Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 167 |
| ensemblid | ENSG00000124812.15 |
| hgncid | 304 |
| symbol | CRISP1 |
| name | cysteine rich secretory protein 1 |
| refseq_nuc | NM_001131.3 |
| refseq_prot | NP_001122.2 |
| ensembl_nuc | ENST00000335847.9 |
| ensembl_prot | ENSP00000338276.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 49834257 |
| end | 49866535 |
| strand | - |
| ver | v1.2 |
| region | chr6:49834257-49866535 |
| region5000 | chr6:49829257-49871535 |
| regionname0 | CRISP1_chr6_49834257_49866535 |
| regionname5000 | CRISP1_chr6_49829257_49871535 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 249 | 369 | 87 | 70 | 154 | 15 | 41 | 120 | CRISP1_chr6_49829257_49871535 | CRISP1 | MEIKH others(244): Show |
chr6 | 49829257 | 49871535 |
| a0002 | 0/0 | 249 | 6 | 0 | 2 | 0 | 3 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | MEIKH others(244): Show |
chr6 | 49829257 | 49871535 |
| a0003 | 0/0 | 249 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | MEIKH others(244): Show |
chr6 | 49829257 | 49871535 |
| a0004 | 0/0 | 249 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | MEIKH others(244): Show |
chr6 | 49829257 | 49871535 |
| a0005 | 0/0 | 249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | MEIKH others(244): Show |
chr6 | 49829257 | 49871535 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 747 | 352 | 73 | 67 | 154 | 15 | 41 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 | ||
| a0001c0002 | 0/0 | 747 | 14 | 12 | 2 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 | ||
| a0001c0004 | 0/0 | 747 | 3 | 2 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 | ||
| a0002c0003 | 0/0 | 747 | 6 | 0 | 2 | 0 | 3 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 | ||
| a0003c0006 | 0/0 | 747 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 | ||
| a0004c0005 | 0/0 | 747 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 | ||
| a0005c0007 | 0/0 | 747 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATGGA others(742): Show |
chr6 | 49829257 | 49871535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1918 | 268 | 47 | 52 | 134 | 8 | 26 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0002 | 0/0 | 1918 | 37 | 16 | 3 | 7 | 2 | 9 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0003 | 0/0 | 1919 | 31 | 2 | 12 | 7 | 5 | 5 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1914): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0005 | 0/0 | 1918 | 4 | 0 | 0 | 4 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0006 | 1/0 | 1918 | 4 | 3 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0007 | 0/0 | 1918 | 4 | 4 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0008 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0009 | 0/0 | 1918 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0010 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0001t0011 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0002t0001 | 0/0 | 1918 | 4 | 3 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0002t0002 | 0/0 | 1918 | 10 | 9 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0001c0004t0002 | 0/0 | 1918 | 3 | 2 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0002c0003t0004 | 0/0 | 1918 | 6 | 0 | 2 | 0 | 3 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0003c0006t0001 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0004c0005t0001 | 0/0 | 1918 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| a0005c0007t0002 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | ATTGA others(1913): Show |
chr6 | 49829257 | 49871535 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 0 | 3 | 19 | 1 | 2 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0002 | 0/0 | 20 | 0 | 3 | 16 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0003 | 0/0 | 12 | 6 | 3 | 3 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0077 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 2 | 2 | 2 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0006g0075 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0007g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0010g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0001t0011g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0002t0001g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0002t0002g0005 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0004t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0004t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0001c0004t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0002c0003t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0002c0003t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0002c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0002c0003t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0002c0003t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0003c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0004c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| a0005c0007t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0004 | g0022 | EUR | GBR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0084 | EUR | GBR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0231 | EUR | FIN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00673 | hp1 | a0003 | c0006 | t0001 | g0190 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01070 | hp2 | a0002 | c0003 | t0004 | g0057 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01071 | hp1 | a0002 | c0003 | t0004 | g0056 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01515 | hp1 | a0002 | c0003 | t0004 | g0054 | EUR | IBS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0239 | EUR | IBS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01884 | hp2 | a0001 | c0004 | t0002 | g0055 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02083 | hp2 | a0004 | c0005 | t0001 | g0156 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02165 | hp1 | a0001 | c0001 | t0011 | g0254 | EAS | CDX | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03540 | hp2 | a0005 | c0007 | t0002 | g0045 | AFR | GWD | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0063 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03710 | hp1 | a0002 | c0003 | t0004 | g0053 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | STU | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0212 | AFR | YRI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18906 | hp2 | a0001 | c0004 | t0002 | g0229 | AFR | YRI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18954 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | LWK | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | LWK | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | YRI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ASW | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ASW | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0244 | EUR | TSI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20752 | hp2 | a0002 | c0003 | t0004 | g0022 | EUR | TSI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0145 | AMR | CLM | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | USA | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | USA | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | USA | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | LWK | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0077 | REF | REF | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0075 | REF | REF | CRISP1_chr6_49829257_49871535 | CRISP1 | chr6 | 49829257 | 49871535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49838443 | G | T | 1 | a0003 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.616C>A | p.Leu206Ile | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/8 | 725/1918 | 616/750 | 206/249 | chr6 | 49838443 | |||
