Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7180 |
| ensemblid | ENSG00000124490.14 |
| hgncid | 12024 |
| symbol | CRISP2 |
| name | cysteine rich secretory protein 2 |
| refseq_nuc | NM_003296.4 |
| refseq_prot | NP_003287.1 |
| ensembl_nuc | ENST00000339139.5 |
| ensembl_prot | ENSP00000339155.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 49692359 |
| end | 49713543 |
| strand | - |
| ver | v1.2 |
| region | chr6:49692359-49713543 |
| region5000 | chr6:49687359-49718543 |
| regionname0 | CRISP2_chr6_49692359_49713543 |
| regionname5000 | CRISP2_chr6_49687359_49718543 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 243 | 392 | 85 | 74 | 174 | 16 | 41 | 137 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0002 | 0/0 | 243 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0003 | 0/0 | 243 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0004 | 0/0 | 243 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0005 | 0/0 | 243 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0006 | 0/0 | 243 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0007 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| a0008 | 0/0 | 243 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | MALLP others(238): Show |
chr6 | 49687359 | 49718543 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 729 | 378 | 72 | 73 | 174 | 16 | 41 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0001c0002 | 0/0 | 729 | 14 | 13 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0002c0003 | 0/0 | 729 | 6 | 5 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0003c0004 | 0/0 | 729 | 3 | 0 | 0 | 0 | 2 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0004c0005 | 0/0 | 729 | 3 | 3 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0005c0007 | 0/0 | 729 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0006c0006 | 0/0 | 729 | 2 | 0 | 0 | 0 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0007c0009 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 | ||
| a0008c0008 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | ATGGC others(724): Show |
chr6 | 49687359 | 49718543 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1365 | 267 | 40 | 51 | 142 | 7 | 26 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0002 | 1/0 | 1365 | 103 | 31 | 18 | 29 | 9 | 15 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0004 | 0/0 | 1365 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0005 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0006 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0007 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0008 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0010 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0001t0012 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0002t0003 | 0/0 | 1365 | 13 | 12 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0001c0002t0011 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0002c0003t0001 | 0/0 | 1365 | 6 | 5 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0003c0004t0002 | 0/0 | 1365 | 3 | 0 | 0 | 0 | 2 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0004c0005t0001 | 0/0 | 1365 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0004c0005t0009 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0005c0007t0001 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0005c0007t0002 | 0/0 | 1365 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0006c0006t0002 | 0/0 | 1365 | 2 | 0 | 0 | 0 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0007c0009t0001 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| a0008c0008t0001 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | GCAGC others(1360): Show |
chr6 | 49687359 | 49718543 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 0 | 3 | 37 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 5 | 5 | 1 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 3 | 2 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0008 | 0/0 | 6 | 2 | 1 | 1 | 1 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0014 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0017 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0002 | 0/0 | 30 | 10 | 1 | 12 | 0 | 7 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0011 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0013 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0015 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0030 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0002t0003g0004 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0002t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0001c0002t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0002c0003t0001g0012 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0003c0004t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0003c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0004c0005t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0004c0005t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0005c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0005c0007t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0006c0006t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0007c0009t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| a0008c0008t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | GBR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0169 | EUR | FIN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | FIN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00673 | hp1 | a0007 | c0009 | t0001 | g0184 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0078 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0012 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0196 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0176 | EUR | IBS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01516 | hp2 | a0003 | c0004 | t0002 | g0039 | EUR | IBS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01517 | hp2 | a0003 | c0004 | t0002 | g0039 | EUR | IBS | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0062 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0012 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0105 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02257 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0153 | EAS | KHV | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02809 | hp2 | a0004 | c0005 | t0009 | g0183 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0049 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03225 | hp2 | a0004 | c0005 | t0001 | g0049 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03491 | hp2 | a0006 | c0006 | t0002 | g0045 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03492 | hp2 | a0006 | c0006 | t0002 | g0045 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0079 | AFR | GWD | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04199 | hp1 | a0003 | c0004 | t0002 | g0108 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0063 | AFR | YRI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18940 | hp2 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18970 | hp2 | a0008 | c0008 | t0001 | g0088 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | LWK | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | LWK | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19043 | hp1 | a0005 | c0007 | t0001 | g0152 | AFR | LWK | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | YRI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ASW | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | TSI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | TSI | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG01123 | hp2 | a0005 | c0007 | t0002 | g0082 | AMR | CLM | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| HG06807 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | USA | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | USA | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | LWK | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0133 | REF | REF | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0167 | REF | REF | CRISP2_chr6_49687359_49718543 | CRISP2 | chr6 | 49687359 | 49718543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49695854 | A | G | 1 | a0003 | 3 | HG01516.hp2 HG01517.hp2 HG04199.hp1 |
missense_variant | MODERATE | c.586T>C | p.Cys196Arg | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/10 | 805/1365 | 586/732 | 196/243 | chr6 | 49695854 | |||
| chr6:49695865 | C | T | 1 | a0007 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.575G>A | p.Cys192Tyr | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/10 | 794/1365 | 575/732 | 192/243 | chr6 | 49695865 | |||
| chr6:49695912 | C | T | 1 | a0006 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.528G>A | p.Met176Ile | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/10 | 747/1365 | 528/732 | 176/243 | chr6 | 49695912 | |||
| chr6:49697957 | G | C | 1 | a0002 | 6 | HG01074.hp2 HG01891.hp1 HG02647.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.418C>G | p.Leu140Val | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/10 | 637/1365 | 418/732 | 140/243 | chr6 | 49697957 | |||
| chr6:49698387 | T | C | 1 | a0004 | 3 | HG02809.hp2 HG03041.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.392A>G | p.Asn131Ser | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 7/10 | 611/1365 | 392/732 | 131/243 | chr6 | 49698387 | |||
| chr6:49699856 | C | A | 1 | a0005 | 2 | HG01123.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.219G>T | p.Arg73Ser | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/10 | 438/1365 | 219/732 | 73/243 | chr6 | 49699856 | |||
| chr6:49709147 | A | G | 1 | a0008 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.50T>C | p.Leu17Ser | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/10 | 269/1365 | 50/732 | 17/243 | chr6 | 49709147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49700692 | T | C | 1 | a0001c0002 | 14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
