Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7268 |
| ensemblid | ENSG00000243725.7 |
| hgncid | 12394 |
| symbol | TTC4 |
| name | tetratricopeptide repeat domain 4 |
| refseq_nuc | NM_004623.5 |
| refseq_prot | NP_004614.3 |
| ensembl_nuc | ENST00000371281.4 |
| ensembl_prot | ENSP00000360329.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 54715861 |
| end | 54742657 |
| strand | + |
| ver | v1.2 |
| region | chr1:54715861-54742657 |
| region5000 | chr1:54710861-54747657 |
| regionname0 | TTC4_chr1_54715861_54742657 |
| regionname5000 | TTC4_chr1_54710861_54747657 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 387 | 289 | 37 | 46 | 170 | 7 | 28 | 131 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0002 | 1/0 | 387 | 91 | 40 | 29 | 2 | 7 | 12 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0003 | 0/0 | 387 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0004 | 0/0 | 387 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0005 | 0/0 | 387 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0006 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0007 | 0/0 | 387 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| a0008 | 0/0 | 387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | MEQPG others(382): Show |
chr1 | 54710861 | 54747657 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1161 | 225 | 22 | 43 | 136 | 6 | 17 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0001c0003 | 0/0 | 1161 | 48 | 8 | 0 | 34 | 0 | 6 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0001c0004 | 0/0 | 1161 | 13 | 6 | 3 | 0 | 1 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0001c0008 | 0/0 | 1161 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0001c0009 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0002c0002 | 1/0 | 1161 | 91 | 40 | 29 | 2 | 7 | 12 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0003c0006 | 0/0 | 1161 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0004c0005 | 0/0 | 1161 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0005c0007 | 0/0 | 1161 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0006c0012 | 0/0 | 1161 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0007c0010 | 0/0 | 1161 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 | ||
| a0008c0011 | 0/0 | 1161 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | ATGGA others(1156): Show |
chr1 | 54710861 | 54747657 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2356 | 217 | 16 | 43 | 135 | 5 | 17 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0001c0001t0002 | 0/0 | 2356 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0001c0001t0006 | 0/0 | 2356 | 2 | 1 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0001c0001t0007 | 0/0 | 2356 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0001c0001t0009 | 0/0 | 2356 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0001c0003t0003 | 0/0 | 2351 | 45 | 5 | 0 | 34 | 0 | 6 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2346): Show |
chr1 | 54710861 | 54747657 |
| a0001c0003t0005 | 0/0 | 2351 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2346): Show |
chr1 | 54710861 | 54747657 |
| a0001c0003t0008 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2346): Show |
chr1 | 54710861 | 54747657 |
| a0001c0004t0003 | 0/0 | 2351 | 13 | 6 | 3 | 0 | 1 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2346): Show |
chr1 | 54710861 | 54747657 |
| a0001c0008t0001 | 0/0 | 2356 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0001c0009t0003 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2346): Show |
chr1 | 54710861 | 54747657 |
| a0002c0002t0001 | 0/0 | 2356 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0002c0002t0002 | 1/0 | 2356 | 73 | 23 | 28 | 2 | 7 | 12 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0002c0002t0003 | 0/0 | 2351 | 12 | 11 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2346): Show |
chr1 | 54710861 | 54747657 |
| a0002c0002t0004 | 0/0 | 2356 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | TCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0003c0006t0002 | 0/0 | 2356 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0004c0005t0001 | 0/0 | 2356 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0005c0007t0001 | 0/0 | 2356 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0006c0012t0001 | 0/0 | 2356 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0007c0010t0001 | 0/0 | 2356 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| a0008c0011t0002 | 0/0 | 2356 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | GCTCG others(2351): Show |
chr1 | 54710861 | 54747657 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 3 | 9 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 6 | 6 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0005 | 0/0 | 11 | 0 | 4 | 5 | 1 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0006 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0007 | 0/0 | 8 | 2 | 3 | 2 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0002g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0006g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0003t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0004t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0008t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0001c0009t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0001 | 0/0 | 27 | 4 | 13 | 0 | 5 | 5 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0008 | 1/0 | 7 | 3 | 1 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0014 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0002c0002t0004g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0003c0006t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0003c0006t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0003c0006t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0004c0005t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0004c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0005c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0005c0007t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0006c0012t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0007c0010t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| a0008c0011t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0007 | EUR | FIN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00408 | hp1 | a0001 | c0003 | t0003 | g0189 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0205 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00621 | hp2 | a0001 | c0003 | t0003 | g0204 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0087 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01074 | hp1 | a0001 | c0004 | t0003 | g0176 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01243 | hp2 | a0001 | c0004 | t0003 | g0052 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0065 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01358 | hp2 | a0006 | c0012 | t0001 | g0023 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01517 | hp2 | a0001 | c0004 | t0003 | g0174 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0016 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01891 | hp2 | a0001 | c0004 | t0003 | g0169 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02056 | hp1 | a0007 | c0010 | t0001 | g0004 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0055 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02135 | hp1 | a0001 | c0003 | t0003 | g0055 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02165 | hp2 | a0001 | c0003 | t0003 | g0011 | EAS | CDX | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02257 | hp1 | a0003 | c0006 | t0002 | g0033 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02258 | hp2 | a0004 | c0005 | t0001 | g0013 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02300 | hp1 | a0001 | c0004 | t0003 | g0173 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02572 | hp1 | a0001 | c0003 | t0005 | g0182 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02602 | hp1 | a0001 | c0004 | t0003 | g0175 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02615 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0061 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02647 | hp1 | a0001 | c0004 | t0003 | g0170 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0184 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0089 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02735 | hp2 | a0001 | c0004 | t0003 | g0053 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02809 | hp2 | a0001 | c0004 | t0003 | g0171 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02818 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0016 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0030 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02895 | hp2 | a0003 | c0006 | t0002 | g0022 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02897 | hp2 | a0003 | c0006 | t0002 | g0022 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02922 | hp1 | a0004 | c0005 | t0001 | g0013 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0068 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0088 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02976 | hp2 | a0002 | c0002 | t0003 | g0086 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03017 | hp1 | a0001 | c0004 | t0003 | g0053 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03017 | hp2 | a0001 | c0003 | t0003 | g0203 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03041 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03098 | hp1 | a0001 | c0004 | t0003 | g0052 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03130 | hp2 | a0004 | c0005 | t0001 | g0013 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03139 | hp2 | a0001 | c0004 | t0003 | g0177 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0179 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03209 | hp2 | a0001 | c0003 | t0005 | g0183 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03453 | hp1 | a0002 | c0002 | t0004 | g0015 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03453 | hp2 | a0004 | c0005 | t0001 | g0013 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03486 | hp1 | a0003 | c0006 | t0002 | g0033 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0036 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0070 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03490 | hp2 | a0001 | c0008 | t0001 | g0012 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03492 | hp1 | a0001 | c0008 | t0001 | g0012 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0060 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03516 | hp2 | a0001 | c0009 | t0003 | g0185 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0062 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03579 | hp2 | a0002 | c0002 | t0004 | g0015 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0200 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0008 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0083 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03834 | hp2 | a0001 | c0003 | t0003 | g0196 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0191 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0201 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0036 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18612 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18906 | hp1 | a0003 | c0006 | t0002 | g0022 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18906 | hp2 | a0001 | c0004 | t0003 | g0172 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18939 | hp2 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18942 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18944 | hp1 | a0005 | c0007 | t0001 | g0005 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18944 | hp2 | a0001 | c0003 | t0003 | g0209 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18946 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18953 | hp1 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18967 | hp2 | a0001 | c0003 | t0003 | g0192 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18970 | hp1 | a0001 | c0001 | t0009 | g0116 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18973 | hp2 | a0001 | c0003 | t0003 | g0197 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18991 | hp1 | a0001 | c0003 | t0003 | g0206 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18992 | hp2 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0193 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19010 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19011 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19043 | hp1 | a0003 | c0006 | t0002 | g0059 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0028 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19058 | hp1 | a0001 | c0003 | t0003 | g0028 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19062 | hp1 | a0001 | c0003 | t0003 | g0210 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19067 | hp1 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19067 | hp2 | a0001 | c0003 | t0003 | g0194 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19072 | hp1 | a0001 | c0003 | t0003 | g0187 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19075 | hp1 | a0001 | c0003 | t0003 | g0207 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19076 | hp2 | a0001 | c0003 | t0003 | g0190 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19079 | hp1 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19084 | hp2 | a0001 | c0003 | t0003 | g0028 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19088 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0168 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0092 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0178 | AFR | ASW | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | ASW | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0076 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0082 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20905 | hp1 | a0001 | c0003 | t0003 | g0188 | SAS | GIH | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | GIH | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02486 | hp1 | a0008 | c0011 | t0002 | g0063 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG02559 | hp2 | a0004 | c0005 | t0001 | g0013 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0085 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG06807 | hp1 | a0001 | c0003 | t0008 | g0186 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0181 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0120 | REF | REF | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0008 | REF | REF | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54715934 | C | T | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.26C>T | p.Thr9Ile | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/10 | 74/2356 | 26/1164 | 9/387 | chr1 | 54715934 | |||
