Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11261 |
| ensemblid | ENSG00000187446.12 |
| hgncid | 17433 |
| symbol | CHP1 |
| name | calcineurin like EF-hand protein 1 |
| refseq_nuc | NM_007236.5 |
| refseq_prot | NP_009167.1 |
| ensembl_nuc | ENST00000334660.10 |
| ensembl_prot | ENSP00000335632.5 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 41231268 |
| end | 41281887 |
| strand | + |
| ver | v1.2 |
| region | chr15:41231268-41281887 |
| region5000 | chr15:41226268-41286887 |
| regionname0 | CHP1_chr15_41231268_41281887 |
| regionname5000 | CHP1_chr15_41226268_41286887 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 585 | 298 | 96 | 50 | 102 | 10 | 38 | CHP1_chr15_41226268_41286887 | CHP1 | ATGGG others(580): Show |
chr15 | 41226268 | 41286887 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3201 | 129 | 35 | 19 | 55 | 4 | 15 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0002 | 0/1 | 3202 | 40 | 2 | 11 | 15 | 1 | 10 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3197): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0003 | 0/0 | 3201 | 31 | 13 | 2 | 15 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0004 | 0/0 | 3201 | 12 | 11 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0005 | 0/0 | 3202 | 10 | 3 | 1 | 6 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3197): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0006 | 0/0 | 3204 | 10 | 0 | 4 | 1 | 1 | 4 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3199): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0007 | 0/0 | 3203 | 9 | 0 | 5 | 0 | 2 | 2 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0008 | 0/0 | 3200 | 8 | 2 | 2 | 3 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0009 | 0/0 | 3201 | 5 | 4 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0010 | 0/0 | 3202 | 4 | 4 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3197): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0011 | 0/0 | 3203 | 4 | 0 | 3 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0012 | 0/0 | 3200 | 4 | 4 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0013 | 0/0 | 3203 | 3 | 3 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0014 | 0/0 | 3201 | 3 | 3 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0015 | 0/0 | 3200 | 3 | 3 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0016 | 0/0 | 3203 | 2 | 0 | 1 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0017 | 0/0 | 3203 | 2 | 2 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0018 | 0/0 | 3204 | 2 | 2 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3199): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0019 | 0/0 | 3200 | 2 | 1 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0020 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0021 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0022 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3197): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0023 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0024 | 0/0 | 3203 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0025 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0026 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0027 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3195): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0028 | 0/0 | 3201 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0029 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0030 | 0/0 | 3202 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3197): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0031 | 0/0 | 3202 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3197): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0032 | 0/0 | 3203 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3198): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0033 | 0/0 | 3201 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| a0001c0001t0034 | 0/0 | 3201 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | AGTGG others(3196): Show |
chr15 | 41226268 | 41286887 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0004 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0008g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0010g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0011g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0012g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0013g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0013g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0014g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0015g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0016g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0016g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0017g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0017g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0018g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0018g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0019g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0020g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0021g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0022g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0023g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0024g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0025g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0026g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0027g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0028g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0029g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0030g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0032g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0033g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| a0001c0001t0034g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0024 | g0035 | EUR | GBR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0184 | EUR | GBR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0038 | EUR | FIN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00544 | hp2 | a0001 | c0001 | t0020 | g0083 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0037 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00642 | hp1 | a0001 | c0001 | t0019 | g0055 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0049 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG00741 | hp2 | a0001 | c0001 | t0011 | g0033 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0136 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0139 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0233 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0100 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01496 | hp2 | a0001 | c0001 | t0030 | g0225 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0018 | EUR | IBS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01928 | hp2 | a0001 | c0001 | t0016 | g0209 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01975 | hp1 | a0001 | c0001 | t0007 | g0039 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0207 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02015 | hp2 | a0001 | c0001 | t0025 | g0268 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0204 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02132 | hp1 | a0001 | c0001 | t0028 | g0269 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02145 | hp2 | a0001 | c0001 | t0010 | g0017 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0198 | EAS | CDX | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0015 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0030 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0048 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0059 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0032 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02698 | hp1 | a0001 | c0001 | t0021 | g0183 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0021 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0053 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02809 | hp1 | a0001 | c0001 | t0013 | g0012 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0052 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02886 | hp2 | a0001 | c0001 | t0013 | g0009 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0163 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0162 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02922 | hp1 | a0001 | c0001 | t0018 | g0157 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0056 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02976 | hp1 | a0001 | c0001 | t0027 | g0061 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0283 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0054 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03098 | hp2 | a0001 | c0001 | t0032 | g0087 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0028 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03195 | hp1 | a0001 | c0001 | t0019 | g0058 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0115 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0011 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0290 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0029 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0278 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0042 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03492 | hp2 | a0001 | c0001 | t0029 | g0267 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0279 | AFR | ESN | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0211 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0171 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03834 | hp1 | a0001 | c0001 | t0033 | g0051 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0040 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0050 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04184 | hp2 | a0001 | c0001 | t0007 | g0044 | SAS | BEB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG04228 | hp2 | a0001 | c0001 | t0009 | g0036 | SAS | STU | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | YRI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0014 | AFR | YRI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18943 | hp1 | a0001 | c0001 | t0016 | g0193 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18962 | hp1 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0206 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18984 | hp2 | a0001 | c0001 | t0026 | g0192 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19030 | hp1 | a0001 | c0001 | t0023 | g0010 | AFR | LWK | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | LWK | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | LWK | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0214 | AFR | LWK | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0043 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0222 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19065 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19082 | hp2 | a0001 | c0001 | t0022 | g0196 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | YRI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ASW | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0081 | EUR | TSI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | TSI | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0164 | SAS | GIH | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0041 | AMR | CLM | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | MSL | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG06807 | hp1 | a0001 | c0001 | t0010 | g0008 | AFR | USA | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | USA | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0252 | AFR | USA | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | USA | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | LWK | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | LWK | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0062 | REF | REF | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | CHP1_chr15_41226268_41286887 | CHP1 | chr15 | 41226268 | 41286887 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41279411 | C | T | 2 | a0001c0001t0012 a0001c0001t0034 |
5 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 22 | chr15 | 41279411 | ||||||
| chr15:41279415 | C | T | 2 | a0001c0001t0012 a0001c0001t0034 |
5 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*26C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 26 | chr15 | 41279415 | ||||||
| chr15:41279473 | C | A | 1 | a0001c0001t0020 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 84 | chr15 | 41279473 | ||||||
| chr15:41280139 | T | A | 1 | a0001c0001t0013 | 3 | HG02630.hp1 HG02809.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750T>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 750 | chr15 | 41280139 | ||||||
| chr15:41280154 | T | C | 2 | a0001c0001t0021 a0001c0001t0022 |
2 | HG02698.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*765T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 765 | chr15 | 41280154 | ||||||
| chr15:41280244 | G | A | 4 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0014 others(1): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*855G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 855 | chr15 | 41280244 | ||||||
| chr15:41280245 | T | C | 1 | a0001c0001t0024 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*856T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 856 | chr15 | 41280245 | ||||||
| chr15:41280504 | A | G | 6 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0009 others(3): Show |
30 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1115A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1115 | chr15 | 41280504 | ||||||
| chr15:41280505 | A | AT | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(3): Show |
56 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1143dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1144 | INFO_REALIGN_3_PRIME | chr15 | 41280505 | |||||
| chr15:41280505 | A | ATT | 8 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0013 others(5): Show |
23 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1142_*1143dupTT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1144 | INFO_REALIGN_3_PRIME | chr15 | 41280505 | |||||
