Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10321 |
| ensemblid | ENSG00000096006.12 |
| hgncid | 16904 |
| symbol | CRISP3 |
| name | cysteine rich secretory protein 3 |
| refseq_nuc | NM_006061.4 |
| refseq_prot | NP_006052.2 |
| ensembl_nuc | ENST00000263045.9 |
| ensembl_prot | ENSP00000263045.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 49727376 |
| end | 49744388 |
| strand | - |
| ver | v1.2 |
| region | chr6:49727376-49744388 |
| region5000 | chr6:49722376-49749388 |
| regionname0 | CRISP3_chr6_49727376_49744388 |
| regionname5000 | CRISP3_chr6_49722376_49749388 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 258 | 143 | 20 | 42 | 62 | 6 | 13 | 45 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0002 | 1/1 | 258 | 137 | 19 | 25 | 70 | 10 | 11 | 58 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0003 | 0/0 | 258 | 112 | 51 | 7 | 33 | 2 | 19 | 24 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0004 | 0/0 | 258 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0005 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0006 | 0/0 | 153 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(148): Show |
chr6 | 49722376 | 49749388 |
| a0007 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0008 | 0/0 | 258 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0009 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| a0010 | 0/0 | 258 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | MKQIL others(253): Show |
chr6 | 49722376 | 49749388 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 774 | 143 | 20 | 42 | 62 | 6 | 13 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0002c0002 | 1/1 | 774 | 135 | 18 | 24 | 70 | 10 | 11 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0002c0005 | 0/0 | 774 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0003c0003 | 0/0 | 774 | 61 | 22 | 3 | 28 | 0 | 8 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0003c0004 | 0/0 | 774 | 49 | 27 | 4 | 5 | 2 | 11 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0003c0007 | 0/0 | 774 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0004c0006 | 0/0 | 774 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0005c0011 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0006c0012 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0007c0010 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0008c0008 | 0/0 | 774 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0009c0009 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 | ||
| a0010c0013 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | ATGAA others(769): Show |
chr6 | 49722376 | 49749388 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2152 | 138 | 16 | 41 | 62 | 6 | 13 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0001c0001t0007 | 0/0 | 2152 | 3 | 3 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0001c0001t0013 | 0/0 | 2152 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0001c0001t0018 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0002c0002t0001 | 0/1 | 2152 | 133 | 17 | 24 | 70 | 10 | 11 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0002c0002t0003 | 1/0 | 2152 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0002c0002t0010 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0002c0005t0008 | 0/0 | 2152 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0003t0002 | 0/0 | 2152 | 55 | 17 | 3 | 27 | 0 | 8 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0003t0006 | 0/0 | 2152 | 3 | 3 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0003t0015 | 0/0 | 2152 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0003t0016 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0003t0017 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0004t0001 | 0/0 | 2152 | 6 | 6 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0004t0003 | 0/0 | 2152 | 25 | 4 | 3 | 5 | 2 | 11 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0004t0004 | 0/0 | 2152 | 11 | 10 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0004t0005 | 0/0 | 2152 | 4 | 4 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0004t0009 | 0/0 | 2152 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0004t0014 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0007t0011 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0003c0007t0012 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0004c0006t0001 | 0/0 | 2152 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0005c0011t0001 | 0/0 | 2152 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0006c0012t0001 | 0/0 | 2152 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0007c0010t0001 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0008c0008t0001 | 0/0 | 2152 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0009c0009t0001 | 0/0 | 2152 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| a0010c0013t0001 | 0/0 | 2152 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | GCACC others(2147): Show |
chr6 | 49722376 | 49749388 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 34 | 0 | 14 | 16 | 1 | 3 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0004 | 0/0 | 12 | 1 | 3 | 3 | 2 | 3 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 2 | 0 | 3 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0013g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0001 | 0/0 | 63 | 9 | 16 | 30 | 3 | 5 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0008 | 0/1 | 6 | 1 | 0 | 2 | 1 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0009 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0020 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0003g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0002t0010g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0005t0008g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0002c0005t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0003 | 0/0 | 23 | 1 | 1 | 15 | 0 | 6 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0006g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0015g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0003t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0005 | 0/0 | 8 | 1 | 0 | 4 | 0 | 3 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0013 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0004g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0004g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0004t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0007t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0003c0007t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0004c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0004c0006t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0005c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0006c0012t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0007c0010t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0008c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0009c0009t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| a0010c0013t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | GBR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0055 | EUR | GBR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0008 | EUR | GBR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00140 | hp2 | a0003 | c0004 | t0003 | g0108 | EUR | GBR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0080 | EUR | FIN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00323 | hp1 | a0003 | c0004 | t0003 | g0013 | EUR | FIN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | FIN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00408 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00597 | hp2 | a0005 | c0011 | t0001 | g0131 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00621 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00621 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00673 | hp1 | a0006 | c0012 | t0001 | g0059 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG00741 | hp2 | a0003 | c0004 | t0003 | g0099 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01069 | hp1 | a0003 | c0004 | t0004 | g0034 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01167 | hp1 | a0003 | c0003 | t0002 | g0162 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01255 | hp1 | a0003 | c0003 | t0002 | g0152 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01346 | hp1 | a0003 | c0004 | t0003 | g0013 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01496 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | IBS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0023 | EUR | IBS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0023 | EUR | IBS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01884 | hp1 | a0003 | c0003 | t0006 | g0039 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01884 | hp2 | a0003 | c0007 | t0012 | g0097 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01934 | hp1 | a0003 | c0004 | t0003 | g0102 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01981 | hp2 | a0001 | c0001 | t0013 | g0132 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02040 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02055 | hp2 | a0003 | c0004 | t0005 | g0111 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02056 | hp2 | a0003 | c0004 | t0003 | g0005 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02083 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02083 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02145 | hp1 | a0003 | c0003 | t0017 | g0143 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02145 | hp2 | a0003 | c0004 | t0005 | g0110 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02165 | hp1 | a0003 | c0003 | t0002 | g0165 | EAS | CDX | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | CDX | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02257 | hp1 | a0003 | c0004 | t0009 | g0075 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02257 | hp2 | a0003 | c0004 | t0004 | g0021 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02258 | hp2 | a0003 | c0003 | t0016 | g0145 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02280 | hp1 | a0003 | c0003 | t0006 | g0039 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02280 | hp2 | a0003 | c0004 | t0005 | g0112 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0166 | EAS | KHV | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02602 | hp2 | a0003 | c0004 | t0003 | g0005 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02615 | hp1 | a0003 | c0003 | t0002 | g0016 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02622 | hp1 | a0003 | c0003 | t0002 | g0142 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02630 | hp1 | a0003 | c0004 | t0004 | g0034 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02630 | hp2 | a0003 | c0003 | t0002 | g0016 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02647 | hp1 | a0007 | c0010 | t0001 | g0158 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02647 | hp2 | a0003 | c0004 | t0003 | g0107 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0003 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02698 | hp2 | a0003 | c0004 | t0003 | g0105 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02717 | hp2 | a0001 | c0001 | t0018 | g0136 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02723 | hp1 | a0003 | c0004 | t0004 | g0021 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0003 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02738 | hp1 | a0003 | c0004 | t0003 | g0005 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0113 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02976 | hp1 | a0003 | c0003 | t0002 | g0116 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03017 | hp2 | a0003 | c0004 | t0003 | g0103 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03041 | hp2 | a0003 | c0003 | t0002 | g0144 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03098 | hp1 | a0003 | c0003 | t0002 | g0159 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03098 | hp2 | a0003 | c0004 | t0004 | g0021 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03130 | hp1 | a0002 | c0002 | t0010 | g0069 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03139 | hp2 | a0003 | c0003 | t0002 | g0122 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03195 | hp1 | a0003 | c0003 | t0002 | g0015 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03195 | hp2 | a0003 | c0004 | t0014 | g0084 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03209 | hp1 | a0003 | c0003 | t0002 | g0015 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03209 | hp2 | a0003 | c0004 | t0005 | g0109 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03225 | hp1 | a0003 | c0004 | t0004 | g0082 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03492 | hp1 | a0003 | c0003 | t0002 | g0003 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03516 | hp1 | a0003 | c0003 | t0002 | g0016 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03516 | hp2 | a0003 | c0004 | t0004 | g0085 | AFR | ESN | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03540 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03540 | hp2 | a0003 | c0004 | t0004 | g0035 | AFR | GWD | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03579 | hp2 | a0003 | c0003 | t0002 | g0003 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03654 | hp1 | a0003 | c0004 | t0003 | g0013 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0003 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0050 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03688 | hp1 | a0003 | c0004 | t0003 | g0106 | SAS | STU | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03688 | hp2 | a0008 | c0008 | t0001 | g0120 | SAS | STU | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03704 | hp1 | a0003 | c0004 | t0003 | g0005 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03831 | hp2 | a0003 | c0003 | t0002 | g0171 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03942 | hp1 | a0003 | c0004 | t0003 | g0013 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03942 | hp2 | a0003 | c0004 | t0003 | g0081 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | STU | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0003 | SAS | STU | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0003 | SAS | BEB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG04204 | hp2 | a0003 | c0003 | t0002 | g0172 | SAS | STU | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18522 | hp1 | a0009 | c0009 | t0001 | g0056 | AFR | YRI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18522 | hp2 | a0003 | c0003 | t0002 | g0146 | AFR | YRI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | CHB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18906 | hp1 | a0003 | c0007 | t0011 | g0096 | AFR | YRI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0168 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18956 | hp1 | a0003 | c0003 | t0015 | g0167 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18961 | hp1 | a0004 | c0006 | t0001 | g0138 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18963 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18969 | hp1 | a0010 | c0013 | t0001 | g0115 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18971 | hp2 | a0003 | c0003 | t0002 | g0170 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18972 | hp2 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18982 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18984 | hp2 | a0003 | c0003 | t0002 | g0161 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19000 | hp2 | a0003 | c0003 | t0002 | g0163 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19001 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19030 | hp1 | a0003 | c0004 | t0004 | g0035 | AFR | LWK | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19030 | hp2 | a0003 | c0003 | t0002 | g0016 | AFR | LWK | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19043 | hp1 | a0002 | c0005 | t0008 | g0041 | AFR | LWK | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19043 | hp2 | a0003 | c0004 | t0003 | g0101 | AFR | LWK | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19055 | hp1 | a0003 | c0003 | t0002 | g0164 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19067 | hp2 | a0003 | c0004 | t0003 | g0098 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19070 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19072 | hp1 | a0003 | c0004 | t0003 | g0005 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19072 | hp2 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19074 | hp1 | a0004 | c0006 | t0001 | g0129 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19076 | hp1 | a0003 | c0003 | t0002 | g0173 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19078 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19083 | hp2 | a0003 | c0003 | t0002 | g0169 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19240 | hp1 | a0003 | c0003 | t0006 | g0160 | AFR | YRI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA19240 | hp2 | a0003 | c0004 | t0004 | g0083 | AFR | YRI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20129 | hp1 | a0003 | c0004 | t0004 | g0021 | AFR | ASW | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20129 | hp2 | a0003 | c0004 | t0003 | g0100 | AFR | ASW | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | TSI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20905 | hp1 | a0003 | c0004 | t0003 | g0104 | SAS | GIH | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20905 | hp2 | a0003 | c0004 | t0003 | g0013 | SAS | GIH | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01123 | hp1 | a0002 | c0005 | t0008 | g0040 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02109 | hp1 | a0003 | c0004 | t0009 | g0074 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02486 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02486 | hp2 | a0003 | c0003 | t0002 | g0015 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0123 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0015 | AFR | ACB | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03471 | hp1 | a0003 | c0003 | t0002 | g0016 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | USA | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | USA | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20300 | hp1 | a0003 | c0004 | t0003 | g0005 | AFR | USA | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0015 | AFR | LWK | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | LWK | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0008 | REF | REF | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0053 | REF | REF | CRISP3_chr6_49722376_49749388 | CRISP3 | chr6 | 49722376 | 49749388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49733217 | A | G | 1 | a0005 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.538T>C | p.Tyr180His | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/8 | 559/2152 | 538/777 | 180/258 | chr6 | 49733217 | |||
| chr6:49733705 | G | A | 1 | a0006 | 1 | HG00673.hp1 | stop_gained&splice_region_variant | HIGH | c.460C>T | p.Gln154* | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/8 | 481/2152 | 460/777 | 154/258 | chr6 | 49733705 | |||
| chr6:49733726 | C | A | 6 | a0001 a0004 a0005 others(3): Show |
149 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
missense_variant | MODERATE | c.439G>T | p.Ala147Ser | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/8 | 460/2152 | 439/777 | 147/258 | chr6 | 49733726 | |||
| chr6:49733743 | C | G | 1 | a0004 | 2 | NA18961.hp1 NA19074.hp1 |
missense_variant | MODERATE | c.422G>C | p.Gly141Ala | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/8 | 443/2152 | 422/777 | 141/258 | chr6 | 49733743 | |||
| chr6:49733756 | C | T | 1 | a0007 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.409G>A | p.Asp137Asn | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/8 | 430/2152 | 409/777 | 137/258 | chr6 | 49733756 | |||
| chr6:49733810 | A | G | 7 | a0001 a0003 a0004 others(4): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
missense_variant | MODERATE | c.355T>C | p.Ser119Pro | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/8 | 376/2152 | 355/777 | 119/258 | chr6 | 49733810 | |||
| chr6:49733824 | T | G | 1 | a0010 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.341A>C | p.Tyr114Ser | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/8 | 362/2152 | 341/777 | 114/258 | chr6 | 49733824 | |||
| chr6:49735508 | C | G | 1 | a0009 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.312G>C | p.Met104Ile | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/8 | 333/2152 | 312/777 | 104/258 | chr6 | 49735508 | |||
| chr6:49735512 | C | T | 1 | a0008 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.308G>A | p.Arg103Gln | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/8 | 329/2152 | 308/777 | 103/258 | chr6 | 49735512 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49728760 | G | T | 1 | a0003c0003 | 61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
synonymous_variant | LOW | c.747C>A | p.Ala249Ala | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 768/2152 | 747/777 | 249/258 | chr6 | 49728760 | |||
| chr6:49728802 | T | C | 1 | a0003c0007 | 2 | HG01884.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.705A>G | p.Thr235Thr | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 726/2152 | 705/777 | 235/258 | chr6 | 49728802 | |||
| chr6:49744350 | A | G | 1 | a0002c0005 | 2 | HG01123.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.18T>C | p.His6His | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/8 | 39/2152 | 18/777 | 6/258 | chr6 | 49744350 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49727389 | C | T | 9 | a0003c0003t0002 a0003c0003t0006 a0003c0003t0015 others(6): Show |
75 | HG00408.hp1 HG00621.hp2 HG01069.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1341G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 1341 | chr6 | 49727389 | ||||||
| chr6:49727408 | C | T | 2 | a0003c0004t0004 a0003c0004t0014 |
12 | HG01069.hp1 HG02257.hp2 HG02630.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1322G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 1322 | chr6 | 49727408 | ||||||
| chr6:49727455 | T | G | 1 | a0003c0003t0016 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1275A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 1275 | chr6 | 49727455 | ||||||
| chr6:49727507 | C | A | 1 | a0001c0001t0007 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1223G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 1223 | chr6 | 49727507 | ||||||
| chr6:49727519 | A | G | 25 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(22): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*1211T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 1211 | chr6 | 49727519 | ||||||
| chr6:49727645 | C | T | 1 | a0003c0003t0015 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 1085 | chr6 | 49727645 | ||||||
| chr6:49727792 | G | C | 1 | a0003c0003t0017 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 938 | chr6 | 49727792 | ||||||
| chr6:49727831 | T | C | 1 | a0003c0007t0012 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 899 | chr6 | 49727831 | ||||||
| chr6:49727853 | C | G | 1 | a0003c0004t0014 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*877G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 877 | chr6 | 49727853 | ||||||
| chr6:49727868 | G | A | 1 | a0003c0004t0005 | 4 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*862C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 862 | chr6 | 49727868 | ||||||
| chr6:49728085 | G | A | 1 | a0002c0005t0008 | 2 | HG01123.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*645C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 645 | chr6 | 49728085 | ||||||
| chr6:49728153 | A | G | 1 | a0001c0001t0013 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*577T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 577 | chr6 | 49728153 | ||||||
| chr6:49728195 | A | G | 1 | a0003c0003t0006 | 3 | HG01884.hp1 HG02280.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*535T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 535 | chr6 | 49728195 | ||||||
| chr6:49728407 | T | G | 1 | a0003c0004t0009 | 2 | HG02109.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*323A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 323 | chr6 | 49728407 | ||||||
| chr6:49728462 | C | G | 2 | a0003c0007t0011 a0003c0007t0012 |
2 | HG01884.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*268G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 268 | chr6 | 49728462 | ||||||
| chr6:49728625 | G | A | 1 | a0001c0001t0018 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 105 | chr6 | 49728625 | ||||||