| chr6:49846585 | T | A | 1 | a0005 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.370A>T | p.Thr124Ser | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/8 | 479/1918 | 370/750 | 124/249 | chr6 | 49846585 | |||
| chr6:49846666 | T | C | 1 | a0002 | 6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.289A>G | p.Thr97Ala | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/8 | 398/1918 | 289/750 | 97/249 | chr6 | 49846666 | |||
| chr6:49848296 | A | G | 1 | a0004 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.199T>C | p.Trp67Arg | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/8 | 308/1918 | 199/750 | 67/249 | chr6 | 49848296 | |||
| chr6:49866429 | C | T | 1 | a0001 | 1 | HG02165.hp1 | splice_region_variant | LOW | c.-3G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | chr6 | 49866429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49838483 | G | A | 2 | a0001c0002 a0005c0007 |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
synonymous_variant | LOW | c.576C>T | p.Gly192Gly | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/8 | 685/1918 | 576/750 | 192/249 | chr6 | 49838483 | |||
| chr6:49846658 | A | G | 1 | a0001c0004 | 3 | HG01123.hp2 HG01884.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.297T>C | p.Cys99Cys | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/8 | 406/1918 | 297/750 | 99/249 | chr6 | 49846658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49834361 | T | C | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(13): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
3_prime_UTR_variant | MODIFIER | c.*955A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 955 | chr6 | 49834361 | ||||||
| chr6:49834496 | G | T | 1 | a0001c0001t0005 | 4 | NA18946.hp2 NA19001.hp1 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*820C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 820 | chr6 | 49834496 | ||||||
| chr6:49834565 | T | A | 1 | a0001c0001t0007 | 4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*751A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 751 | chr6 | 49834565 | ||||||
| chr6:49834626 | A | G | 1 | a0001c0001t0009 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*690T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 690 | chr6 | 49834626 | ||||||
| chr6:49834771 | G | A | 1 | a0001c0001t0008 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*545C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 545 | chr6 | 49834771 | ||||||
| chr6:49834984 | C | T | 7 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 others(4): Show |
279 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 332 | chr6 | 49834984 | ||||||
| chr6:49835089 | A | G | 2 | a0001c0001t0008 a0002c0003t0004 |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*227T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 227 | chr6 | 49835089 | ||||||
| chr6:49835205 | T | C | 1 | a0001c0001t0010 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 8/8 | 111 | chr6 | 49835205 | ||||||
| chr6:49866432 | A | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | chr6 | 49866432 | |||||||
| chr6:49866434 | T | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9034 | chr6 | 49866434 | ||||||
| chr6:49866435 | C | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-9G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9035 | chr6 | 49866435 | ||||||
| chr6:49866437 | A | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9037 | chr6 | 49866437 | ||||||
| chr6:49866438 | C | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-12G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | chr6 | 49866438 | |||||||
| chr6:49866440 | C | G | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | chr6 | 49866440 | |||||||
| chr6:49866443 | C | G | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9043 | chr6 | 49866443 | ||||||
| chr6:49866447 | T | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-21A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9047 | chr6 | 49866447 | ||||||
| chr6:49866451 | T | C | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9051 | chr6 | 49866451 | ||||||
| chr6:49866452 | T | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9052 | chr6 | 49866452 | ||||||
| chr6:49866454 | G | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-28C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9054 | chr6 | 49866454 | ||||||
| chr6:49866456 | G | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9056 | chr6 | 49866456 | ||||||
| chr6:49866458 | C | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9058 | chr6 | 49866458 | ||||||
| chr6:49866460 | T | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-34A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | chr6 | 49866460 | |||||||
| chr6:49866461 | G | C | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-35C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | chr6 | 49866461 | |||||||
| chr6:49866462 | A | T | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9062 | chr6 | 49866462 | ||||||
| chr6:49866465 | A | G | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9065 | chr6 | 49866465 | ||||||
| chr6:49866467 | A | G | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-41T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9067 | chr6 | 49866467 | ||||||
| chr6:49866473 | G | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9073 | chr6 | 49866473 | ||||||
| chr6:49866480 | T | C | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9080 | chr6 | 49866480 | ||||||
| chr6:49866481 | C | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9081 | chr6 | 49866481 | ||||||
| chr6:49866484 | T | G | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9084 | chr6 | 49866484 | ||||||
| chr6:49866494 | T | A | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9094 | chr6 | 49866494 | ||||||
| chr6:49866503 | T | G | 1 | a0001c0001t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-77A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/8 | 9103 | chr6 | 49866503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49835486 | A | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
9 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.623-43T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835486 | |||||||
| chr6:49835657 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.623-214T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835657 | |||||||
| chr6:49835696 | T | C | 1 | a0001c0001t0003g0246 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.623-253A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835696 | |||||||
| chr6:49835779 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.623-336A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835779 | |||||||
