Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6668 |
| ensemblid | ENSG00000167182.16 |
| hgncid | 11207 |
| symbol | SP2 |
| name | Sp2 transcription factor |
| refseq_nuc | NM_003110.6 |
| refseq_prot | NP_003101.3 |
| ensembl_nuc | ENST00000376741.5 |
| ensembl_prot | ENSP00000365931.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 47896236 |
| end | 47928957 |
| strand | + |
| ver | v1.2 |
| region | chr17:47896236-47928957 |
| region5000 | chr17:47891236-47933957 |
| regionname0 | SP2_chr17_47896236_47928957 |
| regionname5000 | SP2_chr17_47891236_47933957 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 613 | 321 | 85 | 61 | 123 | 15 | 35 | 100 | SP2_chr17_47891236_47933957 | SP2 | MSDPQ others(608): Show |
chr17 | 47891236 | 47933957 |
| a0002 | 0/0 | 613 | 35 | 2 | 16 | 10 | 1 | 6 | 9 | SP2_chr17_47891236_47933957 | SP2 | MSDPQ others(608): Show |
chr17 | 47891236 | 47933957 |
| a0003 | 0/0 | 613 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | MSDPQ others(608): Show |
chr17 | 47891236 | 47933957 |
| a0004 | 0/0 | 613 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | MSDPQ others(608): Show |
chr17 | 47891236 | 47933957 |
| a0005 | 0/0 | 613 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | MSDPQ others(608): Show |
chr17 | 47891236 | 47933957 |
| a0006 | 0/0 | 606 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | MAATA others(601): Show |
chr17 | 47891236 | 47933957 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1839 | 173 | 32 | 25 | 89 | 9 | 17 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0001c0002 | 1/0 | 1839 | 122 | 30 | 35 | 32 | 6 | 18 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0001c0004 | 0/0 | 1839 | 19 | 19 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0001c0005 | 0/0 | 1839 | 5 | 4 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0001c0010 | 0/0 | 1839 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0001c0011 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0002c0003 | 0/0 | 1839 | 32 | 2 | 16 | 7 | 1 | 6 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0002c0008 | 0/0 | 1839 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0003c0006 | 0/0 | 1839 | 4 | 3 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0004c0007 | 0/0 | 1839 | 4 | 0 | 0 | 4 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0005c0012 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | ATGAG others(1834): Show |
chr17 | 47891236 | 47933957 | ||
| a0006c0009 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | AGGAG others(1834): Show |
chr17 | 47891236 | 47933957 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3028 | 170 | 31 | 24 | 88 | 9 | 17 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0001c0001t0006 | 0/0 | 3029 | 3 | 1 | 1 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3024): Show |
chr17 | 47891236 | 47933957 |
| a0001c0002t0001 | 0/0 | 3028 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0001c0002t0002 | 1/0 | 3026 | 110 | 29 | 26 | 31 | 5 | 18 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0001c0002t0003 | 0/0 | 3026 | 6 | 0 | 6 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0001c0002t0004 | 0/0 | 3027 | 5 | 1 | 3 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3022): Show |
chr17 | 47891236 | 47933957 |
| a0001c0004t0001 | 0/0 | 3028 | 9 | 9 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0001c0004t0002 | 0/0 | 3026 | 9 | 9 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0001c0004t0007 | 0/0 | 3026 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0001c0005t0001 | 0/0 | 3028 | 5 | 4 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0001c0010t0002 | 0/0 | 3026 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0001c0011t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0002c0003t0002 | 0/0 | 3026 | 31 | 2 | 15 | 7 | 1 | 6 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0002c0003t0004 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3022): Show |
chr17 | 47891236 | 47933957 |
| a0002c0008t0002 | 0/0 | 3026 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| a0003c0006t0005 | 0/0 | 3028 | 4 | 3 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0004c0007t0001 | 0/0 | 3028 | 4 | 0 | 0 | 4 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0005c0012t0001 | 0/0 | 3028 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3023): Show |
chr17 | 47891236 | 47933957 |
| a0006c0009t0002 | 0/0 | 3026 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | AGGCT others(3021): Show |
chr17 | 47891236 | 47933957 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 26 | 2 | 1 | 18 | 2 | 3 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0003 | 0/0 | 14 | 1 | 0 | 13 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0207 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0002 | 0/0 | 9 | 0 | 1 | 4 | 0 | 4 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0004 | 0/0 | 11 | 5 | 3 | 0 | 2 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0005 | 0/0 | 10 | 0 | 8 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0021 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0040 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0003g0002 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0004t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0005t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0010t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0001c0011t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0006 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0003t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0008t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0008t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0002c0008t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0003c0006t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0003c0006t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0004c0007t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0004c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0004c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0005c0012t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| a0006c0009t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0110 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0052 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0049 | EUR | GBR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00544 | hp2 | a0005 | c0012 | t0001 | g0197 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00558 | hp1 | a0001 | c0005 | t0001 | g0105 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0083 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00741 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0103 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01069 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01070 | hp1 | a0002 | c0003 | t0002 | g0077 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01099 | hp1 | a0002 | c0003 | t0002 | g0082 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01106 | hp1 | a0003 | c0006 | t0005 | g0164 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0075 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01257 | hp1 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0042 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0090 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0122 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01358 | hp2 | a0002 | c0003 | t0002 | g0126 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01433 | hp2 | a0002 | c0003 | t0002 | g0006 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01496 | hp2 | a0002 | c0003 | t0002 | g0087 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01515 | hp1 | a0002 | c0003 | t0002 | g0006 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01884 | hp1 | a0001 | c0005 | t0001 | g0013 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01975 | hp2 | a0002 | c0003 | t0002 | g0089 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01978 | hp1 | a0002 | c0003 | t0004 | g0088 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02004 | hp1 | a0001 | c0010 | t0002 | g0121 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02027 | hp2 | a0002 | c0003 | t0002 | g0086 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02074 | hp1 | a0004 | c0007 | t0001 | g0003 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02135 | hp1 | a0004 | c0007 | t0001 | g0130 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02155 | hp1 | a0004 | c0007 | t0001 | g0139 | EAS | CDX | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0096 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0218 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02273 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PEL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02630 | hp1 | a0001 | c0004 | t0002 | g0029 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0098 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0106 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0081 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02818 | hp1 | a0001 | c0004 | t0002 | g0014 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0220 