| chr6:49728657 | C | T | 1 | a0002c0002t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 8/8 | 73 | chr6 | 49728657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49728975 | T | C | 7 | a0003c0004t0004g0021 a0003c0004t0004g0034 a0003c0004t0004g0035 others(4): Show |
12 | HG01069.hp1 HG02257.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.650-118A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49728975 | |||||||
| chr6:49728988 | G | A | 2 | a0003c0007t0011g0096 a0003c0007t0012g0097 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.650-131C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49728988 | |||||||
| chr6:49729013 | T | G | 1 | a0003c0003t0002g0122 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.650-156A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729013 | |||||||
| chr6:49729178 | T | C | 1 | a0002c0002t0001g0057 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.650-321A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729178 | |||||||
| chr6:49729181 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(35): Show |
101 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.650-324C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729181 | |||||||
| chr6:49729253 | C | T | 2 | a0002c0005t0008g0040 a0002c0005t0008g0041 |
2 | HG01123.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.650-396G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729253 | |||||||
| chr6:49729260 | A | C | 4 | a0003c0004t0005g0109 a0003c0004t0005g0110 a0003c0004t0005g0111 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.650-403T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729260 | |||||||
| chr6:49729408 | A | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(38): Show |
105 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.650-551T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729408 | |||||||
| chr6:49729520 | C | A | 4 | a0003c0004t0005g0109 a0003c0004t0005g0110 a0003c0004t0005g0111 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.650-663G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729520 | |||||||
| chr6:49729541 | C | A | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.650-684G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729541 | |||||||
| chr6:49729615 | C | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0151 others(1): Show |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.650-758G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729615 | |||||||
| chr6:49729710 | G | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
112 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.650-853C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729710 | |||||||
| chr6:49729711 | T | G | 1 | a0003c0003t0002g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.650-854A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729711 | |||||||
| chr6:49729764 | A | G | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.650-907T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729764 | |||||||
| chr6:49729853 | C | T | 1 | a0003c0003t0002g0166 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.650-996G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729853 | |||||||
| chr6:49729862 | A | G | 5 | a0003c0004t0001g0113 a0003c0004t0005g0109 a0003c0004t0005g0110 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.650-1005T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729862 | |||||||
| chr6:49729945 | T | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0148 a0001c0001t0007g0037 others(1): Show |
5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-1088A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49729945 | |||||||
| chr6:49730620 | A | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0148 a0001c0001t0007g0037 others(1): Show |
5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.649+543T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49730620 | |||||||
| chr6:49730678 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.649+485A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49730678 | |||||||
| chr6:49730798 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0013g0132 |
2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.649+365G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49730798 | |||||||
| chr6:49730909 | G | A | 2 | a0003c0007t0011g0096 a0003c0007t0012g0097 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.649+254C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49730909 | |||||||
| chr6:49730990 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0151 others(1): Show |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.649+173G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49730990 | |||||||
| chr6:49731037 | CT | C | 6 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0077 others(3): Show |
12 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.649+125delA | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 7/7 | chr6 | 49731037 | |||||||
| chr6:49731578 | C | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0139 a0001c0001t0018g0136 |
4 | HG02717.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.561-327G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731578 | |||||||
| chr6:49731578 | C | G | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.561-327G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731578 | |||||||
| chr6:49731581 | C | A | 37 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(34): Show |
75 | HG00408.hp1 HG00621.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.561-330G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731581 | |||||||
| chr6:49731609 | C | G | 1 | a0003c0004t0005g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.561-358G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731609 | |||||||
| chr6:49731699 | T | TA | 2 | a0002c0002t0001g0058 a0003c0004t0001g0012 |
6 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.561-449dupT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731699 | |||||||
| chr6:49731699 | TA | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
224 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.561-449delT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731699 | |||||||
| chr6:49731751 | C | T | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.561-500G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731751 | |||||||
| chr6:49731752 | G | A | 1 | a0005c0011t0001g0131 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.561-501C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731752 | |||||||
| chr6:49731762 | G | T | 1 | a0003c0004t0003g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.561-511C>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731762 | |||||||
| chr6:49731986 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0151 others(1): Show |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.561-735G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49731986 | |||||||
| chr6:49732047 | G | A | 2 | a0002c0005t0008g0040 a0002c0005t0008g0041 |
2 | HG01123.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.561-796C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732047 | |||||||
| chr6:49732142 | G | A | 2 | a0003c0004t0009g0074 a0003c0004t0009g0075 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.561-891C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732142 | |||||||
| chr6:49732166 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(130): Show |
275 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.561-915A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732166 | |||||||
| chr6:49732335 | A | T | 1 | a0003c0004t0005g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.560+860T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732335 | |||||||
| chr6:49732502 | G | A | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.560+693C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732502 | |||||||
| chr6:49732559 | G | A | 1 | a0003c0004t0005g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.560+636C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732559 | |||||||
| chr6:49732590 | A | T | 37 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(34): Show |