| chr6:49835791 | TA | T | 6 | a0001c0001t0008g0062 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.623-349delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835791 | |||||||
| chr6:49835803 | AT | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-361delA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835803 | |||||||
| chr6:49835913 | G | A | 3 | a0001c0004t0002g0055 a0001c0004t0002g0145 a0001c0004t0002g0229 |
3 | HG01123.hp2 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.623-470C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835913 | |||||||
| chr6:49835948 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.623-505G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49835948 | |||||||
| chr6:49836132 | T | C | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.623-689A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836132 | |||||||
| chr6:49836211 | C | T | 6 | a0001c0001t0008g0062 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.623-768G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836211 | |||||||
| chr6:49836212 | C | T | 6 | a0001c0001t0008g0062 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.623-769G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836212 | |||||||
| chr6:49836281 | G | A | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.623-838C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836281 | |||||||
| chr6:49836317 | A | C | 6 | a0001c0002t0002g0005 a0001c0002t0002g0047 a0001c0002t0002g0048 others(3): Show |
11 | HG01069.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.623-874T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836317 | |||||||
| chr6:49836339 | TA | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0153 |
3 | HG01891.hp1 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.623-897delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836339 | |||||||
| chr6:49836340 | A | T | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.623-897T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836340 | |||||||
| chr6:49836340 | AT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0138 a0001c0001t0008g0062 others(5): Show |
9 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.623-898delA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836340 | |||||||
| chr6:49836342 | T | A | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.623-899A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836342 | |||||||
| chr6:49836345 | T | A | 1 | a0001c0001t0003g0243 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.623-902A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836345 | |||||||
| chr6:49836346 | T | A | 10 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0042 others(7): Show |
14 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.623-903A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836346 | |||||||
| chr6:49836501 | A | AT | 2 | a0001c0001t0001g0027 a0001c0001t0001g0150 |
3 | HG02145.hp2 NA18966.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.623-1059_623-1058i others(3): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836501 | |||||||
| chr6:49836502 | A | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(103): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.623-1059T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836502 | |||||||
| chr6:49836561 | G | A | 1 | a0001c0001t0003g0039 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.623-1118C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836561 | |||||||
| chr6:49836586 | G | A | 6 | a0001c0002t0002g0005 a0001c0002t0002g0047 a0001c0002t0002g0048 others(3): Show |
11 | HG01069.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.623-1143C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836586 | |||||||
| chr6:49836629 | G | A | 21 | a0001c0001t0003g0004 a0001c0001t0003g0037 a0001c0001t0003g0039 others(18): Show |
31 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.623-1186C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836629 | |||||||
| chr6:49836661 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.623-1218T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836661 | |||||||
| chr6:49836841 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.623-1398C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836841 | |||||||
| chr6:49836898 | A | AT | 3 | a0001c0001t0002g0020 a0001c0001t0002g0052 a0001c0001t0002g0096 |
5 | HG01891.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.623-1456dupA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836898 | |||||||
| chr6:49836906 | T | A | 7 | a0001c0001t0001g0206 a0001c0001t0008g0062 a0002c0003t0004g0022 others(4): Show |
8 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.623-1463A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836906 | |||||||
| chr6:49836907 | A | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0208 |
2 | HG02165.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.623-1464T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836907 | |||||||
| chr6:49836923 | A | C | 1 | a0001c0001t0008g0062 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.623-1480T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836923 | |||||||
| chr6:49836931 | C | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.623-1488G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836931 | |||||||
| chr6:49836938 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.623-1495A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49836938 | |||||||
| chr6:49837049 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.622+1388A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837049 | |||||||
| chr6:49837190 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
2 | HG02071.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.622+1247C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837190 | |||||||
| chr6:49837195 | A | G | 36 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
49 | HG00408.hp1 HG00621.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.622+1242T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837195 | |||||||
| chr6:49837229 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.622+1208T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837229 | |||||||
| chr6:49837332 | C | T | 45 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0042 others(42): Show |
66 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.622+1105G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837332 | |||||||
| chr6:49837354 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.622+1083G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837354 | |||||||
| chr6:49837384 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.622+1053A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837384 | |||||||
| chr6:49837441 | AT | A | 12 | a0001c0001t0001g0070 a0001c0001t0001g0111 a0001c0001t0001g0144 others(9): Show |
13 | HG00099.hp1 HG00099.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.622+995delA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837441 | |||||||
| chr6:49837456 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.622+981A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837456 | |||||||
| chr6:49837481 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.622+956T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837481 | |||||||