| chr15:41280505 | A | ATTT | 2 | a0001c0001t0006 a0001c0001t0018 |
12 | HG00642.hp2 HG01123.hp2 HG01358.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1141_*1143dupTTT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1144 | INFO_REALIGN_3_PRIME | chr15 | 41280505 | |||||
| chr15:41280505 | A | T | 1 | a0001c0001t0033 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1116A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1116 | chr15 | 41280505 | ||||||
| chr15:41280505 | AT | A | 7 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0015 others(4): Show |
20 | HG00642.hp1 HG01167.hp1 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1143delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1143 | INFO_REALIGN_3_PRIME | chr15 | 41280505 | |||||
| chr15:41280704 | G | T | 1 | a0001c0001t0031 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1315 | chr15 | 41280704 | ||||||
| chr15:41281110 | C | T | 2 | a0001c0001t0018 a0001c0001t0032 |
3 | HG02922.hp1 HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1721C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1721 | chr15 | 41281110 | ||||||
| chr15:41281149 | G | A | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(5): Show |
48 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1760G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1760 | chr15 | 41281149 | ||||||
| chr15:41281196 | A | G | 1 | a0001c0001t0029 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1807A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 1807 | chr15 | 41281196 | ||||||
| chr15:41281414 | C | A | 10 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(7): Show |
45 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2025C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 2025 | chr15 | 41281414 | ||||||
| chr15:41281853 | C | T | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(3): Show |
46 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2464C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 7/7 | 2464 | chr15 | 41281853 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41231725 | A | G | 2 | a0001c0001t0004g0291 a0001c0001t0018g0290 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.67+276A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41231725 | |||||||
| chr15:41232038 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0177 a0001c0001t0001g0178 others(127): Show |
132 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.67+589C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232038 | |||||||
| chr15:41232208 | AT | A | 20 | a0001c0001t0001g0019 a0001c0001t0001g0270 a0001c0001t0001g0271 others(17): Show |
20 | HG01070.hp1 HG01175.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.67+779delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41232208 | ||||||
| chr15:41232208 | ATT | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0177 a0001c0001t0001g0178 others(118): Show |
123 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.67+778_67+779delTT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41232208 | ||||||
| chr15:41232239 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+790C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232239 | |||||||
| chr15:41232315 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0177 a0001c0001t0001g0178 others(143): Show |
148 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.67+866G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232315 | |||||||
| chr15:41232359 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.67+910T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232359 | |||||||
| chr15:41232364 | C | T | 2 | a0001c0001t0025g0268 a0001c0001t0028g0269 |
2 | HG02015.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.67+915C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232364 | |||||||
| chr15:41232517 | A | AT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0212 a0001c0001t0001g0215 others(56): Show |
61 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.67+1079dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41232517 | ||||||
| chr15:41232619 | A | G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1170A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232619 | |||||||
| chr15:41232734 | G | C | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1285G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232734 | |||||||
| chr15:41232895 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.67+1446A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232895 | |||||||
| chr15:41232957 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67+1508C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41232957 | |||||||
| chr15:41233013 | C | T | 1 | a0001c0001t0012g0211 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67+1564C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233013 | |||||||
| chr15:41233126 | C | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+1677C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233126 | |||||||
| chr15:41233159 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0158 others(144): Show |
149 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.67+1710G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233159 | |||||||
| chr15:41233223 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1774G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233223 | |||||||
| chr15:41233240 | T | C | 1 | a0001c0001t0014g0006 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.67+1791T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233240 | |||||||
| chr15:41233357 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.67+1908G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233357 | |||||||
| chr15:41233406 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0158 others(144): Show |
149 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.67+1957A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233406 | |||||||
| chr15:41233751 | C | T | 1 | a0001c0001t0007g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67+2302C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233751 | |||||||
| chr15:41233824 | C | T | 51 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(48): Show |
51 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.67+2375C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233824 | |||||||
| chr15:41233906 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.67+2457G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233906 | |||||||
| chr15:41233930 | C | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG02109.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67+2481C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41233930 | |||||||
| chr15:41234178 | T | G | 4 | a0001c0001t0009g0029 a0001c0001t0009g0031 a0001c0001t0015g0028 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2729T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41234178 | |||||||
| chr15:41234831 | T | C | 1 | a0001c0001t0017g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67+3382T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41234831 | |||||||
| chr15:41235176 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0060 a0001c0001t0001g0158 others(59): Show |
64 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3727T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235176 | |||||||
| chr15:41235247 | AG | A | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3799delG | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235247 | |||||||
| chr15:41235250 | G | A | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3801G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235250 | |||||||
| chr15:41235251 | G | A | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3802G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235251 | |||||||
| chr15:41235253 | T | TA | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3804_67+3805ins others(1): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235253 | |||||||
| chr15:41235255 | A | AGG | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3806_67+3807ins others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235255 | |||||||
| chr15:41235256 | C | A | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+3807C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235256 | |||||||
| chr15:41235298 | G | A | 1 | a0001c0001t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67+3849G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235298 | |||||||
| chr15:41235523 | A | C | 1 | a0001c0001t0029g0267 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.67+4074A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235523 | |||||||
| chr15:41235559 | T | G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+4110T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235559 | |||||||
| chr15:41235581 | A | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01255.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.67+4132A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235581 | |||||||
| chr15:41235867 | C | T | 1 | a0001c0001t0004g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.67+4418C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41235867 | |||||||
| chr15:41236003 | C | T | 1 | a0001c0001t0003g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.67+4554C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236003 | |||||||
| chr15:41236079 | CT | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(174): Show |
179 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.67+4647delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41236079 | ||||||
| chr15:41236102 | A | C | 1 | a0001c0001t0002g0279 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.67+4653A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236102 | |||||||
| chr15:41236352 | T | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(176): Show |
181 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.67+4903T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236352 | |||||||
| chr15:41236385 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01255.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.67+4936C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236385 | |||||||
| chr15:41236450 | T | C | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.67+5001T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236450 | |||||||
| chr15:41236547 | C | G | 117 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.67+5098C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236547 | |||||||
| chr15:41236600 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+5151A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236600 | |||||||
| chr15:41236662 | A | T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+5213A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236662 | |||||||
| chr15:41236713 | A | G | 1 | a0001c0001t0028g0269 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.67+5264A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236713 | |||||||
| chr15:41236785 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.67+5336A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41236785 | |||||||
| chr15:41236832 | C | CT | 175 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(172): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.67+5397dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41236832 | ||||||
| chr15:41237036 | G | A | 1 | a0001c0001t0006g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.67+5587G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237036 | |||||||
| chr15:41237126 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.67+5677T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237126 | |||||||
| chr15:41237238 | C | T | 1 | a0001c0001t0009g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+5789C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237238 | |||||||
| chr15:41237514 | T | C | 105 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(102): Show |
105 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.67+6065T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237514 | |||||||
| chr15:41237641 | C | G | 1 | a0001c0001t0029g0267 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.68-6026C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237641 | |||||||
| chr15:41237666 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.68-6001A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237666 | |||||||
| chr15:41237834 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.68-5833T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41237834 | |||||||
| chr15:41238161 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(111): Show |
116 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.68-5506G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238161 | |||||||
| chr15:41238182 | G | T | 1 | a0001c0001t0028g0269 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.68-5485G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238182 | |||||||
| chr15:41238197 | A | G | 11 | a0001c0001t0001g0057 a0001c0001t0009g0029 a0001c0001t0009g0031 others(8): Show |
11 | HG00642.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-5470A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238197 | |||||||
| chr15:41238311 | C | T | 13 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0202 others(10): Show |
13 | HG01928.hp2 HG01975.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-5356C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238311 | |||||||
| chr15:41238453 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.68-5214G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238453 | |||||||
| chr15:41238622 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0158 a0001c0001t0001g0159 others(58): Show |
63 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.68-5045C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238622 | |||||||
| chr15:41238629 | G | T | 1 | a0001c0001t0017g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-5038G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238629 | |||||||
| chr15:41238684 | C | CA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0158 a0001c0001t0001g0159 others(59): Show |
64 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.68-4968dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41238684 | ||||||
