Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54902 |
| ensemblid | ENSG00000011295.16 |
| hgncid | 26006 |
| symbol | TTC19 |
| name | tetratricopeptide repeat domain 19 |
| refseq_nuc | NM_017775.4 |
| refseq_prot | NP_060245.3 |
| ensembl_nuc | ENST00000261647.10 |
| ensembl_prot | ENSP00000261647.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 15999824 |
| end | 16029404 |
| strand | + |
| ver | v1.2 |
| region | chr17:15999824-16029404 |
| region5000 | chr17:15994824-16034404 |
| regionname0 | TTC19_chr17_15999824_16029404 |
| regionname5000 | TTC19_chr17_15994824_16034404 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 380 | 322 | 92 | 67 | 116 | 12 | 33 | 90 | TTC19_chr17_15994824_16034404 | TTC19 | MFRLL others(375): Show |
chr17 | 15994824 | 16034404 |
| a0002 | 0/0 | 380 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | MFRLL others(375): Show |
chr17 | 15994824 | 16034404 |
| a0003 | 0/0 | 380 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | MFRLL others(375): Show |
chr17 | 15994824 | 16034404 |
| a0004 | 0/0 | 380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | MFRLL others(375): Show |
chr17 | 15994824 | 16034404 |
| a0005 | 0/0 | 380 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | MFRLL others(375): Show |
chr17 | 15994824 | 16034404 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1140 | 304 | 76 | 65 | 116 | 12 | 33 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0001c0002 | 0/0 | 1140 | 14 | 13 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0001c0004 | 0/0 | 1140 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0001c0007 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0001c0009 | 0/0 | 1140 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0002c0003 | 0/0 | 1140 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0003c0006 | 0/0 | 1140 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0004c0008 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 | ||
| a0005c0005 | 0/0 | 1140 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | ATGTT others(1135): Show |
chr17 | 15994824 | 16034404 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3050 | 93 | 11 | 18 | 49 | 5 | 8 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0002 | 0/0 | 3051 | 25 | 1 | 5 | 9 | 0 | 10 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3046): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0003 | 0/0 | 3049 | 25 | 9 | 4 | 10 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3044): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0004 | 0/0 | 3060 | 22 | 0 | 9 | 6 | 4 | 3 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3055): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0005 | 0/0 | 3062 | 15 | 3 | 2 | 10 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3057): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0006 | 0/0 | 3054 | 12 | 5 | 3 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3049): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0007 | 0/0 | 3061 | 10 | 1 | 2 | 4 | 1 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3056): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0008 | 0/0 | 3063 | 8 | 1 | 1 | 6 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3058): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0010 | 0/0 | 3045 | 5 | 4 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3040): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0011 | 0/0 | 3053 | 5 | 5 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3048): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0012 | 0/0 | 3066 | 5 | 0 | 4 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3061): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0013 | 0/0 | 3062 | 4 | 0 | 2 | 0 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3057): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0014 | 0/0 | 3059 | 4 | 0 | 0 | 2 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3054): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0015 | 0/0 | 3044 | 4 | 1 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3039): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0016 | 0/0 | 3055 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3050): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0017 | 0/0 | 3055 | 3 | 1 | 1 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3050): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0018 | 0/0 | 3054 | 3 | 0 | 1 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3049): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0019 | 0/0 | 3053 | 3 | 1 | 1 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3048): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0020 | 0/0 | 3053 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3048): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0021 | 0/0 | 3065 | 3 | 0 | 1 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3060): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0022 | 0/0 | 3060 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3055): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0023 | 0/0 | 3052 | 3 | 0 | 1 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0027 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0028 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3039): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0029 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0030 | 0/0 | 3074 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3069): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0031 | 0/0 | 3055 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3050): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0032 | 0/0 | 3061 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3056): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0033 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0037 | 0/0 | 3060 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3055): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0038 | 0/0 | 3059 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3054): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0039 | 0/0 | 3055 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3050): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0040 | 0/0 | 3053 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3048): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0041 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0042 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0043 | 0/0 | 3042 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3037): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0044 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0045 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0046 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3044): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0047 | 0/0 | 3051 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3046): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0048 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0049 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0050 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3046): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0051 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0052 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3070): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0053 | 0/0 | 3064 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3059): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0054 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3058): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0055 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3058): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0057 | 0/0 | 3053 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3048): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0058 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0059 | 0/0 | 3054 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3049): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0060 | 0/0 | 3037 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3032): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0062 | 0/0 | 3061 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3056): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0063 | 0/0 | 3055 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3050): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0065 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3046): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0066 | 0/0 | 3041 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3036): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0067 | 0/0 | 3049 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3044): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0068 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0069 | 0/0 | 3061 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3056): Show |
chr17 | 15994824 | 16034404 |
| a0001c0001t0070 | 0/0 | 3050 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0001c0002t0009 | 0/0 | 3061 | 6 | 6 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3056): Show |
chr17 | 15994824 | 16034404 |
| a0001c0002t0024 | 0/0 | 3060 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3055): Show |
chr17 | 15994824 | 16034404 |
| a0001c0002t0025 | 0/0 | 3059 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3054): Show |
chr17 | 15994824 | 16034404 |
| a0001c0002t0026 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0002t0034 | 0/0 | 3067 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3062): Show |
chr17 | 15994824 | 16034404 |
| a0001c0002t0036 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3058): Show |
chr17 | 15994824 | 16034404 |
| a0001c0004t0010 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3040): Show |
chr17 | 15994824 | 16034404 |
| a0001c0004t0028 | 0/0 | 3044 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3039): Show |
chr17 | 15994824 | 16034404 |
| a0001c0007t0027 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0001c0009t0061 | 0/0 | 3064 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3059): Show |
chr17 | 15994824 | 16034404 |
| a0002c0003t0001 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0002c0003t0056 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0002c0003t0064 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3047): Show |
chr17 | 15994824 | 16034404 |
| a0003c0006t0035 | 0/0 | 3064 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3059): Show |
chr17 | 15994824 | 16034404 |
| a0004c0008t0001 | 0/0 | 3050 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3045): Show |
chr17 | 15994824 | 16034404 |
| a0005c0005t0004 | 0/0 | 3060 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | AGTGC others(3055): Show |
chr17 | 15994824 | 16034404 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 6 | 3 | 7 | 3 | 4 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0004 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0015 | 0/0 | 4 | 2 | 0 | 1 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0041 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0001 | 0/0 | 7 | 1 | 2 | 1 | 0 | 3 