| chr1:54716627 | T | A | 5 | a0001 a0004 a0005 others(2): Show |
299 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(296): Show |
missense_variant | MODERATE | c.139T>A | p.Ser47Thr | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/10 | 187/2356 | 139/1164 | 47/387 | chr1 | 54716627 | |||
| chr1:54717617 | C | T | 1 | a0005 | 3 | NA18944.hp1 NA19067.hp1 NA19079.hp1 |
missense_variant | MODERATE | c.355C>T | p.Leu119Phe | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/10 | 403/2356 | 355/1164 | 119/387 | chr1 | 54717617 | |||
| chr1:54717627 | A | G | 1 | a0007 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.365A>G | p.Asn122Ser | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/10 | 413/2356 | 365/1164 | 122/387 | chr1 | 54717627 | |||
| chr1:54722716 | G | A | 1 | a0008 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.511G>A | p.Val171Met | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/10 | 559/2356 | 511/1164 | 171/387 | chr1 | 54722716 | |||
| chr1:54722764 | C | T | 1 | a0004 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
missense_variant | MODERATE | c.559C>T | p.Leu187Phe | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/10 | 607/2356 | 559/1164 | 187/387 | chr1 | 54722764 | |||
| chr1:54741484 | C | T | 1 | a0003 | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.1135C>T | p.Arg379Trp | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 1183/2356 | 1135/1164 | 379/387 | chr1 | 54741484 | |||
| chr1:54742657 | A | C | 1 | a0001 | 2 | HG02922.hp2 NA20129.hp2 |
splice_region_variant | LOW | c.*1144A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | chr1 | 54742657 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54722709 | C | T | 3 | a0001c0003 a0001c0004 a0001c0009 |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
synonymous_variant | LOW | c.504C>T | p.Ala168Ala | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/10 | 552/2356 | 504/1164 | 168/387 | chr1 | 54722709 | |||
| chr1:54731647 | G | A | 1 | a0001c0004 | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
synonymous_variant | LOW | c.843G>A | p.Leu281Leu | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/10 | 891/2356 | 843/1164 | 281/387 | chr1 | 54731647 | |||
| chr1:54731647 | G | C | 1 | a0001c0008 | 2 | HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.843G>C | p.Leu281Leu | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/10 | 891/2356 | 843/1164 | 281/387 | chr1 | 54731647 | |||
| chr1:54737612 | C | T | 1 | a0001c0009 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1009C>T | p.Leu337Leu | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/10 | 1057/2356 | 1009/1164 | 337/387 | chr1 | 54737612 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54715861 | G | T | 1 | a0002c0002t0004 | 4 | HG02615.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-48G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/10 | 48 | chr1 | 54715861 | ||||||
| chr1:54741543 | T | C | 7 | a0001c0001t0009 a0001c0003t0003 a0001c0003t0005 others(4): Show |
75 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*30T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 30 | chr1 | 54741543 | ||||||
| chr1:54741861 | T | G | 1 | a0001c0001t0006 | 2 | HG00323.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*348T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 348 | chr1 | 54741861 | ||||||
| chr1:54741865 | G | A | 6 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0008 others(3): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*352G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 352 | chr1 | 54741865 | ||||||
| chr1:54741911 | CACAA | C | 6 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0008 others(3): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*407_*410delACAA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 407 | INFO_REALIGN_3_PRIME | chr1 | 54741911 | |||||
| chr1:54742081 | C | G | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(14): Show |
314 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*568C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 568 | chr1 | 54742081 | ||||||
| chr1:54742112 | A | G | 1 | a0001c0003t0005 | 2 | HG02572.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 599 | chr1 | 54742112 | ||||||
| chr1:54742150 | CT | C | 6 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0008 others(3): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*640delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 640 | INFO_REALIGN_3_PRIME | chr1 | 54742150 | |||||
| chr1:54742245 | C | T | 5 | a0001c0003t0003 a0001c0003t0005 a0001c0004t0003 others(2): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*732C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 732 | chr1 | 54742245 | ||||||
| chr1:54742310 | T | C | 6 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0008 others(3): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*797T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 797 | chr1 | 54742310 | ||||||
| chr1:54742311 | T | C | 6 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0008 others(3): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*798T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 798 | chr1 | 54742311 | ||||||
| chr1:54742531 | C | T | 6 | a0001c0003t0003 a0001c0003t0005 a0001c0003t0008 others(3): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1018C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 1018 | chr1 | 54742531 | ||||||
| chr1:54742626 | G | C | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(14): Show |
314 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1113G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 1113 | chr1 | 54742626 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:54716170 | G | T | 38 | a0001c0001t0002g0054 a0001c0001t0002g0180 a0001c0003t0003g0011 others(35): Show |
51 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.111+151G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716170 | |||||||
| chr1:54716257 | TACTTA | T | 12 | a0001c0003t0003g0168 a0001c0004t0003g0052 a0001c0004t0003g0053 others(9): Show |
14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+243_111+247del others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 54716257 | ||||||
| chr1:54716363 | G | C | 2 | a0002c0002t0002g0056 a0002c0002t0002g0057 |
2 | HG00639.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.112-237G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716363 | |||||||
| chr1:54716393 | T | C | 1 | a0002c0002t0002g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.112-207T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716393 | |||||||
| chr1:54716556 | A | G | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-44A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716556 | |||||||
| chr1:54716775 | G | A | 38 | a0001c0001t0002g0054 a0001c0001t0002g0180 a0001c0003t0003g0011 others(35): Show |
51 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.229+58G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54716775 | |||||||
| chr1:54716877 | C | T | 50 | a0001c0001t0002g0054 a0001c0001t0002g0180 a0001c0003t0003g0011 others(47): Show |
65 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.229+160C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54716877 | |||||||
| chr1:54716905 | G | A | 50 | a0001c0001t0002g0054 a0001c0001t0002g0180 a0001c0003t0003g0011 others(47): Show |
65 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.229+188G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54716905 | |||||||
| chr1:54717022 | G | A | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.229+305G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717022 | |||||||
| chr1:54717031 | A | G | 1 | a0001c0003t0008g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.229+314A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717031 | |||||||
| chr1:54717428 | A | G | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.230-64A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717428 | |||||||
| chr1:54717459 | A | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.230-33A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717459 | |||||||
| chr1:54717855 | C | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+202C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54717855 | |||||||
| chr1:54718137 | T | C | 12 | a0001c0003t0003g0168 a0001c0004t0003g0052 a0001c0004t0003g0053 others(9): Show |
14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+484T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718137 | |||||||
| chr1:54718280 | C | T | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+627C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718280 | |||||||
| chr1:54718287 | C | T | 32 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(29): Show |
44 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.391+634C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718287 | |||||||
| chr1:54718288 | G | A | 9 | a0001c0004t0003g0169 a0002c0002t0002g0029 a0002c0002t0002g0030 others(6): Show |
12 | HG01175.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+635G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718288 | |||||||
| chr1:54718414 | T | G | 2 | a0001c0001t0001g0064 a0001c0003t0003g0168 |
2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.391+761T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718414 | |||||||
| chr1:54718416 | T | C | 36 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(33): Show |
48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.391+763T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718416 | |||||||
| chr1:54718458 | G | A | 5 | a0001c0003t0003g0181 a0001c0003t0003g0184 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+805G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718458 | |||||||
| chr1:54718468 | C | T | 4 | a0001c0003t0003g0181 a0001c0003t0005g0182 a0001c0003t0005g0183 others(1): Show |
4 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+815C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718468 | |||||||
| chr1:54718502 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0166 a0001c0001t0001g0167 |
5 | HG02055.hp2 HG02258.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+849C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718502 | |||||||
| chr1:54718536 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
232 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.391+883C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718536 | |||||||
| chr1:54718613 | C | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+960C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718613 | |||||||
| chr1:54718787 | A | T | 49 | a0001c0001t0001g0051 a0001c0003t0003g0011 a0001c0003t0003g0021 others(46): Show |
64 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.391+1134A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718787 | |||||||
| chr1:54718788 | A | G | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+1135A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718788 | |||||||
| chr1:54718788 | A | T | 32 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(29): Show |
44 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.391+1135A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718788 | |||||||
| chr1:54718823 | C | A | 1 | a0002c0002t0002g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.391+1170C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718823 | |||||||
| chr1:54718896 | T | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1243T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718896 | |||||||
| chr1:54718954 | G | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1301G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718954 | |||||||
| chr1:54718984 | C | CT | 5 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0003t0003g0178 others(2): Show |
5 | HG02922.hp2 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+1337dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54718984 | ||||||
| chr1:54719116 | T | C | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1463T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719116 | |||||||
| chr1:54719206 | G | A | 2 | a0004c0005t0001g0013 a0004c0005t0001g0092 |
6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+1553G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719206 | |||||||
| chr1:54719264 | C | T | 1 | a0001c0001t0001g0027 | 3 | HG02258.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391+1611C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719264 | |||||||
| chr1:54719301 | G | GTACTTTG others(54): Show |
28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.391+1663_391+1664i others(63): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719301 | ||||||
| chr1:54719301 | G | GTACTTTG others(179): Show |
8 | a0001c0003t0003g0178 a0001c0003t0003g0179 a0001c0003t0003g0181 others(5): Show |
8 | HG02572.hp1 HG02723.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.391+1698_391+1699i others(188): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719301 | ||||||
| chr1:54719301 | G | GTACTTTG others(179): Show |
12 | a0001c0003t0003g0168 a0001c0004t0003g0052 a0001c0004t0003g0053 others(9): Show |
14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+1698_391+1699i others(188): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719301 | ||||||
| chr1:54719307 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.391+1654T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719307 | |||||||
| chr1:54719352 | A | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1699A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719352 | |||||||
| chr1:54719531 | C | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1632C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719531 | |||||||
| chr1:54719689 | A | C | 1 | a0001c0004t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.392-1474A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719689 | |||||||
| chr1:54719794 | G | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1369G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719794 | |||||||
| chr1:54719811 | A | T | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.392-1352A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719811 | |||||||
| chr1:54719896 | C | CT | 10 | a0001c0003t0003g0028 a0001c0003t0003g0184 a0001c0003t0003g0206 others(7): Show |
12 | HG01891.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.392-1248dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719896 | ||||||