| chr15:41238710 | ATGG | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.68-4950_68-4948del others(3): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41238710 | ||||||
| chr15:41238742 | C | T | 6 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-4925C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238742 | |||||||
| chr15:41238753 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-4914G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238753 | |||||||
| chr15:41238796 | G | T | 1 | a0001c0001t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.68-4871G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238796 | |||||||
| chr15:41238886 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0003g0045 others(30): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.68-4781C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238886 | |||||||
| chr15:41238897 | G | C | 1 | a0001c0001t0008g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.68-4770G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41238897 | |||||||
| chr15:41239320 | G | GT | 174 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.68-4334dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41239320 | ||||||
| chr15:41239552 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.68-4115C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239552 | |||||||
| chr15:41239651 | C | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-4016C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239651 | |||||||
| chr15:41239670 | T | G | 1 | a0001c0001t0014g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.68-3997T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239670 | |||||||
| chr15:41239793 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.68-3874C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239793 | |||||||
| chr15:41239837 | C | T | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.68-3830C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239837 | |||||||
| chr15:41239846 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(179): Show |
184 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.68-3821A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239846 | |||||||
| chr15:41239938 | G | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-3729G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239938 | |||||||
| chr15:41239959 | G | T | 1 | a0001c0001t0033g0051 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.68-3708G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41239959 | |||||||
| chr15:41240022 | C | T | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-3645C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240022 | |||||||
| chr15:41240241 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.68-3426G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240241 | |||||||
| chr15:41240361 | A | G | 2 | a0001c0001t0010g0017 a0001c0001t0014g0015 |
2 | HG02145.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.68-3306A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240361 | |||||||
| chr15:41240411 | A | G | 39 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(36): Show |
39 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.68-3256A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240411 | |||||||
| chr15:41240523 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68-3144G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240523 | |||||||
| chr15:41240651 | G | T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-3016G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240651 | |||||||
| chr15:41240671 | G | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.68-2996G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240671 | |||||||
| chr15:41240753 | CA | C | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0003g0210 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2894delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41240753 | ||||||
| chr15:41240754 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68-2913A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240754 | |||||||
| chr15:41240766 | A | T | 64 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(61): Show |
64 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.68-2901A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240766 | |||||||
| chr15:41240858 | T | TTA | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2808_68-2807ins others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41240858 | ||||||
| chr15:41240860 | C | CTT | 172 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.68-2797_68-2796dup others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41240860 | ||||||
| chr15:41240860 | C | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2807C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240860 | |||||||
| chr15:41240938 | C | T | 2 | a0001c0001t0006g0050 a0001c0001t0007g0049 |
2 | HG00741.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.68-2729C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41240938 | |||||||
| chr15:41241272 | C | T | 1 | a0001c0001t0004g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.68-2395C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41241272 | |||||||
| chr15:41241694 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.68-1973C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41241694 | |||||||
| chr15:41241753 | A | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1914A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41241753 | |||||||
| chr15:41241879 | C | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG01081.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.68-1788C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41241879 | |||||||
| chr15:41242004 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.68-1663T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242004 | |||||||
| chr15:41242234 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.68-1433A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242234 | |||||||
| chr15:41242376 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.68-1291G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242376 | |||||||
| chr15:41242462 | A | G | 1 | a0001c0001t0014g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.68-1205A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242462 | |||||||
| chr15:41242541 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0158 a0001c0001t0001g0159 others(58): Show |
63 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.68-1126C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242541 | |||||||
| chr15:41242596 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68-1071G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242596 | |||||||
| chr15:41242597 | C | T | 3 | a0001c0001t0003g0169 a0001c0001t0003g0174 a0001c0001t0005g0282 |
3 | HG02257.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.68-1070C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242597 | |||||||
| chr15:41242755 | T | C | 1 | a0001c0001t0024g0035 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.68-912T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242755 | |||||||
| chr15:41242817 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0284 a0001c0001t0001g0285 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-850C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41242817 | |||||||
| chr15:41242961 | T | TA | 32 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0003g0045 others(29): Show |
32 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.68-699dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr15 | 41242961 | ||||||
| chr15:41243008 | C | G | 67 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(64): Show |
67 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.68-659C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243008 | |||||||
| chr15:41243169 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-498G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243169 | |||||||
| chr15:41243247 | A | G | 1 | a0001c0001t0011g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.68-420A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243247 | |||||||
| chr15:41243295 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.68-372G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243295 | |||||||
| chr15:41243478 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-189G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243478 | |||||||
| chr15:41243553 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.68-114A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243553 | |||||||
| chr15:41243638 | C | T | 10 | a0001c0001t0001g0159 a0001c0001t0001g0270 a0001c0001t0001g0271 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.68-29C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 1/6 | chr15 | 41243638 | |||||||
| chr15:41243971 | G | A | 1 | a0001c0001t0004g0278 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.140+232G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41243971 | |||||||
| chr15:41244067 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.140+328A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244067 | |||||||
| chr15:41244154 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.140+415C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244154 | |||||||
| chr15:41244196 | T | TA | 159 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0057 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.140+474dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41244196 | ||||||
| chr15:41244207 | A | AC | 13 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(10): Show |
13 | HG01515.hp1 HG02074.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.140+468_140+469ins others(1): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244207 | |||||||
| chr15:41244425 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.140+686T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244425 | |||||||
| chr15:41244426 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.140+687T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244426 | |||||||
| chr15:41244435 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.140+696C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244435 | |||||||
| chr15:41244591 | T | C | 8 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0220 others(5): Show |
8 | HG01891.hp1 HG02922.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+852T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244591 | |||||||
| chr15:41244969 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0277 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.140+1230G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41244969 | |||||||
| chr15:41245130 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0158 a0001c0001t0001g0159 others(58): Show |
63 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+1391C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245130 | |||||||
| chr15:41245157 | C | A | 1 | a0001c0001t0002g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.140+1418C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245157 | |||||||
| chr15:41245219 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.140+1480G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245219 | |||||||
| chr15:41245325 | G | A | 1 | a0001c0001t0011g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.140+1586G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245325 | |||||||
| chr15:41245341 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.140+1602C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245341 | |||||||
| chr15:41245378 | G | A | 1 | a0001c0001t0014g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.140+1639G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245378 | |||||||
| chr15:41245459 | C | T | 11 | a0001c0001t0001g0057 a0001c0001t0009g0029 a0001c0001t0009g0031 others(8): Show |
11 | HG00642.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+1720C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245459 | |||||||
| chr15:41245788 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.140+2049C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245788 | |||||||
| chr15:41245942 | A | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+2203A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245942 | |||||||
| chr15:41245952 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.140+2213C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245952 | |||||||
| chr15:41245955 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0158 a0001c0001t0001g0159 others(58): Show |
63 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.140+2216T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41245955 | |||||||
| chr15:41246130 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.140+2391C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246130 | |||||||
| chr15:41246326 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 others(54): Show |
59 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.140+2587C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246326 | |||||||
| chr15:41246412 | C | T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+2673C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246412 | |||||||
| chr15:41246531 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.140+2792G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246531 | |||||||
| chr15:41246593 | A | C | 1 | a0001c0001t0017g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.140+2854A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246593 | |||||||
| chr15:41246614 | G | A | 1 | a0001c0001t0005g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140+2875G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246614 | |||||||
| chr15:41246624 | C | CT | 68 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0057 others(65): Show |
68 | HG00597.hp1 HG00597.hp2 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.140+2911dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41246624 | ||||||
| chr15:41246624 | CT | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0069 others(60): Show |