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0010g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0011g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0012g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0013g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0013g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0015g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0015g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0015g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0016g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0016g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0017g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0017g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0017g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0018g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0019g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0019g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0020g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0021g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0021g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0021g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0022g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0022g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0022g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0023g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0023g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0023g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0027g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0028g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0029g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0030g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0030g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0031g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0031g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0032g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0032g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0033g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0033g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0037g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0038g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0039g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0040g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0041g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0042g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0043g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0044g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0045g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0046g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0047g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0048g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0049g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0050g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0051g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0052g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0053g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0054g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0055g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0057g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0058g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0059g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0060g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0062g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0063g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0065g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0066g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0067g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0068g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0069g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0001t0070g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0009g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0024g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0024g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0025g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0025g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0026g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0034g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0002t0036g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0004t0010g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0004t0028g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0007t0027g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0001c0009t0061g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0002c0003t0056g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0002c0003t0064g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0003c0006t0035g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0004c0008t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| a0005c0005t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00323 | hp2 | a0001 | c0001 | t0018 | g0010 | EUR | FIN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00408 | hp1 | a0001 | c0001 | t0022 | g0072 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00639 | hp2 | a0001 | c0001 | t0052 | g0061 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0085 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01071 | hp1 | a0001 | c0001 | t0013 | g0027 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01106 | hp1 | a0001 | c0001 | t0018 | g0010 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01109 | hp1 | a0001 | c0001 | t0053 | g0059 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01109 | hp2 | a0003 | c0006 | t0035 | g0183 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01168 | hp1 | a0001 | c0001 | t0023 | g0048 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01168 | hp2 | a0001 | c0001 | t0019 | g0165 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0174 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01192 | hp1 | a0001 | c0001 | t0032 | g0002 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01243 | hp1 | a0001 | c0001 | t0054 | g0055 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0007 | AMR | PUR | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0025 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0062 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01358 | hp1 | a0001 | c0001 | t0012 | g0002 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0049 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01516 | hp2 | a0001 | c0001 | t0014 | g0011 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01884 | hp1 | a0001 | c0002 | t0026 | g0181 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01891 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0091 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01928 | hp2 | a0001 | c0001 | t0012 | g0063 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01934 | hp1 | a0001 | c0001 | t0030 | g0002 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01934 | hp2 | a0001 | c0002 | t0034 | g0005 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01952 | hp2 | a0001 | c0001 | t0030 | g0044 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01975 | hp2 | a0001 | c0001 | t0021 | g0002 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01978 | hp2 | a0001 | c0009 | t0061 | g0028 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01981 | hp2 | a0001 | c0001 | t0012 | g0002 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01993 | hp1 | a0001 | c0001 | t0055 | g0043 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02027 | hp1 | a0001 | c0001 | t0015 | g0029 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02040 | hp1 | a0001 | c0001 | t0023 | g0074 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0067 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02056 | hp2 | a0001 | c0001 | t0015 | g0029 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02145 | hp1 | a0001 | c0001 | t0042 | g0178 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0160 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02148 | hp2 | a0001 | c0001 | t0039 | g0010 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02257 | hp1 | a0001 | c0001 | t0032 | g0028 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02258 | hp1 | a0001 | c0001 | t0069 | g0078 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02280 | hp1 | a0001 | c0001 | t0037 | g0080 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02280 | hp2 | a0001 | c0001 | t0020 | g0008 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02293 | hp1 | a0001 | c0001 | t0065 | g0060 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0082 | AMR | PEL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02451 | hp1 | a0001 | c0001 | t0059 | g0090 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02523 | hp2 | a0001 | c0001 | t0015 | g0069 | EAS | KHV | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02572 | hp2 | a0001 | c0001 | t0043 | g0093 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02615 | hp1 | a0001 | c0007 | t0027 | g0171 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02630 | hp1 | a0001 | c0001 | t0027 | g0168 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02630 | hp2 | a0001 | c0001 | t0062 | g0070 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02647 | hp2 | a0001 | c0001 | t0046 | g0014 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02698 | hp1 | a0001 | c0001 | t0066 | g0057 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02723 | hp2 | a0001 | c0001 | t0031 | g0124 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02809 | hp2 | a0002 | c0003 | t0064 | g0087 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02886 | hp1 | a0004 | c0008 | t0001 | g0116 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0161 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02895 | hp2 | a0001 | c0004 | t0010 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02896 | hp1 | a0001 | c0001 | t0028 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02897 | hp1 | a0001 | c0004 | t0028 | g0007 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02922 | hp1 | a0001 | c0001 | t0049 | g0032 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02965 | hp1 | a0001 | c0001 | t0050 | g0092 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02965 | hp2 | a0001 | c0002 | t0009 | g0005 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02970 | hp1 | a0001 | c0002 | t0036 | g0005 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02976 | hp1 | a0001 | c0001 | t0057 | g0105 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0162 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03041 | hp1 | a0001 | c0001 | t0029 | g0008 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03041 | hp2 | a0001 | c0002 | t0024 | g0186 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03139 | hp2 | a0001 | c0002 | t0009 | g0005 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03195 | hp1 | a0001 | c0001 | t0033 | g0159 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0018 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0187 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03225 | hp1 | a0001 | c0001 | t0029 | g0008 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03225 | hp2 | a0001 | c0001 | t0060 | g0121 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03453 | hp1 | a0001 | c0001 | t0031 | g0089 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03486 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03486 | hp2 | a0002 | c0003 | t0001 | g0096 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0103 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03491 | hp2 | a0001 | c0001 | t0013 | g0002 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03492 | hp1 | a0001 | c0001 | t0013 | g0002 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03516 | hp1 | a0001 | c0001 | t0038 | g0172 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03516 | hp2 | a0001 | c0001 | t0063 | g0158 | AFR | ESN | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03540 | hp2 | a0001 | c0002 | t0025 | g0184 | AFR | GWD | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03579 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03579 | hp2 | a0001 | c0002 | t0026 | g0005 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03704 | hp1 | a0001 | c0001 | t0014 | g0065 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0010 | SAS | PJL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04115 | hp1 | a0001 | c0001 | t0040 | g0167 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04184 | hp1 | a0001 | c0001 | t0019 | g0023 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04204 | hp1 | a0005 | c0005 | t0004 | g0053 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0045 | SAS | STU | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18522 | hp2 | a0001 | c0001 | t0044 | g0180 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18747 | hp1 | a0001 | c0001 | t0021 | g0047 | EAS | CHB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0030 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18906 | hp2 | a0001 | c0002 | t0009 | g0005 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18949 | hp2 | a0001 | c0001 | t0022 | g0079 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18960 | hp2 | a0001 | c0001 | t0023 | g0013 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18961 | hp1 | a0001 | c0001 | t0012 | g0026 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18963 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18964 | hp2 | a0001 | c0001 | t0051 | g0017 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18986 | hp2 | a0001 | c0001 | t0014 | g0076 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18995 | hp1 | a0001 | c0001 | t0014 | g0068 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA18999 | hp2 | a0001 | c0001 | t0022 | g0020 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19000 | hp1 | a0001 | c0001 | t0070 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19030 | hp1 | a0001 | c0001 | t0048 | g0179 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19030 | hp2 | a0002 | c0003 | t0056 | g0086 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0176 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19043 | hp2 | a0001 | c0001 | t0067 | g0133 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19054 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19060 | hp1 | a0001 | c0001 | t0068 