75 | HG00408.hp1 HG00621.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.560+605T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732590 | |||||||
| chr6:49732757 | G | C | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.560+438C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732757 | |||||||
| chr6:49732855 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0139 |
3 | HG02809.hp1 HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.560+340A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732855 | |||||||
| chr6:49732933 | G | A | 9 | a0003c0004t0004g0021 a0003c0004t0004g0034 a0003c0004t0004g0035 others(6): Show |
14 | HG01069.hp1 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.560+262C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49732933 | |||||||
| chr6:49733127 | GT | G | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.560+67delA | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 6/7 | chr6 | 49733127 | |||||||
| chr6:49733304 | T | G | 2 | a0004c0006t0001g0129 a0004c0006t0001g0138 |
2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.463-12A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733304 | |||||||
| chr6:49733321 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.463-29C>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733321 | |||||||
| chr6:49733389 | C | T | 1 | a0003c0004t0003g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.463-97G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733389 | |||||||
| chr6:49733443 | C | T | 2 | a0003c0007t0011g0096 a0003c0007t0012g0097 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.463-151G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733443 | |||||||
| chr6:49733496 | C | T | 1 | a0003c0004t0004g0083 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.463-204G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733496 | |||||||
| chr6:49733524 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.462+179T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733524 | |||||||
| chr6:49733681 | G | T | 4 | a0003c0004t0005g0109 a0003c0004t0005g0110 a0003c0004t0005g0111 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+22C>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 5/7 | chr6 | 49733681 | |||||||
| chr6:49733864 | C | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0148 a0001c0001t0007g0037 others(1): Show |
5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-16G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49733864 | |||||||
| chr6:49733865 | C | T | 9 | a0003c0004t0004g0021 a0003c0004t0004g0034 a0003c0004t0004g0035 others(6): Show |
14 | HG01069.hp1 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-17G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49733865 | |||||||
| chr6:49733881 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.317-33T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49733881 | |||||||
| chr6:49733972 | C | T | 9 | a0003c0004t0004g0021 a0003c0004t0004g0034 a0003c0004t0004g0035 others(6): Show |
14 | HG01069.hp1 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.317-124G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49733972 | |||||||
| chr6:49734128 | C | T | 1 | a0003c0004t0004g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.317-280G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734128 | |||||||
| chr6:49734141 | A | G | 1 | a0002c0002t0001g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.317-293T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734141 | |||||||
| chr6:49734237 | T | C | 1 | a0002c0002t0001g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.317-389A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734237 | |||||||
| chr6:49734495 | C | T | 1 | a0003c0004t0003g0106 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.317-647G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734495 | |||||||
| chr6:49734663 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0076 others(14): Show |
32 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.317-815G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734663 | |||||||
| chr6:49734724 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
149 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.316+780C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734724 | |||||||
| chr6:49734724 | G | C | 16 | a0003c0004t0003g0005 a0003c0004t0003g0013 a0003c0004t0003g0081 others(13): Show |
27 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.316+780C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734724 | |||||||
| chr6:49734725 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(63): Show |
149 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.316+779T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734725 | |||||||
| chr6:49734740 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.316+764G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49734740 | |||||||
| chr6:49735011 | G | A | 4 | a0003c0004t0003g0101 a0003c0004t0003g0107 a0003c0004t0009g0074 others(1): Show |
4 | HG02109.hp1 HG02257.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+493C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49735011 | |||||||
| chr6:49735195 | A | T | 1 | a0002c0002t0001g0047 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.316+309T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49735195 | |||||||
| chr6:49735314 | G | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(62): Show |
147 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.316+190C>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49735314 | |||||||
| chr6:49735316 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.316+188T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49735316 | |||||||
| chr6:49735388 | A | G | 1 | a0003c0007t0011g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.316+116T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 4/7 | chr6 | 49735388 | |||||||
| chr6:49735910 | G | C | 7 | a0003c0004t0004g0021 a0003c0004t0004g0034 a0003c0004t0004g0035 others(4): Show |
12 | HG01069.hp1 HG02257.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.229-319C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 3/7 | chr6 | 49735910 | |||||||
| chr6:49735933 | G | A | 1 | a0003c0007t0012g0097 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.229-342C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 3/7 | chr6 | 49735933 | |||||||
| chr6:49735998 | C | T | 1 | a0002c0002t0001g0029 | 2 | NA18999.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.228+393G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 3/7 | chr6 | 49735998 | |||||||
| chr6:49736075 | G | GAA | 14 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0076 others(11): Show |
29 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.228+314_228+315dup others(2): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 3/7 | chr6 | 49736075 | |||||||
| chr6:49736144 | C | T | 37 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(34): Show |
75 | HG00408.hp1 HG00621.hp2 HG01069.hp1 others(72): Show |
intron_variant | MODIFIER | c.228+247G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 3/7 | chr6 | 49736144 | |||||||
| chr6:49736206 | C | T | 10 | a0003c0003t0002g0170 a0003c0004t0004g0021 a0003c0004t0004g0034 others(7): Show |
15 | HG01069.hp1 HG01884.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.228+185G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 3/7 | chr6 | 49736206 | |||||||
| chr6:49736553 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.112-46A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49736553 | |||||||
| chr6:49736593 | A | C | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.112-86T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49736593 | |||||||
| chr6:49736763 | G | C | 1 | a0003c0004t0003g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.112-256C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49736763 | |||||||
| chr6:49736833 | T | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(122): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.112-326A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49736833 | |||||||