synonymous_variant | LOW | c.159A>G | p.Pro53Pro | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/10 | 378/1365 | 159/732 | 53/243 | chr6 | 49700692 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49692367 | A | G | 1 | a0001c0001t0008 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 10/10 | 406 | chr6 | 49692367 | ||||||
| chr6:49692391 | C | T | 1 | a0001c0001t0007 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*382G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 10/10 | 382 | chr6 | 49692391 | ||||||
| chr6:49692506 | A | G | 1 | a0001c0001t0006 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*267T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 10/10 | 267 | chr6 | 49692506 | ||||||
| chr6:49692547 | G | A | 1 | a0004c0005t0009 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 10/10 | 226 | chr6 | 49692547 | ||||||
| chr6:49692705 | A | C | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*68T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 10/10 | 68 | chr6 | 49692705 | ||||||
| chr6:49692762 | C | A | 1 | a0001c0001t0010 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 10/10 | 11 | chr6 | 49692762 | ||||||
| chr6:49709197 | T | C | 2 | a0001c0002t0003 a0001c0002t0011 |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-1A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/10 | 1 | chr6 | 49709197 | ||||||
| chr6:49712504 | T | C | 1 | a0001c0001t0012 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/10 | 3308 | chr6 | 49712504 | ||||||
| chr6:49713497 | A | C | 1 | a0001c0001t0005 | 1 | HG02135.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/10 | 4301 | chr6 | 49713497 | ||||||
| chr6:49713499 | A | G | 1 | a0001c0001t0004 | 2 | HG00733.hp1 HG01257.hp2 |
5_prime_UTR_variant | MODIFIER | c.-175T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/10 | 4303 | chr6 | 49713499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49693010 | C | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0022 others(12): Show |
29 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.605-110G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49693010 | |||||||
| chr6:49693429 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0125 |
2 | NA18978.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.605-529G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49693429 | |||||||
| chr6:49693491 | C | G | 1 | a0001c0001t0002g0071 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.605-591G>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49693491 | |||||||
| chr6:49693643 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.605-743C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49693643 | |||||||
| chr6:49693756 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.605-856C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49693756 | |||||||
| chr6:49694107 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG01243.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.605-1207G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694107 | |||||||
| chr6:49694182 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0161 a0001c0001t0001g0203 |
3 | HG00741.hp2 HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.605-1282A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694182 | |||||||
| chr6:49694184 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.605-1284G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694184 | |||||||
| chr6:49694207 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0085 |
3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.605-1307G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694207 | |||||||
| chr6:49694295 | C | T | 1 | a0001c0001t0002g0055 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.605-1395G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694295 | |||||||
| chr6:49694379 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
138 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.604+1457A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694379 | |||||||
| chr6:49694391 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.604+1445C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694391 | |||||||
| chr6:49694400 | A | G | 16 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0091 others(13): Show |
27 | HG01069.hp2 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.604+1436T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694400 | |||||||
| chr6:49694408 | TTGGTGCT others(4): Show |
T | 1 | a0001c0001t0002g0170 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.604+1417_604+1427d others(13): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694408 | |||||||
| chr6:49694444 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.604+1392C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694444 | |||||||
| chr6:49694544 | C | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0140 others(2): Show |
6 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.604+1292G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694544 | |||||||
| chr6:49694740 | C | CT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.604+1095dupA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694740 | |||||||
| chr6:49694740 | C | CTT | 2 | a0001c0001t0001g0178 a0002c0003t0001g0012 |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.604+1094_604+1095d others(4): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694740 | |||||||
| chr6:49694748 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.604+1088A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694748 | |||||||
| chr6:49694766 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.604+1070C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694766 | |||||||
| chr6:49694775 | C | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0043 others(7): Show |
16 | HG00280.hp1 HG00738.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.604+1061G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694775 | |||||||
| chr6:49694802 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.604+1034G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694802 | |||||||
| chr6:49694836 | C | A | 17 | a0001c0001t0001g0172 a0001c0001t0001g0175 a0001c0001t0002g0011 others(14): Show |
31 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.604+1000G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694836 | |||||||
| chr6:49694912 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.604+924A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694912 | |||||||
| chr6:49694933 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): Show |
213 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.604+903G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49694933 | |||||||
| chr6:49695043 | A | G | 1 | a0001c0002t0003g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.604+793T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695043 | |||||||
| chr6:49695138 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0151 |
5 | HG02109.hp2 HG02145.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.604+698G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695138 | |||||||
| chr6:49695475 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.604+361T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695475 | |||||||
| chr6:49695503 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
11 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.604+333G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695503 | |||||||
| chr6:49695515 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.604+321A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695515 | |||||||
| chr6:49695523 | T | C | 2 | a0005c0007t0001g0152 a0005c0007t0002g0082 |
2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.604+313A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695523 | |||||||
| chr6:49695556 | G | A | 1 | a0001c0001t0002g0171 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.604+280C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695556 | |||||||
| chr6:49695646 | C | G | 1 | a0001c0001t0002g0073 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.604+190G>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695646 | |||||||
| chr6:49695752 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.604+84C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695752 | |||||||
| chr6:49695806 | A | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
11 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.604+30T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 9/9 | chr6 | 49695806 | |||||||
| chr6:49696236 | TA | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.516-313delT | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696236 | |||||||
| chr6:49696468 | G | GGT | 3 | a0001c0002t0003g0004 a0001c0002t0003g0078 a0001c0002t0003g0079 |
12 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.516-546_516-545dup others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696468 | |||||||
| chr6:49696581 | TTAAAG | T | 14 | a0001c0001t0001g0175 a0001c0001t0002g0011 a0001c0001t0002g0015 others(11): Show |
27 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.516-662_516-658del others(5): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696581 | |||||||
| chr6:49696587 | T | TA | 5 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0151 others(2): Show |
7 | HG00323.hp1 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-664dupT | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696587 | |||||||
| chr6:49696587 | TA | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
122 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.516-664delT | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696587 | |||||||
| chr6:49696601 | A | G | 26 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(23): Show |
65 | HG00408.hp2 HG00621.hp2 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.516-677T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696601 | |||||||