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19062 | hp2 | a0001 | c0001 | t0017 | g0173 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19064 | hp1 | a0001 | c0001 | t0021 | g0054 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19077 | hp2 | a0001 | c0001 | t0058 | g0036 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19083 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19240 | hp1 | a0001 | c0002 | t0025 | g0185 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA19240 | hp2 | a0001 | c0002 | t0024 | g0182 | AFR | YRI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ASW | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0011 | EUR | TSI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | TSI | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0051 | SAS | GIH | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20905 | hp2 | a0001 | c0001 | t0047 | g0041 | SAS | GIH | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01123 | hp1 | a0001 | c0001 | t0017 | g0010 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0019 | AMR | CLM | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02109 | hp2 | a0001 | c0001 | t0015 | g0071 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02486 | hp1 | a0001 | c0001 | t0045 | g0014 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0005 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG02559 | hp2 | a0001 | c0001 | t0010 | g0177 | AFR | ACB | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03471 | hp1 | a0001 | c0001 | t0020 | g0008 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0022 | AFR | MSL | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG06807 | hp1 | a0001 | c0002 | t0009 | g0005 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | USA | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA21309 | hp1 | a0001 | c0001 | t0041 | g0163 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | LWK | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0041 | REF | REF | TTC19_chr17_15994824_16034404 | TTC19 | chr17 | 15994824 | 16034404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15999994 | C | T | 1 | a0004 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.146C>T | p.Pro49Leu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 171/3050 | 146/1143 | 49/380 | chr17 | 15999994 | |||
| chr17:16000227 | G | C | 1 | a0005 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.294G>C | p.Gln98His | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/10 | 319/3050 | 294/1143 | 98/380 | chr17 | 16000227 | |||
| chr17:16025098 | C | T | 1 | a0002 | 3 | HG02809.hp2 HG03486.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.758C>T | p.Pro253Leu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/10 | 783/3050 | 758/1143 | 253/380 | chr17 | 16025098 | |||
| chr17:16027383 | C | T | 1 | a0003 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1004C>T | p.Thr335Ile | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1029/3050 | 1004/1143 | 335/380 | chr17 | 16027383 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15999873 | C | T | 1 | a0001c0009 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.25C>T | p.Leu9Leu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 50/3050 | 25/1143 | 9/380 | chr17 | 15999873 | |||
| chr17:16001965 | C | T | 1 | a0001c0004 | 2 | HG02895.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.363C>T | p.Asp121Asp | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/10 | 388/3050 | 363/1143 | 121/380 | chr17 | 16001965 | |||
| chr17:16004254 | G | A | 2 | a0001c0002 a0003c0006 |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
synonymous_variant | LOW | c.573G>A | p.Ala191Ala | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/10 | 598/3050 | 573/1143 | 191/380 | chr17 | 16004254 | |||
| chr17:16025021 | A | G | 1 | a0001c0007 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.681A>G | p.Glu227Glu | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/10 | 706/3050 | 681/1143 | 227/380 | chr17 | 16025021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:15999834 | G | A | 7 | a0001c0002t0009 a0001c0002t0024 a0001c0002t0025 others(4): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 15 | chr17 | 15999834 | ||||||
| chr17:15999848 | C | T | 1 | a0001c0001t0070 | 1 | NA19000.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 1/10 | 1 | chr17 | 15999848 | ||||||
| chr17:16027549 | G | A | 1 | a0001c0001t0037 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 27 | chr17 | 16027549 | ||||||
| chr17:16027568 | T | C | 18 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0016 others(15): Show |
41 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*46T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 46 | chr17 | 16027568 | ||||||
| chr17:16027594 | C | G | 1 | a0001c0001t0069 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 72 | chr17 | 16027594 | ||||||
| chr17:16027605 | G | A | 2 | a0001c0001t0045 a0001c0001t0046 |
2 | HG02486.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*83G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 83 | chr17 | 16027605 | ||||||
| chr17:16027633 | G | A | 1 | a0001c0001t0047 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 111 | chr17 | 16027633 | ||||||
| chr17:16027717 | A | G | 1 | a0001c0001t0033 | 2 | HG02145.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*195A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 195 | chr17 | 16027717 | ||||||
| chr17:16027735 | G | T | 1 | a0001c0001t0044 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*213G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 213 | chr17 | 16027735 | ||||||
| chr17:16027748 | T | C | 6 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0029 others(3): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*226T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 226 | chr17 | 16027748 | ||||||
| chr17:16027823 | G | A | 1 | a0001c0001t0051 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 301 | chr17 | 16027823 | ||||||
| chr17:16027872 | A | G | 1 | a0001c0001t0068 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*350A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 350 | chr17 | 16027872 | ||||||
| chr17:16028100 | C | T | 1 | a0001c0001t0067 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 578 | chr17 | 16028100 | ||||||
| chr17:16028122 | G | A | 11 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0017 others(8): Show |
30 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*600G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 600 | chr17 | 16028122 | ||||||
| chr17:16028231 | T | A | 11 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0017 others(8): Show |
30 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*709T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 709 | chr17 | 16028231 | ||||||
| chr17:16028379 | G | A | 6 | a0001c0001t0013 a0001c0001t0030 a0001c0001t0052 others(3): Show |
10 | HG00639.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*857G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 857 | chr17 | 16028379 | ||||||
| chr17:16028493 | G | A | 11 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0017 others(8): Show |
30 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*971G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 971 | chr17 | 16028493 | ||||||
| chr17:16028534 | T | C | 6 | a0001c0001t0011 a0001c0001t0020 a0001c0001t0029 others(3): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1012 | chr17 | 16028534 | ||||||
| chr17:16028674 | C | T | 2 | a0001c0001t0020 a0001c0001t0029 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1152C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1152 | chr17 | 16028674 | ||||||
| chr17:16028716 | T | A | 1 | a0002c0003t0056 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1194T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1194 | chr17 | 16028716 | ||||||
| chr17:16028757 | C | CTT | 59 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(56): Show |
170 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1236_*1237dupTT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1238 | INFO_REALIGN_3_PRIME | chr17 | 16028757 | |||||
| chr17:16028818 | C | CA | 7 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0019 others(4): Show |
40 | HG00673.hp2 HG01168.hp2 HG01261.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1324dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAA | 3 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0058 |
16 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1323_*1324dupAA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAA | 5 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0039 others(2): Show |
9 | HG01123.hp1 HG01891.hp1 HG02148.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1322_*1324dupAAA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA | 3 | a0001c0001t0014 a0001c0001t0038 a0001c0002t0025 |
7 | HG01516.hp2 HG03516.hp1 HG03540.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1318_*1324dupAAAA others(3): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(1): Show |
5 | a0001c0001t0004 a0001c0001t0022 a0001c0001t0037 others(2): Show |
29 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1317_*1324dupAAAA others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0007 a0001c0001t0032 a0001c0001t0062 others(2): Show |
20 | HG01099.hp2 HG01192.hp1 HG01361.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1316_*1324dupAAAA others(5): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005 a0001c0001t0013 |
19 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1315_*1324dupAAAA others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0008 a0001c0001t0030 a0001c0001t0054 others(1): Show |
12 | HG01123.hp2 HG01243.hp1 HG01934.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1314_*1324dupAAAA others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0052 a0001c0001t0053 a0001c0009t0061 others(1): Show |
4 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1313_*1324dupAAAA others(8): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0021 | 3 | HG01975.hp2 NA18747.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1312_*1324dupAAAA others(9): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0012 | 5 | HG01261.hp1 HG01358.hp1 HG01928.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1311_*1324dupAAAA others(10): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0034 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310_*1324dupAAAA others(11): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1325 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | CA | C | 5 | a0001c0001t0003 a0001c0001t0046 a0001c0001t0050 others(2): Show |
29 | HG01070.hp2 HG01192.hp2 HG01433.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1324delA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1324 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | CAAAAAAA | C | 2 | a0001c0001t0010 a0001c0004t0010 |
6 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1318_*1324delAAAA others(3): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1318 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | CAAAAAAA others(1): Show |
C | 3 | a0001c0001t0015 a0001c0001t0028 a0001c0004t0028 |
6 | HG02027.hp1 HG02056.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1317_*1324delAAAA others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1317 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315_*1324delAAAA others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1315 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0066 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314_*1324delAAAA others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1314 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028818 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0060 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1312_*1324delAAAA others(9): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1312 | INFO_REALIGN_3_PRIME | chr17 | 16028818 | |||||
| chr17:16028855 | A | G | 1 | a0001c0001t0022 | 3 | HG00408.hp1 NA18949.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1333A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1333 | chr17 | 16028855 | ||||||
| chr17:16028880 | G | C | 3 | a0001c0001t0016 a0001c0001t0027 a0001c0007t0027 |
5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1358G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1358 | chr17 | 16028880 | ||||||
| chr17:16028991 | G | A | 1 | a0001c0001t0048 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1469 | chr17 | 16028991 | ||||||
| chr17:16029065 | A | G | 3 | a0001c0001t0018 a0001c0001t0039 a0001c0001t0040 |
5 | HG00323.hp2 HG01106.hp1 HG02148.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1543A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1543 | chr17 | 16029065 | ||||||