| chr6:49736917 | A | G | 1 | a0002c0002t0001g0063 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.111+408T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49736917 | |||||||
| chr6:49737005 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.111+320C>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49737005 | |||||||
| chr6:49737091 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.111+234C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49737091 | |||||||
| chr6:49737121 | C | T | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.111+204G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 2/7 | chr6 | 49737121 | |||||||
| chr6:49737464 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.38-66G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737464 | |||||||
| chr6:49737465 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.38-67T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737465 | |||||||
| chr6:49737466 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.38-68A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737466 | |||||||
| chr6:49737466 | TG | T | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.38-69delC | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737466 | |||||||
| chr6:49737469 | G | A | 11 | a0003c0004t0003g0005 a0003c0004t0003g0013 a0003c0004t0003g0081 others(8): Show |
22 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.38-71C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737469 | |||||||
| chr6:49737611 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-213T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737611 | |||||||
| chr6:49737612 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-214T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737612 | |||||||
| chr6:49737613 | A | T | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-215T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737613 | |||||||
| chr6:49737615 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-217A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737615 | |||||||
| chr6:49737620 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-222C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737620 | |||||||
| chr6:49737623 | T | G | 2 | a0002c0005t0008g0040 a0002c0005t0008g0041 |
2 | HG01123.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.38-225A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737623 | |||||||
| chr6:49737628 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-230G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737628 | |||||||
| chr6:49737646 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-248T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737646 | |||||||
| chr6:49737649 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-251A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737649 | |||||||
| chr6:49737653 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-255T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737653 | |||||||
| chr6:49737660 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-262A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737660 | |||||||
| chr6:49737663 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-265A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737663 | |||||||
| chr6:49737666 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-268G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737666 | |||||||
| chr6:49737669 | C | A | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-271G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737669 | |||||||
| chr6:49737674 | T | G | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-276A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737674 | |||||||
| chr6:49737676 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-278G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737676 | |||||||
| chr6:49737679 | A | C | 1 | a0003c0003t0002g0003 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.38-281T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737679 | |||||||
| chr6:49737684 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.38-286G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737684 | |||||||
| chr6:49737685 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.38-287C>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737685 | |||||||
| chr6:49737957 | T | C | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.38-559A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49737957 | |||||||
| chr6:49738329 | A | G | 1 | a0002c0002t0001g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.38-931T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49738329 | |||||||
| chr6:49738475 | T | C | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1077A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49738475 | |||||||
| chr6:49738546 | A | T | 1 | a0003c0004t0003g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.38-1148T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49738546 | |||||||
| chr6:49738697 | C | T | 1 | a0003c0004t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.38-1299G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49738697 | |||||||
| chr6:49738721 | C | A | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1323G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49738721 | |||||||
| chr6:49738906 | T | C | 1 | a0002c0002t0001g0030 | 2 | NA18944.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.38-1508A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49738906 | |||||||
| chr6:49739001 | G | GA | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
104 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.38-1604dupT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739001 | |||||||
| chr6:49739003 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0151 others(1): Show |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.38-1605T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739003 | |||||||
| chr6:49739012 | A | C | 4 | a0003c0004t0005g0109 a0003c0004t0005g0110 a0003c0004t0005g0111 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-1614T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739012 | |||||||
| chr6:49739197 | C | T | 1 | a0003c0004t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.38-1799G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739197 | |||||||
| chr6:49739261 | A | G | 2 | a0003c0004t0009g0074 a0003c0004t0009g0075 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.38-1863T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739261 | |||||||
| chr6:49739369 | T | A | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-1971A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739369 | |||||||
| chr6:49739404 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.38-2006G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739404 | |||||||
| chr6:49739405 | G | A | 1 | a0003c0004t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.38-2007C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739405 | |||||||
| chr6:49739462 | A | G | 1 | a0003c0003t0002g0165 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.38-2064T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739462 | |||||||
| chr6:49739559 | G | A | 2 | a0002c0005t0008g0040 a0002c0005t0008g0041 |
2 | HG01123.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.38-2161C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739559 | |||||||
| chr6:49739766 | G | GA | 29 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(26): Show |
62 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.38-2369dupT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739766 | |||||||
| chr6:49739773 | A | G | 2 | a0002c0002t0001g0045 a0002c0002t0001g0062 |
2 | HG02615.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.38-2375T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739773 | |||||||
| chr6:49739936 | A | G | 1 | a0003c0004t0003g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.38-2538T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49739936 | |||||||
| chr6:49740146 | C | T | 1 | a0001c0001t0001g0007 | 7 | HG00423.hp2 HG00558.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-2748G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740146 | |||||||