65 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.140+2911delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41246624 | ||||||
| chr15:41246697 | C | T | 75 | a0001c0001t0001g0026 a0001c0001t0001g0177 a0001c0001t0001g0178 others(72): Show |
75 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.140+2958C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246697 | |||||||
| chr15:41246765 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.140+3026C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246765 | |||||||
| chr15:41246794 | A | G | 6 | a0001c0001t0006g0041 a0001c0001t0006g0042 a0001c0001t0006g0047 others(3): Show |
6 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+3055A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246794 | |||||||
| chr15:41246836 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0006g0032 |
2 | HG01074.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.140+3097C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41246836 | |||||||
| chr15:41247014 | CA | C | 112 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.140+3291delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41247014 | ||||||
| chr15:41247031 | T | G | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+3292T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247031 | |||||||
| chr15:41247132 | G | T | 1 | a0001c0001t0003g0262 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.140+3393G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247132 | |||||||
| chr15:41247139 | C | T | 1 | a0001c0001t0004g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.140+3400C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247139 | |||||||
| chr15:41247173 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.140+3434G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247173 | |||||||
| chr15:41247206 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.140+3467G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247206 | |||||||
| chr15:41247247 | G | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.140+3508G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247247 | |||||||
| chr15:41247269 | T | C | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.140+3530T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247269 | |||||||
| chr15:41247369 | TA | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(26): Show |
29 | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.140+3644delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41247369 | ||||||
| chr15:41247698 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0264 |
3 | HG01891.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.140+3959C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247698 | |||||||
| chr15:41247699 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+3960G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247699 | |||||||
| chr15:41247787 | G | A | 108 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.140+4048G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247787 | |||||||
| chr15:41247913 | G | C | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+4174G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247913 | |||||||
| chr15:41247951 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.140+4212A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247951 | |||||||
| chr15:41247964 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0223 others(8): Show |
13 | HG02040.hp2 HG02155.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.140+4225G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247964 | |||||||
| chr15:41247976 | A | AAAAT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0158 a0001c0001t0001g0159 others(68): Show |
73 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(70): Show |
intron_variant | MODIFIER | c.140+4249_140+4252d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41247976 | ||||||
| chr15:41247989 | A | AAAAT | 108 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.140+4269_140+4272d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41247989 | ||||||
| chr15:41247992 | A | T | 26 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(23): Show |
26 | HG00609.hp1 HG01081.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.140+4253A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247992 | |||||||
| chr15:41247993 | T | A | 26 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(23): Show |
26 | HG00609.hp1 HG01081.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.140+4254T>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41247993 | |||||||
| chr15:41248148 | AT | A | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+4423delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41248148 | ||||||
| chr15:41248268 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.140+4529C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41248268 | |||||||
| chr15:41248418 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.140+4679C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41248418 | |||||||
| chr15:41248655 | G | A | 1 | a0001c0001t0009g0036 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.140+4916G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41248655 | |||||||
| chr15:41248726 | C | G | 75 | a0001c0001t0001g0026 a0001c0001t0001g0177 a0001c0001t0001g0178 others(72): Show |
75 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.140+4987C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41248726 | |||||||
| chr15:41248973 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.140+5234G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41248973 | |||||||
| chr15:41249135 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.140+5396A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249135 | |||||||
| chr15:41249206 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.140+5467G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249206 | |||||||
| chr15:41249429 | C | CAGATGTG others(1): Show |
8 | a0001c0001t0001g0026 a0001c0001t0001g0284 a0001c0001t0001g0285 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+5691_140+5698d others(10): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249429 | ||||||
| chr15:41249461 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.140+5722T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249461 | |||||||
| chr15:41249462 | C | CT | 53 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0093 others(50): Show |
55 | HG01106.hp2 HG01109.hp1 HG01123.hp1 others(52): Show |
intron_variant | MODIFIER | c.140+5751dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249462 | C | CTT | 11 | a0001c0001t0001g0097 a0001c0001t0001g0224 a0001c0001t0001g0255 others(8): Show |
11 | HG01175.hp2 HG02040.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+5750_140+5751d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249462 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.140+5723C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249462 | |||||||
| chr15:41249462 | CTT | C | 8 | a0001c0001t0001g0276 a0001c0001t0001g0289 a0001c0001t0004g0291 others(5): Show |
8 | HG00642.hp1 HG00642.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+5750_140+5751d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249462 | CTTT | C | 47 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(44): Show |
47 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.140+5749_140+5751d others(5): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249462 | CTTTT | C | 61 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(58): Show |
61 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.140+5748_140+5751d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249462 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+5741_140+5751d others(13): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249462 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.140+5740_140+5751d others(14): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249462 | ||||||
| chr15:41249504 | G | A | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.140+5765G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249504 | |||||||
| chr15:41249559 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.140+5820G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249559 | |||||||
| chr15:41249695 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.140+5956A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249695 | |||||||
| chr15:41249764 | G | A | 1 | a0001c0001t0018g0157 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.140+6025G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249764 | |||||||
| chr15:41249768 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.140+6029G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249768 | |||||||
| chr15:41249830 | A | AT | 12 | a0001c0001t0001g0134 a0001c0001t0001g0254 a0001c0001t0001g0270 others(9): Show |
12 | HG01433.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.140+6109dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249830 | ||||||
| chr15:41249830 | AT | A | 10 | a0001c0001t0001g0070 a0001c0001t0001g0158 a0001c0001t0001g0159 others(7): Show |
10 | HG01081.hp2 HG01515.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+6109delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41249830 | ||||||
| chr15:41249957 | C | T | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.140+6218C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41249957 | |||||||
| chr15:41250034 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.140+6295C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250034 | |||||||
| chr15:41250056 | C | T | 1 | a0001c0001t0011g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.140+6317C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250056 | |||||||
| chr15:41250090 | T | TA | 7 | a0001c0001t0001g0180 a0001c0001t0001g0287 a0001c0001t0002g0020 others(4): Show |
7 | HG01175.hp1 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.140+6368dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41250090 | ||||||
| chr15:41250090 | TA | T | 12 | a0001c0001t0001g0090 a0001c0001t0001g0158 a0001c0001t0001g0159 others(9): Show |
12 | HG02258.hp1 HG02738.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+6368delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41250090 | ||||||
| chr15:41250090 | TAA | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 others(52): Show |
57 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(54): Show |
intron_variant | MODIFIER | c.140+6367_140+6368d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41250090 | ||||||
| chr15:41250304 | C | T | 5 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(2): Show |
5 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+6565C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250304 | |||||||
| chr15:41250380 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0009g0053 a0001c0001t0009g0056 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-6530C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250380 | |||||||
| chr15:41250393 | G | A | 184 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.141-6517G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250393 | |||||||
| chr15:41250477 | G | T | 1 | a0001c0001t0008g0089 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.141-6433G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250477 | |||||||
| chr15:41250585 | A | T | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141-6325A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250585 | |||||||
| chr15:41250644 | A | G | 1 | a0001c0001t0007g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.141-6266A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250644 | |||||||
| chr15:41250660 | CA | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.141-6236delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41250660 | ||||||
| chr15:41250839 | T | C | 3 | a0001c0001t0002g0247 a0001c0001t0003g0172 a0001c0001t0004g0283 |
3 | HG02071.hp1 HG03017.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.141-6071T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250839 | |||||||
| chr15:41250854 | A | T | 1 | a0001c0001t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141-6056A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250854 | |||||||
| chr15:41250861 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(177): Show |
182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.141-6049C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250861 | |||||||
| chr15:41250911 | C | G | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-5999C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41250911 | |||||||
| chr15:41251161 | G | A | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141-5749G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41251161 | |||||||
| chr15:41251220 | C | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-5690C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41251220 | |||||||
| chr15:41251573 | C | T | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141-5337C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41251573 | |||||||
| chr15:41251804 | CT | C | 9 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-5089delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41251804 | ||||||
| chr15:41252108 | G | A | 1 | a0001c0001t0005g0261 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.141-4802G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252108 | |||||||
| chr15:41252239 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141-4671G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252239 | |||||||
| chr15:41252317 | C | T | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-4593C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252317 | |||||||
| chr15:41252360 | G | A | 1 | a0001c0001t0002g0246 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.141-4550G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252360 | |||||||
| chr15:41252416 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0264 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-4494C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252416 | |||||||