| chr17:16029106 | T | TGAG | 3 | a0001c0001t0030 a0001c0001t0052 a0001c0001t0055 |
4 | HG00639.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1584_*1585insGAG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1585 | chr17 | 16029106 | ||||||
| chr17:16029108 | G | GAGTAAAA others(1): Show |
3 | a0001c0001t0030 a0001c0001t0052 a0001c0001t0055 |
4 | HG00639.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1586_*1587insAGTA others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1587 | chr17 | 16029108 | ||||||
| chr17:16029111 | T | C | 1 | a0001c0001t0032 | 2 | HG01192.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1589T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1589 | chr17 | 16029111 | ||||||
| chr17:16029188 | T | G | 1 | a0001c0001t0062 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1666 | chr17 | 16029188 | ||||||
| chr17:16029260 | T | C | 3 | a0001c0001t0011 a0001c0001t0049 a0001c0001t0050 |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1738T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1738 | chr17 | 16029260 | ||||||
| chr17:16029313 | T | C | 34 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(31): Show |
115 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1791T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1791 | chr17 | 16029313 | ||||||
| chr17:16029342 | C | CTGAT | 2 | a0001c0001t0031 a0001c0001t0059 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1823_*1826dupATTG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 10/10 | 1827 | INFO_REALIGN_3_PRIME | chr17 | 16029342 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:16000288 | C | A | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.312+43C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000288 | |||||||
| chr17:16000555 | C | A | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+310C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000555 | |||||||
| chr17:16000612 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.312+367G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000612 | |||||||
| chr17:16000714 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18973.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.312+469G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000714 | |||||||
| chr17:16000891 | A | G | 1 | a0002c0003t0064g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312+646A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16000891 | |||||||
| chr17:16001012 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.312+767A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001012 | |||||||
| chr17:16001136 | C | T | 1 | a0001c0001t0005g0085 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.313-779C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001136 | |||||||
| chr17:16001179 | C | G | 1 | a0001c0001t0004g0084 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.313-736C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001179 | |||||||
| chr17:16001187 | C | T | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-728C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001187 | |||||||
| chr17:16001288 | C | T | 2 | a0001c0001t0004g0082 a0001c0001t0007g0083 |
2 | HG02293.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.313-627C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001288 | |||||||
| chr17:16001337 | A | G | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-578A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001337 | |||||||
| chr17:16001734 | G | A | 2 | a0001c0001t0031g0089 a0001c0001t0059g0090 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.313-181G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001734 | |||||||
| chr17:16001764 | T | C | 10 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(7): Show |
15 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-151T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001764 | |||||||
| chr17:16001788 | G | C | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.313-127G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001788 | |||||||
| chr17:16001876 | A | G | 88 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(85): Show |
107 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.313-39A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 2/9 | chr17 | 16001876 | |||||||
| chr17:16002119 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.423+94G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002119 | |||||||
| chr17:16002121 | T | C | 2 | a0001c0001t0031g0089 a0001c0001t0059g0090 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.423+96T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002121 | |||||||
| chr17:16002282 | G | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(23): Show |
33 | HG01192.hp2 HG01891.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.423+257G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002282 | |||||||
| chr17:16002396 | C | T | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.423+371C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002396 | |||||||
| chr17:16002638 | C | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(44): Show |
63 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(60): Show |
intron_variant | MODIFIER | c.424-155C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002638 | |||||||
| chr17:16002643 | G | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424-150G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002643 | |||||||
| chr17:16002646 | T | G | 6 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | HG02056.hp1 NA18961.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.424-147T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002646 | |||||||
| chr17:16002721 | G | A | 1 | a0001c0001t0004g0024 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.424-72G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 3/9 | chr17 | 16002721 | |||||||
| chr17:16003077 | C | T | 161 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(158): Show |
202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.462+246C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003077 | |||||||
| chr17:16003078 | T | C | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.462+247T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003078 | |||||||
| chr17:16003114 | G | A | 35 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(32): Show |
46 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.462+283G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003114 | |||||||
| chr17:16003239 | A | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(44): Show |
60 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.462+408A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003239 | |||||||
| chr17:16003250 | T | C | 7 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(4): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+419T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003250 | |||||||
| chr17:16003332 | C | T | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.463-499C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003332 | |||||||
| chr17:16003404 | C | T | 1 | a0001c0001t0006g0175 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.463-427C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003404 | |||||||
| chr17:16003405 | A | G | 31 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(28): Show |
42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.463-426A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003405 | |||||||
| chr17:16003422 | C | CTTAT | 4 | a0001c0001t0020g0008 a0001c0001t0029g0008 a0001c0001t0031g0089 others(1): Show |
7 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-379_463-376dup others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | ||||||
| chr17:16003422 | C | CTTATTTA others(5): Show |
1 | a0001c0001t0059g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.463-387_463-376dup others(12): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | ||||||
| chr17:16003422 | CTTAT | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(211): Show |
294 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.463-379_463-376del others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | ||||||
| chr17:16003422 | CTTATTTA others(1): Show |
C | 7 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(4): Show |
9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.463-383_463-376del others(8): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003422 | ||||||
| chr17:16003466 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.463-365G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003466 | |||||||
| chr17:16003518 | T | C | 5 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(2): Show |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-313T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003518 | |||||||
| chr17:16003572 | T | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(53): Show |
74 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(71): Show |
intron_variant | MODIFIER | c.463-259T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003572 | |||||||
| chr17:16003598 | G | A | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.463-233G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003598 | |||||||
| chr17:16003706 | G | A | 2 | a0001c0001t0030g0044 a0001c0001t0055g0043 |
2 | HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.463-125G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003706 | |||||||
| chr17:16003719 | T | A | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.463-112T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003719 | |||||||
| chr17:16003743 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.463-88A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003743 | |||||||
| chr17:16003770 | C | CAT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0111 a0001c0001t0001g0141 others(12): Show |
20 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.463-47_463-46dupTA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr17 | 16003770 | ||||||
| chr17:16003805 | G | T | 1 | a0001c0001t0004g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.463-26G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 4/9 | chr17 | 16003805 | |||||||
| chr17:16003994 | G | A | 1 | a0001c0001t0005g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.519+107G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 5/9 | chr17 | 16003994 | |||||||
| chr17:16004016 | T | C | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.519+129T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 5/9 | chr17 | 16004016 | |||||||
| chr17:16004153 | G | GA | 57 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(54): Show |
72 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.520-42dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr17 | 16004153 | ||||||
| chr17:16004450 | G | A | 26 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(23): Show |
32 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.581+188G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004450 | |||||||
| chr17:16004581 | G | A | 1 | a0002c0003t0056g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.581+319G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004581 | |||||||
| chr17:16004870 | G | T | 2 | a0001c0001t0033g0159 a0001c0001t0033g0160 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.581+608G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004870 | |||||||
| chr17:16004940 | C | G | 7 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(4): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.581+678C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004940 | |||||||
| chr17:16004997 | C | A | 2 | a0001c0001t0031g0089 a0001c0001t0059g0090 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.581+735C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16004997 | |||||||
| chr17:16005049 | G | A | 1 | a0001c0001t0010g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.581+787G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005049 | |||||||
| chr17:16005116 | T | C | 1 | a0001c0002t0026g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.581+854T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005116 | |||||||
| chr17:16005143 | CAATT | C | 3 | a0001c0001t0031g0089 a0001c0001t0043g0093 a0001c0001t0059g0090 |
3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.581+883_581+886del others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr17 | 16005143 | ||||||
| chr17:16005254 | G | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.581+992G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005254 | |||||||
| chr17:16005397 | C | T | 3 | a0001c0001t0033g0159 a0001c0001t0033g0160 a0001c0001t0063g0158 |