| chr6:49696611 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.516-687T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696611 | |||||||
| chr6:49696625 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.516-701A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696625 | |||||||
| chr6:49696725 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-801A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696725 | |||||||
| chr6:49696750 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-826G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696750 | |||||||
| chr6:49696756 | G | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-832C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696756 | |||||||
| chr6:49696851 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.516-927A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49696851 | |||||||
| chr6:49697014 | T | C | 1 | a0005c0007t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.515+846A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697014 | |||||||
| chr6:49697061 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.515+799G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697061 | |||||||
| chr6:49697150 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.515+710G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697150 | |||||||
| chr6:49697181 | A | G | 2 | a0001c0001t0001g0178 a0002c0003t0001g0012 |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+679T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697181 | |||||||
| chr6:49697191 | G | T | 25 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(22): Show |
64 | HG00408.hp2 HG00621.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.515+669C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697191 | |||||||
| chr6:49697404 | G | GTGTGTGT others(10): Show |
1 | a0001c0002t0011g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.515+455_515+456ins others(17): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697404 | |||||||
| chr6:49697404 | G | GTGTGTGT others(12): Show |
2 | a0001c0002t0003g0063 a0001c0002t0003g0078 |
2 | HG01069.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.515+455_515+456ins others(19): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697404 | |||||||
| chr6:49697404 | G | GTGTGTGT others(14): Show |
1 | a0001c0002t0003g0004 | 10 | HG02257.hp1 HG02630.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.515+455_515+456ins others(21): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697404 | |||||||
| chr6:49697404 | G | GTGTGTGT others(16): Show |
1 | a0001c0002t0003g0079 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.515+455_515+456ins others(23): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697404 | |||||||
| chr6:49697407 | G | GT | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.515+452_515+453ins others(1): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697407 | |||||||
| chr6:49697407 | GGT | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.515+451_515+452del others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697407 | |||||||
| chr6:49697560 | A | G | 1 | a0001c0001t0002g0033 | 2 | HG02486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.515+300T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697560 | |||||||
| chr6:49697577 | A | G | 1 | a0001c0002t0011g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.515+283T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697577 | |||||||
| chr6:49697744 | G | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.515+116C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697744 | |||||||
| chr6:49697756 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.515+104G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 8/9 | chr6 | 49697756 | |||||||
| chr6:49698013 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0151 others(1): Show |
6 | HG02109.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.418-56T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 7/9 | chr6 | 49698013 | |||||||
| chr6:49698017 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0145 others(8): Show |
16 | HG00280.hp1 HG00280.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.418-60T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 7/9 | chr6 | 49698017 | |||||||
| chr6:49698037 | A | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0084 others(2): Show |
8 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.418-80T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 7/9 | chr6 | 49698037 | |||||||
| chr6:49698052 | T | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0189 |
3 | NA18946.hp2 NA19001.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.418-95A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 7/9 | chr6 | 49698052 | |||||||
| chr6:49698280 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0159 |
5 | HG02056.hp1 NA19001.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+82T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 7/9 | chr6 | 49698280 | |||||||
| chr6:49698668 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.272-161C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49698668 | |||||||
| chr6:49698723 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.272-216G>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49698723 | |||||||
| chr6:49698745 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.272-238G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49698745 | |||||||
| chr6:49698904 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(26): Show |
92 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.272-397T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49698904 | |||||||
| chr6:49698942 | G | T | 1 | a0001c0001t0001g0050 | 2 | NA18954.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.272-435C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49698942 | |||||||
| chr6:49699062 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.272-555G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699062 | |||||||
| chr6:49699144 | T | A | 2 | a0005c0007t0001g0152 a0005c0007t0002g0082 |
2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.272-637A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699144 | |||||||
| chr6:49699219 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.271+585A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699219 | |||||||
| chr6:49699430 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.271+374C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699430 | |||||||
| chr6:49699454 | TA | T | 3 | a0001c0002t0003g0004 a0001c0002t0003g0078 a0001c0002t0003g0079 |
12 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+349delT | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699454 | |||||||
| chr6:49699615 | T | C | 2 | a0001c0001t0001g0178 a0002c0003t0001g0012 |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+189A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699615 | |||||||
| chr6:49699752 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.271+52T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 6/9 | chr6 | 49699752 | |||||||
| chr6:49699897 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.184-6G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49699897 | |||||||
| chr6:49700113 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.184-222A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49700113 | |||||||
| chr6:49700123 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-232A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49700123 | |||||||
| chr6:49700231 | A | G | 3 | a0001c0001t0001g0182 a0004c0005t0001g0049 a0004c0005t0009g0183 |
4 | HG02717.hp2 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-340T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49700231 | |||||||
| chr6:49700420 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.183+248T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49700420 | |||||||
| chr6:49700463 | T | A | 1 | a0001c0001t0002g0072 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.183+205A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49700463 | |||||||
| chr6:49700603 | G | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.183+65C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 5/9 | chr6 | 49700603 | |||||||
| chr6:49700870 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.67-86C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49700870 | |||||||
| chr6:49700919 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.67-135T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49700919 | |||||||
| chr6:49700977 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0151 |
5 | HG02109.hp2 HG02145.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-193C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49700977 | |||||||
| chr6:49701030 | G | T | 3 | a0001c0002t0003g0004 a0001c0002t0003g0078 a0001c0002t0003g0079 |
12 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-246C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701030 | |||||||
| chr6:49701077 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
208 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.67-293C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701077 | |||||||
| chr6:49701092 | C | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-308G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701092 | |||||||
| chr6:49701096 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.67-312A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701096 | |||||||
| chr6:49701243 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.67-459A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701243 | |||||||
| chr6:49701485 | CGT | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0094 others(14): Show |
35 | HG00408.hp2 HG00438.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-703_67-702delAC | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701485 | |||||||
| chr6:49701496 | GTGTGTA | G | 4 | a0001c0001t0001g0182 a0001c0002t0003g0004 a0001c0002t0003g0078 others(1): Show |