| chr6:49837509 | T | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0210 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+928A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837509 | |||||||
| chr6:49837525 | T | C | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0210 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.622+912A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837525 | |||||||
| chr6:49837573 | C | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0228 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.622+864G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837573 | |||||||
| chr6:49837580 | A | C | 1 | a0001c0001t0002g0020 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.622+857T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837580 | |||||||
| chr6:49837713 | A | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.622+724T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837713 | |||||||
| chr6:49837856 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(104): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.622+581G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837856 | |||||||
| chr6:49837858 | A | C | 1 | a0001c0001t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.622+579T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837858 | |||||||
| chr6:49837869 | G | A | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.622+568C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837869 | |||||||
| chr6:49837901 | T | TA | 23 | a0001c0001t0002g0023 a0001c0001t0002g0059 a0001c0001t0002g0060 others(20): Show |
24 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.622+535dupT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837901 | |||||||
| chr6:49837901 | TA | T | 17 | a0001c0001t0001g0033 a0001c0001t0001g0092 a0001c0001t0001g0115 others(14): Show |
25 | HG01069.hp2 HG01106.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.622+535delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49837901 | |||||||
| chr6:49838004 | A | G | 6 | a0001c0001t0008g0062 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.622+433T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49838004 | |||||||
| chr6:49838104 | T | C | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.622+333A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49838104 | |||||||
| chr6:49838190 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.622+247T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49838190 | |||||||
| chr6:49838272 | T | C | 39 | a0001c0001t0002g0021 a0001c0001t0002g0038 a0001c0001t0002g0042 others(36): Show |
59 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.622+165A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49838272 | |||||||
| chr6:49838408 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0002g0104 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.622+29C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 7/7 | chr6 | 49838408 | |||||||
| chr6:49838694 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-169A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49838694 | |||||||
| chr6:49838741 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.534-216A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49838741 | |||||||
| chr6:49838803 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.534-278G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49838803 | |||||||
| chr6:49839153 | G | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-628C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839153 | |||||||
| chr6:49839180 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.534-655T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839180 | |||||||
| chr6:49839272 | C | CA | 20 | a0001c0001t0001g0210 a0001c0001t0001g0249 a0001c0001t0002g0023 others(17): Show |
21 | HG00621.hp1 HG01243.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.534-748dupT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839272 | |||||||
| chr6:49839272 | CA | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(71): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.534-748delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839272 | |||||||
| chr6:49839272 | CAA | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(105): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.534-749_534-748del others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839272 | |||||||
| chr6:49839272 | CAAA | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0095 a0001c0001t0001g0110 others(16): Show |
29 | HG00323.hp2 HG00642.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.534-750_534-748del others(3): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839272 | |||||||
| chr6:49839272 | CAAAA | C | 5 | a0001c0002t0002g0047 a0002c0003t0004g0022 a0002c0003t0004g0053 others(2): Show |
6 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.534-751_534-748del others(4): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839272 | |||||||
| chr6:49839272 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-757_534-748del others(10): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839272 | |||||||
| chr6:49839273 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.534-748T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839273 | |||||||
| chr6:49839325 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.534-800G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839325 | |||||||
| chr6:49839376 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0249 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.534-851T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839376 | |||||||
| chr6:49839427 | G | A | 24 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0038 others(21): Show |
35 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.534-902C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839427 | |||||||
| chr6:49839604 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0153 |
2 | HG01891.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.534-1079T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839604 | |||||||
| chr6:49839709 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.534-1184T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839709 | |||||||
| chr6:49839714 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.533+1184C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839714 | |||||||
| chr6:49839809 | T | G | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.533+1089A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839809 | |||||||
| chr6:49839894 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0094 a0001c0001t0001g0200 |
6 | HG00609.hp2 NA18940.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.533+1004C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839894 | |||||||
| chr6:49839972 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.533+926A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49839972 | |||||||
| chr6:49840085 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0153 |
3 | HG01891.hp1 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.533+813A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49840085 | |||||||
