T>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137893 | |||||||
| chr5:134137944 | CT | C | 35 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(32): Show |
61 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.442-114delT | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137944 | |||||||
| chr5:134137992 | C | A | 4 | a0001c0002t0006g0010 a0001c0002t0006g0020 a0001c0002t0006g0169 others(1): Show |
10 | HG01099.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-67C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134137992 | |||||||
| chr5:134138006 | T | C | 89 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(86): Show |
165 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.442-53T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 3/9 | chr5 | 134138006 | |||||||
| chr5:134138220 | C | T | 3 | a0001c0001t0035g0112 a0001c0001t0050g0061 a0001c0007t0021g0023 |
4 | HG00741.hp2 HG02809.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+56C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/9 | chr5 | 134138220 | |||||||
| chr5:134138226 | TTC | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.547+64_547+65delCT | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 134138226 | ||||||
| chr5:134138584 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0004g0017 a0001c0001t0005g0055 |
4 | HG02056.hp1 HG02083.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-367G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/9 | chr5 | 134138584 | |||||||
| chr5:134138647 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.548-304G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/9 | chr5 | 134138647 | |||||||
| chr5:134138782 | G | A | 1 | a0001c0001t0047g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.548-169G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/9 | chr5 | 134138782 | |||||||
| chr5:134138900 | A | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.548-51A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 4/9 | chr5 | 134138900 | |||||||
| chr5:134139236 | A | G | 1 | a0002c0003t0001g0089 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.635+198A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139236 | |||||||
| chr5:134139260 | G | C | 1 | a0001c0001t0002g0125 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.635+222G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139260 | |||||||
| chr5:134139264 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.635+226G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139264 | |||||||
| chr5:134139531 | G | A | 1 | a0001c0007t0021g0023 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.635+493G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139531 | |||||||
| chr5:134139773 | T | G | 2 | a0001c0001t0035g0112 a0001c0001t0050g0061 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.635+735T>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139773 | |||||||
| chr5:134139809 | A | G | 2 | a0001c0001t0032g0062 a0001c0002t0043g0168 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.635+771A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139809 | |||||||
| chr5:134139902 | C | T | 11 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(8): Show |
12 | HG01433.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.635+864C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139902 | |||||||
| chr5:134139962 | G | C | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.635+924G>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134139962 | |||||||
| chr5:134140352 | T | C | 6 | a0001c0001t0032g0062 a0001c0002t0006g0010 a0001c0002t0006g0020 others(3): Show |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.635+1314T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134140352 | |||||||
| chr5:134140578 | G | A | 1 | a0002c0003t0001g0088 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.635+1540G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134140578 | |||||||
| chr5:134141066 | A | G | 3 | a0001c0001t0015g0024 a0001c0001t0015g0066 a0001c0001t0015g0067 |
4 | HG01496.hp2 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-1119A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141066 | |||||||
| chr5:134141125 | G | T | 50 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.636-1060G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141125 | |||||||
| chr5:134141143 | C | T | 7 | a0001c0001t0020g0153 a0001c0001t0020g0161 a0001c0001t0028g0162 others(4): Show |
7 | HG01433.hp1 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.636-1042C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141143 | |||||||
| chr5:134141146 | G | A | 11 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(8): Show |
12 | HG01433.hp1 HG02451.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.636-1039G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141146 | |||||||
| chr5:134141359 | G | T | 1 | a0001c0001t0024g0100 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.636-826G>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141359 | |||||||
| chr5:134141364 | T | C | 2 | a0001c0001t0035g0112 a0001c0001t0050g0061 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.636-821T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141364 | |||||||
| chr5:134141411 | G | GC | 39 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(36): Show |
66 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.636-773dupC | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 134141411 | ||||||
| chr5:134141489 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.636-696A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141489 | |||||||
| chr5:134141566 | G | A | 1 | a0001c0001t0010g0160 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.636-619G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141566 | |||||||
| chr5:134141599 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02055.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.636-586C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141599 | |||||||
| chr5:134141638 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.636-547G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141638 | |||||||
| chr5:134141644 | C | T | 3 | a0001c0001t0035g0112 a0001c0001t0050g0061 a0001c0007t0021g0023 |
4 | HG00741.hp2 HG02809.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-541C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134141644 | |||||||
| chr5:134141782 | AG | A | 1 | a0001c0002t0006g0010 | 5 | HG01099.hp2 HG02647.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-401delG | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 134141782 | ||||||