3 | HG02145.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.582-1077C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005397 | |||||||
| chr17:16005458 | G | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.582-1016G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005458 | |||||||
| chr17:16005508 | A | AC | 79 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(76): Show |
103 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(100): Show |
intron_variant | MODIFIER | c.582-966_582-965ins others(1): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005508 | |||||||
| chr17:16005533 | T | C | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.582-941T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005533 | |||||||
| chr17:16005559 | C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.582-915C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005559 | |||||||
| chr17:16005597 | C | G | 1 | a0001c0002t0009g0187 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.582-877C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005597 | |||||||
| chr17:16005842 | G | A | 23 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(20): Show |
29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.582-632G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005842 | |||||||
| chr17:16005892 | G | T | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.582-582G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005892 | |||||||
| chr17:16005945 | G | A | 6 | a0001c0001t0010g0007 a0001c0001t0010g0177 a0001c0001t0028g0007 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.582-529G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005945 | |||||||
| chr17:16005991 | G | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.582-483G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16005991 | |||||||
| chr17:16006135 | C | T | 2 | a0001c0001t0002g0140 a0001c0001t0003g0040 |
3 | NA18947.hp1 NA18962.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.582-339C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16006135 | |||||||
| chr17:16006414 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(143): Show |
183 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.582-60A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 6/9 | chr17 | 16006414 | |||||||
| chr17:16006664 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.676+96A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006664 | |||||||
| chr17:16006670 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.676+102A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006670 | |||||||
| chr17:16006674 | A | G | 34 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(31): Show |
42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.676+106A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006674 | |||||||
| chr17:16006735 | A | C | 5 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(2): Show |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+167A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006735 | |||||||
| chr17:16006764 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.676+196G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006764 | |||||||
| chr17:16006819 | T | C | 3 | a0001c0001t0033g0159 a0001c0001t0033g0160 a0001c0001t0063g0158 |
3 | HG02145.hp2 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.676+251T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006819 | |||||||
| chr17:16006827 | T | C | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+259T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006827 | |||||||
| chr17:16006972 | A | G | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.676+404A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16006972 | |||||||
| chr17:16007084 | G | A | 2 | a0001c0001t0031g0089 a0001c0001t0059g0090 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.676+516G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007084 | |||||||
| chr17:16007111 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.676+543T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007111 | |||||||
| chr17:16007127 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.676+559G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007127 | |||||||
| chr17:16007376 | CT | C | 26 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(23): Show |
32 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.676+809delT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007376 | |||||||
| chr17:16007439 | AGTTTTTT | A | 51 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(48): Show |
66 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.676+891_676+897del others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16007439 | ||||||
| chr17:16007439 | AGTTTTTT others(7): Show |
A | 1 | a0001c0001t0004g0084 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.676+884_676+897del others(14): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16007439 | ||||||
| chr17:16007470 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(63): Show |
86 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.676+902C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007470 | |||||||
| chr17:16007666 | C | T | 1 | a0001c0001t0003g0138 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.676+1098C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007666 | |||||||
| chr17:16007752 | C | T | 3 | a0001c0001t0031g0089 a0001c0001t0043g0093 a0001c0001t0059g0090 |
3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.676+1184C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007752 | |||||||
| chr17:16007791 | T | G | 158 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(155): Show |
199 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.676+1223T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007791 | |||||||
| chr17:16007889 | A | G | 1 | a0001c0001t0048g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.676+1321A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007889 | |||||||
| chr17:16007945 | A | G | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.676+1377A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16007945 | |||||||
| chr17:16008118 | C | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+1550C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008118 | |||||||
| chr17:16008211 | C | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+1643C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008211 | |||||||
| chr17:16008377 | T | G | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+1809T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008377 | |||||||
| chr17:16008600 | C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+2032C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008600 | |||||||
| chr17:16008619 | C | T | 23 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(20): Show |
29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+2051C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008619 | |||||||
| chr17:16008658 | G | A | 1 | a0001c0001t0010g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676+2090G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008658 | |||||||
| chr17:16008666 | C | T | 1 | a0001c0001t0057g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676+2098C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008666 | |||||||
| chr17:16008781 | C | T | 1 | a0001c0001t0031g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.676+2213C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008781 | |||||||
| chr17:16008796 | T | C | 1 | a0001c0001t0016g0161 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.676+2228T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008796 | |||||||
| chr17:16008825 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+2257G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16008825 | |||||||
| chr17:16009014 | ATCCATTA others(25): Show |
A | 2 | a0001c0001t0033g0159 a0001c0001t0033g0160 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.676+2448_676+2479d others(34): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009014 | ||||||
| chr17:16009021 | A | G | 1 | a0001c0001t0004g0013 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.676+2453A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009021 | |||||||
| chr17:16009041 | G | A | 8 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(5): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.676+2473G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009041 | |||||||
| chr17:16009115 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0058g0036 |
2 | NA18950.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.676+2547G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009115 | |||||||
| chr17:16009139 | G | C | 1 | a0001c0002t0026g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.676+2571G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009139 | |||||||
| chr17:16009198 | CAAGT | C | 2 | a0001c0001t0001g0017 a0001c0001t0051g0017 |
4 | HG02074.hp1 NA18964.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2635_676+2638d others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009198 | ||||||
| chr17:16009270 | A | AGT | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2705_676+2706d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009270 | ||||||
| chr17:16009400 | G | A | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+2832G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009400 | |||||||
| chr17:16009442 | C | A | 1 | a0001c0001t0019g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.676+2874C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009442 | |||||||
| chr17:16009500 | C | CT | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+2941dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16009500 | ||||||
| chr17:16009565 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG00621.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.676+2997T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009565 | |||||||
| chr17:16009801 | A | G | 2 | a0001c0001t0031g0089 a0001c0001t0059g0090 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.676+3233A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16009801 | |||||||
| chr17:16010126 | T | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(143): Show |
183 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.676+3558T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010126 | |||||||
| chr17:16010129 | C | T | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+3561C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010129 | |||||||
| chr17:16010167 | A | AT | 20 | a0001c0001t0001g0088 a0001c0001t0001g0110 a0001c0001t0001g0135 others(17): Show |
21 | HG00642.hp1 HG00673.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.676+3623dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16010167 | ||||||
| chr17:16010167 | AT | A | 19 | a0001c0001t0001g0015 a0001c0001t0001g0108 a0001c0001t0001g0113 others(16): Show |
26 | HG01109.hp2 HG01168.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.676+3623delT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16010167 | ||||||
| chr17:16010167 | ATTTTT | A | 61 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(58): Show |
81 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(78): Show |
intron_variant | MODIFIER | c.676+3619_676+3623d others(7): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16010167 | ||||||
| chr17:16010206 | C | G | 1 | a0001c0007t0027g0171 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.676+3638C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010206 | |||||||
| chr17:16010234 | T | A | 23 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(20): Show |
29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+3666T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010234 | |||||||
| chr17:16010242 | C | T | 1 | a0001c0001t0005g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.676+3674C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010242 | |||||||
| chr17:16010306 | C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+3738C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010306 | |||||||
| chr17:16010432 | A | G | 34 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(31): Show |
42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.676+3864A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010432 | |||||||
| chr17:16010462 | G | A | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+3894G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010462 | |||||||
| chr17:16010505 | C | T | 23 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(20): Show |
29 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+3937C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010505 | |||||||
| chr17:16010589 | C | G | 2 | a0001c0001t0005g0077 a0001c0001t0069g0078 |