| chr1:54719896 | C | CTT | 9 | a0001c0003t0003g0168 a0001c0004t0003g0052 a0001c0004t0003g0053 others(6): Show |
11 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.392-1249_392-1248d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719896 | ||||||
| chr1:54719896 | CT | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0094 a0001c0001t0001g0095 others(11): Show |
15 | HG01168.hp2 HG01256.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.392-1248delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719896 | ||||||
| chr1:54719959 | T | C | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1204T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719959 | |||||||
| chr1:54719971 | A | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1192A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719971 | |||||||
| chr1:54720025 | A | C | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1138A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720025 | |||||||
| chr1:54720090 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.392-1073G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720090 | |||||||
| chr1:54720285 | A | G | 3 | a0001c0001t0001g0165 a0001c0003t0003g0204 a0001c0003t0003g0205 |
3 | HG00423.hp1 HG00621.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.392-878A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720285 | |||||||
| chr1:54720314 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.392-849C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720314 | |||||||
| chr1:54720437 | CT | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(29): Show |
59 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.392-711delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54720437 | ||||||
| chr1:54720452 | T | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-711T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720452 | |||||||
| chr1:54720489 | T | C | 2 | a0002c0002t0002g0029 a0003c0006t0002g0059 |
3 | HG01175.hp2 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.392-674T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720489 | |||||||
| chr1:54720493 | GT | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(42): Show |
85 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.392-655delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54720493 | ||||||
| chr1:54720505 | TTTTA | T | 13 | a0001c0003t0003g0168 a0001c0003t0003g0187 a0001c0004t0003g0052 others(10): Show |
15 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.392-657_392-654del others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720505 | |||||||
| chr1:54720506 | TTTA | T | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.392-656_392-654del others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720506 | |||||||
| chr1:54720507 | TTA | T | 7 | a0001c0003t0003g0178 a0001c0003t0003g0179 a0001c0003t0003g0184 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-655_392-654del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720507 | |||||||
| chr1:54720722 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.392-441C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720722 | |||||||
| chr1:54720818 | C | G | 8 | a0002c0002t0003g0016 a0002c0002t0003g0036 a0002c0002t0003g0068 others(5): Show |
12 | HG00642.hp2 HG01891.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.392-345C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720818 | |||||||
| chr1:54720942 | C | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-221C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720942 | |||||||
| chr1:54720989 | G | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0041 others(8): Show |
23 | HG00621.hp1 HG01255.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.392-174G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720989 | |||||||
| chr1:54721013 | G | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-150G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54721013 | |||||||
| chr1:54721252 | G | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.469+12G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721252 | |||||||
| chr1:54721468 | T | G | 36 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(33): Show |
48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.469+228T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721468 | |||||||
| chr1:54721493 | C | T | 12 | a0001c0003t0003g0168 a0001c0004t0003g0052 a0001c0004t0003g0053 others(9): Show |
14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.469+253C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721493 | |||||||
| chr1:54721494 | C | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.469+254C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721494 | |||||||
| chr1:54721624 | G | T | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.469+384G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721624 | |||||||
| chr1:54721829 | A | C | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.469+589A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721829 | |||||||
| chr1:54721926 | G | T | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.469+686G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721926 | |||||||
| chr1:54722016 | A | G | 8 | a0001c0003t0003g0178 a0001c0003t0003g0179 a0001c0003t0003g0181 others(5): Show |
8 | HG02572.hp1 HG02723.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-659A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722016 | |||||||
| chr1:54722052 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.470-623T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722052 | |||||||
| chr1:54722129 | A | AT | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
195 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.470-529dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54722129 | ||||||
| chr1:54722129 | A | ATT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(11): Show |
20 | HG00673.hp1 HG00673.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-530_470-529dup others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54722129 | ||||||
| chr1:54722129 | ATT | A | 43 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(40): Show |
57 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.470-530_470-529del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54722129 | ||||||
| chr1:54722349 | C | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.470-326C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722349 | |||||||
| chr1:54722516 | G | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.470-159G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722516 | |||||||
| chr1:54722518 | A | G | 36 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(33): Show |
48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.470-157A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722518 | |||||||
| chr1:54722576 | G | A | 36 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(33): Show |
48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.470-99G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722576 | |||||||
| chr1:54722581 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.470-94T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722581 | |||||||
| chr1:54722596 | G | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.470-79G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722596 | |||||||
| chr1:54722819 | CAATTAGC others(17): Show |
C | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+31_594+54delTG others(22): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54722819 | ||||||
| chr1:54722974 | G | T | 1 | a0001c0001t0001g0050 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.594+175G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54722974 | |||||||
| chr1:54723110 | CTGTGTTT others(3): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.594+321_594+330del others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54723110 | ||||||
| chr1:54723121 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.594+322T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723121 | |||||||
| chr1:54723158 | G | A | 1 | a0001c0004t0003g0172 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.594+359G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723158 | |||||||
| chr1:54723165 | A | G | 1 | a0002c0002t0004g0015 | 4 | HG02615.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+366A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723165 | |||||||
| chr1:54723169 | G | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+370G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723169 | |||||||
| chr1:54723205 | T | C | 50 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0003t0003g0011 others(47): Show |
64 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.594+406T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723205 | |||||||
| chr1:54723268 | G | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+469G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723268 | |||||||
| chr1:54723347 | C | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+548C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723347 | |||||||
| chr1:54723406 | G | C | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.594+607G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723406 | |||||||
| chr1:54723456 | C | T | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.594+657C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723456 | |||||||
| chr1:54723457 | G | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0100 |
4 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+658G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723457 | |||||||
| chr1:54723512 | G | A | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+713G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723512 | |||||||
| chr1:54723525 | A | G | 1 | a0002c0002t0002g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.594+726A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723525 | |||||||
| chr1:54723550 | A | G | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+751A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723550 | |||||||
| chr1:54723735 | G | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+936G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723735 | |||||||
| chr1:54723796 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+997A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723796 | |||||||
| chr1:54723826 | T | C | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.594+1027T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723826 | |||||||
| chr1:54723955 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0162 a0001c0001t0001g0163 |
4 | HG02523.hp1 NA19012.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1156A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723955 | |||||||
| chr1:54724040 | T | C | 1 | a0001c0003t0003g0188 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.594+1241T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724040 | |||||||
| chr1:54724107 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.594+1308A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724107 | |||||||
| chr1:54724120 | C | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1321C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724120 | |||||||
| chr1:54724125 | G | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.594+1326G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724125 | |||||||
| chr1:54724197 | G | A | 1 | a0001c0003t0003g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.594+1398G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724197 | |||||||
| chr1:54724268 | C | CT | 17 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(14): Show |
19 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.594+1481dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54724268 | ||||||
| chr1:54724268 | C | CTT | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1480_594+1481d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54724268 | ||||||
| chr1:54724410 | C | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1611C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724410 | |||||||
| chr1:54724428 | G | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1629G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724428 | |||||||
| chr1:54724574 | C | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+1775C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724574 | |||||||
| chr1:54724644 | C | T | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.594+1845C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724644 | |||||||
| chr1:54724677 | CTT | C | 2 | a0004c0005t0001g0013 a0004c0005t0001g0092 |
6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1879_594+1880d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724677 | |||||||
| chr1:54724679 | T | G | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1880T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724679 | |||||||
| chr1:54724780 | G | A | 38 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(35): Show |
54 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.594+1981G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724780 | |||||||
| chr1:54724865 | C | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.594+2066C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724865 | |||||||
| chr1:54725003 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
309 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.594+2204T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725003 | |||||||
| chr1:54725217 | G | C | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+2418G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725217 | |||||||
| chr1:54725330 | C | G | 1 | a0001c0001t0001g0020 | 4 | HG00423.hp2 HG00438.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+2531C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725330 | |||||||
| chr1:54725369 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.594+2570A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725369 | |||||||
| chr1:54725400 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+2601C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725400 | |||||||
| chr1:54725728 | A | G | 59 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0099 others(56): Show |
80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.595-2618A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725728 | |||||||
| chr1:54725732 | G | A | 4 | a0001c0004t0003g0052 a0001c0004t0003g0170 a0001c0004t0003g0171 others(1): Show |
5 | HG01243.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-2614G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725732 | |||||||