| chr15:41252419 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.141-4491G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252419 | |||||||
| chr15:41252600 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0002g0176 |
2 | NA18944.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.141-4310G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252600 | |||||||
| chr15:41252925 | TG | T | 3 | a0001c0001t0014g0006 a0001c0001t0014g0015 a0001c0001t0023g0010 |
3 | HG02257.hp1 HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.141-3983delG | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41252925 | ||||||
| chr15:41252926 | GGT | G | 8 | a0001c0001t0008g0016 a0001c0001t0010g0008 a0001c0001t0010g0011 others(5): Show |
8 | HG02145.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.141-3983_141-3982d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252926 | |||||||
| chr15:41252927 | G | GT | 10 | a0001c0001t0001g0109 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG00609.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.141-3953dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41252927 | ||||||
| chr15:41252927 | GT | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
137 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.141-3953delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41252927 | ||||||
| chr15:41252927 | GTT | G | 74 | a0001c0001t0001g0019 a0001c0001t0001g0069 a0001c0001t0001g0072 others(71): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.141-3954_141-3953d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41252927 | ||||||
| chr15:41252927 | GTTTTTTT others(10): Show |
G | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-3969_141-3953d others(19): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41252927 | ||||||
| chr15:41252990 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0158 others(59): Show |
64 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.141-3920G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41252990 | |||||||
| chr15:41253036 | T | C | 1 | a0001c0001t0006g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.141-3874T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253036 | |||||||
| chr15:41253052 | T | C | 1 | a0001c0001t0011g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.141-3858T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253052 | |||||||
| chr15:41253415 | T | G | 118 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.141-3495T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253415 | |||||||
| chr15:41253423 | G | GTATT | 9 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG00544.hp2 HG01175.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-3441_141-3438d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41253423 | ||||||
| chr15:41253423 | GTATT | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0026 others(112): Show |
117 | HG00323.hp1 HG00597.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.141-3441_141-3438d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41253423 | ||||||
| chr15:41253423 | GTATTTAT others(1): Show |
G | 80 | a0001c0001t0001g0019 a0001c0001t0001g0177 a0001c0001t0001g0178 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.141-3445_141-3438d others(10): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41253423 | ||||||
| chr15:41253423 | GTATTTAT others(5): Show |
G | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.141-3449_141-3438d others(14): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41253423 | ||||||
| chr15:41253426 | T | TTTAC | 8 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-3481_141-3480i others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41253426 | ||||||
| chr15:41253430 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.141-3480T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253430 | |||||||
| chr15:41253486 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0060 others(60): Show |
65 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(62): Show |
intron_variant | MODIFIER | c.141-3424T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253486 | |||||||
| chr15:41253516 | G | A | 1 | a0001c0001t0007g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.141-3394G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253516 | |||||||
| chr15:41253555 | T | C | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141-3355T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253555 | |||||||
| chr15:41253594 | A | G | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.141-3316A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253594 | |||||||
| chr15:41253669 | T | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0060 others(60): Show |
65 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(62): Show |
intron_variant | MODIFIER | c.141-3241T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253669 | |||||||
| chr15:41253746 | G | A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0093 |
3 | NA18975.hp2 NA18984.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.141-3164G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253746 | |||||||
| chr15:41253896 | C | T | 2 | a0001c0001t0003g0124 a0001c0001t0007g0154 |
2 | HG01081.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.141-3014C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253896 | |||||||
| chr15:41253951 | AT | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0060 others(76): Show |
81 | HG00099.hp1 HG01081.hp1 HG01106.hp2 others(78): Show |
intron_variant | MODIFIER | c.141-2943delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41253951 | ||||||
| chr15:41253968 | A | T | 8 | a0001c0001t0001g0098 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG01081.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.141-2942A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41253968 | |||||||
| chr15:41254022 | A | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-2888A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254022 | |||||||
| chr15:41254096 | T | A | 1 | a0001c0001t0002g0257 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.141-2814T>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254096 | |||||||
| chr15:41254217 | G | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-2693G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254217 | |||||||
| chr15:41254398 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.141-2512G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254398 | |||||||
| chr15:41254433 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.141-2477G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254433 | |||||||
| chr15:41254553 | A | C | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-2357A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254553 | |||||||
| chr15:41254932 | T | G | 76 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(73): Show |
76 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.141-1978T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41254932 | |||||||
| chr15:41255121 | A | G | 1 | a0001c0001t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.141-1789A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255121 | |||||||
| chr15:41255494 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.141-1416A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255494 | |||||||
| chr15:41255539 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.141-1371A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255539 | |||||||
| chr15:41255546 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.141-1364G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255546 | |||||||
| chr15:41255740 | C | T | 33 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0003g0045 others(30): Show |
33 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.141-1170C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255740 | |||||||
| chr15:41255741 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-1169G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255741 | |||||||
| chr15:41255758 | TC | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0060 others(55): Show |
60 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.141-1149delC | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr15 | 41255758 | ||||||
| chr15:41255763 | C | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0018g0157 others(1): Show |
4 | HG02922.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1147C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255763 | |||||||
| chr15:41255781 | C | T | 7 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG01081.hp1 HG01106.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-1129C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255781 | |||||||
| chr15:41255845 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-1065G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41255845 | |||||||
| chr15:41256046 | T | C | 1 | a0001c0001t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.141-864T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41256046 | |||||||
| chr15:41256396 | C | G | 1 | a0001c0001t0007g0038 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.141-514C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41256396 | |||||||
| chr15:41256750 | A | C | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.141-160A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 2/6 | chr15 | 41256750 | |||||||
| chr15:41257098 | CCT | C | 76 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(73): Show |
76 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.221+109_221+110del others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41257098 | |||||||
| chr15:41257484 | T | C | 1 | a0001c0001t0002g0020 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.221+494T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41257484 | |||||||
| chr15:41257745 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.221+755A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41257745 | |||||||
| chr15:41258107 | C | T | 7 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(4): Show |
7 | HG02280.hp1 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+1117C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41258107 | |||||||
| chr15:41258127 | TACAC | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0082 a0001c0001t0001g0112 others(3): Show |
6 | HG00558.hp1 HG02080.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+1139_221+1142d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41258127 | ||||||
| chr15:41258135 | C | T | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.221+1145C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41258135 | |||||||
| chr15:41258144 | A | G | 1 | a0001c0001t0002g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.221+1154A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41258144 | |||||||
| chr15:41258183 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.221+1193G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41258183 | |||||||
| chr15:41258687 | C | A | 67 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(64): Show |
67 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.221+1697C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41258687 | |||||||
| chr15:41258974 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.221+1984C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41258974 | |||||||
| chr15:41259150 | A | C | 1 | a0001c0001t0003g0148 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.221+2160A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259150 | |||||||
| chr15:41259237 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.221+2247C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259237 | |||||||
| chr15:41259387 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.221+2397C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259387 | |||||||
| chr15:41259443 | CGACTCTG others(2): Show |
C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+2454_221+2462d others(11): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259443 | |||||||
| chr15:41259444 | G | C | 1 | a0001c0001t0006g0050 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.221+2454G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259444 | |||||||
| chr15:41259525 | C | CT | 14 | a0001c0001t0001g0057 a0001c0001t0001g0285 a0001c0001t0001g0286 others(11): Show |
14 | HG00597.hp1 HG01109.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.221+2553dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41259525 | ||||||
| chr15:41259525 | C | CTT | 28 | a0001c0001t0001g0019 a0001c0001t0003g0045 a0001c0001t0006g0032 others(25): Show |
28 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.221+2552_221+2553d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41259525 | ||||||
| chr15:41259525 | CT | C | 14 | a0001c0001t0001g0069 a0001c0001t0001g0099 a0001c0001t0001g0144 others(11): Show |
14 | HG01257.hp2 HG02132.hp2 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.221+2553delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41259525 | ||||||
| chr15:41259663 | T | C | 5 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
5 | HG02280.hp1 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+2673T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259663 | |||||||
| chr15:41259729 | A | G | 2 | a0001c0001t0003g0167 a0001c0001t0012g0171 |
2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.221+2739A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259729 | |||||||
| chr15:41259910 | C | T | 1 | a0001c0001t0007g0037 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.222-2846C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259910 | |||||||
| chr15:41259965 | G | A | 6 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.222-2791G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41259965 | |||||||
| chr15:41260170 | G | GT | 11 | a0001c0001t0001g0147 a0001c0001t0002g0105 a0001c0001t0002g0113 others(8): Show |
11 | HG01081.hp2 HG01243.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.222-2572dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41260170 | ||||||
| chr15:41260394 | CT | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0057 others(175): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.222-2344delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41260394 | ||||||