| chr6:49840214 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.533+684G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49840214 | |||||||
| chr6:49840270 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.533+628C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49840270 | |||||||
| chr6:49840656 | C | T | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.533+242G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49840656 | |||||||
| chr6:49840776 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.533+122G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49840776 | |||||||
| chr6:49840788 | A | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0087 |
2 | NA18939.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.533+110T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 6/7 | chr6 | 49840788 | |||||||
| chr6:49841003 | G | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.436-8C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841003 | |||||||
| chr6:49841049 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.436-54T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841049 | |||||||
| chr6:49841227 | C | T | 1 | a0001c0001t0002g0020 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.436-232G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841227 | |||||||
| chr6:49841228 | G | A | 3 | a0001c0004t0002g0055 a0001c0004t0002g0145 a0001c0004t0002g0229 |
3 | HG01123.hp2 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.436-233C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841228 | |||||||
| chr6:49841328 | A | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-333T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841328 | |||||||
| chr6:49841574 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.436-579G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841574 | |||||||
| chr6:49841616 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.436-621T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841616 | |||||||
| chr6:49841736 | G | A | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.436-741C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841736 | |||||||
| chr6:49841863 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.436-868C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841863 | |||||||
| chr6:49841874 | C | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-879G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49841874 | |||||||
| chr6:49842077 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.436-1082A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842077 | |||||||
| chr6:49842265 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0117 |
2 | HG02451.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.436-1270C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842265 | |||||||
| chr6:49842332 | G | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-1337C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842332 | |||||||
| chr6:49842365 | C | A | 1 | a0001c0001t0002g0064 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.436-1370G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842365 | |||||||
| chr6:49842437 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02027.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.436-1442A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842437 | |||||||
| chr6:49842527 | T | G | 2 | a0001c0004t0002g0055 a0001c0004t0002g0229 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.436-1532A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842527 | |||||||
| chr6:49842608 | G | C | 1 | a0001c0004t0002g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.436-1613C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842608 | |||||||
| chr6:49842853 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0214 |
3 | HG01516.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.436-1858G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842853 | |||||||
| chr6:49842983 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.436-1988T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842983 | |||||||
| chr6:49842984 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.436-1989G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49842984 | |||||||
| chr6:49843008 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436-2013G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843008 | |||||||
| chr6:49843145 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.436-2150G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843145 | |||||||
| chr6:49843213 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(97): Show |
155 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.436-2218C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843213 | |||||||
| chr6:49843273 | C | T | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.436-2278G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843273 | |||||||
| chr6:49843427 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.436-2432A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843427 | |||||||
| chr6:49843447 | G | A | 46 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0020 others(43): Show |
69 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.436-2452C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843447 | |||||||
| chr6:49843462 | G | T | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.436-2467C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843462 | |||||||
| chr6:49843545 | C | A | 2 | a0001c0004t0002g0055 a0001c0004t0002g0229 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.436-2550G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843545 | |||||||
| chr6:49843550 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-2555G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843550 | |||||||
| chr6:49843607 | C | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-2612G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843607 | |||||||
| chr6:49843614 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.436-2619C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843614 | |||||||
| chr6:49843855 | A | T | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.435+2665T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49843855 | |||||||
| chr6:49844027 | A | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0112 |
2 | NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.435+2493T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844027 | |||||||
| chr6:49844034 | G | A | 1 | a0001c0001t0007g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.435+2486C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844034 | |||||||
| chr6:49844041 | A | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0076 others(3): Show |
7 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+2479T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844041 | |||||||
| chr6:49844078 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0144 |
2 | HG01074.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.435+2442T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844078 | |||||||
| chr6:49844088 | C | T | 3 | a0001c0004t0002g0055 a0001c0004t0002g0145 a0001c0004t0002g0229 |
3 | HG01123.hp2 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.435+2432G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844088 | |||||||