13 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-718_67-713delTA others(4): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701496 | |||||||
| chr6:49701498 | GTGTA | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.67-718_67-715delTA others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701498 | |||||||
| chr6:49701498 | GTGTATA | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0115 others(12): Show |
21 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-720_67-715delTA others(4): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701498 | |||||||
| chr6:49701498 | GTGTATAT others(1): Show |
G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0146 others(2): Show |
6 | HG02145.hp2 HG02486.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-722_67-715delTA others(6): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701498 | |||||||
| chr6:49701498 | GTGTATAT others(3): Show |
G | 1 | a0001c0001t0001g0001 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.67-724_67-715delTA others(8): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701498 | |||||||
| chr6:49701500 | G | A | 21 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0096 others(18): Show |
35 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.67-716C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701500 | |||||||
| chr6:49701500 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.67-726_67-717dupTA others(8): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701500 | |||||||
| chr6:49701500 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0047 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.67-728_67-717dupTA others(10): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701500 | |||||||
| chr6:49701500 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67-717_67-716insTA others(8): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701500 | |||||||
| chr6:49701500 | GTA | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
23 | HG00323.hp1 HG00733.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.67-718_67-717delTA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701500 | |||||||
| chr6:49701500 | GTATA | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0162 others(2): Show |
6 | HG01346.hp2 HG02738.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-720_67-717delTA others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701500 | |||||||
| chr6:49701502 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.67-718T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701502 | |||||||
| chr6:49701504 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-720T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701504 | |||||||
| chr6:49701513 | T | TATATATA others(10): Show |
1 | a0001c0001t0002g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.67-730_67-729insTG others(15): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701513 | |||||||
| chr6:49701515 | TATATATA others(11): Show |
T | 1 | a0001c0001t0002g0059 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.67-749_67-732delGT others(16): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701515 | |||||||
| chr6:49701521 | TATATACA others(3): Show |
T | 1 | a0001c0001t0002g0055 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-747_67-738delGT others(8): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701521 | |||||||
| chr6:49701523 | T | C | 9 | a0001c0001t0001g0168 a0001c0001t0002g0011 a0001c0001t0002g0015 others(6): Show |
15 | HG00733.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-739A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701523 | |||||||
| chr6:49701523 | TATACAC | T | 2 | a0001c0001t0001g0178 a0002c0003t0001g0012 |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-745_67-740delGT others(4): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701523 | |||||||
| chr6:49701525 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0050 others(20): Show |
39 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.67-741A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701525 | |||||||
| chr6:49701525 | TACAC | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0148 a0001c0002t0003g0004 others(2): Show |
15 | HG01069.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-745_67-742delGT others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701525 | |||||||
| chr6:49701527 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(86): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.67-743G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701527 | |||||||
| chr6:49701528 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67-744T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701528 | |||||||
| chr6:49701529 | C | T | 2 | a0005c0007t0001g0152 a0005c0007t0002g0082 |
2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-745G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701529 | |||||||
| chr6:49701596 | TAC | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0156 a0001c0001t0001g0203 others(1): Show |
5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-814_67-813delGT | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701596 | |||||||
| chr6:49701606 | C | CGGTATAT others(64): Show |
1 | a0001c0001t0001g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67-823_67-822insAT others(69): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701606 | |||||||
| chr6:49701609 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67-825C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701609 | |||||||
| chr6:49701610 | G | GTATATAT others(8): Show |
1 | a0001c0001t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67-827_67-826insAT others(13): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATAT others(23): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
8 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(28): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATAT others(38): Show |
1 | a0001c0001t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.67-827_67-826insAT others(43): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(6): Show |
1 | a0001c0001t0001g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.67-827_67-826insAT others(11): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(68): Show |
1 | a0001c0001t0001g0132 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.67-827_67-826insAT others(73): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(36): Show |
8 | a0001c0001t0001g0021 a0001c0001t0001g0090 a0001c0001t0001g0091 others(5): Show |
10 | HG00673.hp2 HG02135.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(41): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(51): Show |
14 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
24 | HG00099.hp1 HG00738.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(56): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(66): Show |
20 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(17): Show |
42 | HG00140.hp1 HG00323.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(71): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(81): Show |
15 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0025 others(12): Show |
28 | HG00642.hp2 HG01515.hp1 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(86): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(96): Show |
6 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0087 others(3): Show |
9 | HG00423.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(101): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(111): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
5 | NA18943.hp2 NA18957.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(116): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(126): Show |
6 | a0001c0001t0001g0041 a0001c0001t0001g0095 a0001c0001t0001g0098 others(3): Show |
7 | HG00408.hp1 HG00438.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(131): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(141): Show |
3 | a0001c0001t0001g0027 a0001c0001t0001g0099 a0001c0001t0012g0199 |
5 | HG00544.hp1 HG00544.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-827_67-826insAT others(146): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(156): Show |
1 | a0001c0001t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.67-827_67-826insAT others(161): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(171): Show |
2 | a0001c0001t0001g0042 a0001c0001t0002g0140 |
3 | HG02615.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.67-827_67-826insAT others(176): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | GTATATGT others(216): Show |
1 | a0001c0001t0001g0131 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.67-827_67-826insAT others(221): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | G | T | 1 | a0001c0001t0001g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.67-826C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | GTA | G | 36 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0085 others(33): Show |
89 | HG00280.hp2 HG00408.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.67-828_67-827delTA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701610 | GTATATAT others(10): Show |
G | 1 | a0001c0001t0001g0104 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.67-843_67-827delTA others(15): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701610 | |||||||
| chr6:49701616 | ATATATAC others(10): Show |
A | 7 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(4): Show |
12 | HG01074.hp2 HG01891.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-849_67-833delCA others(15): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701616 | |||||||
| chr6:49701616 | ATATATAC others(25): Show |
A | 6 | a0001c0001t0002g0035 a0001c0001t0002g0058 a0001c0001t0002g0060 others(3): Show |
7 | HG02622.hp1 HG02630.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-864_67-833delCA others(30): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701616 | |||||||