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02896 | hp2 | a0003 | c0006 | t0005 | g0017 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02965 | hp2 | a0001 | c0004 | t0002 | g0129 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0215 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0216 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03209 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0221 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0013 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03239 | hp2 | a0002 | c0003 | t0002 | g0080 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03453 | hp2 | a0001 | c0004 | t0002 | g0028 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03486 | hp2 | a0002 | c0003 | t0002 | g0079 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03492 | hp1 | a0002 | c0003 | t0002 | g0125 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0029 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0014 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0069 | AFR | GWD | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03579 | hp1 | a0003 | c0006 | t0005 | g0017 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03579 | hp2 | a0001 | c0004 | t0002 | g0014 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0006 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0084 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0104 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04228 | hp1 | a0002 | c0003 | t0002 | g0085 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0091 | SAS | STU | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18522 | hp2 | a0003 | c0006 | t0005 | g0017 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18942 | hp2 | a0001 | c0011 | t0001 | g0228 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18943 | hp2 | a0002 | c0003 | t0002 | g0222 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18946 | hp1 | a0002 | c0008 | t0002 | g0199 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0117 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18978 | hp1 | a0002 | c0003 | t0002 | g0223 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18995 | hp1 | a0002 | c0008 | t0002 | g0200 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18995 | hp2 | a0004 | c0007 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19000 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19005 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19030 | hp2 | a0001 | c0004 | t0007 | g0127 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19057 | hp2 | a0002 | c0008 | t0002 | g0190 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA19240 | hp2 | a0002 | c0003 | t0002 | g0078 | AFR | YRI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | ASW | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ASW | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0101 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | GIH | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20905 | hp2 | a0006 | c0009 | t0002 | g0055 | SAS | GIH | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0230 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0128 | AFR | MSL | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA18955 | hp2 | a0002 | c0003 | t0002 | g0039 | EAS | JPT | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0109 | AFR | USA | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | LWK | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0207 | REF | REF | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0021 | REF | REF | SP2_chr17_47891236_47933957 | SP2 | chr17 | 47891236 | 47933957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47896288 | T | G | 1 | a0006 | 1 | NA20905.hp2 | start_lost | HIGH | c.2T>G | p.Met1? | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/7 | 53/3026 | 2/1842 | 1/613 | chr17 | 47896288 | |||
| chr17:47916750 | G | T | 1 | a0004 | 4 | HG02074.hp1 HG02135.hp1 HG02155.hp1 others(1): Show |
missense_variant | MODERATE | c.679G>T | p.Ala227Ser | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 730/3026 | 679/1842 | 227/613 | chr17 | 47916750 | |||
| chr17:47923040 | T | C | 1 | a0002 | 35 | HG00735.hp2 HG00741.hp1 HG01069.hp1 others(32): Show |
missense_variant | MODERATE | c.1138T>C | p.Ser380Pro | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/7 | 1189/3026 | 1138/1842 | 380/613 | chr17 | 47923040 | |||
| chr17:47923046 | A | G | 1 | a0003 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.1144A>G | p.Thr382Ala | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/7 | 1195/3026 | 1144/1842 | 382/613 | chr17 | 47923046 | |||
| chr17:47925410 | G | T | 1 | a0005 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.1610G>T | p.Arg537Leu | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/7 | 1661/3026 | 1610/1842 | 537/613 | chr17 | 47925410 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47916678 | C | T | 7 | a0001c0001 a0001c0004 a0001c0011 others(4): Show |
204 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(201): Show |
synonymous_variant | LOW | c.607C>T | p.Leu203Leu | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 658/3026 | 607/1842 | 203/613 | chr17 | 47916678 | |||
| chr17:47916683 | A | G | 1 | a0001c0010 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.612A>G | p.Thr204Thr | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 663/3026 | 612/1842 | 204/613 | chr17 | 47916683 | |||
| chr17:47916728 | T | C | 7 | a0001c0001 a0001c0004 a0001c0011 others(4): Show |
204 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(201): Show |
synonymous_variant | LOW | c.657T>C | p.Leu219Leu | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 708/3026 | 657/1842 | 219/613 | chr17 | 47916728 | |||
| chr17:47916788 | G | A | 5 | a0001c0001 a0001c0011 a0002c0008 others(2): Show |
181 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(178): Show |
synonymous_variant | LOW | c.717G>A | p.Pro239Pro | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 768/3026 | 717/1842 | 239/613 | chr17 | 47916788 | |||
| chr17:47917106 | G | A | 1 | a0001c0011 | 1 | NA18942.hp2 | synonymous_variant | LOW | c.1035G>A | p.Gln345Gln | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/7 | 1086/3026 | 1035/1842 | 345/613 | chr17 | 47917106 | |||
| chr17:47925378 | G | T | 5 | a0001c0001 a0001c0005 a0001c0011 others(2): Show |
183 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(180): Show |
synonymous_variant | LOW | c.1578G>T | p.Val526Val | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/7 | 1629/3026 | 1578/1842 | 526/613 | chr17 | 47925378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47928098 | G | A | 1 | a0001c0002t0003 | 6 | HG00738.hp1 HG01106.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 274 | chr17 | 47928098 | ||||||
| chr17:47928164 | A | AC | 3 | a0001c0001t0006 a0001c0002t0004 a0002c0003t0004 |
9 | HG00741.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*346dupC | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 347 | INFO_REALIGN_3_PRIME | chr17 | 47928164 | |||||
| chr17:47928426 | A | ACT | 9 | a0001c0001t0001 a0001c0001t0006 a0001c0002t0001 others(6): Show |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*606dupCT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 607 | INFO_REALIGN_3_PRIME | chr17 | 47928426 | |||||
| chr17:47928485 | T | C | 1 | a0001c0004t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*661T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 661 | chr17 | 47928485 | ||||||
| chr17:47928602 | T | C | 1 | a0003c0006t0005 | 4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*778T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 778 | chr17 | 47928602 | ||||||
| chr17:47928932 | T | G | 1 | a0001c0004t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1108T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 7/7 | 1108 | chr17 | 47928932 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:47896319 | G | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0230 |
3 | HG00639.hp1 HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.7+26G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896319 | |||||||
| chr17:47896398 | G | A | 1 | a0001c0002t0002g0041 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.7+105G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896398 | |||||||
| chr17:47896427 | A | T | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+134A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896427 | |||||||
| chr17:47896592 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7+299C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896592 | |||||||
| chr17:47896650 | C | T | 3 | a0002c0003t0002g0039 a0002c0003t0002g0222 a0002c0003t0002g0223 |
4 | NA18943.hp2 NA18955.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+357C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896650 | |||||||
| chr17:47896721 | G | A | 1 | a0002c0003t0002g0042 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.7+428G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896721 | |||||||