| chr5:134142020 | A | G | 29 | a0001c0001t0003g0003 a0001c0001t0003g0037 a0001c0001t0003g0038 others(26): Show |
49 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.636-165A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134142020 | |||||||
| chr5:134142111 | C | T | 36 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
84 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.636-74C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 5/9 | chr5 | 134142111 | |||||||
| chr5:134142407 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.755+103G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 6/9 | chr5 | 134142407 | |||||||
| chr5:134142494 | G | A | 1 | a0001c0001t0039g0097 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.755+190G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 6/9 | chr5 | 134142494 | |||||||
| chr5:134142597 | G | A | 1 | a0001c0001t0022g0033 | 2 | NA18964.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.756-124G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 6/9 | chr5 | 134142597 | |||||||
| chr5:134142650 | G | A | 90 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(87): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.756-71G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 6/9 | chr5 | 134142650 | |||||||
| chr5:134142668 | A | C | 94 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.756-53A>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 6/9 | chr5 | 134142668 | |||||||
| chr5:134142922 | C | T | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.918+39C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 7/9 | chr5 | 134142922 | |||||||
| chr5:134142959 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.919-34G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 7/9 | chr5 | 134142959 | |||||||
| chr5:134143205 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1026+105C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 8/9 | chr5 | 134143205 | |||||||
| chr5:134143669 | G | A | 1 | a0001c0001t0003g0037 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1075+29G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143669 | |||||||
| chr5:134143702 | C | G | 16 | a0001c0001t0001g0095 a0001c0001t0013g0036 a0001c0001t0013g0146 others(13): Show |
18 | HG00741.hp2 HG01167.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.1075+62C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143702 | |||||||
| chr5:134143726 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1075+86G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143726 | |||||||
| chr5:134143764 | T | C | 1 | a0001c0001t0024g0098 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1075+124T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143764 | |||||||
| chr5:134143775 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1075+135C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143775 | |||||||
| chr5:134143830 | C | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1075+190C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143830 | |||||||
| chr5:134143897 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1075+257T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134143897 | |||||||
| chr5:134144053 | C | G | 4 | a0001c0002t0006g0010 a0001c0002t0006g0020 a0001c0002t0006g0169 others(1): Show |
10 | HG01099.hp2 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1075+413C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134144053 | |||||||
| chr5:134144177 | T | C | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1075+537T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134144177 | |||||||
| chr5:134144218 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1075+578G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134144218 | |||||||
| chr5:134144295 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1075+655C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134144295 | |||||||
| chr5:134144533 | G | A | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1075+893G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134144533 | |||||||
| chr5:134144897 | C | G | 4 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(1): Show |
5 | HG02630.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1075+1257C>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134144897 | |||||||
| chr5:134145045 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1076-1179G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145045 | |||||||
| chr5:134145097 | T | C | 4 | a0001c0001t0035g0112 a0001c0001t0041g0171 a0001c0001t0050g0061 others(1): Show |
5 | HG00741.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076-1127T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145097 | |||||||
| chr5:134145102 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1076-1122G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145102 | |||||||
| chr5:134145184 | C | T | 1 | a0001c0007t0021g0023 | 2 | HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1076-1040C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145184 | |||||||
| chr5:134145637 | A | G | 2 | a0001c0001t0046g0050 a0004c0005t0027g0147 |
2 | HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1076-587A>G | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145637 | |||||||
| chr5:134145702 | C | A | 1 | a0001c0001t0010g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1076-522C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145702 | |||||||
| chr5:134145744 | C | T | 15 | a0001c0001t0013g0036 a0001c0001t0013g0146 a0001c0001t0013g0148 others(12): Show |
17 | HG00741.hp2 HG01433.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1076-480C>T | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145744 | |||||||
| chr5:134145775 | T | C | 1 | a0001c0001t0004g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1076-449T>C | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145775 | |||||||
| chr5:134145776 | G | A | 36 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(33): Show |
84 | HG00280.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1076-448G>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134145776 | |||||||
| chr5:134145926 | GGAGATGA others(18): Show |
G | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1076-274_1076-250d others(27): Show |
TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 134145926 | ||||||
| chr5:134146058 | C | A | 6 | a0001c0001t0032g0062 a0001c0002t0006g0010 a0001c0002t0006g0020 others(3): Show |
12 | HG01099.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1076-166C>A | TCF7 | ENSG00000081059.20 | transcript | ENST00000342854.10 | protein_coding | 9/9 | chr5 | 134146058 |