| chr6:49701616 | ATATATAC others(40): Show |
A | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.67-879_67-833delCA others(45): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701616 | |||||||
| chr6:49701618 | A | ATACATTA others(6): Show |
2 | a0001c0001t0001g0190 a0001c0001t0002g0061 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.67-835_67-834insCA others(11): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(21): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0155 others(3): Show |
8 | HG00621.hp1 HG00733.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-835_67-834insCA others(26): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(36): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(7): Show |
20 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.67-835_67-834insCA others(41): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(51): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(13): Show |
47 | HG00558.hp2 HG00639.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.67-835_67-834insCA others(56): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(66): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0005c0007t0001g0152 |
6 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-835_67-834insCA others(71): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(81): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(3): Show |
10 | HG00642.hp1 HG01074.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-835_67-834insCA others(86): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(96): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0195 others(3): Show |
7 | HG00741.hp1 HG01099.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-835_67-834insCA others(101): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATACATTA others(156): Show |
1 | a0001c0001t0001g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.67-835_67-834insCA others(161): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | ATATACAT others(8): Show |
1 | a0001c0001t0001g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-849_67-835dupCA others(13): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | A | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.67-834T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | ATATACAT others(8): Show |
A | 17 | a0001c0001t0001g0057 a0001c0001t0002g0002 a0001c0001t0002g0013 others(14): Show |
55 | HG00323.hp1 HG00408.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.67-849_67-835delCA others(13): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701618 | ATATACAT others(23): Show |
A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0151 |
3 | HG02109.hp2 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.67-864_67-835delCA others(28): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701618 | |||||||
| chr6:49701643 | T | TATATGTA others(3): Show |
1 | a0001c0001t0001g0165 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67-869_67-860dupGT others(8): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701643 | |||||||
| chr6:49701646 | A | C | 1 | a0001c0001t0002g0044 | 2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.67-862T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701646 | |||||||
| chr6:49701674 | A | ATATGTAT others(165): Show |
1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-891_67-890insAT others(170): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701674 | |||||||
| chr6:49701689 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0002g0164 |
2 | HG00140.hp2 HG00423.hp2 |
intron_variant | MODIFIER | c.67-905T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701689 | |||||||
| chr6:49701689 | ATATGTAT others(4): Show |
A | 3 | a0001c0001t0001g0203 a0001c0002t0003g0004 a0001c0002t0003g0079 |
3 | HG02647.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.67-916_67-906delAT others(9): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701689 | |||||||
| chr6:49701690 | T | TATGTATA others(23): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0148 a0001c0001t0002g0149 |
4 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-907_67-906insTA others(28): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701690 | |||||||
| chr6:49701698 | CATTATGT others(15): Show |
C | 1 | a0001c0001t0002g0055 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.67-936_67-915delAC others(20): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701698 | |||||||
| chr6:49701700 | T | TTATA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0144 others(3): Show |
21 | HG00558.hp1 HG01069.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.67-917_67-916insTA others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701700 | |||||||
| chr6:49701700 | T | TTATATAT others(72): Show |
1 | a0001c0002t0003g0063 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.67-917_67-916insTA others(77): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701700 | |||||||
| chr6:49701700 | T | TTATATAT others(87): Show |
1 | a0001c0002t0011g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-917_67-916insTA others(92): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701700 | |||||||
| chr6:49701704 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.67-920C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701704 | |||||||
| chr6:49701708 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-924T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701708 | |||||||
| chr6:49701709 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-925G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701709 | |||||||
| chr6:49701709 | CATATATA others(4): Show |
C | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67-936_67-926delAC others(9): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701709 | |||||||
| chr6:49701713 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-929A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701713 | |||||||
| chr6:49701716 | A | ATGTATAC others(22): Show |
1 | a0001c0001t0001g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67-933_67-932insAC others(27): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701716 | |||||||
| chr6:49701716 | A | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-932T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701716 | |||||||
| chr6:49701719 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67-935C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701719 | |||||||
| chr6:49701720 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67-936A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701720 | |||||||
| chr6:49701720 | T | TATAC | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-937_67-936insGT others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701720 | |||||||
| chr6:49701730 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.67-946C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701730 | |||||||
| chr6:49701743 | GTA | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0148 a0001c0001t0002g0149 |
4 | HG02055.hp1 HG02145.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-961_67-960delTA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701743 | |||||||
| chr6:49701749 | A | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-965T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701749 | |||||||
| chr6:49701752 | T | C | 3 | a0001c0002t0003g0004 a0001c0002t0003g0078 a0001c0002t0003g0079 |
12 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-968A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701752 | |||||||
| chr6:49701764 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.67-980A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701764 | |||||||
| chr6:49701790 | G | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1006C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701790 | |||||||
| chr6:49701791 | T | C | 2 | a0005c0007t0001g0152 a0005c0007t0002g0082 |
2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-1007A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701791 | |||||||
| chr6:49701806 | T | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1022A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701806 | |||||||
| chr6:49701852 | TAA | T | 18 | a0001c0001t0001g0046 a0001c0001t0001g0168 a0001c0001t0001g0172 others(15): Show |
32 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.67-1070_67-1069del others(2): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701852 | |||||||
| chr6:49701860 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0151 |
5 | HG02109.hp2 HG02145.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-1076T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701860 | |||||||
| chr6:49701872 | T | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1088A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701872 | |||||||
| chr6:49701934 | A | AT | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG02083.hp2 HG02165.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1151dupA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701934 | |||||||
| chr6:49701935 | TAATATAT others(32): Show |
T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.67-1190_67-1152del others(39): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701935 | |||||||
| chr6:49701943 | G | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG02083.hp2 HG02165.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1159C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701943 | |||||||
| chr6:49701967 | ATAATATA others(36): Show |
A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG02083.hp2 HG02165.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1226_67-1184del others(43): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49701967 | |||||||
| chr6:49702007 | ATAT | A | 21 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0020 others(18): Show |
60 | HG00408.hp2 HG00621.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.67-1226_67-1224del others(3): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702007 | |||||||