| chr17:47896758 | C | T | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+465C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896758 | |||||||
| chr17:47896885 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
104 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.7+592C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896885 | |||||||
| chr17:47896886 | A | C | 1 | a0001c0001t0001g0169 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.7+593A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896886 | |||||||
| chr17:47896919 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
202 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.7+626C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47896919 | |||||||
| chr17:47897128 | C | T | 2 | a0002c0003t0002g0125 a0002c0003t0002g0126 |
2 | HG01358.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.7+835C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897128 | |||||||
| chr17:47897684 | G | A | 4 | a0001c0002t0002g0011 a0001c0002t0002g0043 a0001c0002t0002g0044 others(1): Show |
6 | NA18747.hp1 NA18956.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+1391G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897684 | |||||||
| chr17:47897819 | C | T | 1 | a0001c0002t0002g0124 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.7+1526C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897819 | |||||||
| chr17:47897910 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7+1617C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47897910 | |||||||
| chr17:47898026 | A | T | 1 | a0001c0002t0002g0122 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7+1733A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898026 | |||||||
| chr17:47898157 | C | T | 1 | a0001c0010t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.7+1864C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898157 | |||||||
| chr17:47898167 | G | T | 1 | a0001c0002t0002g0027 | 2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.7+1874G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898167 | |||||||
| chr17:47898209 | A | T | 1 | a0001c0002t0002g0120 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.7+1916A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898209 | |||||||
| chr17:47898333 | T | G | 1 | a0001c0004t0007g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+2040T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898333 | |||||||
| chr17:47898489 | T | C | 5 | a0001c0004t0002g0014 a0001c0004t0002g0028 a0001c0004t0002g0029 others(2): Show |
9 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+2196T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898489 | |||||||
| chr17:47898623 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(25): Show |
47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+2330T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898623 | |||||||
| chr17:47898792 | A | G | 2 | a0001c0002t0002g0118 a0001c0002t0002g0119 |
2 | NA18950.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.7+2499A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47898792 | |||||||
| chr17:47899023 | T | G | 28 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(25): Show |
47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+2730T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899023 | |||||||
| chr17:47899105 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.7+2812C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899105 | |||||||
| chr17:47899199 | T | C | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+2906T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899199 | |||||||
| chr17:47899234 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.7+2941C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899234 | |||||||
| chr17:47899257 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7+2964C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899257 | |||||||
| chr17:47899340 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+3047A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899340 | |||||||
| chr17:47899372 | T | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(41): Show |
65 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.7+3079T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899372 | |||||||
| chr17:47899458 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
115 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.7+3165A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899458 | |||||||
| chr17:47899483 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG02148.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7+3190A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899483 | |||||||
| chr17:47899526 | T | C | 1 | a0004c0007t0001g0130 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.7+3233T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899526 | |||||||
| chr17:47899722 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0170 a0001c0001t0001g0171 |
4 | HG00438.hp2 HG00639.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3429G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899722 | |||||||
| chr17:47899818 | C | T | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3525C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47899818 | |||||||
| chr17:47900136 | A | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0154 others(12): Show |
17 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+3843A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900136 | |||||||
| chr17:47900259 | A | G | 1 | a0002c0003t0002g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.7+3966A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900259 | |||||||
| chr17:47900266 | A | G | 15 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0154 others(12): Show |
17 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+3973A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900266 | |||||||
| chr17:47900326 | G | T | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+4033G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900326 | |||||||
| chr17:47900347 | C | T | 1 | a0001c0002t0002g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7+4054C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900347 | |||||||
| chr17:47900470 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01993.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.7+4177C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900470 | |||||||
| chr17:47900500 | G | A | 3 | a0001c0004t0001g0215 a0001c0004t0001g0216 a0001c0004t0001g0217 |
3 | HG02970.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.7+4207G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900500 | |||||||
| chr17:47900745 | C | T | 72 | a0001c0002t0001g0110 a0001c0002t0002g0002 a0001c0002t0002g0005 others(69): Show |
109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.7+4452C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47900745 | |||||||
| chr17:47901077 | AGTCAC | A | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+4787_7+4791delCA others(3): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47901077 | ||||||
| chr17:47901149 | C | CT | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
127 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.7+4870dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47901149 | ||||||
| chr17:47901240 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.7+4947C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901240 | |||||||
| chr17:47901280 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(25): Show |
47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+4987T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901280 | |||||||
| chr17:47901335 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.7+5042C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901335 | |||||||
| chr17:47901421 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
115 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.7+5128A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901421 | |||||||
| chr17:47901447 | G | GT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0155 others(10): Show |
15 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.7+5162dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47901447 | ||||||
| chr17:47901513 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+5220C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901513 | |||||||
| chr17:47901869 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.7+5576T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47901869 | |||||||
| chr17:47902053 | A | G | 1 | a0001c0002t0002g0114 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.7+5760A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47902053 | |||||||
| chr17:47902491 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.7+6198G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47902491 | |||||||
| chr17:47902894 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+6601T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47902894 | |||||||
| chr17:47903036 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.7+6743G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903036 | |||||||