2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.676+4021C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010589 | |||||||
| chr17:16010626 | C | T | 5 | a0001c0001t0004g0012 a0001c0001t0004g0049 a0001c0001t0004g0081 others(2): Show |
7 | HG00735.hp2 HG01099.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+4058C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010626 | |||||||
| chr17:16010640 | A | G | 2 | a0001c0002t0025g0184 a0001c0002t0025g0185 |
2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.676+4072A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010640 | |||||||
| chr17:16010704 | C | G | 1 | a0001c0001t0052g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.676+4136C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010704 | |||||||
| chr17:16010785 | C | T | 6 | a0001c0001t0006g0018 a0001c0001t0006g0042 a0001c0001t0006g0169 others(3): Show |
9 | HG00741.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+4217C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16010785 | |||||||
| chr17:16011153 | A | G | 2 | a0001c0001t0002g0134 a0001c0001t0002g0137 |
2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.676+4585A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011153 | |||||||
| chr17:16011215 | C | G | 1 | a0002c0003t0056g0086 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.676+4647C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011215 | |||||||
| chr17:16011462 | C | T | 23 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(20): Show |
29 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+4894C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011462 | |||||||
| chr17:16011465 | G | A | 3 | a0001c0001t0031g0089 a0001c0001t0043g0093 a0001c0001t0059g0090 |
3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.676+4897G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011465 | |||||||
| chr17:16011498 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+4930G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011498 | |||||||
| chr17:16011672 | A | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+5104A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011672 | |||||||
| chr17:16011758 | A | G | 145 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(142): Show |
182 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.676+5190A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16011758 | |||||||
| chr17:16012021 | CT | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(20): Show |
29 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(26): Show |
intron_variant | MODIFIER | c.676+5464delT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16012021 | ||||||
| chr17:16012144 | G | T | 3 | a0001c0001t0016g0161 a0001c0001t0027g0168 a0001c0007t0027g0171 |
3 | HG02615.hp1 HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.676+5576G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012144 | |||||||
| chr17:16012260 | G | A | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+5692G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012260 | |||||||
| chr17:16012595 | A | G | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+6027A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012595 | |||||||
| chr17:16012600 | A | G | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+6032A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012600 | |||||||
| chr17:16012708 | T | C | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+6140T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012708 | |||||||
| chr17:16012758 | G | A | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+6190G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012758 | |||||||
| chr17:16012829 | C | T | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.676+6261C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16012829 | |||||||
| chr17:16013094 | C | T | 1 | a0001c0001t0067g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.676+6526C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013094 | |||||||
| chr17:16013178 | C | T | 3 | a0001c0001t0031g0089 a0001c0001t0043g0093 a0001c0001t0059g0090 |
3 | HG02451.hp1 HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.676+6610C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013178 | |||||||
| chr17:16013312 | C | T | 7 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(4): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.676+6744C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013312 | |||||||
| chr17:16013326 | A | T | 6 | a0001c0001t0006g0018 a0001c0001t0006g0042 a0001c0001t0006g0169 others(3): Show |
9 | HG00741.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+6758A>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013326 | |||||||
| chr17:16013422 | T | C | 1 | a0001c0001t0004g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.676+6854T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013422 | |||||||
| chr17:16013440 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.676+6872T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013440 | |||||||
| chr17:16013532 | A | G | 1 | a0001c0001t0016g0161 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.676+6964A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013532 | |||||||
| chr17:16013683 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.676+7115A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013683 | |||||||
| chr17:16013955 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG00738.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.676+7387G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16013955 | |||||||
| chr17:16014114 | T | C | 1 | a0001c0001t0004g0050 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.676+7546T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014114 | |||||||
| chr17:16014212 | C | T | 1 | a0001c0001t0016g0030 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.676+7644C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014212 | |||||||
| chr17:16014225 | T | C | 2 | a0001c0001t0001g0094 a0004c0008t0001g0116 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.676+7657T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014225 | |||||||
| chr17:16014404 | C | G | 32 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(29): Show |
41 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.676+7836C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014404 | |||||||
| chr17:16014568 | T | C | 7 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(4): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.676+8000T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014568 | |||||||
| chr17:16014591 | G | A | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+8023G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014591 | |||||||
| chr17:16014682 | G | A | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.676+8114G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014682 | |||||||
| chr17:16014814 | C | G | 1 | a0001c0001t0048g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.676+8246C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014814 | |||||||
| chr17:16014884 | G | T | 1 | a0002c0003t0064g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.676+8316G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014884 | |||||||
| chr17:16014908 | G | A | 159 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(156): Show |
200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.676+8340G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16014908 | |||||||
| chr17:16015087 | T | C | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+8519T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015087 | |||||||
| chr17:16015100 | G | T | 1 | a0001c0001t0002g0130 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.676+8532G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015100 | |||||||
| chr17:16015103 | T | C | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.676+8535T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015103 | |||||||
| chr17:16015196 | A | T | 1 | a0001c0001t0057g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676+8628A>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015196 | |||||||
| chr17:16015249 | C | T | 1 | a0001c0001t0042g0178 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676+8681C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015249 | |||||||
| chr17:16015349 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0002g0188 |
2 | HG00673.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.676+8781A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015349 | |||||||
| chr17:16015387 | C | CT | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.676+8820dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16015387 | ||||||
| chr17:16015448 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0136 |
2 | NA18967.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.676+8880C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015448 | |||||||
| chr17:16015481 | T | A | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.676+8913T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015481 | |||||||
| chr17:16015797 | G | C | 1 | a0001c0001t0007g0051 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.677-9220G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16015797 | |||||||
| chr17:16016030 | T | C | 2 | a0001c0001t0038g0172 a0001c0001t0041g0163 |
2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.677-8987T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016030 | |||||||
| chr17:16016098 | C | T | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-8919C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016098 | |||||||
| chr17:16016120 | T | C | 1 | a0002c0003t0064g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.677-8897T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016120 | |||||||
| chr17:16016234 | G | T | 6 | a0001c0001t0010g0007 a0001c0001t0010g0177 a0001c0001t0028g0007 others(3): Show |
8 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.677-8783G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016234 | |||||||
| chr17:16016295 | C | G | 34 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(31): Show |
42 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.677-8722C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016295 | |||||||
| chr17:16016295 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.677-8722C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016295 | |||||||
| chr17:16016552 | A | AT | 60 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0088 others(57): Show |
74 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.677-8442dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16016552 | ||||||
| chr17:16016552 | A | ATT | 16 | a0001c0001t0001g0034 a0001c0001t0003g0034 a0001c0001t0003g0101 others(13): Show |
18 | HG01192.hp2 HG01243.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-8443_677-8442d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16016552 | ||||||
| chr17:16016575 | T | G | 10 | a0001c0001t0001g0117 a0001c0001t0048g0179 a0001c0002t0009g0005 others(7): Show |
14 | HG00323.hp1 HG01109.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.677-8442T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016575 | |||||||
| chr17:16016575 | T | TG | 10 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(7): Show |
15 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-8439dupG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16016575 | ||||||
| chr17:16016596 | C | T | 3 | a0001c0001t0016g0030 a0002c0003t0056g0086 a0002c0003t0064g0087 |
4 | HG01891.hp1 HG02809.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.677-8421C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016596 | |||||||
| chr17:16016646 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(7): Show |
14 | HG03491.hp1 HG03654.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.677-8371C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016646 | |||||||
| chr17:16016707 | A | G | 68 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(65): Show |
88 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(85): Show |
intron_variant | MODIFIER | c.677-8310A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016707 | |||||||
| chr17:16016789 | C | T | 1 | a0001c0001t0022g0072 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.677-8228C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016789 | |||||||
| chr17:16016801 | G | A | 1 | a0001c0001t0012g0063 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.677-8216G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016801 | |||||||
| chr17:16016865 | G | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.677-8152G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016865 | |||||||