| chr1:54725864 | A | C | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.595-2482A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725864 | |||||||
| chr1:54725923 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0094 a0001c0001t0001g0101 others(56): Show |
88 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.595-2423G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725923 | |||||||
| chr1:54725958 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.595-2388A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725958 | |||||||
| chr1:54725971 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(173): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.595-2375T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725971 | |||||||
| chr1:54725976 | C | G | 1 | a0001c0003t0008g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.595-2370C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725976 | |||||||
| chr1:54726029 | G | A | 1 | a0001c0003t0003g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.595-2317G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726029 | |||||||
| chr1:54726212 | C | T | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.595-2134C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726212 | |||||||
| chr1:54726337 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.595-2009A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726337 | |||||||
| chr1:54726608 | T | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
309 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.595-1738T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726608 | |||||||
| chr1:54726676 | T | C | 3 | a0003c0006t0002g0022 a0003c0006t0002g0033 a0003c0006t0002g0059 |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-1670T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726676 | |||||||
| chr1:54726767 | C | T | 48 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(45): Show |
62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.595-1579C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726767 | |||||||
| chr1:54726863 | C | CCTGG | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(23): Show |
52 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.595-1482_595-1479d others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54726863 | ||||||
| chr1:54727055 | C | CA | 5 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0002c0002t0002g0030 others(2): Show |
6 | HG01981.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-1275dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727055 | ||||||
| chr1:54727055 | CA | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.595-1275delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727055 | ||||||
| chr1:54727068 | A | AC | 41 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(38): Show |
57 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.595-1278_595-1277i others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727068 | |||||||
| chr1:54727068 | A | C | 10 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(7): Show |
12 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-1278A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727068 | |||||||
| chr1:54727074 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-1272A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727074 | |||||||
| chr1:54727112 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-1234G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727112 | |||||||
| chr1:54727265 | C | G | 1 | a0004c0005t0001g0092 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.595-1081C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727265 | |||||||
| chr1:54727362 | G | T | 1 | a0001c0001t0007g0091 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.595-984G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727362 | |||||||
| chr1:54727509 | T | G | 9 | a0001c0003t0003g0184 a0002c0002t0003g0016 a0002c0002t0003g0036 others(6): Show |
13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.595-837T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727509 | |||||||
| chr1:54727539 | A | AAAGTT | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-804_595-803ins others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727539 | ||||||
| chr1:54727554 | G | GA | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-786dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727554 | ||||||
| chr1:54727607 | T | G | 1 | a0002c0002t0002g0061 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.595-739T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727607 | |||||||
| chr1:54727649 | C | T | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.595-697C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727649 | |||||||
| chr1:54727688 | C | CA | 29 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
45 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.595-636dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727688 | ||||||
| chr1:54727688 | CA | C | 6 | a0001c0001t0001g0115 a0001c0001t0001g0158 a0001c0001t0007g0090 others(3): Show |
6 | HG01070.hp1 HG02922.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-636delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727688 | ||||||
| chr1:54727688 | CAAAAAAA others(4): Show |
C | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.595-646_595-636del others(11): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727688 | ||||||
| chr1:54727736 | C | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-610C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727736 | |||||||
| chr1:54727743 | G | T | 58 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0003t0003g0011 others(55): Show |
76 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.595-603G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727743 | |||||||
| chr1:54727804 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0154 |
4 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-542A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727804 | |||||||
| chr1:54727845 | C | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.595-501C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727845 | |||||||
| chr1:54727953 | C | A | 1 | a0001c0001t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.595-393C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727953 | |||||||
| chr1:54728016 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-330A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728016 | |||||||
| chr1:54728023 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-323G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728023 | |||||||
| chr1:54728041 | G | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-305G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728041 | |||||||
| chr1:54728043 | C | G | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.595-303C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728043 | |||||||
| chr1:54728199 | T | G | 9 | a0001c0003t0003g0184 a0002c0002t0003g0016 a0002c0002t0003g0036 others(6): Show |
13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.595-147T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728199 | |||||||
| chr1:54728515 | C | G | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+83C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728515 | |||||||
| chr1:54728620 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+188A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728620 | |||||||
| chr1:54728682 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+250T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728682 | |||||||
| chr1:54728710 | C | G | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+278C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728710 | |||||||
| chr1:54728831 | T | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0139 |
3 | NA18957.hp1 NA18993.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.681+399T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728831 | |||||||
| chr1:54728851 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+419T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728851 | |||||||
| chr1:54729021 | C | A | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+589C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729021 | |||||||
| chr1:54729140 | G | A | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+708G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729140 | |||||||
| chr1:54729169 | C | T | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.681+737C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729169 | |||||||
| chr1:54729198 | C | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+766C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729198 | |||||||
| chr1:54729298 | GGTAACTG others(7): Show |
G | 1 | a0001c0003t0003g0190 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.681+868_681+881del others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54729298 | ||||||
| chr1:54729308 | T | A | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.681+876T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729308 | |||||||
| chr1:54729514 | C | T | 1 | a0001c0001t0001g0051 | 2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.681+1082C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729514 | |||||||
| chr1:54729675 | A | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+1243A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729675 | |||||||
| chr1:54729727 | G | GT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(83): Show |
134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.681+1309dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54729727 | ||||||
| chr1:54729845 | C | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+1413C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729845 | |||||||
| chr1:54729913 | G | A | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.681+1481G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729913 | |||||||
| chr1:54730001 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1485G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730001 | |||||||
| chr1:54730006 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(25): Show |
57 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.682-1480C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730006 | |||||||
| chr1:54730021 | G | A | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.682-1465G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730021 | |||||||
| chr1:54730024 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1462G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730024 | |||||||
| chr1:54730027 | G | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1459G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730027 | |||||||
| chr1:54730155 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1331T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730155 | |||||||
| chr1:54730235 | T | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1251T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730235 | |||||||
| chr1:54730241 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.682-1245A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730241 | |||||||
| chr1:54730247 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1239A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730247 | |||||||
| chr1:54730280 | C | CT | 45 | a0001c0001t0001g0132 a0001c0001t0001g0144 a0001c0001t0001g0154 others(42): Show |
66 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.682-1189dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730280 | ||||||
| chr1:54730280 | CT | C | 22 | a0001c0001t0001g0151 a0001c0001t0002g0054 a0001c0001t0002g0180 others(19): Show |
26 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.682-1189delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730280 | ||||||
| chr1:54730342 | A | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1144A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730342 | |||||||
| chr1:54730426 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
307 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.682-1060G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730426 | |||||||
| chr1:54730434 | A | G | 1 | a0001c0001t0001g0019 | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-1052A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730434 | |||||||
| chr1:54730664 | A | G | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.682-822A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730664 | |||||||
| chr1:54730789 | T | TTTC | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.682-694_682-692dup others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730789 | ||||||
| chr1:54730793 | T | TTC | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.682-692_682-691ins others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730793 | ||||||
| chr1:54730807 | T | A | 1 | a0003c0006t0002g0033 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.682-679T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730807 | |||||||
| chr1:54731063 | G | C | 1 | a0002c0002t0002g0075 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.682-423G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731063 | |||||||
| chr1:54731066 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-420G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731066 | |||||||
| chr1:54731134 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.682-352G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731134 | |||||||
| chr1:54731218 | GTTT | G | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.682-261_682-259del others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54731218 | ||||||
| chr1:54731224 | T | TG | 12 | a0001c0003t0003g0178 a0001c0003t0003g0179 a0001c0003t0003g0184 others(9): Show |
16 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.682-262_682-261ins others(1): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731224 | |||||||
| chr1:54731476 | T | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(58): Show |
120 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.682-10T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731476 | |||||||
| chr1:54731849 | T | C | 5 | a0001c0004t0003g0053 a0001c0004t0003g0173 a0001c0004t0003g0174 others(2): Show |
6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+149T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731849 | |||||||
| chr1:54731855 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+155T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731855 | |||||||
| chr1:54731859 | T | TGAACCTT others(5): Show |