| chr17:47903136 | G | A | 2 | a0001c0002t0002g0046 a0001c0002t0002g0047 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.7+6843G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903136 | |||||||
| chr17:47903394 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+7101G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903394 | |||||||
| chr17:47903527 | C | T | 5 | a0001c0004t0002g0014 a0001c0004t0002g0028 a0001c0004t0002g0029 others(2): Show |
9 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+7234C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903527 | |||||||
| chr17:47903541 | C | T | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+7248C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903541 | |||||||
| chr17:47903590 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.7+7297C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903590 | |||||||
| chr17:47903638 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
94 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.7+7345A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903638 | |||||||
| chr17:47903739 | A | C | 2 | a0001c0002t0002g0040 a0001c0002t0002g0230 |
3 | HG00639.hp1 HG01123.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.7+7446A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903739 | |||||||
| chr17:47903912 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
128 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.7+7619T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903912 | |||||||
| chr17:47903957 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(25): Show |
47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+7664T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903957 | |||||||
| chr17:47903991 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
128 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.7+7698A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47903991 | |||||||
| chr17:47904058 | C | T | 1 | a0001c0002t0002g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7+7765C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904058 | |||||||
| chr17:47904144 | A | C | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+7851A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904144 | |||||||
| chr17:47904170 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(124): Show |
202 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.7+7877T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904170 | |||||||
| chr17:47904178 | T | TG | 2 | a0001c0001t0001g0037 a0001c0001t0001g0210 |
3 | HG00558.hp2 NA18987.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.7+7887dupG | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904178 | ||||||
| chr17:47904262 | C | CA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
122 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.7+7987dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904262 | ||||||
| chr17:47904262 | C | CAA | 8 | a0001c0001t0001g0034 a0001c0001t0001g0170 a0001c0001t0001g0172 others(5): Show |
10 | HG00597.hp1 HG01175.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+7986_7+7987dupAA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904262 | ||||||
| chr17:47904282 | A | T | 1 | a0001c0002t0002g0113 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.7+7989A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904282 | |||||||
| chr17:47904553 | G | A | 26 | a0001c0002t0002g0040 a0001c0002t0002g0230 a0002c0003t0002g0006 others(23): Show |
35 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.7+8260G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904553 | |||||||
| chr17:47904569 | T | G | 1 | a0002c0003t0002g0076 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.7+8276T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904569 | |||||||
| chr17:47904570 | G | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG02486.hp1 HG02698.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.7+8277G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904570 | |||||||
| chr17:47904647 | C | T | 1 | a0001c0002t0002g0112 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7+8354C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904647 | |||||||
| chr17:47904648 | G | A | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+8355G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904648 | |||||||
| chr17:47904713 | G | GT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
128 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.7+8424dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904713 | ||||||
| chr17:47904768 | A | AT | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+8480dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47904768 | ||||||
| chr17:47904881 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7+8588C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904881 | |||||||
| chr17:47904893 | C | T | 2 | a0001c0004t0001g0038 a0001c0004t0001g0221 |
3 | HG02818.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.7+8600C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904893 | |||||||
| chr17:47904953 | G | A | 2 | a0001c0002t0002g0020 a0001c0002t0002g0048 |
3 | HG02109.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7+8660G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904953 | |||||||
| chr17:47904980 | C | G | 72 | a0001c0002t0001g0110 a0001c0002t0002g0002 a0001c0002t0002g0005 others(69): Show |
109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.7+8687C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904980 | |||||||
| chr17:47904994 | A | T | 9 | a0001c0002t0001g0110 a0001c0002t0002g0005 a0001c0002t0002g0108 others(6): Show |
18 | HG00099.hp1 HG00738.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+8701A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47904994 | |||||||
| chr17:47905071 | T | A | 1 | a0001c0001t0001g0156 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.7+8778T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905071 | |||||||
| chr17:47905107 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(25): Show |
47 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+8814C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905107 | |||||||
| chr17:47905431 | G | A | 72 | a0001c0002t0001g0110 a0001c0002t0002g0002 a0001c0002t0002g0005 others(69): Show |
109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.7+9138G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905431 | |||||||
| chr17:47905674 | A | G | 1 | a0001c0005t0001g0013 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+9381A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905674 | |||||||
| chr17:47905708 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0166 |
3 | HG01243.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.7+9415C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905708 | |||||||
| chr17:47905817 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.8-9495C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905817 | |||||||
| chr17:47905911 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.8-9401G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47905911 | |||||||
| chr17:47906391 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.8-8921C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906391 | |||||||
| chr17:47906529 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.8-8783C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906529 | |||||||
| chr17:47906660 | C | T | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-8652C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906660 | |||||||
| chr17:47906894 | C | T | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-8418C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47906894 | |||||||
| chr17:47907072 | T | C | 1 | a0001c0002t0002g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.8-8240T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907072 | |||||||
| chr17:47907243 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.8-8069G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907243 | |||||||
| chr17:47907555 | A | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0155 others(10): Show |
15 | HG02080.hp2 HG02148.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-7757A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907555 | |||||||
| chr17:47907583 | A | G | 44 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(41): Show |
65 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.8-7729A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907583 | |||||||
| chr17:47907699 | G | A | 1 | a0001c0004t0007g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8-7613G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907699 | |||||||
| chr17:47907877 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.8-7435C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47907877 | |||||||
| chr17:47908048 | A | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
128 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.8-7264A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908048 | |||||||