| chr6:49844327 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.435+2193G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844327 | |||||||
| chr6:49844462 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
10 | HG00597.hp1 HG01978.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.435+2058C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844462 | |||||||
| chr6:49844472 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.435+2048G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844472 | |||||||
| chr6:49844510 | G | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+2010C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844510 | |||||||
| chr6:49844563 | T | TGAGGCTG others(20): Show |
5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+1930_435+1956d others(29): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844563 | |||||||
| chr6:49844594 | G | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0141 others(2): Show |
8 | HG00639.hp2 HG00741.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.435+1926C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844594 | |||||||
| chr6:49844670 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.435+1850G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844670 | |||||||
| chr6:49844673 | A | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1847T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844673 | |||||||
| chr6:49844754 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435+1766G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844754 | |||||||
| chr6:49844873 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.435+1647C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844873 | |||||||
| chr6:49844927 | AT | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1592delA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844927 | |||||||
| chr6:49844932 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+1588C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49844932 | |||||||
| chr6:49845074 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.435+1446A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845074 | |||||||
| chr6:49845078 | T | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+1442A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845078 | |||||||
| chr6:49845126 | A | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
112 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.435+1394T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845126 | |||||||
| chr6:49845219 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+1301G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845219 | |||||||
| chr6:49845364 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+1156T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845364 | |||||||
| chr6:49845499 | T | A | 1 | a0001c0001t0002g0020 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.435+1021A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845499 | |||||||
| chr6:49845707 | C | CA | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.435+812dupT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845707 | |||||||
| chr6:49845707 | C | CAA | 8 | a0001c0001t0001g0074 a0001c0001t0001g0133 a0001c0001t0001g0138 others(5): Show |
8 | HG00438.hp1 HG00741.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.435+811_435+812dup others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845707 | |||||||
| chr6:49845719 | T | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+801A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845719 | |||||||
| chr6:49845719 | T | C | 1 | a0001c0004t0002g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.435+801A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845719 | |||||||
| chr6:49845784 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0228 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.435+736C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845784 | |||||||
| chr6:49845826 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.435+694T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845826 | |||||||
| chr6:49845963 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.435+557C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49845963 | |||||||
| chr6:49846054 | C | T | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+466G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846054 | |||||||
| chr6:49846055 | G | A | 3 | a0001c0004t0002g0055 a0001c0004t0002g0145 a0001c0004t0002g0229 |
3 | HG01123.hp2 HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.435+465C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846055 | |||||||
| chr6:49846170 | C | T | 6 | a0001c0001t0001g0131 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.435+350G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846170 | |||||||
| chr6:49846183 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.435+337T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846183 | |||||||
| chr6:49846218 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+302A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846218 | |||||||
| chr6:49846391 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.435+129C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846391 | |||||||
| chr6:49846456 | G | C | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+64C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846456 | |||||||
| chr6:49846461 | G | A | 6 | a0001c0001t0002g0084 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG00140.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+59C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 5/7 | chr6 | 49846461 | |||||||
| chr6:49846903 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.287-235T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49846903 | |||||||
| chr6:49846905 | C | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0152 others(1): Show |
4 | HG01891.hp1 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.287-237G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49846905 | |||||||
| chr6:49847034 | T | G | 1 | a0001c0002t0002g0047 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.287-366A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847034 | |||||||
| chr6:49847207 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-539G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847207 | |||||||
| chr6:49847216 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.287-548A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847216 | |||||||
| chr6:49847231 | A | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.287-563T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847231 | |||||||
| chr6:49847343 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0011g0254 |
2 | HG02040.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.287-675C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847343 | |||||||
| chr6:49847350 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.287-682G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847350 | |||||||
| chr6:49847447 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+762T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847447 | |||||||