56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+160_896+171dup others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54731859 | ||||||
| chr1:54731874 | T | C | 4 | a0001c0003t0003g0028 a0001c0003t0003g0206 a0001c0003t0003g0207 others(1): Show |
6 | NA18953.hp1 NA18991.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+174T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731874 | |||||||
| chr1:54731875 | A | G | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.896+175A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731875 | |||||||
| chr1:54732046 | T | G | 54 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(51): Show |
72 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.896+346T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732046 | |||||||
| chr1:54732227 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.896+527A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732227 | |||||||
| chr1:54732287 | C | T | 1 | a0001c0001t0001g0048 | 2 | NA18968.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.896+587C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732287 | |||||||
| chr1:54732316 | G | C | 5 | a0001c0004t0003g0053 a0001c0004t0003g0173 a0001c0004t0003g0174 others(2): Show |
6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+616G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732316 | |||||||
| chr1:54732334 | AAT | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0099 others(6): Show |
9 | HG01069.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+636_896+637del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54732334 | ||||||
| chr1:54732335 | AT | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.896+636delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732335 | |||||||
| chr1:54732336 | T | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0104 others(44): Show |
61 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.896+636T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732336 | |||||||
| chr1:54732393 | G | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+693G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732393 | |||||||
| chr1:54732448 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+748G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732448 | |||||||
| chr1:54732452 | T | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
177 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.896+752T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732452 | |||||||
| chr1:54732459 | A | AT | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0135 others(6): Show |
9 | HG00597.hp2 HG01175.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+775dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54732459 | ||||||
| chr1:54732459 | AT | A | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.896+775delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54732459 | ||||||
| chr1:54732464 | T | C | 2 | a0004c0005t0001g0013 a0004c0005t0001g0092 |
6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+764T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732464 | |||||||
| chr1:54732542 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.896+842T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732542 | |||||||
| chr1:54732568 | C | T | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.896+868C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732568 | |||||||
| chr1:54732660 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+960A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732660 | |||||||
| chr1:54732694 | G | A | 57 | a0001c0001t0001g0110 a0001c0003t0003g0011 a0001c0003t0003g0021 others(54): Show |
75 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.897-935G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732694 | |||||||
| chr1:54732709 | C | G | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.897-920C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732709 | |||||||
| chr1:54732777 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-852T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732777 | |||||||
| chr1:54732778 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-851T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732778 | |||||||
| chr1:54732813 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-816T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732813 | |||||||
| chr1:54732931 | T | C | 9 | a0001c0003t0003g0184 a0002c0002t0003g0016 a0002c0002t0003g0036 others(6): Show |
13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.897-698T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732931 | |||||||
| chr1:54732950 | G | A | 4 | a0001c0003t0003g0181 a0001c0003t0005g0182 a0001c0003t0005g0183 others(1): Show |
4 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-679G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732950 | |||||||
| chr1:54732960 | G | T | 2 | a0004c0005t0001g0013 a0004c0005t0001g0092 |
6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.897-669G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732960 | |||||||
| chr1:54732961 | C | A | 1 | a0002c0002t0002g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.897-668C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732961 | |||||||
| chr1:54732994 | C | T | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.897-635C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732994 | |||||||
| chr1:54732995 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.897-634G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732995 | |||||||
| chr1:54733093 | C | CA | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-525dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733093 | ||||||
| chr1:54733155 | C | T | 1 | a0002c0002t0002g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.897-474C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733155 | |||||||
| chr1:54733156 | C | T | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.897-473C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733156 | |||||||
| chr1:54733168 | TA | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-459delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733168 | ||||||
| chr1:54733216 | A | G | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.897-413A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733216 | |||||||
| chr1:54733246 | C | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.897-383C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733246 | |||||||
| chr1:54733247 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-382A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733247 | |||||||
| chr1:54733254 | CA | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-367delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733254 | ||||||
| chr1:54733309 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.897-320A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733309 | |||||||
| chr1:54733323 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0108 |
3 | NA18955.hp2 NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.897-306G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733323 | |||||||
| chr1:54733418 | CAA | C | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.897-200_897-199del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733418 | ||||||
| chr1:54733418 | CAAAAAAA | C | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.897-205_897-199del others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733418 | ||||||
| chr1:54733426 | A | T | 17 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(14): Show |
19 | HG01074.hp1 HG01175.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.897-203A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733426 | |||||||
| chr1:54733426 | AAAAAT | A | 3 | a0003c0006t0002g0022 a0003c0006t0002g0033 a0003c0006t0002g0059 |
6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.897-182_897-178del others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733426 | ||||||
| chr1:54733427 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.897-202A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733427 | |||||||
| chr1:54733431 | T | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
234 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.897-198T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733431 | |||||||
| chr1:54733432 | A | AT | 4 | a0001c0001t0001g0026 a0001c0001t0001g0100 a0001c0001t0001g0144 others(1): Show |
6 | HG01516.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.897-197_897-196ins others(1): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733432 | |||||||
| chr1:54733432 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
225 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.897-197A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733432 | |||||||
| chr1:54733743 | ATTAATTT others(4): Show |
A | 1 | a0002c0002t0003g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.978+36_978+46delAA others(9): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733743 | ||||||
| chr1:54733746 | AATTTTTT others(2): Show |
A | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+37_978+45delAT others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | |||||||
| chr1:54733746 | AATTTTTT others(3): Show |
A | 15 | a0001c0003t0003g0178 a0001c0003t0003g0179 a0001c0003t0003g0193 others(12): Show |
17 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.978+37_978+46delAT others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | |||||||
| chr1:54733746 | AATTTTTT others(4): Show |
A | 34 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(31): Show |
50 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.978+37_978+47delAT others(9): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | |||||||
| chr1:54733746 | AATTTTTT others(5): Show |
A | 1 | a0002c0002t0003g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.978+37_978+48delAT others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | |||||||
| chr1:54733747 | A | AT | 12 | a0002c0002t0001g0072 a0002c0002t0001g0084 a0002c0002t0002g0001 others(9): Show |
21 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.978+63dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | ||||||
| chr1:54733747 | AT | A | 6 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0002c0002t0002g0001 others(3): Show |
8 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+63delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | ||||||
| chr1:54733747 | ATTTTTTT | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
16 | HG01358.hp2 HG02056.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.978+57_978+63delTT others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | ||||||
| chr1:54733747 | ATTTTTTT others(1): Show |
A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
168 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.978+56_978+63delTT others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | ||||||
| chr1:54733747 | ATTTTTTT others(2): Show |
A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(19): Show |
39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.978+55_978+63delTT others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | ||||||
| chr1:54733747 | ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0095 others(4): Show |
8 | HG02129.hp1 NA18951.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+54_978+63delTT others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | ||||||
| chr1:54733758 | T | A | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+48T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733758 | |||||||
| chr1:54733759 | T | A | 15 | a0001c0003t0003g0178 a0001c0003t0003g0179 a0001c0003t0003g0193 others(12): Show |
17 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.978+49T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733759 | |||||||
| chr1:54733760 | T | A | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.978+50T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733760 | |||||||
| chr1:54733761 | T | A | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+51T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733761 | |||||||
| chr1:54733762 | T | A | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+52T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733762 | |||||||
| chr1:54733764 | T | A | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+54T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733764 | |||||||
| chr1:54733814 | T | G | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.978+104T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733814 | |||||||
| chr1:54733858 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.978+148T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733858 | |||||||
| chr1:54733907 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.978+197A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733907 | |||||||
| chr1:54734043 | T | C | 2 | a0001c0001t0007g0090 a0001c0001t0007g0091 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.978+333T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734043 | |||||||
| chr1:54734079 | T | A | 5 | a0001c0003t0003g0181 a0001c0003t0005g0182 a0001c0003t0005g0183 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+369T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734079 | |||||||
| chr1:54734080 | T | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+370T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734080 | |||||||
| chr1:54734081 | T | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+371T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734081 | |||||||
| chr1:54734095 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.978+385G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734095 | |||||||
| chr1:54734186 | C | T | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+476C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734186 | |||||||
| chr1:54734212 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+502T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734212 | |||||||
| chr1:54734272 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.978+562A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734272 | |||||||
| chr1:54734325 | G | A | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.978+615G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734325 | |||||||
| chr1:54734347 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+637T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734347 | |||||||
| chr1:54734363 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+653T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734363 | |||||||
| chr1:54734463 | G | A | 58 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0003t0003g0011 others(55): Show |