| chr6:49740363 | A | G | 2 | a0001c0001t0007g0037 a0001c0001t0007g0123 |
3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.38-2965T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740363 | |||||||
| chr6:49740393 | C | G | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
61 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.38-2995G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740393 | |||||||
| chr6:49740446 | A | AC | 5 | a0001c0001t0001g0086 a0002c0002t0001g0054 a0003c0003t0002g0142 others(2): Show |
5 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-3049dupG | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740446 | |||||||
| chr6:49740510 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.38-3112A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740510 | |||||||
| chr6:49740575 | A | ATG | 29 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0086 others(26): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.38-3179_38-3178dup others(2): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740575 | A | ATGTG | 13 | a0001c0001t0001g0088 a0001c0001t0001g0125 a0003c0003t0002g0164 others(10): Show |
13 | HG00639.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.38-3181_38-3178dup others(4): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740575 | A | ATGTGTG | 5 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0087 others(2): Show |
9 | HG00733.hp2 HG01123.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.38-3183_38-3178dup others(6): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740575 | ATG | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0022 others(43): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.38-3179_38-3178del others(2): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740575 | ATGTG | A | 14 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0001g0139 others(11): Show |
26 | HG00423.hp1 HG00741.hp2 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.38-3181_38-3178del others(4): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740575 | ATGTGTG | A | 3 | a0002c0002t0001g0032 a0002c0002t0001g0046 a0002c0002t0001g0061 |
4 | HG06807.hp1 NA18956.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-3183_38-3178del others(6): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740575 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0018g0136 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.38-3187_38-3178del others(10): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740575 | |||||||
| chr6:49740650 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.38-3252G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740650 | |||||||
| chr6:49740714 | C | CATT | 132 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
274 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.38-3317_38-3316ins others(3): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740714 | |||||||
| chr6:49740723 | T | A | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.38-3325A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740723 | |||||||
| chr6:49740732 | A | G | 1 | a0003c0004t0003g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.38-3334T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740732 | |||||||
| chr6:49740889 | C | G | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+3442G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740889 | |||||||
| chr6:49740928 | C | A | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.37+3403G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49740928 | |||||||
| chr6:49741033 | A | G | 1 | a0002c0002t0001g0050 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.37+3298T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741033 | |||||||
| chr6:49741057 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(37): Show |
104 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.37+3274G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741057 | |||||||
| chr6:49741124 | C | CA | 21 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0022 others(18): Show |
39 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.37+3206dupT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741124 | |||||||
| chr6:49741128 | A | AC | 6 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0077 others(3): Show |
12 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+3202_37+3203ins others(1): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741128 | |||||||
| chr6:49741129 | A | C | 1 | a0002c0002t0001g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.37+3202T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741129 | |||||||
| chr6:49741133 | C | A | 42 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
107 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.37+3198G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741133 | |||||||
| chr6:49741134 | A | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(38): Show |
106 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.37+3197T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741134 | |||||||
| chr6:49741135 | A | C | 2 | a0001c0001t0001g0139 a0004c0006t0001g0138 |
2 | HG03225.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.37+3196T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741135 | |||||||
| chr6:49741135 | AAC | A | 5 | a0003c0004t0001g0012 a0003c0004t0005g0109 a0003c0004t0005g0110 others(2): Show |
9 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.37+3194_37+3195del others(2): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741135 | |||||||
| chr6:49741136 | A | C | 28 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(25): Show |
60 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.37+3195T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741136 | |||||||
| chr6:49741136 | AC | A | 17 | a0003c0004t0001g0113 a0003c0004t0003g0005 a0003c0004t0003g0013 others(14): Show |
28 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.37+3194delG | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741136 | |||||||
| chr6:49741137 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(91): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.37+3194G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741137 | |||||||
| chr6:49741137 | CA | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0151 others(1): Show |
7 | HG01074.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+3193delT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741137 | |||||||
| chr6:49741151 | C | CAAA | 24 | a0003c0003t0002g0003 a0003c0003t0002g0015 a0003c0003t0002g0016 others(21): Show |
57 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.37+3177_37+3179dup others(3): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741151 | |||||||
| chr6:49741151 | CA | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0121 a0001c0001t0001g0140 others(9): Show |
15 | HG00140.hp2 HG01074.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.37+3179delT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741151 | |||||||
| chr6:49741151 | CAA | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(80): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.37+3178_37+3179del others(2): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741151 | |||||||
| chr6:49741293 | T | G | 1 | a0003c0004t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37+3038A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741293 | |||||||
| chr6:49741334 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.37+2997C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741334 | |||||||
| chr6:49741452 | T | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0148 a0001c0001t0007g0037 others(1): Show |
5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+2879A>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741452 | |||||||
| chr6:49741461 | T | C | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+2870A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741461 | |||||||
| chr6:49741544 | C | T | 1 | a0003c0004t0001g0012 | 5 | HG02109.hp2 HG02486.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+2787G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741544 | |||||||