| chr15:41260584 | G | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0270 others(39): Show |
42 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.222-2172G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41260584 | |||||||
| chr15:41260733 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.222-2023G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41260733 | |||||||
| chr15:41260810 | A | G | 7 | a0001c0001t0001g0057 a0001c0001t0009g0053 a0001c0001t0009g0056 others(4): Show |
7 | HG00642.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1946A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41260810 | |||||||
| chr15:41260945 | G | A | 14 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0122 others(11): Show |
14 | HG00609.hp1 HG01109.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.222-1811G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41260945 | |||||||
| chr15:41261316 | A | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-1440A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261316 | |||||||
| chr15:41261368 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.222-1388G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261368 | |||||||
| chr15:41261435 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.222-1321C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261435 | |||||||
| chr15:41261674 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.222-1082C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261674 | |||||||
| chr15:41261720 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0158 others(58): Show |
63 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.222-1036G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261720 | |||||||
| chr15:41261878 | G | C | 1 | a0001c0001t0010g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.222-878G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261878 | |||||||
| chr15:41261887 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.222-869G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261887 | |||||||
| chr15:41261919 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0135 a0001c0001t0011g0033 |
3 | HG00741.hp2 HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.222-837G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41261919 | |||||||
| chr15:41261992 | CA | C | 9 | a0001c0001t0001g0086 a0001c0001t0003g0200 a0001c0001t0004g0234 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.222-746delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41261992 | ||||||
| chr15:41261992 | CAA | C | 78 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(75): Show |
78 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.222-747_222-746del others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr15 | 41261992 | ||||||
| chr15:41262113 | G | A | 74 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.222-643G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41262113 | |||||||
| chr15:41262371 | T | C | 74 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.222-385T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41262371 | |||||||
| chr15:41262389 | G | A | 81 | a0001c0001t0001g0145 a0001c0001t0001g0177 a0001c0001t0001g0178 others(78): Show |
81 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.222-367G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41262389 | |||||||
| chr15:41262448 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.222-308C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41262448 | |||||||
| chr15:41262690 | A | T | 2 | a0001c0001t0001g0108 a0001c0001t0002g0131 |
2 | NA18943.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.222-66A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 3/6 | chr15 | 41262690 | |||||||
| chr15:41263051 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(182): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.349+168T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41263051 | |||||||
| chr15:41263052 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+169C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41263052 | |||||||
| chr15:41263294 | A | G | 4 | a0001c0001t0001g0180 a0001c0001t0003g0179 a0001c0001t0003g0187 others(1): Show |
4 | NA18984.hp2 NA18989.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+411A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41263294 | |||||||
| chr15:41263668 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.349+785A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41263668 | |||||||
| chr15:41263817 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0026 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.349+934A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41263817 | |||||||
| chr15:41264050 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.349+1167G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264050 | |||||||
| chr15:41264145 | T | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1262T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264145 | |||||||
| chr15:41264195 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349+1312T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264195 | |||||||
| chr15:41264196 | C | T | 1 | a0001c0001t0004g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.349+1313C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264196 | |||||||
| chr15:41264197 | G | A | 18 | a0001c0001t0001g0232 a0001c0001t0001g0237 a0001c0001t0001g0238 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+1314G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264197 | |||||||
| chr15:41264336 | G | C | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.349+1453G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264336 | |||||||
| chr15:41264962 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0130 |
2 | HG02004.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.349+2079C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41264962 | |||||||
| chr15:41265065 | G | C | 1 | a0001c0001t0001g0094 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.349+2182G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265065 | |||||||
| chr15:41265172 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.349+2289G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265172 | |||||||
| chr15:41265206 | C | CA | 6 | a0001c0001t0001g0134 a0001c0001t0001g0220 a0001c0001t0001g0221 others(3): Show |
6 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+2331dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265206 | ||||||
| chr15:41265235 | A | G | 80 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(77): Show |
80 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.349+2352A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265235 | |||||||
| chr15:41265256 | C | T | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.349+2373C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265256 | |||||||
| chr15:41265269 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.349+2386C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265269 | |||||||
| chr15:41265363 | C | CA | 13 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0065 others(10): Show |
13 | HG01175.hp1 HG01243.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.349+2512dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CA | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0086 a0001c0001t0001g0088 others(39): Show |
42 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.349+2512delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAA | C | 43 | a0001c0001t0001g0130 a0001c0001t0001g0145 a0001c0001t0001g0146 others(40): Show |
43 | HG00544.hp1 HG00609.hp2 HG01517.hp2 others(40): Show |
intron_variant | MODIFIER | c.349+2511_349+2512d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAAA | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0177 others(81): Show |
86 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.349+2510_349+2512d others(5): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAAAA | C | 48 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0232 others(45): Show |
48 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.349+2509_349+2512d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0153 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.349+2502_349+2512d others(13): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01255.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.349+2500_349+2512d others(15): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0002g0106 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.349+2499_349+2512d others(16): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265363 | CAAAAAAA others(10): Show |
C | 8 | a0001c0001t0001g0277 a0001c0001t0001g0284 a0001c0001t0001g0285 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+2496_349+2512d others(19): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265363 | ||||||
| chr15:41265434 | G | C | 1 | a0001c0001t0007g0044 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349+2551G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265434 | |||||||
| chr15:41265525 | CATGGTGA others(28): Show |
C | 1 | a0001c0001t0002g0081 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.349+2645_349+2679d others(37): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265525 | ||||||
| chr15:41265710 | C | CA | 43 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0270 others(40): Show |
43 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.349+2841dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41265710 | ||||||
| chr15:41265839 | A | G | 42 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0270 others(39): Show |
42 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.349+2956A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265839 | |||||||
| chr15:41265840 | C | T | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.349+2957C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41265840 | |||||||
| chr15:41266049 | C | T | 1 | a0001c0001t0007g0154 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.349+3166C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266049 | |||||||
| chr15:41266359 | T | TA | 6 | a0001c0001t0006g0041 a0001c0001t0006g0042 a0001c0001t0006g0047 others(3): Show |
6 | HG00741.hp1 HG01074.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+3488dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41266359 | ||||||
| chr15:41266360 | A | T | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+3477A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266360 | |||||||
| chr15:41266422 | G | T | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.349+3539G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266422 | |||||||
| chr15:41266490 | C | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0060 others(59): Show |
64 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.349+3607C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266490 | |||||||
| chr15:41266531 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.349+3648T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266531 | |||||||
| chr15:41266643 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.349+3760G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266643 | |||||||
| chr15:41266730 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.350-3827G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266730 | |||||||
| chr15:41266797 | C | T | 4 | a0001c0001t0001g0085 a0001c0001t0002g0133 a0001c0001t0017g0059 others(1): Show |
4 | HG01496.hp2 HG02293.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-3760C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266797 | |||||||
| chr15:41266956 | C | T | 1 | a0001c0001t0003g0165 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.350-3601C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266956 | |||||||
| chr15:41266978 | C | T | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-3579C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41266978 | |||||||
| chr15:41267064 | G | A | 1 | a0001c0001t0006g0048 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.350-3493G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267064 | |||||||
| chr15:41267200 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.350-3357G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267200 | |||||||
| chr15:41267204 | T | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-3353T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267204 | |||||||
| chr15:41267376 | A | C | 5 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG01255.hp1 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-3181A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267376 | |||||||
| chr15:41267587 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0005g0198 |
2 | HG00558.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.350-2970G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267587 | |||||||
| chr15:41267633 | G | T | 42 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0270 others(39): Show |
42 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.350-2924G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267633 | |||||||
| chr15:41267769 | C | CA | 10 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-2774dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41267769 | ||||||
| chr15:41267894 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.350-2663A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41267894 | |||||||
| chr15:41267929 | T | TA | 22 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0134 others(19): Show |
22 | HG01109.hp2 HG01169.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.350-2610dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41267929 | ||||||
| chr15:41267929 | T | TAA | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0060 others(59): Show |
64 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.350-2611_350-2610d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41267929 | ||||||
| chr15:41267929 | T | TAAA | 49 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0181 others(46): Show |
49 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.350-2612_350-2610d others(5): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41267929 | ||||||