| chr6:49702021 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.67-1237T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702021 | |||||||
| chr6:49702060 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.67-1276A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702060 | |||||||
| chr6:49702072 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1288A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702072 | |||||||
| chr6:49702139 | C | CA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0047 others(7): Show |
15 | HG01081.hp2 HG01099.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-1356_67-1355ins others(1): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | C | CATA | 3 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0019 |
4 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1356_67-1355ins others(3): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | C | CATATATA others(6): Show |
1 | a0001c0001t0001g0150 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.67-1356_67-1355ins others(13): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(16): Show |
35 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.67-1356delA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTAT | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(34): Show |
58 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.67-1358_67-1356del others(3): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATAT | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0018 others(9): Show |
15 | HG00140.hp2 HG01934.hp1 HG02698.hp1 others(12): Show |
intron_variant | MODIFIER | c.67-1360_67-1356del others(5): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(16): Show |
34 | HG00423.hp2 HG00438.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.67-1362_67-1356del others(7): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(2): Show |
C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(22): Show |
47 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.67-1364_67-1356del others(9): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(4): Show |
C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0179 a0001c0001t0001g0197 others(13): Show |
33 | HG00639.hp1 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-1366_67-1356del others(11): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(6): Show |
C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0106 others(8): Show |
13 | HG01884.hp2 HG02165.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-1368_67-1356del others(13): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(8): Show |
C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(12): Show |
29 | HG00323.hp2 HG00735.hp1 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.67-1370_67-1356del others(15): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(10): Show |
C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.67-1372_67-1356del others(17): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(12): Show |
C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0100 others(2): Show |
7 | HG01256.hp2 HG01993.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1374_67-1356del others(19): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(14): Show |
C | 2 | a0001c0001t0001g0121 a0001c0001t0012g0199 |
2 | HG06807.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.67-1376_67-1356del others(21): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(16): Show |
C | 1 | a0001c0001t0002g0015 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.67-1378_67-1356del others(23): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702139 | CTATATAT others(20): Show |
C | 1 | a0001c0001t0002g0054 | 2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.67-1382_67-1356del others(27): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702139 | |||||||
| chr6:49702152 | T | TATGTGTA others(21): Show |
2 | a0001c0001t0001g0047 a0001c0001t0001g0085 |
3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-1369_67-1368ins others(28): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702152 | |||||||
| chr6:49702153 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67-1369T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702153 | |||||||
| chr6:49702155 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67-1371T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702155 | |||||||
| chr6:49702158 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.67-1374A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702158 | |||||||
| chr6:49702175 | A | G | 26 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(23): Show |
65 | HG00408.hp2 HG00621.hp2 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.67-1391T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702175 | |||||||
| chr6:49702178 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0085 |
3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.67-1394A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702178 | |||||||
| chr6:49702180 | T | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1396A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702180 | |||||||
| chr6:49702185 | C | A | 1 | a0001c0001t0002g0193 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.67-1401G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702185 | |||||||
| chr6:49702218 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1434G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702218 | |||||||
| chr6:49702271 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1487C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702271 | |||||||
| chr6:49702411 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-1627C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702411 | |||||||
| chr6:49702415 | A | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1631T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702415 | |||||||
| chr6:49702462 | C | A | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.67-1678G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702462 | |||||||
| chr6:49702577 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1793G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702577 | |||||||
| chr6:49702599 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.67-1815G>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702599 | |||||||
| chr6:49702627 | T | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-1843A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702627 | |||||||
| chr6:49702639 | A | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0145 others(7): Show |
15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-1855T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702639 | |||||||
| chr6:49702645 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.67-1861A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702645 | |||||||
| chr6:49702693 | G | A | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.67-1909C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702693 | |||||||
| chr6:49702767 | G | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
99 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.67-1983C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702767 | |||||||
| chr6:49702849 | G | C | 18 | a0001c0001t0001g0046 a0001c0001t0001g0168 a0001c0001t0001g0172 others(15): Show |
32 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.67-2065C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702849 | |||||||
| chr6:49702892 | CT | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-2109delA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49702892 | |||||||
| chr6:49703068 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.67-2284T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703068 | |||||||
| chr6:49703138 | C | T | 1 | a0001c0001t0002g0030 | 3 | HG00733.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.67-2354G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703138 | |||||||
| chr6:49703188 | TA | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.67-2405delT | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703188 | |||||||
| chr6:49703221 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-2437G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703221 | |||||||
| chr6:49703281 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0060 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.67-2497C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703281 | |||||||
| chr6:49703301 | G | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-2517C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703301 | |||||||
| chr6:49703302 | C | CT | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-2519dupA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703302 | |||||||
| chr6:49703390 | A | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0065 |
3 | HG02040.hp2 NA18966.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.67-2606T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703390 | |||||||
| chr6:49703418 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67-2634G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703418 | |||||||
| chr6:49703419 | A | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-2635T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703419 | |||||||
| chr6:49703510 | A | G | 1 | a0001c0001t0008g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.67-2726T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703510 | |||||||
| chr6:49703540 | G | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-2756C>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703540 | |||||||
| chr6:49703640 | T | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.67-2856A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703640 | |||||||
| chr6:49703756 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
99 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.67-2972G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703756 | |||||||