| chr17:47908228 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0166 |
3 | HG01243.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.8-7084A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908228 | |||||||
| chr17:47908458 | C | G | 1 | a0001c0002t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.8-6854C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908458 | |||||||
| chr17:47908586 | C | G | 1 | a0001c0002t0002g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8-6726C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908586 | |||||||
| chr17:47908783 | G | C | 1 | a0001c0002t0002g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.8-6529G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908783 | |||||||
| chr17:47908850 | C | T | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-6462C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908850 | |||||||
| chr17:47908916 | C | A | 72 | a0001c0002t0001g0110 a0001c0002t0002g0002 a0001c0002t0002g0005 others(69): Show |
109 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.8-6396C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908916 | |||||||
| chr17:47908962 | G | A | 4 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0052 others(1): Show |
4 | HG00099.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-6350G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908962 | |||||||
| chr17:47908973 | G | C | 1 | a0001c0002t0002g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8-6339G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47908973 | |||||||
| chr17:47909092 | C | G | 3 | a0001c0004t0001g0218 a0001c0004t0001g0219 a0001c0004t0001g0220 |
3 | HG02258.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.8-6220C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909092 | |||||||
| chr17:47909130 | A | G | 9 | a0001c0001t0001g0033 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
10 | HG01081.hp2 HG01169.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-6182A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909130 | |||||||
| chr17:47909498 | C | T | 3 | a0001c0004t0001g0215 a0001c0004t0001g0216 a0001c0004t0001g0217 |
3 | HG02970.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.8-5814C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909498 | |||||||
| chr17:47909917 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.8-5395G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909917 | |||||||
| chr17:47909959 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.8-5353T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47909959 | |||||||
| chr17:47910008 | C | T | 7 | a0001c0001t0001g0165 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-5304C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910008 | |||||||
| chr17:47910130 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.8-5182C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910130 | |||||||
| chr17:47910240 | T | C | 1 | a0001c0002t0002g0054 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.8-5072T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910240 | |||||||
| chr17:47910294 | C | T | 4 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0052 others(1): Show |
4 | HG00099.hp2 HG01255.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-5018C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47910294 | |||||||
| chr17:47910896 | A | AGTTACCT others(15): Show |
1 | a0001c0002t0002g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.8-4415_8-4394dupGT others(20): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47910896 | ||||||
| chr17:47911008 | TTGAGCCC others(22): Show |
T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4302_8-4274delGA others(27): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47911008 | ||||||
| chr17:47911038 | T | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4274T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911038 | |||||||
| chr17:47911039 | A | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4273A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911039 | |||||||
| chr17:47911044 | G | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4268G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911044 | |||||||
| chr17:47911046 | C | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4266C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911046 | |||||||
| chr17:47911050 | A | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4262A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911050 | |||||||
| chr17:47911051 | C | G | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4261C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911051 | |||||||
| chr17:47911052 | C | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4260C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911052 | |||||||
| chr17:47911053 | C | T | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.8-4259C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911053 | |||||||
| chr17:47911090 | G | C | 1 | a0002c0003t0002g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.8-4222G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911090 | |||||||
| chr17:47911167 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
104 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.8-4145G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911167 | |||||||
| chr17:47911182 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0150 |
5 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-4130C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911182 | |||||||
| chr17:47911465 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.8-3847A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911465 | |||||||
| chr17:47911467 | C | G | 3 | a0001c0002t0002g0091 a0001c0002t0002g0106 a0001c0002t0002g0122 |
3 | HG01358.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.8-3845C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911467 | |||||||
| chr17:47911506 | C | CA | 13 | a0001c0001t0001g0170 a0001c0002t0002g0024 a0001c0002t0002g0092 others(10): Show |
15 | HG00597.hp2 HG00621.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.8-3790dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47911506 | ||||||
| chr17:47911549 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.8-3763C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911549 | |||||||
| chr17:47911584 | G | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
94 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.8-3728G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911584 | |||||||
| chr17:47911659 | A | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
104 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.8-3653A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911659 | |||||||
| chr17:47911680 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
128 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.8-3632T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911680 | |||||||
| chr17:47911729 | C | T | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.8-3583C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911729 | |||||||
| chr17:47911736 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-3576C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911736 | |||||||
| chr17:47911804 | C | CA | 11 | a0001c0001t0001g0134 a0001c0001t0001g0166 a0001c0001t0001g0183 others(8): Show |
12 | HG00639.hp1 HG01123.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3491dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47911804 | ||||||
| chr17:47911880 | C | G | 3 | a0001c0002t0002g0067 a0001c0002t0002g0068 a0001c0002t0002g0069 |
3 | HG02486.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.8-3432C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911880 | |||||||
| chr17:47911911 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-3401A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911911 | |||||||
| chr17:47911972 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-3340A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47911972 | |||||||
| chr17:47912442 | C | CT | 7 | a0001c0001t0001g0149 a0001c0001t0001g0170 a0001c0001t0001g0204 others(4): Show |
7 | HG01123.hp1 HG02080.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2853dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912442 | ||||||
| chr17:47912442 | C | CTTTTT | 4 | a0001c0004t0002g0014 a0001c0004t0002g0028 a0001c0004t0002g0029 others(1): Show |
8 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-2857_8-2853dupTT others(3): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912442 | ||||||
| chr17:47912442 | CT | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0150 others(4): Show |
7 | HG01070.hp1 HG01175.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2853delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912442 | ||||||
| chr17:47912457 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | HG01256.hp2 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.8-2855T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47912457 | |||||||