| chr15:41267929 | T | TAAAA | 15 | a0001c0001t0003g0172 a0001c0001t0005g0007 a0001c0001t0005g0206 others(12): Show |
15 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-2613_350-2610d others(6): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41267929 | ||||||
| chr15:41268001 | T | A | 1 | a0001c0001t0001g0186 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.350-2556T>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268001 | |||||||
| chr15:41268606 | C | T | 6 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(3): Show |
6 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1951C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268606 | |||||||
| chr15:41268641 | C | CA | 10 | a0001c0001t0001g0063 a0001c0001t0001g0255 a0001c0001t0001g0271 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1902dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41268641 | ||||||
| chr15:41268680 | G | A | 67 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(64): Show |
67 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.350-1877G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268680 | |||||||
| chr15:41268725 | C | T | 69 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(66): Show |
69 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.350-1832C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268725 | |||||||
| chr15:41268750 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.350-1807C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268750 | |||||||
| chr15:41268806 | A | C | 1 | a0001c0001t0002g0135 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.350-1751A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268806 | |||||||
| chr15:41268852 | C | T | 2 | a0001c0001t0003g0262 a0001c0001t0005g0261 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.350-1705C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268852 | |||||||
| chr15:41268902 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.350-1655G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268902 | |||||||
| chr15:41268980 | A | G | 1 | a0001c0001t0027g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.350-1577A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41268980 | |||||||
| chr15:41269001 | G | A | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1556G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269001 | |||||||
| chr15:41269253 | G | GA | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1295dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41269253 | ||||||
| chr15:41269266 | A | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1291A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269266 | |||||||
| chr15:41269596 | A | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-961A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269596 | |||||||
| chr15:41269684 | A | G | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.350-873A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269684 | |||||||
| chr15:41269687 | G | T | 1 | a0001c0001t0008g0214 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.350-870G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269687 | |||||||
| chr15:41269716 | G | A | 67 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(64): Show |
67 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.350-841G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269716 | |||||||
| chr15:41269832 | C | A | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.350-725C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269832 | |||||||
| chr15:41269854 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 others(53): Show |
58 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.350-703G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269854 | |||||||
| chr15:41269962 | A | G | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.350-595A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41269962 | |||||||
| chr15:41270020 | A | G | 121 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.350-537A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270020 | |||||||
| chr15:41270145 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-412G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270145 | |||||||
| chr15:41270157 | T | A | 1 | a0001c0001t0004g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.350-400T>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270157 | |||||||
| chr15:41270158 | C | A | 1 | a0001c0001t0004g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.350-399C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270158 | |||||||
| chr15:41270195 | C | T | 76 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(73): Show |
76 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.350-362C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270195 | |||||||
| chr15:41270265 | T | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-292T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270265 | |||||||
| chr15:41270266 | T | TG | 22 | a0001c0001t0001g0088 a0001c0001t0001g0129 a0001c0001t0001g0212 others(19): Show |
22 | HG00642.hp1 HG01106.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.350-282dupG | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr15 | 41270266 | ||||||
| chr15:41270269 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.350-288G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270269 | |||||||
| chr15:41270421 | A | G | 6 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0264 others(3): Show |
6 | HG01891.hp1 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-136A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270421 | |||||||
| chr15:41270462 | T | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0226 others(4): Show |
7 | HG01496.hp2 HG02922.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-95T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270462 | |||||||
| chr15:41270545 | T | C | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-12T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 4/6 | chr15 | 41270545 | |||||||
| chr15:41270726 | G | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG01891.hp2 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+108G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41270726 | |||||||
| chr15:41270974 | G | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.411+356G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41270974 | |||||||
| chr15:41270982 | G | C | 1 | a0001c0001t0014g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411+364G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41270982 | |||||||
| chr15:41271016 | A | G | 121 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(118): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.411+398A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271016 | |||||||
| chr15:41271016 | A | T | 1 | a0001c0001t0013g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.411+398A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271016 | |||||||
| chr15:41271021 | C | T | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.411+403C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271021 | |||||||
| chr15:41271110 | C | A | 70 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(67): Show |
70 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.411+492C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271110 | |||||||
| chr15:41271113 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.411+495G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271113 | |||||||
| chr15:41271148 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.411+530C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271148 | |||||||
| chr15:41271250 | G | A | 32 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0003g0124 others(29): Show |
32 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.411+632G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271250 | |||||||
| chr15:41271254 | C | CA | 11 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0121 others(8): Show |
11 | HG01109.hp2 HG01243.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.411+660dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41271254 | ||||||
| chr15:41271254 | CA | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0091 others(63): Show |
68 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(65): Show |
intron_variant | MODIFIER | c.411+660delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41271254 | ||||||
| chr15:41271254 | CAA | C | 33 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0003g0124 others(30): Show |
33 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.411+659_411+660del others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41271254 | ||||||
| chr15:41271254 | CAAAA | C | 11 | a0001c0001t0005g0007 a0001c0001t0008g0016 a0001c0001t0010g0008 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.411+657_411+660del others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41271254 | ||||||
| chr15:41271254 | CAAAAA | C | 57 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(54): Show |
57 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.411+656_411+660del others(5): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41271254 | ||||||
| chr15:41271342 | C | T | 70 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(67): Show |
70 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.411+724C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271342 | |||||||
| chr15:41271357 | G | A | 117 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0156 others(114): Show |
117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.411+739G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271357 | |||||||
| chr15:41271419 | A | T | 68 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(65): Show |
68 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.411+801A>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271419 | |||||||
| chr15:41271482 | A | G | 1 | a0001c0001t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.411+864A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271482 | |||||||
| chr15:41271720 | A | C | 3 | a0001c0001t0003g0185 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | NA18955.hp1 NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.411+1102A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271720 | |||||||
| chr15:41271752 | A | G | 41 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0270 others(38): Show |
41 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.411+1134A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271752 | |||||||
| chr15:41271772 | C | G | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.411+1154C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41271772 | |||||||
| chr15:41272186 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.411+1568C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272186 | |||||||
| chr15:41272195 | A | G | 123 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0057 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.411+1577A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272195 | |||||||
| chr15:41272217 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG01255.hp2 HG01258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.411+1599C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272217 | |||||||
| chr15:41272309 | T | A | 70 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(67): Show |
70 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.411+1691T>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272309 | |||||||
| chr15:41272394 | C | T | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.411+1776C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272394 | |||||||
| chr15:41272612 | G | A | 41 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0270 others(38): Show |
41 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.411+1994G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272612 | |||||||
| chr15:41272618 | G | A | 122 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0177 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.411+2000G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272618 | |||||||
| chr15:41272628 | C | T | 2 | a0001c0001t0012g0162 a0001c0001t0034g0163 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.411+2010C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272628 | |||||||
| chr15:41272640 | C | T | 1 | a0001c0001t0007g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.411+2022C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272640 | |||||||
| chr15:41272747 | C | G | 32 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0003g0124 others(29): Show |
32 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.411+2129C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272747 | |||||||
| chr15:41272791 | G | T | 74 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(71): Show |
74 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.411+2173G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272791 | |||||||
| chr15:41272815 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0008g0089 |
2 | NA18968.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.411+2197G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272815 | |||||||
| chr15:41272833 | G | A | 1 | a0001c0001t0012g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.411+2215G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41272833 | |||||||
| chr15:41273013 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0002g0132 |
2 | HG00597.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.411+2395C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273013 | |||||||
| chr15:41273062 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0212 others(57): Show |
62 | HG01081.hp1 HG01106.hp2 HG01167.hp2 others(59): Show |
intron_variant | MODIFIER | c.411+2444A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273062 | |||||||
| chr15:41273127 | C | A | 9 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 others(6): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.411+2509C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273127 | |||||||