| chr17:16016882 | C | T | 4 | a0001c0001t0031g0089 a0001c0001t0043g0093 a0001c0001t0059g0090 others(1): Show |
4 | HG02451.hp1 HG02572.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.677-8135C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16016882 | |||||||
| chr17:16017152 | T | G | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-7865T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017152 | |||||||
| chr17:16017172 | A | C | 1 | a0001c0001t0006g0166 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.677-7845A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017172 | |||||||
| chr17:16017341 | C | T | 1 | a0001c0001t0048g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-7676C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017341 | |||||||
| chr17:16017448 | C | CA | 26 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0110 others(23): Show |
27 | HG00621.hp1 HG00735.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-7547dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | ||||||
| chr17:16017448 | CA | C | 16 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(13): Show |
18 | HG01243.hp2 HG02080.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-7547delA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | ||||||
| chr17:16017448 | CAA | C | 33 | a0001c0001t0003g0099 a0001c0001t0003g0101 a0001c0001t0006g0018 others(30): Show |
44 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.677-7548_677-7547d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | ||||||
| chr17:16017448 | CAAA | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(17): Show |
27 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-7549_677-7547d others(5): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | ||||||
| chr17:16017448 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.677-7558_677-7547d others(14): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017448 | ||||||
| chr17:16017638 | G | A | 9 | a0001c0001t0005g0003 a0001c0001t0005g0026 a0001c0001t0005g0052 others(6): Show |
14 | NA18950.hp2 NA18956.hp2 NA18959.hp1 others(11): Show |
intron_variant | MODIFIER | c.677-7379G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017638 | |||||||
| chr17:16017688 | G | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(18): Show |
27 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-7329G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017688 | |||||||
| chr17:16017688 | G | T | 1 | a0001c0001t0048g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.677-7329G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017688 | |||||||
| chr17:16017757 | A | G | 141 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(138): Show |
177 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.677-7260A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16017757 | |||||||
| chr17:16017854 | G | GT | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-7159dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16017854 | ||||||
| chr17:16018050 | C | T | 7 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(4): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-6967C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018050 | |||||||
| chr17:16018105 | G | A | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-6912G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018105 | |||||||
| chr17:16018255 | T | TG | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-6760dupG | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16018255 | ||||||
| chr17:16018304 | A | G | 1 | a0001c0001t0015g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.677-6713A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018304 | |||||||
| chr17:16018335 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.677-6682C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018335 | |||||||
| chr17:16018383 | C | T | 1 | a0001c0001t0006g0170 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.677-6634C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018383 | |||||||
| chr17:16018413 | C | A | 1 | a0001c0001t0027g0168 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.677-6604C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018413 | |||||||
| chr17:16018519 | T | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(18): Show |
27 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-6498T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018519 | |||||||
| chr17:16018678 | C | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(64): Show |
87 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.677-6339C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018678 | |||||||
| chr17:16018819 | T | C | 1 | a0002c0003t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.677-6198T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018819 | |||||||
| chr17:16018891 | C | G | 2 | a0001c0001t0006g0174 a0001c0001t0019g0165 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.677-6126C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16018891 | |||||||
| chr17:16018996 | AGTTTGGT others(3): Show |
A | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-6015_677-6006d others(12): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16018996 | ||||||
| chr17:16019072 | C | T | 1 | a0001c0001t0015g0071 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.677-5945C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019072 | |||||||
| chr17:16019153 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(18): Show |
27 | HG01192.hp2 HG02109.hp1 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.677-5864C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019153 | |||||||
| chr17:16019202 | G | A | 7 | a0001c0001t0004g0020 a0001c0001t0007g0020 a0001c0001t0015g0029 others(4): Show |
8 | HG00408.hp1 HG02015.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.677-5815G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019202 | |||||||
| chr17:16019330 | T | A | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-5687T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019330 | |||||||
| chr17:16019533 | G | A | 7 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(4): Show |
12 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.677-5484G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019533 | |||||||
| chr17:16019552 | C | G | 1 | a0001c0001t0014g0068 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.677-5465C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019552 | |||||||
| chr17:16019593 | CTG | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(156): Show |
200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.677-5422_677-5421d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16019593 | ||||||
| chr17:16019658 | A | G | 1 | a0001c0001t0044g0180 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.677-5359A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019658 | |||||||
| chr17:16019791 | G | A | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-5226G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16019791 | |||||||
| chr17:16019965 | T | TA | 53 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(50): Show |
66 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(63): Show |
intron_variant | MODIFIER | c.677-5034dupA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16019965 | ||||||
| chr17:16019965 | T | TAA | 7 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(4): Show |
9 | HG01243.hp2 HG02559.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-5035_677-5034d others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16019965 | ||||||
| chr17:16020012 | C | T | 60 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(57): Show |
75 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(72): Show |
intron_variant | MODIFIER | c.677-5005C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020012 | |||||||
| chr17:16020103 | T | G | 1 | a0001c0001t0016g0161 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.677-4914T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020103 | |||||||
| chr17:16020360 | TTGTC | T | 11 | a0001c0002t0009g0005 a0001c0002t0009g0187 a0001c0002t0024g0182 others(8): Show |
15 | HG01109.hp2 HG01884.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.677-4655_677-4652d others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16020360 | ||||||
| chr17:16020395 | C | T | 159 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(156): Show |
200 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.677-4622C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020395 | |||||||
| chr17:16020460 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.677-4557G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020460 | |||||||
| chr17:16020560 | A | C | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-4457A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020560 | |||||||
| chr17:16020575 | A | C | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-4442A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020575 | |||||||
| chr17:16020606 | T | A | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-4411T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020606 | |||||||
| chr17:16020667 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.677-4350C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020667 | |||||||
| chr17:16020776 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.677-4241G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020776 | |||||||
| chr17:16020860 | T | C | 18 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(15): Show |
24 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.677-4157T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020860 | |||||||
| chr17:16020978 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0003g0102 a0001c0001t0045g0014 others(1): Show |
5 | HG01192.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.677-4039C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16020978 | |||||||
| chr17:16021008 | GTTCA | G | 7 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(4): Show |
9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-4000_677-3997d others(6): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16021008 | ||||||
| chr17:16021056 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(159): Show |
203 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.677-3961A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021056 | |||||||
| chr17:16021094 | T | C | 4 | a0001c0001t0016g0030 a0001c0001t0016g0161 a0001c0001t0027g0168 others(1): Show |
5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-3923T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021094 | |||||||
| chr17:16021109 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.677-3908T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021109 | |||||||
| chr17:16021401 | CA | C | 2 | a0001c0001t0020g0008 a0001c0001t0029g0008 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-3609delA | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16021401 | ||||||
| chr17:16021409 | C | G | 3 | a0001c0001t0031g0089 a0001c0001t0031g0124 a0001c0001t0059g0090 |
3 | HG02451.hp1 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.677-3608C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021409 | |||||||
| chr17:16021478 | T | C | 1 | a0001c0001t0060g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-3539T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021478 | |||||||
| chr17:16021613 | G | C | 7 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(4): Show |
9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.677-3404G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021613 | |||||||
| chr17:16021684 | G | A | 1 | a0001c0001t0063g0158 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.677-3333G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16021684 | |||||||
| chr17:16022025 | G | A | 25 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(22): Show |
32 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.677-2992G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022025 | |||||||
| chr17:16022028 | G | T | 8 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(5): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-2989G>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022028 | |||||||
| chr17:16022038 | G | A | 2 | a0002c0003t0056g0086 a0002c0003t0064g0087 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.677-2979G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022038 | |||||||
| chr17:16022087 | G | GGGTTGT | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-2926_677-2921d others(8): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16022087 | ||||||
| chr17:16022116 | G | GT | 69 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(66): Show |
89 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.677-2898dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16022116 | ||||||