| chr17:47912513 | C | T | 1 | a0001c0002t0002g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8-2799C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47912513 | |||||||
| chr17:47912850 | T | TTTTG | 2 | a0001c0004t0001g0215 a0001c0004t0002g0028 |
3 | HG02976.hp2 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.8-2438_8-2435dupGT others(2): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47912850 | ||||||
| chr17:47913231 | T | C | 73 | a0001c0002t0001g0110 a0001c0002t0002g0002 a0001c0002t0002g0005 others(70): Show |
110 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.8-2081T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913231 | |||||||
| chr17:47913789 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8-1523T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913789 | |||||||
| chr17:47913874 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
102 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.8-1438C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913874 | |||||||
| chr17:47913887 | T | C | 1 | a0002c0008t0002g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.8-1425T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47913887 | |||||||
| chr17:47914059 | C | T | 3 | a0001c0004t0001g0218 a0001c0004t0001g0219 a0001c0004t0001g0220 |
3 | HG02258.hp2 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.8-1253C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47914059 | |||||||
| chr17:47914357 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.8-955G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47914357 | |||||||
| chr17:47914371 | C | CA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0135 a0001c0001t0001g0183 others(7): Show |
12 | HG02258.hp2 HG02559.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-926dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47914371 | ||||||
| chr17:47915011 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.8-301G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915011 | |||||||
| chr17:47915043 | G | A | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-269G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915043 | |||||||
| chr17:47915214 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(51): Show |
99 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.8-85dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47915214 | ||||||
| chr17:47915214 | C | CAA | 5 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(2): Show |
6 | HG02818.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-86_8-85dupAA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr17 | 47915214 | ||||||
| chr17:47915256 | G | A | 26 | a0001c0002t0002g0040 a0001c0002t0002g0230 a0002c0003t0002g0006 others(23): Show |
35 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.8-56G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915256 | |||||||
| chr17:47915266 | C | G | 8 | a0002c0003t0002g0023 a0002c0003t0002g0042 a0002c0003t0002g0076 others(5): Show |
9 | HG01109.hp1 HG01261.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-46C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 1/6 | chr17 | 47915266 | |||||||
| chr17:47915550 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(42): Show |
66 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.84+162C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915550 | |||||||
| chr17:47915635 | G | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.84+247G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915635 | |||||||
| chr17:47915813 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.85-343C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915813 | |||||||
| chr17:47915834 | C | G | 10 | a0001c0002t0002g0020 a0001c0002t0002g0048 a0001c0004t0001g0038 others(7): Show |
12 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.85-322C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915834 | |||||||
| chr17:47915870 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.85-286C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47915870 | |||||||
| chr17:47916101 | C | T | 6 | a0001c0001t0001g0165 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-55C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47916101 | |||||||
| chr17:47916117 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.85-39C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 2/6 | chr17 | 47916117 | |||||||
| chr17:47917158 | T | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0064 others(12): Show |
17 | HG00140.hp1 HG01167.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1059+28T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917158 | |||||||
| chr17:47917169 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1059+39G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917169 | |||||||
| chr17:47917332 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+202T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917332 | |||||||
| chr17:47917358 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(127): Show |
207 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.1059+228A>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917358 | |||||||
| chr17:47917625 | GT | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(214): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1059+509delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47917625 | ||||||
| chr17:47917625 | GTT | G | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+508_1059+509d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47917625 | ||||||
| chr17:47917901 | G | A | 3 | a0001c0002t0002g0067 a0001c0002t0002g0068 a0001c0002t0002g0069 |
3 | HG02486.hp2 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1059+771G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917901 | |||||||
| chr17:47917939 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1059+809G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47917939 | |||||||
| chr17:47918114 | GT | G | 7 | a0001c0001t0001g0135 a0001c0002t0002g0025 a0001c0002t0002g0026 others(4): Show |
10 | HG01256.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059+997delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47918114 | ||||||
| chr17:47918525 | C | G | 1 | a0002c0003t0002g0126 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1059+1395C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918525 | |||||||
| chr17:47918538 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1059+1408G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918538 | |||||||
| chr17:47918769 | A | T | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+1639A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918769 | |||||||
| chr17:47918898 | C | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(42): Show |
66 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.1059+1768C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918898 | |||||||
| chr17:47918937 | G | A | 4 | a0001c0004t0002g0014 a0001c0004t0002g0028 a0001c0004t0002g0029 others(1): Show |
8 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1059+1807G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47918937 | |||||||
| chr17:47919002 | T | TAC | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(174): Show |
282 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.1059+1884_1059+188 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919002 | ||||||
| chr17:47919002 | TAC | T | 26 | a0001c0002t0002g0040 a0001c0002t0002g0230 a0002c0003t0002g0006 others(23): Show |
35 | HG00639.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1059+1884_1059+188 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919002 | ||||||
| chr17:47919028 | T | TAC | 4 | a0001c0001t0001g0182 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+1912_1059+191 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919028 | ||||||
| chr17:47919306 | A | G | 1 | a0001c0005t0001g0013 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1059+2176A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919306 | |||||||
| chr17:47919359 | A | G | 1 | a0001c0002t0002g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1059+2229A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919359 | |||||||
| chr17:47919421 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0152 |
2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1059+2291A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919421 | |||||||
| chr17:47919422 | A | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(122): Show |
198 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.1059+2292A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919422 | |||||||
| chr17:47919608 | C | T | 1 | a0001c0011t0001g0228 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1059+2478C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919608 | |||||||
| chr17:47919666 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0161 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1059+2536A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919666 | |||||||