| chr15:41273165 | A | AAT | 4 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG01515.hp1 HG02074.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2558_411+2559d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41273165 | ||||||
| chr15:41273228 | A | G | 10 | a0001c0001t0001g0057 a0001c0001t0009g0029 a0001c0001t0009g0031 others(7): Show |
10 | HG00642.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.411+2610A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273228 | |||||||
| chr15:41273296 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.411+2678C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273296 | |||||||
| chr15:41273418 | G | A | 1 | a0001c0001t0022g0196 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.411+2800G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273418 | |||||||
| chr15:41273528 | T | C | 8 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+2910T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273528 | |||||||
| chr15:41273562 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.411+2944G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273562 | |||||||
| chr15:41273687 | TA | T | 6 | a0001c0001t0001g0241 a0001c0001t0001g0244 a0001c0001t0003g0210 others(3): Show |
6 | HG01257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+3083delA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41273687 | ||||||
| chr15:41273699 | AAAG | A | 7 | a0001c0001t0001g0026 a0001c0001t0003g0262 a0001c0001t0004g0249 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+3085_411+3087d others(5): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41273699 | ||||||
| chr15:41273766 | C | A | 3 | a0001c0001t0012g0171 a0001c0001t0012g0211 a0001c0001t0012g0252 |
3 | HG03579.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.411+3148C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41273766 | |||||||
| chr15:41274017 | A | G | 23 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(20): Show |
23 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.411+3399A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41274017 | |||||||
| chr15:41274031 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0096 |
2 | HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.411+3413A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41274031 | |||||||
| chr15:41274084 | C | T | 24 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(21): Show |
24 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.411+3466C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41274084 | |||||||
| chr15:41274118 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.411+3500G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41274118 | |||||||
| chr15:41274149 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.411+3531C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41274149 | |||||||
| chr15:41274352 | C | G | 2 | a0001c0001t0004g0143 a0001c0001t0027g0061 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.411+3734C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41274352 | |||||||
| chr15:41274790 | G | GT | 31 | a0001c0001t0001g0126 a0001c0001t0006g0032 a0001c0001t0006g0034 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.412-3959dupT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41274790 | ||||||
| chr15:41274790 | GT | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(62): Show |
67 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.412-3959delT | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41274790 | ||||||
| chr15:41274790 | GTT | G | 87 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0216 others(84): Show |
87 | HG00099.hp2 HG00544.hp1 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.412-3960_412-3959d others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41274790 | ||||||
| chr15:41275024 | G | A | 1 | a0001c0001t0007g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.412-3743G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275024 | |||||||
| chr15:41275171 | G | T | 118 | a0001c0001t0001g0026 a0001c0001t0001g0216 a0001c0001t0001g0217 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.412-3596G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275171 | |||||||
| chr15:41275196 | C | T | 11 | a0001c0001t0001g0026 a0001c0001t0004g0234 a0001c0001t0004g0235 others(8): Show |
11 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.412-3571C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275196 | |||||||
| chr15:41275197 | G | A | 75 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(72): Show |
75 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.412-3570G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275197 | |||||||
| chr15:41275327 | G | A | 5 | a0001c0001t0012g0162 a0001c0001t0012g0171 a0001c0001t0012g0211 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-3440G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275327 | |||||||
| chr15:41275406 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.412-3361C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275406 | |||||||
| chr15:41275600 | G | A | 1 | a0001c0001t0006g0046 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.412-3167G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275600 | |||||||
| chr15:41275634 | T | C | 8 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0080 others(5): Show |
8 | HG00544.hp2 NA18949.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-3133T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275634 | |||||||
| chr15:41275728 | C | T | 7 | a0001c0001t0010g0008 a0001c0001t0010g0011 a0001c0001t0010g0014 others(4): Show |
7 | HG02630.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.412-3039C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275728 | |||||||
| chr15:41275825 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.412-2942C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275825 | |||||||
| chr15:41275841 | G | A | 3 | a0001c0001t0018g0157 a0001c0001t0018g0290 a0001c0001t0032g0087 |
3 | HG02922.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.412-2926G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41275841 | |||||||
| chr15:41276192 | G | A | 48 | a0001c0001t0003g0045 a0001c0001t0003g0124 a0001c0001t0003g0140 others(45): Show |
48 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.412-2575G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41276192 | |||||||
| chr15:41276240 | C | CA | 119 | a0001c0001t0001g0026 a0001c0001t0001g0216 a0001c0001t0001g0217 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.412-2513dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41276240 | ||||||
| chr15:41276659 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01255.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.412-2108C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41276659 | |||||||
| chr15:41277074 | T | C | 3 | a0001c0001t0018g0157 a0001c0001t0018g0290 a0001c0001t0032g0087 |
3 | HG02922.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.412-1693T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41277074 | |||||||
| chr15:41277262 | A | G | 23 | a0001c0001t0001g0026 a0001c0001t0001g0216 a0001c0001t0001g0217 others(20): Show |
23 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.412-1505A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41277262 | |||||||
| chr15:41277446 | C | A | 31 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0041 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.412-1321C>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41277446 | |||||||
| chr15:41277710 | C | T | 23 | a0001c0001t0001g0026 a0001c0001t0001g0216 a0001c0001t0001g0217 others(20): Show |
23 | HG01081.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.412-1057C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41277710 | |||||||
| chr15:41277791 | G | GA | 13 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0001g0096 others(10): Show |
13 | HG02145.hp2 HG02698.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.412-960dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41277791 | ||||||
| chr15:41277791 | G | GAA | 9 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0251 others(6): Show |
9 | HG01515.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-961_412-960dup others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41277791 | ||||||
| chr15:41277791 | G | GAAA | 72 | a0001c0001t0001g0217 a0001c0001t0003g0045 a0001c0001t0003g0124 others(69): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.412-962_412-960dup others(3): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41277791 | ||||||
| chr15:41277791 | G | GAAAA | 28 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0219 others(25): Show |
28 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.412-963_412-960dup others(4): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41277791 | ||||||
| chr15:41277791 | G | GAAAAA | 6 | a0001c0001t0001g0026 a0001c0001t0001g0289 a0001c0001t0012g0162 others(3): Show |
6 | HG01109.hp2 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-964_412-960dup others(5): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41277791 | ||||||
| chr15:41277951 | G | C | 1 | a0001c0001t0003g0201 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.412-816G>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41277951 | |||||||
| chr15:41277955 | C | CA | 14 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0134 others(11): Show |
14 | HG00323.hp1 HG01123.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.412-802dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41277955 | ||||||
| chr15:41277965 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.412-802A>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41277965 | |||||||
| chr15:41278103 | C | T | 76 | a0001c0001t0001g0026 a0001c0001t0001g0216 a0001c0001t0001g0217 others(73): Show |
76 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.412-664C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278103 | |||||||
| chr15:41278205 | C | T | 2 | a0001c0001t0018g0157 a0001c0001t0018g0290 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.412-562C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278205 | |||||||
| chr15:41278250 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.412-517G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278250 | |||||||
| chr15:41278332 | C | CA | 49 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0121 others(46): Show |
49 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.412-417dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41278332 | ||||||
| chr15:41278485 | TTC | T | 48 | a0001c0001t0003g0045 a0001c0001t0003g0124 a0001c0001t0003g0140 others(45): Show |
48 | HG00099.hp2 HG00544.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.412-280_412-279del others(2): Show |
CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr15 | 41278485 | ||||||
| chr15:41278512 | A | G | 31 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0041 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.412-255A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278512 | |||||||
| chr15:41278557 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.412-210A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278557 | |||||||
| chr15:41278690 | T | C | 1 | a0001c0001t0008g0016 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.412-77T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278690 | |||||||
| chr15:41278711 | T | G | 22 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0041 others(19): Show |
22 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.412-56T>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 5/6 | chr15 | 41278711 | |||||||
| chr15:41278937 | G | A | 2 | a0001c0001t0004g0251 a0001c0001t0004g0266 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.534+48G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41278937 | |||||||
| chr15:41278938 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02572.hp1 HG02738.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.534+49C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41278938 | |||||||
| chr15:41278941 | G | A | 61 | a0001c0001t0001g0026 a0001c0001t0001g0216 a0001c0001t0001g0217 others(58): Show |
61 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.534+52G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41278941 | |||||||
| chr15:41278948 | T | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0001g0146 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.534+59T>C | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41278948 | |||||||
| chr15:41278988 | G | A | 31 | a0001c0001t0006g0032 a0001c0001t0006g0034 a0001c0001t0006g0041 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.534+99G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41278988 | |||||||
| chr15:41278998 | G | T | 1 | a0001c0001t0004g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.534+109G>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41278998 | |||||||
| chr15:41279079 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0134 |
2 | NA18949.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.534+190C>T | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41279079 | |||||||
| chr15:41279080 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.534+191G>A | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41279080 | |||||||
| chr15:41279101 | C | G | 7 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG01081.hp1 HG01106.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+212C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41279101 | |||||||
| chr15:41279210 | C | CA | 10 | a0001c0001t0001g0071 a0001c0001t0001g0197 a0001c0001t0001g0259 others(7): Show |
10 | HG00544.hp2 HG02055.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-110dupA | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr15 | 41279210 | ||||||
| chr15:41279261 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.535-75A>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41279261 | |||||||
| chr15:41279313 | C | G | 2 | a0001c0001t0009g0056 a0001c0001t0015g0054 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.535-23C>G | CHP1 | ENSG00000187446.12 | transcript | ENST00000334660.10 | protein_coding | 6/6 | chr15 | 41279313 |