76 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.978+753G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734463 | |||||||
| chr1:54734535 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+825T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734535 | |||||||
| chr1:54734579 | G | A | 1 | a0001c0004t0003g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.978+869G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734579 | |||||||
| chr1:54735063 | C | CT | 9 | a0002c0002t0002g0083 a0002c0002t0003g0016 a0002c0002t0003g0036 others(6): Show |
13 | HG00642.hp2 HG01891.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+1364dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54735063 | ||||||
| chr1:54735125 | G | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1415G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735125 | |||||||
| chr1:54735127 | C | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1417C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735127 | |||||||
| chr1:54735156 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.978+1446G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735156 | |||||||
| chr1:54735156 | G | T | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+1446G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735156 | |||||||
| chr1:54735163 | G | A | 1 | a0002c0002t0002g0080 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.978+1453G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735163 | |||||||
| chr1:54735310 | C | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1600C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735310 | |||||||
| chr1:54735338 | C | G | 2 | a0001c0001t0007g0090 a0001c0001t0007g0091 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.978+1628C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735338 | |||||||
| chr1:54735370 | A | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1660A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735370 | |||||||
| chr1:54735377 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0166 |
2 | HG00408.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.978+1667G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735377 | |||||||
| chr1:54735438 | C | G | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.978+1728C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735438 | |||||||
| chr1:54735461 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.978+1751T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735461 | |||||||
| chr1:54735516 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.978+1806C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735516 | |||||||
| chr1:54735575 | C | T | 1 | a0001c0004t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978+1865C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735575 | |||||||
| chr1:54735588 | G | A | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.978+1878G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735588 | |||||||
| chr1:54735592 | A | ATAATCTC others(4): Show |
1 | a0001c0003t0003g0190 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.978+1884_978+1894d others(13): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54735592 | ||||||
| chr1:54735719 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.979-1863C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735719 | |||||||
| chr1:54735748 | C | T | 1 | a0001c0004t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.979-1834C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735748 | |||||||
| chr1:54735765 | A | G | 16 | a0002c0002t0002g0001 a0002c0002t0002g0014 a0002c0002t0002g0032 others(13): Show |
50 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.979-1817A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735765 | |||||||
| chr1:54735891 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.979-1691T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735891 | |||||||
| chr1:54736147 | G | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1435G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736147 | |||||||
| chr1:54736149 | G | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1433G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736149 | |||||||
| chr1:54736155 | A | C | 9 | a0001c0003t0003g0184 a0002c0002t0003g0016 a0002c0002t0003g0036 others(6): Show |
13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.979-1427A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736155 | |||||||
| chr1:54736156 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1426A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736156 | |||||||
| chr1:54736157 | G | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1425G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736157 | |||||||
| chr1:54736158 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1424A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736158 | |||||||
| chr1:54736160 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1422A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736160 | |||||||
| chr1:54736163 | G | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1419G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736163 | |||||||
| chr1:54736164 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1418A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736164 | |||||||
| chr1:54736164 | AAAGAAAG others(4): Show |
A | 15 | a0001c0003t0003g0178 a0001c0003t0003g0184 a0001c0003t0003g0201 others(12): Show |
19 | HG00642.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.979-1417_979-1407d others(13): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736164 | |||||||
| chr1:54736165 | A | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1417A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736165 | |||||||
| chr1:54736165 | A | G | 41 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(38): Show |
55 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.979-1417A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736165 | |||||||
| chr1:54736168 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1414A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736168 | |||||||
| chr1:54736168 | AAAGAAAG | A | 16 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0179 others(13): Show |
22 | HG00408.hp1 HG00621.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.979-1413_979-1407d others(9): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736168 | |||||||
| chr1:54736169 | A | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1413A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736169 | |||||||
| chr1:54736169 | A | G | 25 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0168 others(22): Show |
33 | HG00423.hp1 HG01074.hp1 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-1413A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736169 | |||||||
| chr1:54736170 | A | C | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1412A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736170 | |||||||
| chr1:54736172 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1410A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736172 | |||||||
| chr1:54736172 | AAAG | A | 23 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0168 others(20): Show |
29 | HG00423.hp1 HG01074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.979-1409_979-1407d others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736172 | |||||||
| chr1:54736173 | A | G | 3 | a0001c0003t0003g0011 a0001c0003t0003g0199 a0001c0004t0003g0053 |
4 | HG02083.hp2 HG02735.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1409A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736173 | |||||||
| chr1:54736173 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1409A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736173 | |||||||
| chr1:54736173 | AAGGAGAG others(6): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0047 |
3 | NA18940.hp1 NA18940.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.979-1406_979-1394d others(15): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736173 | ||||||
| chr1:54736174 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1408A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736174 | |||||||
| chr1:54736174 | AG | A | 3 | a0001c0003t0003g0011 a0001c0003t0003g0199 a0001c0004t0003g0053 |
4 | HG02083.hp2 HG02735.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1406delG | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736174 | ||||||
| chr1:54736175 | G | GGA | 9 | a0001c0001t0001g0136 a0001c0001t0002g0054 a0002c0002t0002g0001 others(6): Show |
15 | HG00140.hp1 HG01081.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1360_979-1359d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | G | GGAGA | 9 | a0001c0001t0002g0054 a0002c0002t0002g0001 a0002c0002t0002g0008 others(6): Show |
12 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.979-1362_979-1359d others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | G | GGAGAGA | 4 | a0002c0002t0002g0001 a0002c0002t0002g0032 a0002c0002t0002g0075 others(1): Show |
8 | HG01106.hp1 HG01167.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1364_979-1359d others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | G | GGAGAGAG others(1): Show |
8 | a0002c0002t0002g0001 a0002c0002t0002g0014 a0002c0002t0002g0065 others(5): Show |
12 | HG01123.hp1 HG01169.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-1366_979-1359d others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | G | GGAGAGAG others(3): Show |
1 | a0002c0002t0002g0001 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.979-1368_979-1359d others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | G | GGAGAGAG others(5): Show |
1 | a0002c0002t0002g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.979-1370_979-1359d others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | G | GGAGAGAG others(7): Show |
3 | a0002c0002t0002g0001 a0002c0002t0002g0079 a0003c0006t0002g0022 |
3 | HG01175.hp1 HG02698.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.979-1372_979-1359d others(16): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGA | G | 4 | a0002c0002t0002g0001 a0002c0002t0002g0008 a0002c0002t0002g0014 others(1): Show |
5 | HG01243.hp1 HG02602.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-1360_979-1359d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGA | G | 5 | a0002c0002t0002g0001 a0002c0002t0002g0008 a0002c0002t0002g0030 others(2): Show |
6 | HG01109.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1362_979-1359d others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGA | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(5): Show |
10 | HG00423.hp2 HG01175.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.979-1364_979-1359d others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(1): Show |
G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(9): Show |
24 | HG00438.hp1 HG00558.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.979-1366_979-1359d others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(3): Show |
G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0160 others(2): Show |
7 | HG01975.hp1 HG01981.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-1368_979-1359d others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(5): Show |
G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(18): Show |
33 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.979-1370_979-1359d others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(7): Show |
G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
133 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.979-1372_979-1359d others(16): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(9): Show |
G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | NA18954.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1374_979-1359d others(18): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(11): Show |
G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(8): Show |
16 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.979-1376_979-1359d others(20): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(13): Show |
G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0165 |
2 | NA18953.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.979-1378_979-1359d others(22): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(15): Show |
G | 1 | a0002c0002t0004g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.979-1380_979-1359d others(24): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736175 | GGAGAGAG others(19): Show |
G | 2 | a0004c0005t0001g0013 a0004c0005t0001g0092 |
6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1384_979-1359d others(28): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | ||||||
| chr1:54736177 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1405A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736177 | |||||||
| chr1:54736183 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1399A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736183 | |||||||
| chr1:54736186 | G | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1396G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736186 | |||||||
| chr1:54736187 | A | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1395A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736187 | |||||||
| chr1:54736189 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1393A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736189 | |||||||
| chr1:54736190 | G | T | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1392G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736190 | |||||||
| chr1:54736191 | A | T | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-1391A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736191 | |||||||
| chr1:54736193 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1389A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736193 | |||||||
| chr1:54736193 | A | T | 2 | a0001c0004t0003g0052 a0001c0009t0003g0185 |
3 | HG01243.hp2 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.979-1389A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736193 | |||||||
| chr1:54736195 | A | T | 8 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0187 others(5): Show |
16 | HG01243.hp2 HG02080.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.979-1387A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736195 | |||||||
| chr1:54736197 | A | T | 13 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0187 others(10): Show |
21 | HG01243.hp2 HG01891.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.979-1385A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736197 | |||||||
| chr1:54736199 | A | T | 17 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0187 others(14): Show |