| chr17:47919710 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(119): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1059+2580G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919710 | |||||||
| chr17:47919825 | C | CTTTT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(31): Show |
58 | HG00642.hp1 HG01167.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.1059+2714_1059+271 others(8): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | C | CTTTTT | 18 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0065 others(15): Show |
20 | HG00140.hp1 HG01074.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1059+2713_1059+271 others(9): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | C | CTTTTTT | 36 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(33): Show |
76 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1059+2712_1059+271 others(10): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | C | CTTTTTTT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0170 others(13): Show |
20 | HG01081.hp2 HG01123.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1059+2711_1059+271 others(11): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | C | CTTTTTTT others(2): Show |
5 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0219 others(2): Show |
6 | HG02559.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059+2709_1059+271 others(13): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | C | CTTTTTTT others(3): Show |
2 | a0001c0004t0001g0216 a0001c0004t0001g0217 |
2 | HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1059+2708_1059+271 others(14): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | CTT | C | 25 | a0001c0001t0001g0165 a0001c0002t0002g0027 a0001c0002t0002g0053 others(22): Show |
31 | HG00741.hp2 HG01109.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059+2716_1059+271 others(6): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919825 | CTTT | C | 87 | a0001c0001t0001g0138 a0001c0002t0001g0110 a0001c0002t0002g0002 others(84): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1059+2715_1059+271 others(7): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47919825 | ||||||
| chr17:47919847 | T | C | 1 | a0002c0008t0002g0190 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1059+2717T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919847 | |||||||
| chr17:47919940 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1059+2810G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919940 | |||||||
| chr17:47919993 | C | T | 1 | a0005c0012t0001g0197 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1059+2863C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47919993 | |||||||
| chr17:47920141 | C | T | 1 | a0002c0003t0002g0086 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1060-2821C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920141 | |||||||
| chr17:47920209 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0140 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1060-2753G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920209 | |||||||
| chr17:47920264 | C | T | 3 | a0001c0002t0002g0026 a0001c0002t0002g0093 a0001c0002t0002g0112 |
4 | HG02055.hp1 HG02109.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-2698C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920264 | |||||||
| chr17:47920290 | A | AT | 15 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0224 others(12): Show |
16 | HG00597.hp2 HG02027.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1060-2656dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47920290 | ||||||
| chr17:47920452 | G | A | 2 | a0001c0004t0001g0038 a0001c0004t0001g0221 |
3 | HG02818.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1060-2510G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920452 | |||||||
| chr17:47920574 | C | G | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-2388C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920574 | |||||||
| chr17:47920582 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1060-2380G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920582 | |||||||
| chr17:47920648 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(225): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1060-2314T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920648 | |||||||
| chr17:47920684 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(110): Show |
181 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1060-2278G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920684 | |||||||
| chr17:47920739 | T | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02486.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1060-2223T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920739 | |||||||
| chr17:47920762 | T | C | 8 | a0001c0004t0001g0038 a0001c0004t0001g0215 a0001c0004t0001g0216 others(5): Show |
9 | HG02258.hp2 HG02559.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-2200T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47920762 | |||||||
| chr17:47921127 | G | A | 2 | a0001c0002t0002g0097 a0001c0002t0002g0098 |
2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1060-1835G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921127 | |||||||
| chr17:47921319 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG00438.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1060-1643A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921319 | |||||||
| chr17:47921401 | A | G | 1 | a0001c0005t0001g0013 | 3 | HG01884.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1060-1561A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921401 | |||||||
| chr17:47921464 | C | A | 2 | a0001c0002t0002g0099 a0001c0002t0002g0100 |
2 | NA18964.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1060-1498C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921464 | |||||||
| chr17:47921674 | C | A | 1 | a0001c0002t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1060-1288C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921674 | |||||||
| chr17:47921754 | A | G | 46 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(43): Show |
67 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.1060-1208A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47921754 | |||||||
| chr17:47922073 | G | A | 5 | a0001c0004t0002g0014 a0001c0004t0002g0028 a0001c0004t0002g0029 others(2): Show |
9 | HG02630.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-889G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922073 | |||||||
| chr17:47922205 | T | C | 1 | a0001c0004t0002g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1060-757T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922205 | |||||||
| chr17:47922216 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1060-746T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922216 | |||||||
| chr17:47922257 | C | T | 1 | a0002c0003t0002g0117 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1060-705C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922257 | |||||||
| chr17:47922467 | G | C | 1 | a0001c0002t0002g0111 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1060-495G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922467 | |||||||
| chr17:47922524 | CTT | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(43): Show |
67 | HG00140.hp1 HG01167.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.1060-427_1060-426d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr17 | 47922524 | ||||||
| chr17:47922713 | G | A | 1 | a0001c0010t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1060-249G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922713 | |||||||
| chr17:47922831 | G | A | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(2): Show |
5 | HG01175.hp2 HG01192.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-131G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922831 | |||||||
| chr17:47922906 | G | A | 1 | a0002c0003t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060-56G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 3/6 | chr17 | 47922906 | |||||||
| chr17:47923282 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01081.hp2 | splice_region_variant&intron_variant | LOW | c.1372+8T>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923282 | |||||||
| chr17:47923335 | C | T | 1 | a0001c0010t0002g0121 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1372+61C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923335 | |||||||
| chr17:47923505 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1372+231G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923505 | |||||||
| chr17:47923539 | C | T | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+265C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923539 | |||||||
| chr17:47923739 | C | T | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+465C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923739 | |||||||
| chr17:47923862 | C | T | 1 | a0002c0003t0002g0085 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1372+588C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923862 | |||||||
| chr17:47923946 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1372+672C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47923946 | |||||||