| chr6:49703819 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67-3035A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703819 | |||||||
| chr6:49703822 | C | T | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-3038G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703822 | |||||||
| chr6:49703887 | T | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-3103A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703887 | |||||||
| chr6:49703924 | C | A | 2 | a0001c0002t0003g0063 a0001c0002t0011g0062 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67-3140G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703924 | |||||||
| chr6:49703989 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.67-3205T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49703989 | |||||||
| chr6:49704032 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
6 | NA18951.hp2 NA18986.hp1 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-3248C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704032 | |||||||
| chr6:49704080 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0151 |
5 | HG02109.hp2 HG02145.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-3296A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704080 | |||||||
| chr6:49704144 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.67-3360A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704144 | |||||||
| chr6:49704355 | A | G | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
4 | HG00423.hp1 HG00544.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3571T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704355 | |||||||
| chr6:49704481 | T | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67-3697A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704481 | |||||||
| chr6:49704540 | C | T | 2 | a0001c0002t0003g0063 a0001c0002t0011g0062 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67-3756G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704540 | |||||||
| chr6:49704655 | G | T | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.67-3871C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704655 | |||||||
| chr6:49704677 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.67-3893T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704677 | |||||||
| chr6:49704709 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
12 | HG00639.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-3925T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704709 | |||||||
| chr6:49704763 | T | A | 2 | a0001c0002t0003g0063 a0001c0002t0011g0062 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.67-3979A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704763 | |||||||
| chr6:49704775 | G | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0145 others(7): Show |
15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-3991C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704775 | |||||||
| chr6:49704834 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.67-4050A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49704834 | |||||||
| chr6:49705169 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.66+3962C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705169 | |||||||
| chr6:49705181 | C | A | 3 | a0001c0002t0003g0004 a0001c0002t0003g0078 a0001c0002t0003g0079 |
12 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+3950G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705181 | |||||||
| chr6:49705191 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.66+3940A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705191 | |||||||
| chr6:49705231 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0085 |
3 | HG02451.hp2 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.66+3900A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705231 | |||||||
| chr6:49705293 | A | AGCCAGAA others(58): Show |
1 | a0001c0001t0001g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.66+3773_66+3837dup others(65): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705293 | |||||||
| chr6:49705412 | T | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+3719A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705412 | |||||||
| chr6:49705454 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
5 | HG00642.hp2 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+3677G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705454 | |||||||
| chr6:49705482 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(176): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.66+3649A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705482 | |||||||
| chr6:49705667 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.66+3464A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705667 | |||||||
| chr6:49705672 | T | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+3459A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705672 | |||||||
| chr6:49705787 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.66+3344A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705787 | |||||||
| chr6:49705844 | A | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3287T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705844 | |||||||
| chr6:49705901 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+3230A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49705901 | |||||||
| chr6:49706102 | C | T | 3 | a0001c0002t0003g0004 a0001c0002t0003g0078 a0001c0002t0003g0079 |
12 | HG01069.hp2 HG02257.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+3029G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706102 | |||||||
| chr6:49706226 | A | G | 2 | a0001c0001t0001g0178 a0002c0003t0001g0012 |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+2905T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706226 | |||||||
| chr6:49706324 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.66+2807T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706324 | |||||||
| chr6:49706363 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
10 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+2768T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706363 | |||||||
| chr6:49706667 | A | G | 1 | a0001c0001t0002g0180 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.66+2464T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706667 | |||||||
| chr6:49706745 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.66+2386A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706745 | |||||||
| chr6:49706899 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
99 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.66+2232T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706899 | |||||||
| chr6:49706900 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.66+2231G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706900 | |||||||
| chr6:49706982 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.66+2149A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49706982 | |||||||
| chr6:49707039 | A | G | 2 | a0005c0007t0001g0152 a0005c0007t0002g0082 |
2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.66+2092T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707039 | |||||||
| chr6:49707263 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.66+1868T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707263 | |||||||
| chr6:49707285 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.66+1846A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707285 | |||||||
| chr6:49707342 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.66+1789T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707342 | |||||||
| chr6:49707389 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+1742G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707389 | |||||||
| chr6:49707454 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0203 a0001c0001t0002g0055 |
4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+1677A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707454 | |||||||
| chr6:49707581 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.66+1550C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707581 | |||||||
| chr6:49707624 | T | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+1507A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707624 | |||||||
| chr6:49707831 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
208 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.66+1300A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707831 | |||||||
| chr6:49707854 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.66+1277G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707854 | |||||||
| chr6:49707927 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.66+1204A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49707927 | |||||||
| chr6:49708059 | C | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+1072G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708059 | |||||||
| chr6:49708088 | A | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+1043T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708088 | |||||||
| chr6:49708131 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.66+1000T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708131 | |||||||
| chr6:49708394 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0145 others(7): Show |
15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.66+737G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708394 | |||||||
| chr6:49708473 | C | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+658G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708473 | |||||||
| chr6:49708539 | C | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.66+592G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708539 | |||||||
| chr6:49708590 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0090 |
4 | HG00673.hp2 NA18975.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+541T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708590 | |||||||