| chr17:16022264 | T | C | 1 | a0001c0001t0044g0180 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.677-2753T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022264 | |||||||
| chr17:16022362 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.677-2655T>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022362 | |||||||
| chr17:16022370 | C | T | 2 | a0002c0003t0056g0086 a0002c0003t0064g0087 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.677-2647C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022370 | |||||||
| chr17:16022389 | C | A | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-2628C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022389 | |||||||
| chr17:16022420 | A | G | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-2597A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022420 | |||||||
| chr17:16022460 | G | C | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-2557G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022460 | |||||||
| chr17:16022464 | T | C | 1 | a0001c0001t0004g0075 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.677-2553T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022464 | |||||||
| chr17:16022495 | A | G | 1 | a0001c0001t0011g0022 | 3 | HG02622.hp1 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.677-2522A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022495 | |||||||
| chr17:16022551 | G | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02273.hp2 NA18968.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-2466G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022551 | |||||||
| chr17:16022627 | A | C | 1 | a0001c0002t0025g0185 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.677-2390A>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022627 | |||||||
| chr17:16022719 | T | C | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-2298T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022719 | |||||||
| chr17:16022933 | G | A | 4 | a0001c0001t0004g0021 a0001c0001t0005g0021 a0001c0001t0005g0066 others(1): Show |
4 | HG00621.hp2 NA18982.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-2084G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16022933 | |||||||
| chr17:16023007 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.677-2010T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023007 | |||||||
| chr17:16023049 | G | C | 69 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(66): Show |
89 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.677-1968G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023049 | |||||||
| chr17:16023074 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0002g0039 |
2 | NA18982.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.677-1943A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023074 | |||||||
| chr17:16023155 | C | T | 1 | a0002c0003t0064g0087 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.677-1862C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023155 | |||||||
| chr17:16023467 | G | C | 22 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(19): Show |
28 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.677-1550G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023467 | |||||||
| chr17:16023521 | C | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(22): Show |
31 | HG01192.hp2 HG02109.hp1 HG02451.hp1 others(28): Show |
intron_variant | MODIFIER | c.677-1496C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023521 | |||||||
| chr17:16023548 | A | G | 8 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(5): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-1469A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023548 | |||||||
| chr17:16023561 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.677-1456G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023561 | |||||||
| chr17:16023563 | G | A | 5 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(2): Show |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.677-1454G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023563 | |||||||
| chr17:16023649 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.677-1368A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023649 | |||||||
| chr17:16023741 | CTCAAAGA others(3): Show |
C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(7): Show |
14 | HG03491.hp1 HG03654.hp2 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.677-1274_677-1265d others(12): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16023741 | ||||||
| chr17:16023775 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0003g0097 a0001c0001t0003g0106 |
3 | HG02809.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.677-1242G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023775 | |||||||
| chr17:16023909 | C | A | 161 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(158): Show |
202 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.677-1108C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16023909 | |||||||
| chr17:16024228 | G | A | 24 | a0001c0001t0001g0164 a0001c0001t0006g0018 a0001c0001t0006g0023 others(21): Show |
31 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.677-789G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024228 | |||||||
| chr17:16024290 | CTTTTTTT others(3): Show |
C | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.677-713_677-704del others(10): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024290 | ||||||
| chr17:16024364 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.677-653C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024364 | |||||||
| chr17:16024462 | A | AT | 44 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0034 others(41): Show |
55 | HG00621.hp1 HG01109.hp2 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.677-539dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | ||||||
| chr17:16024462 | A | ATT | 14 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0042g0178 others(11): Show |
20 | HG01884.hp1 HG01934.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.677-540_677-539dup others(2): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | ||||||
| chr17:16024462 | A | ATTTT | 73 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(70): Show |
89 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.677-542_677-539dup others(4): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | ||||||
| chr17:16024462 | A | ATTTTT | 5 | a0001c0001t0004g0081 a0001c0001t0008g0073 a0001c0001t0015g0029 others(2): Show |
6 | HG00735.hp2 HG02027.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.677-543_677-539dup others(5): Show |
TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | 16024462 | ||||||
| chr17:16024495 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.677-522C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024495 | |||||||
| chr17:16024551 | C | T | 1 | a0001c0001t0019g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.677-466C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024551 | |||||||
| chr17:16024754 | A | G | 1 | a0001c0001t0043g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.677-263A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024754 | |||||||
| chr17:16024864 | T | C | 8 | a0001c0001t0011g0022 a0001c0001t0011g0032 a0001c0001t0011g0091 others(5): Show |
13 | HG01891.hp2 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.677-153T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024864 | |||||||
| chr17:16024901 | T | C | 8 | a0001c0001t0010g0007 a0001c0001t0010g0176 a0001c0001t0010g0177 others(5): Show |
10 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-116T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024901 | |||||||
| chr17:16024908 | T | C | 37 | a0001c0001t0003g0097 a0001c0001t0004g0013 a0001c0001t0004g0020 others(34): Show |
44 | HG00408.hp1 HG00621.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.677-109T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024908 | |||||||
| chr17:16024975 | C | G | 1 | a0001c0001t0005g0046 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.677-42C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 7/9 | chr17 | 16024975 | |||||||
| chr17:16025270 | T | G | 116 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0038 others(113): Show |
145 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.831+99T>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025270 | |||||||
| chr17:16025286 | G | C | 98 | a0001c0001t0001g0038 a0001c0001t0003g0014 a0001c0001t0003g0102 others(95): Show |
123 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.831+115G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025286 | |||||||
| chr17:16025288 | C | A | 2 | a0001c0001t0031g0089 a0001c0001t0059g0090 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.831+117C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025288 | |||||||
| chr17:16025519 | C | T | 20 | a0001c0001t0006g0018 a0001c0001t0006g0023 a0001c0001t0006g0166 others(17): Show |
26 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.831+348C>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025519 | |||||||
| chr17:16025571 | A | G | 94 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(91): Show |
118 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.831+400A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025571 | |||||||
| chr17:16025676 | A | T | 5 | a0001c0001t0006g0023 a0001c0001t0006g0166 a0001c0001t0006g0175 others(2): Show |
6 | HG02015.hp2 HG04184.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+505A>T | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025676 | |||||||
| chr17:16025689 | C | A | 50 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(47): Show |
65 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.831+518C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025689 | |||||||
| chr17:16025715 | G | A | 1 | a0005c0005t0004g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.831+544G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025715 | |||||||
| chr17:16025822 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0123 others(5): Show |
11 | HG00408.hp2 HG00673.hp2 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+651A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025822 | |||||||
| chr17:16025842 | G | C | 4 | a0001c0001t0016g0030 a0001c0001t0016g0161 a0001c0001t0027g0168 others(1): Show |
5 | HG01891.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+671G>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025842 | |||||||
| chr17:16025903 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG00621.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.832-637T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16025903 | |||||||
| chr17:16026086 | C | A | 1 | a0001c0001t0057g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-454C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026086 | |||||||
| chr17:16026146 | C | A | 2 | a0001c0001t0001g0146 a0001c0001t0002g0145 |
2 | HG00673.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.832-394C>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026146 | |||||||
| chr17:16026153 | A | AT | 79 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(76): Show |
96 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.832-386dupT | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr17 | 16026153 | ||||||
| chr17:16026272 | T | C | 1 | a0001c0001t0048g0179 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832-268T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026272 | |||||||
| chr17:16026322 | T | C | 6 | a0001c0001t0006g0018 a0001c0001t0006g0042 a0001c0001t0006g0169 others(3): Show |
9 | HG00741.hp1 HG01433.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-218T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 8/9 | chr17 | 16026322 | |||||||
| chr17:16026773 | G | A | 134 | a0001c0001t0004g0002 a0001c0001t0004g0011 a0001c0001t0004g0012 others(131): Show |
169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.994+71G>A | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026773 | |||||||
| chr17:16026819 | A | G | 32 | a0001c0001t0006g0018 a0001c0001t0006g0023 a0001c0001t0006g0042 others(29): Show |
41 | HG00323.hp2 HG00741.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.994+117A>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026819 | |||||||
| chr17:16026833 | T | C | 1 | a0001c0001t0015g0069 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.994+131T>C | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026833 | |||||||
| chr17:16026944 | C | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0002g0035 |
3 | NA18961.hp2 NA18999.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.994+242C>G | TTC19 | ENSG00000011295.16 | transcript | ENST00000261647.10 | protein_coding | 9/9 | chr17 | 16026944 |