| chr17:47924127 | T | A | 1 | a0001c0001t0001g0214 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1373-792T>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924127 | |||||||
| chr17:47924134 | G | GT | 15 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0001c0001t0001g0152 others(12): Show |
15 | HG01175.hp2 HG01261.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.1373-772dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 47924134 | ||||||
| chr17:47924169 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(110): Show |
183 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.1373-750G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924169 | |||||||
| chr17:47924309 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1373-610A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924309 | |||||||
| chr17:47924339 | A | AT | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(226): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1373-579dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr17 | 47924339 | ||||||
| chr17:47924502 | C | A | 1 | a0001c0002t0002g0092 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1373-417C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924502 | |||||||
| chr17:47924652 | C | G | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-267C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924652 | |||||||
| chr17:47924798 | C | G | 2 | a0001c0004t0001g0215 a0001c0004t0001g0217 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1373-121C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 4/6 | chr17 | 47924798 | |||||||
| chr17:47925822 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(120): Show |
196 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1741+281A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925822 | |||||||
| chr17:47925882 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1741+341A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925882 | |||||||
| chr17:47925904 | C | CATTTT | 1 | a0003c0006t0005g0017 | 3 | HG02896.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1741+363_1741+364i others(7): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925904 | |||||||
| chr17:47925905 | C | CT | 38 | a0001c0002t0002g0012 a0001c0002t0002g0044 a0001c0002t0002g0047 others(35): Show |
43 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1741+392dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | C | CTT | 5 | a0001c0001t0001g0168 a0001c0002t0002g0104 a0001c0004t0001g0220 others(2): Show |
6 | HG01978.hp1 HG02630.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+391_1741+392d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | C | T | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+364C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47925905 | |||||||
| chr17:47925905 | CT | C | 9 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0144 others(6): Show |
10 | HG02109.hp1 HG02109.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1741+392delT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | CTT | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0131 others(17): Show |
37 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1741+391_1741+392d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | CTTTTTT | C | 11 | a0001c0001t0001g0007 a0001c0001t0001g0165 a0001c0001t0001g0174 others(8): Show |
18 | HG01175.hp2 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1741+387_1741+392d others(8): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | CTTTTTTT | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(46): Show |
88 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1741+386_1741+392d others(9): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0166 a0001c0001t0001g0181 others(2): Show |
6 | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+385_1741+392d others(10): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47925905 | CTTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0064 others(14): Show |
19 | HG00140.hp1 HG01167.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1741+382_1741+392d others(13): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47925905 | ||||||
| chr17:47926161 | C | G | 2 | a0003c0006t0005g0017 a0003c0006t0005g0164 |
4 | HG01106.hp1 HG02896.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1741+620C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926161 | |||||||
| chr17:47926192 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+651G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926192 | |||||||
| chr17:47926193 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+652A>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926193 | |||||||
| chr17:47926194 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+653G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926194 | |||||||
| chr17:47926195 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+654G>C | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926195 | |||||||
| chr17:47926196 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1741+655C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926196 | |||||||
| chr17:47926315 | G | GT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(117): Show |
191 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.1741+789dupT | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47926315 | ||||||
| chr17:47926315 | G | GTT | 4 | a0001c0001t0001g0193 a0001c0001t0001g0210 a0003c0006t0005g0017 others(1): Show |
6 | HG01106.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1741+788_1741+789d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47926315 | ||||||
| chr17:47926315 | G | T | 1 | a0001c0004t0007g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1741+774G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926315 | |||||||
| chr17:47926334 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0171 |
3 | HG00438.hp2 HG00639.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1741+793A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926334 | |||||||
| chr17:47926433 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0064 others(12): Show |
17 | HG00140.hp1 HG01167.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1741+892C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926433 | |||||||
| chr17:47926440 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1741+899G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926440 | |||||||
| chr17:47926493 | T | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(120): Show |
196 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1741+952T>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926493 | |||||||
| chr17:47926523 | C | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(120): Show |
196 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.1741+982C>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926523 | |||||||
| chr17:47926548 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1741+1007A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926548 | |||||||
| chr17:47926744 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0166 |
3 | HG01243.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1742-980C>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47926744 | |||||||
| chr17:47927172 | A | G | 1 | a0001c0004t0002g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1742-552A>G | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927172 | |||||||
| chr17:47927300 | A | AAGGTGGG others(16): Show |
1 | a0001c0001t0001g0211 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1742-420_1742-398d others(25): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927300 | ||||||
| chr17:47927431 | G | T | 4 | a0001c0002t0002g0022 a0001c0002t0002g0092 a0001c0002t0002g0095 others(1): Show |
5 | NA18940.hp2 NA18975.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1742-293G>T | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927431 | |||||||
| chr17:47927462 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1742-262G>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927462 | |||||||
| chr17:47927531 | C | CA | 8 | a0001c0002t0002g0050 a0001c0002t0002g0058 a0001c0002t0002g0104 others(5): Show |
8 | HG00735.hp2 HG01099.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1742-172dupA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927531 | ||||||
| chr17:47927531 | CA | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0193 a0001c0002t0002g0098 |
6 | HG01346.hp2 HG01891.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1742-172delA | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927531 | ||||||
| chr17:47927531 | CAA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(116): Show |
189 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.1742-173_1742-172d others(4): Show |
SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | 47927531 | ||||||
| chr17:47927644 | C | A | 1 | a0001c0002t0002g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1742-80C>A | SP2 | ENSG00000167182.16 | transcript | ENST00000376741.5 | protein_coding | 6/6 | chr17 | 47927644 |