| chr6:49708720 | A | G | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+411T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708720 | |||||||
| chr6:49708823 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.66+308G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708823 | |||||||
| chr6:49708929 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.66+202G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49708929 | |||||||
| chr6:49709014 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.66+117A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49709014 | |||||||
| chr6:49709054 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0002g0077 a0001c0001t0002g0140 |
4 | HG02615.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+77G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49709054 | |||||||
| chr6:49709125 | C | G | 1 | a0001c0001t0001g0048 | 2 | HG01168.hp1 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.66+6G>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 4/9 | chr6 | 49709125 | |||||||
| chr6:49709241 | T | A | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-36A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709241 | |||||||
| chr6:49709492 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
208 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.-9-287G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709492 | |||||||
| chr6:49709501 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0085 a0001c0001t0002g0200 others(1): Show |
5 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-296G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709501 | |||||||
| chr6:49709597 | T | C | 5 | a0001c0002t0003g0004 a0001c0002t0003g0063 a0001c0002t0003g0078 others(2): Show |
14 | HG01069.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-392A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709597 | |||||||
| chr6:49709625 | G | A | 2 | a0005c0007t0001g0152 a0005c0007t0002g0082 |
2 | HG01123.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-420C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709625 | |||||||
| chr6:49709636 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-9-431G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709636 | |||||||
| chr6:49709710 | A | C | 1 | a0001c0001t0002g0202 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-9-505T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709710 | |||||||
| chr6:49709819 | A | C | 2 | a0001c0002t0003g0063 a0001c0002t0011g0062 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-9-614T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709819 | |||||||
| chr6:49709831 | A | T | 1 | a0001c0001t0002g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-9-626T>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709831 | |||||||
| chr6:49709882 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18956.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-9-677G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49709882 | |||||||
| chr6:49710129 | C | A | 1 | a0001c0001t0001g0141 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9-924G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710129 | |||||||
| chr6:49710148 | C | T | 4 | a0001c0001t0002g0020 a0001c0001t0002g0058 a0001c0001t0002g0059 others(1): Show |
6 | HG01255.hp1 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-943G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710148 | |||||||
| chr6:49710238 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0007g0153 |
2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-9-1033C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710238 | |||||||
| chr6:49710463 | C | T | 18 | a0001c0001t0001g0046 a0001c0001t0001g0168 a0001c0001t0001g0172 others(15): Show |
32 | HG00280.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10+822G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710463 | |||||||
| chr6:49710494 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0007g0153 |
2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-10+791C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710494 | |||||||
| chr6:49710654 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(185): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-10+631G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710654 | |||||||
| chr6:49710717 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-10+568A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710717 | |||||||
| chr6:49710734 | T | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
142 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-10+551A>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710734 | |||||||
| chr6:49710736 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-10+549C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710736 | |||||||
| chr6:49710745 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-10+540G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710745 | |||||||
| chr6:49710746 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-10+539C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710746 | |||||||
| chr6:49710802 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-10+483G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710802 | |||||||
| chr6:49710808 | C | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.-10+477G>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710808 | |||||||
| chr6:49710821 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
12 | HG00639.hp1 HG00741.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+464A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710821 | |||||||
| chr6:49710980 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-10+305G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49710980 | |||||||
| chr6:49711004 | G | A | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10+281C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49711004 | |||||||
| chr6:49711005 | C | T | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10+280G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49711005 | |||||||
| chr6:49711160 | AACAG | A | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10+121_-10+124del others(4): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 3/9 | chr6 | 49711160 | |||||||
| chr6:49711554 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-46-233A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49711554 | |||||||
| chr6:49711879 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-46-558G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49711879 | |||||||
| chr6:49711884 | A | G | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-46-563T>C | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49711884 | |||||||
| chr6:49711962 | T | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(30): Show |
98 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-47+539A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49711962 | |||||||
| chr6:49712218 | G | A | 1 | a0001c0001t0002g0054 | 2 | HG00735.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-47+283C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49712218 | |||||||
| chr6:49712262 | G | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-47+239C>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49712262 | |||||||
| chr6:49712293 | T | C | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-47+208A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49712293 | |||||||
| chr6:49712343 | C | T | 1 | a0005c0007t0002g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-47+158G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49712343 | |||||||
| chr6:49712472 | G | A | 1 | a0001c0001t0012g0199 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-47+29C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49712472 | |||||||
| chr6:49712479 | A | AT | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-47+21dupA | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 2/9 | chr6 | 49712479 | |||||||
| chr6:49712637 | G | A | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-150-33C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49712637 | |||||||
| chr6:49712794 | C | T | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-150-190G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49712794 | |||||||
| chr6:49712883 | C | A | 1 | a0001c0001t0002g0202 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-150-279G>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49712883 | |||||||
| chr6:49713022 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0002g0055 |
3 | HG02109.hp1 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-150-418A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713022 | |||||||
| chr6:49713111 | T | C | 31 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(28): Show |
79 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.-151+364A>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713111 | |||||||
| chr6:49713207 | TATGTACT others(55): Show |
T | 1 | a0001c0001t0001g0081 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-151+206_-151+267d others(64): Show |
CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713207 | |||||||
| chr6:49713271 | A | C | 32 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
80 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.-151+204T>G | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713271 | |||||||
| chr6:49713298 | C | T | 32 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0067 others(29): Show |
80 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.-151+177G>A | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713298 | |||||||
| chr6:49713327 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-151+148A>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713327 | |||||||
| chr6:49713366 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-151+109C>T | CRISP2 | ENSG00000124490.14 | transcript | ENST00000339139.5 | protein_coding | 1/9 | chr6 | 49713366 |