25 | HG01243.hp2 HG01891.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.979-1383A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736199 | |||||||
| chr1:54736201 | A | T | 20 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0187 others(17): Show |
28 | HG00423.hp1 HG01243.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-1381A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736201 | |||||||
| chr1:54736203 | A | T | 31 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(28): Show |
44 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.979-1379A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736203 | |||||||
| chr1:54736205 | A | T | 36 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(33): Show |
50 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.979-1377A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736205 | |||||||
| chr1:54736207 | A | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
54 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.979-1375A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736207 | |||||||
| chr1:54736209 | A | T | 42 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(39): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.979-1373A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736209 | |||||||
| chr1:54736209 | AGAGAGAG others(21): Show |
A | 1 | a0001c0001t0001g0042 | 2 | NA18980.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.979-1372_979-1345d others(30): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736209 | |||||||
| chr1:54736211 | A | T | 45 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(42): Show |
59 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.979-1371A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736211 | |||||||
| chr1:54736213 | A | T | 45 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(42): Show |
59 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.979-1369A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736213 | |||||||
| chr1:54736215 | A | T | 47 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(44): Show |
61 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.979-1367A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736215 | |||||||
| chr1:54736217 | A | T | 50 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(47): Show |
67 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.979-1365A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736217 | |||||||
| chr1:54736218 | GAGAGAAG others(27): Show |
G | 2 | a0001c0004t0003g0169 a0001c0004t0003g0177 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.979-1363_979-1330d others(36): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736218 | |||||||
| chr1:54736219 | A | T | 50 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(47): Show |
68 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.979-1363A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736219 | |||||||
| chr1:54736220 | GAGAAGAG others(18): Show |
G | 13 | a0001c0003t0003g0181 a0001c0003t0003g0188 a0001c0003t0003g0192 others(10): Show |
13 | HG00423.hp1 HG01074.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.979-1361_979-1337d others(27): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736220 | |||||||
| chr1:54736220 | GAGAAGAG others(25): Show |
G | 3 | a0001c0003t0003g0198 a0001c0003t0003g0210 a0001c0004t0003g0052 |
4 | HG01243.hp2 HG03098.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1361_979-1330d others(34): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736220 | |||||||
| chr1:54736221 | A | T | 35 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(32): Show |
52 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-1361A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736221 | |||||||
| chr1:54736222 | GAAGAGGA others(2): Show |
G | 5 | a0001c0003t0003g0201 a0001c0003t0003g0202 a0001c0003t0003g0203 others(2): Show |
8 | HG01891.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1359_979-1351d others(11): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736222 | |||||||
| chr1:54736222 | GAAGAGGA others(16): Show |
G | 10 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0189 others(7): Show |
15 | HG00408.hp1 HG00621.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1359_979-1337d others(25): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736222 | |||||||
| chr1:54736222 | GAAGAGGA others(23): Show |
G | 14 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0178 others(11): Show |
22 | HG02080.hp2 HG02083.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.979-1359_979-1330d others(32): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736222 | |||||||
| chr1:54736223 | A | T | 6 | a0001c0003t0003g0184 a0001c0003t0005g0182 a0001c0003t0005g0183 others(3): Show |
7 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-1359A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736223 | |||||||
| chr1:54736224 | A | G | 5 | a0001c0003t0003g0184 a0001c0003t0005g0182 a0001c0003t0005g0183 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-1358A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736224 | |||||||
| chr1:54736224 | AGAGGAGA others(37): Show |
A | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-1357_979-1314d others(46): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736224 | |||||||
| chr1:54736225 | G | T | 5 | a0001c0003t0003g0184 a0001c0003t0005g0182 a0001c0003t0005g0183 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-1357G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736225 | |||||||
| chr1:54736226 | A | G | 5 | a0001c0003t0003g0184 a0001c0003t0005g0182 a0001c0003t0005g0183 others(2): Show |
6 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-1356A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736226 | |||||||
| chr1:54736227 | G | T | 7 | a0001c0003t0003g0184 a0001c0003t0005g0182 a0001c0003t0005g0183 others(4): Show |
8 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1355G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736227 | |||||||
| chr1:54736229 | A | T | 8 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0005g0182 others(5): Show |
9 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1353A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736229 | |||||||
| chr1:54736231 | A | T | 8 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0005g0182 others(5): Show |
9 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1351A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736231 | |||||||
| chr1:54736232 | G | GT | 8 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0005g0182 others(5): Show |
9 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1350_979-1349i others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736232 | |||||||
| chr1:54736232 | G | T | 5 | a0001c0003t0003g0201 a0001c0003t0003g0202 a0001c0003t0003g0203 others(2): Show |
8 | HG01891.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1350G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736232 | |||||||
| chr1:54736234 | A | T | 13 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0003g0201 others(10): Show |
17 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-1348A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736234 | |||||||
| chr1:54736236 | A | T | 13 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0003g0201 others(10): Show |
17 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-1346A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736236 | |||||||
| chr1:54736238 | A | T | 13 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0003g0201 others(10): Show |
17 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-1344A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736238 | |||||||
| chr1:54736239 | GAAGAGA | G | 9 | a0001c0003t0003g0184 a0001c0003t0003g0201 a0001c0003t0003g0202 others(6): Show |
12 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-1342_979-1337d others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736239 | |||||||
| chr1:54736239 | GAAGAGAG others(6): Show |
G | 2 | a0002c0002t0003g0036 a0002c0002t0003g0089 |
3 | HG02723.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.979-1342_979-1330d others(15): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736239 | |||||||
| chr1:54736241 | A | G | 1 | a0001c0001t0001g0042 | 2 | NA18980.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.979-1341A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736241 | |||||||
| chr1:54736241 | A | T | 2 | a0001c0003t0003g0168 a0002c0002t0003g0087 |
2 | HG00642.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979-1341A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736241 | |||||||
| chr1:54736243 | A | T | 2 | a0001c0003t0003g0168 a0002c0002t0003g0087 |
2 | HG00642.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979-1339A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736243 | |||||||
| chr1:54736245 | A | T | 2 | a0001c0003t0003g0168 a0002c0002t0003g0087 |
2 | HG00642.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979-1337A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736245 | |||||||
| chr1:54736246 | G | T | 32 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0181 others(29): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1336G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736246 | |||||||
| chr1:54736248 | A | T | 34 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0168 others(31): Show |
42 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.979-1334A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736248 | |||||||
| chr1:54736250 | A | T | 34 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0168 others(31): Show |
42 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.979-1332A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736250 | |||||||
| chr1:54736252 | A | T | 32 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0168 others(29): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1330A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736252 | |||||||
| chr1:54736253 | G | GT | 32 | a0001c0003t0003g0021 a0001c0003t0003g0028 a0001c0003t0003g0168 others(29): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1329_979-1328i others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736253 | |||||||
| chr1:54736253 | G | T | 23 | a0001c0003t0003g0011 a0001c0003t0003g0055 a0001c0003t0003g0178 others(20): Show |
33 | HG01243.hp2 HG01891.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-1329G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736253 | |||||||
| chr1:54736253 | GGA | G | 7 | a0002c0002t0002g0029 a0002c0002t0002g0030 a0002c0002t0002g0031 others(4): Show |
10 | HG01175.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.979-1312_979-1311d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736253 | ||||||
| chr1:54736254 | G | A | 1 | a0001c0001t0001g0042 | 2 | NA18980.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.979-1328G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736254 | |||||||
| chr1:54736255 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1327A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736255 | |||||||
| chr1:54736257 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1325A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736257 | |||||||
| chr1:54736259 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1323A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736259 | |||||||
| chr1:54736261 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1321A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736261 | |||||||
| chr1:54736263 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1319A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736263 | |||||||
| chr1:54736265 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1317A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736265 | |||||||
| chr1:54736267 | A | T | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1315A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736267 | |||||||
| chr1:54736268 | G | A | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1314G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736268 | |||||||
| chr1:54736270 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1312G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736270 | |||||||
| chr1:54736290 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.979-1292A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736290 | |||||||
| chr1:54736400 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1182A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736400 | |||||||
| chr1:54736438 | TG | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1142delG | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736438 | ||||||
| chr1:54736442 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(55): Show |
112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.979-1140T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736442 | |||||||
| chr1:54736473 | C | T | 1 | a0001c0003t0003g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.979-1109C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736473 | |||||||
| chr1:54736474 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1108A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736474 | |||||||
| chr1:54736509 | C | T | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1073C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736509 | |||||||
| chr1:54736525 | C | T | 1 | a0002c0002t0002g0076 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.979-1057C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736525 | |||||||
| chr1:54736561 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1021A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736561 | |||||||
| chr1:54736578 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.979-1004C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736578 | |||||||
| chr1:54736607 | G | C | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.979-975G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736607 | |||||||
| chr1:54736790 | C | T | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.979-792C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736790 | |||||||
| chr1:54736972 | C | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-610C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736972 | |||||||
| chr1:54737040 | T | C | 1 | a0004c0005t0001g0092 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.979-542T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737040 | |||||||
| chr1:54737117 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-465G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737117 | |||||||