| chr6:49741611 | G | GT | 18 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0117 others(15): Show |
34 | HG00140.hp1 HG00423.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.37+2719dupA | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741611 | |||||||
| chr6:49741611 | GT | G | 34 | a0001c0001t0001g0025 a0001c0001t0001g0094 a0001c0001t0001g0149 others(31): Show |
54 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.37+2719delA | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741611 | |||||||
| chr6:49741611 | GTT | G | 7 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0077 others(4): Show |
13 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.37+2718_37+2719del others(2): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741611 | |||||||
| chr6:49741611 | GTTTTTTT others(4): Show |
G | 1 | a0003c0004t0004g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.37+2709_37+2719del others(11): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741611 | |||||||
| chr6:49741613 | T | A | 1 | a0002c0002t0001g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.37+2718A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741613 | |||||||
| chr6:49741637 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.37+2694T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741637 | |||||||
| chr6:49741653 | A | T | 2 | a0002c0002t0001g0032 a0002c0002t0001g0046 |
3 | NA18956.hp2 NA19006.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.37+2678T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741653 | |||||||
| chr6:49741684 | A | T | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.37+2647T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741684 | |||||||
| chr6:49741837 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(124): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.37+2494T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741837 | |||||||
| chr6:49741842 | T | A | 1 | a0002c0002t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.37+2489A>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49741842 | |||||||
| chr6:49742101 | T | TA | 3 | a0001c0001t0001g0017 a0001c0001t0001g0153 a0001c0001t0001g0154 |
7 | HG00558.hp2 HG02027.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.37+2229dupT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742101 | |||||||
| chr6:49742371 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | NA18991.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.37+1960G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742371 | |||||||
| chr6:49742392 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
219 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.37+1939C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742392 | |||||||
| chr6:49742434 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0076 others(10): Show |
28 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.37+1897G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742434 | |||||||
| chr6:49742461 | G | A | 1 | a0003c0004t0003g0103 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.37+1870C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742461 | |||||||
| chr6:49742583 | G | A | 20 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0077 others(17): Show |
33 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.37+1748C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742583 | |||||||
| chr6:49742631 | C | CA | 16 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(13): Show |
20 | HG02055.hp2 HG02056.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.37+1699dupT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742631 | |||||||
| chr6:49742631 | CA | C | 17 | a0001c0001t0001g0036 a0002c0002t0001g0045 a0002c0002t0001g0077 others(14): Show |
25 | HG00621.hp1 HG00741.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.37+1699delT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742631 | |||||||
| chr6:49742631 | CAAA | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0076 others(19): Show |
41 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.37+1697_37+1699del others(3): Show |
CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742631 | |||||||
| chr6:49742811 | GA | G | 7 | a0003c0004t0004g0021 a0003c0004t0004g0034 a0003c0004t0004g0035 others(4): Show |
12 | HG01069.hp1 HG02257.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+1519delT | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742811 | |||||||
| chr6:49742822 | G | A | 1 | a0001c0001t0001g0026 | 3 | NA18944.hp2 NA18952.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.37+1509C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49742822 | |||||||
| chr6:49743075 | C | A | 1 | a0002c0002t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.37+1256G>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743075 | |||||||
| chr6:49743257 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0076 others(21): Show |
44 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.37+1074T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743257 | |||||||
| chr6:49743417 | T | C | 1 | a0003c0004t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.37+914A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743417 | |||||||
| chr6:49743419 | A | G | 6 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0077 others(3): Show |
12 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+912T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743419 | |||||||
| chr6:49743478 | C | G | 1 | a0003c0004t0003g0081 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.37+853G>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743478 | |||||||
| chr6:49743738 | A | G | 1 | a0003c0003t0002g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.37+593T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743738 | |||||||
| chr6:49743750 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.37+581T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743750 | |||||||
| chr6:49743781 | CT | C | 15 | a0003c0003t0002g0003 a0003c0003t0002g0027 a0003c0003t0002g0161 others(12): Show |
39 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.37+549delA | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743781 | |||||||
| chr6:49743809 | A | G | 6 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0077 others(3): Show |
12 | HG00280.hp1 HG00738.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+522T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743809 | |||||||
| chr6:49743828 | A | T | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.37+503T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743828 | |||||||
| chr6:49743841 | G | A | 1 | a0003c0003t0002g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.37+490C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743841 | |||||||
| chr6:49743930 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.37+401C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49743930 | |||||||
| chr6:49744025 | T | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
181 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.37+306A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744025 | |||||||
| chr6:49744051 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.37+280T>C | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744051 | |||||||
| chr6:49744073 | T | C | 1 | a0002c0002t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.37+258A>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744073 | |||||||
| chr6:49744142 | C | T | 2 | a0003c0004t0009g0074 a0003c0004t0009g0075 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.37+189G>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744142 | |||||||
| chr6:49744146 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
274 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.37+185C>T | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744146 | |||||||
| chr6:49744173 | A | T | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.37+158T>A | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744173 | |||||||
| chr6:49744197 | A | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.37+134T>G | CRISP3 | ENSG00000096006.12 | transcript | ENST00000263045.9 | protein_coding | 1/7 | chr6 | 49744197 |