| chr1:54737201 | T | C | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-381T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737201 | |||||||
| chr1:54737219 | C | T | 20 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(17): Show |
32 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.979-363C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737219 | |||||||
| chr1:54737321 | G | C | 1 | a0001c0001t0001g0019 | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-261G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737321 | |||||||
| chr1:54737423 | C | T | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-159C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737423 | |||||||
| chr1:54737462 | A | G | 55 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(52): Show |
73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-120A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737462 | |||||||
| chr1:54737483 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-99A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737483 | |||||||
| chr1:54737757 | T | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1061+93T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737757 | |||||||
| chr1:54737760 | G | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1061+96G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737760 | |||||||
| chr1:54737825 | C | A | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1061+161C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737825 | |||||||
| chr1:54737871 | G | A | 17 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(14): Show |
19 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1061+207G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737871 | |||||||
| chr1:54737908 | C | CT | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061+253dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54737908 | ||||||
| chr1:54737908 | CT | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0143 a0001c0001t0001g0153 others(1): Show |
7 | HG02080.hp1 NA18939.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061+253delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54737908 | ||||||
| chr1:54737957 | A | G | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1061+293A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737957 | |||||||
| chr1:54737995 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1061+331G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737995 | |||||||
| chr1:54738045 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1061+381C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738045 | |||||||
| chr1:54738057 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1061+393C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738057 | |||||||
| chr1:54738058 | G | A | 3 | a0001c0001t0002g0054 a0001c0001t0002g0180 a0002c0002t0002g0058 |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+394G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738058 | |||||||
| chr1:54738061 | C | T | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1061+397C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738061 | |||||||
| chr1:54738062 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0009g0116 |
2 | NA18942.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1061+398G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738062 | |||||||
| chr1:54738068 | CTT | C | 2 | a0004c0005t0001g0013 a0004c0005t0001g0092 |
6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+407_1061+408d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738068 | ||||||
| chr1:54738089 | C | T | 1 | a0001c0004t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061+425C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738089 | |||||||
| chr1:54738138 | T | G | 2 | a0001c0003t0005g0182 a0001c0003t0005g0183 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1061+474T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738138 | |||||||
| chr1:54738156 | C | G | 1 | a0001c0001t0001g0044 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1061+492C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738156 | |||||||
| chr1:54738196 | C | T | 40 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(37): Show |
56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1061+532C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738196 | |||||||
| chr1:54738198 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1061+534G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738198 | |||||||
| chr1:54738249 | A | G | 5 | a0001c0004t0003g0053 a0001c0004t0003g0173 a0001c0004t0003g0174 others(2): Show |
6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+585A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738249 | |||||||
| chr1:54738260 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1061+596A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738260 | |||||||
| chr1:54738276 | AC | A | 5 | a0001c0004t0003g0053 a0001c0004t0003g0173 a0001c0004t0003g0174 others(2): Show |
6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+617delC | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738276 | ||||||
| chr1:54738277 | C | A | 1 | a0001c0003t0003g0011 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1061+613C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738277 | |||||||
| chr1:54738354 | G | A | 1 | a0002c0002t0002g0034 | 2 | HG01109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1061+690G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738354 | |||||||
| chr1:54738448 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1061+784C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738448 | |||||||
| chr1:54738511 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1061+847T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738511 | |||||||
| chr1:54738590 | G | A | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1061+926G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738590 | |||||||
| chr1:54738661 | C | CT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
75 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1061+1011dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | ||||||
| chr1:54738661 | C | CTTTTTTT others(1): Show |
29 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(26): Show |
44 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1061+1004_1061+101 others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | ||||||
| chr1:54738661 | C | CTTTTTTT others(2): Show |
23 | a0001c0003t0003g0055 a0001c0003t0003g0181 a0001c0003t0003g0184 others(20): Show |
26 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1061+1003_1061+101 others(13): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | ||||||
| chr1:54738661 | C | CTTTTTTT others(3): Show |
1 | a0001c0003t0003g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1061+1002_1061+101 others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | ||||||
| chr1:54738689 | G | A | 1 | a0001c0004t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061+1025G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738689 | |||||||
| chr1:54738758 | G | T | 1 | a0001c0001t0001g0045 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1061+1094G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738758 | |||||||
| chr1:54738780 | A | C | 1 | a0002c0002t0002g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1061+1116A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738780 | |||||||
| chr1:54738838 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1061+1174T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738838 | |||||||
| chr1:54738844 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1061+1180G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738844 | |||||||
| chr1:54738975 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1061+1311T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738975 | |||||||
| chr1:54738992 | A | G | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061+1328A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738992 | |||||||
| chr1:54739011 | CTTTT | C | 2 | a0002c0002t0001g0084 a0002c0002t0004g0015 |
5 | HG02615.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1061+1348_1061+135 others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739011 | |||||||
| chr1:54739037 | A | ATTT | 25 | a0001c0003t0003g0168 a0001c0003t0003g0184 a0001c0003t0003g0207 others(22): Show |
31 | HG00642.hp2 HG01074.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1061+1384_1061+138 others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54739037 | ||||||
| chr1:54739037 | A | ATTTT | 29 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(26): Show |
41 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1061+1383_1061+138 others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54739037 | ||||||
| chr1:54739092 | G | A | 1 | a0001c0004t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1061+1428G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739092 | |||||||
| chr1:54739111 | A | G | 1 | a0001c0003t0003g0055 | 2 | HG02080.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1061+1447A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739111 | |||||||
| chr1:54739187 | T | A | 1 | a0001c0004t0003g0169 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061+1523T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739187 | |||||||
| chr1:54739412 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(19): Show |
47 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1061+1748C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739412 | |||||||
| chr1:54739526 | A | G | 58 | a0001c0001t0007g0090 a0001c0001t0007g0091 a0001c0003t0003g0011 others(55): Show |
76 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1061+1862A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739526 | |||||||
| chr1:54739625 | C | T | 28 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(25): Show |
40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1062-1786C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739625 | |||||||
| chr1:54739684 | C | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1727C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739684 | |||||||
| chr1:54739699 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1062-1712G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739699 | |||||||
| chr1:54739727 | A | G | 7 | a0002c0002t0003g0016 a0002c0002t0003g0036 a0002c0002t0003g0068 others(4): Show |
11 | HG01891.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1062-1684A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739727 | |||||||
| chr1:54739807 | G | T | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1062-1604G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739807 | |||||||
| chr1:54739907 | C | T | 2 | a0001c0003t0003g0178 a0001c0003t0003g0179 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1062-1504C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739907 | |||||||
| chr1:54739912 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1062-1499A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739912 | |||||||
| chr1:54739920 | T | C | 1 | a0002c0002t0003g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1062-1491T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739920 | |||||||
| chr1:54740027 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1062-1384A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740027 | |||||||
| chr1:54740029 | C | T | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1382C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740029 | |||||||
| chr1:54740122 | C | G | 2 | a0002c0002t0001g0084 a0002c0002t0004g0015 |
5 | HG02615.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-1289C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740122 | |||||||
| chr1:54740139 | CACTCCAG others(16): Show |
C | 11 | a0001c0004t0003g0052 a0001c0004t0003g0053 a0001c0004t0003g0169 others(8): Show |
13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1062-1269_1062-124 others(27): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54740139 | ||||||
| chr1:54740146 | G | A | 1 | a0001c0009t0003g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1062-1265G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740146 | |||||||
| chr1:54740168 | C | A | 56 | a0001c0003t0003g0011 a0001c0003t0003g0021 a0001c0003t0003g0028 others(53): Show |
74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1243C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740168 | |||||||
| chr1:54740192 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1062-1219A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740192 | |||||||
| chr1:54740277 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1062-1134T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740277 | |||||||
| chr1:54740283 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1062-1128G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740283 | |||||||
| chr1:54740490 | T | C | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-921T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740490 | |||||||
| chr1:54740564 | C | T | 3 | a0001c0003t0003g0191 a0001c0003t0003g0196 a0001c0003t0003g0201 |
3 | HG03834.hp2 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1062-847C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740564 | |||||||
| chr1:54740624 | C | G | 5 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(2): Show |
5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-787C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740624 | |||||||
| chr1:54740764 | C | G | 1 | a0001c0003t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1062-647C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740764 | |||||||
| chr1:54740926 | G | T | 2 | a0002c0002t0002g0066 a0002c0002t0002g0081 |
2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1062-485G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740926 | |||||||
| chr1:54740974 | G | A | 2 | a0001c0004t0003g0053 a0001c0004t0003g0175 |
3 | HG02602.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1062-437G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740974 | |||||||
| chr1:54741157 | T | A | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062-254T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54741157 | |||||||
| chr1:54741379 | T | C | 16 | a0001c0003t0003g0168 a0001c0003t0003g0181 a0001c0003t0005g0182 others(13): Show |
18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062-32T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54741379 | |||||||
| chr1:54741405 | C | T | 1 | a0001c0001t0007g0090 | 1 | HG02922.hp2 | splice_region_variant&intron_variant | LOW | c.1062-6C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54741405 |