| chr6:49847488 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.286+721T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847488 | |||||||
| chr6:49847566 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.286+643T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847566 | |||||||
| chr6:49847618 | C | A | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+591G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847618 | |||||||
| chr6:49847657 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+552G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847657 | |||||||
| chr6:49847694 | G | GT | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+514dupA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847694 | |||||||
| chr6:49847694 | GT | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(168): Show |
269 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.286+514delA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847694 | |||||||
| chr6:49847754 | T | C | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.286+455A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847754 | |||||||
| chr6:49847804 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0249 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.286+405G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847804 | |||||||
| chr6:49847892 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.286+317T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847892 | |||||||
| chr6:49847909 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.286+300C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49847909 | |||||||
| chr6:49848042 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+167T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848042 | |||||||
| chr6:49848158 | C | CTG | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+50_286+51insCA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848158 | |||||||
| chr6:49848160 | A | AT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0070 others(3): Show |
9 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+48dupA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848160 | |||||||
| chr6:49848160 | A | ATTTT | 5 | a0001c0001t0003g0037 a0001c0001t0003g0234 a0001c0001t0003g0236 others(2): Show |
6 | HG00639.hp1 HG01123.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+45_286+48dupAA others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848160 | |||||||
| chr6:49848160 | A | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+49T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848160 | |||||||
| chr6:49848186 | G | A | 1 | a0001c0004t0002g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.286+23C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848186 | |||||||
| chr6:49848193 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.286+16T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 4/7 | chr6 | 49848193 | |||||||
| chr6:49848336 | T | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-37A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848336 | |||||||
| chr6:49848368 | T | C | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-69A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848368 | |||||||
| chr6:49848379 | C | T | 12 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(9): Show |
21 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.196-80G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848379 | |||||||
| chr6:49848392 | C | A | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.196-93G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848392 | |||||||
| chr6:49848398 | T | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-99A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848398 | |||||||
| chr6:49848439 | C | T | 8 | a0001c0001t0001g0123 a0001c0001t0001g0210 a0001c0001t0001g0249 others(5): Show |
8 | HG01123.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-140G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848439 | |||||||
| chr6:49848460 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196-161T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848460 | |||||||
| chr6:49848781 | C | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-482G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848781 | |||||||
| chr6:49848913 | A | AT | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-615_196-614ins others(1): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848913 | |||||||
| chr6:49848949 | C | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.196-650G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848949 | |||||||
| chr6:49848973 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.196-674C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49848973 | |||||||
| chr6:49849194 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.196-895G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849194 | |||||||
| chr6:49849408 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0249 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.196-1109G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849408 | |||||||
| chr6:49849551 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196-1252G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849551 | |||||||
| chr6:49849565 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196-1266T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849565 | |||||||
| chr6:49849708 | G | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1409C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849708 | |||||||
| chr6:49849767 | T | G | 2 | a0001c0001t0002g0215 a0001c0001t0002g0217 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.196-1468A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849767 | |||||||
| chr6:49849796 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0228 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.196-1497A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849796 | |||||||
| chr6:49849829 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.196-1530A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849829 | |||||||
| chr6:49849861 | T | C | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1562A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849861 | |||||||
| chr6:49849881 | C | CA | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1583dupT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849881 | |||||||
| chr6:49849991 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.196-1692T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49849991 | |||||||
| chr6:49850073 | G | A | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.196-1774C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850073 | |||||||
| chr6:49850084 | T | G | 1 | a0001c0001t0003g0244 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.196-1785A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850084 | |||||||
| chr6:49850091 | A | G | 2 | a0001c0004t0002g0055 a0001c0004t0002g0229 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.196-1792T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850091 | |||||||
| chr6:49850092 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.196-1793G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850092 | |||||||
| chr6:49850103 | T | TG | 28 | a0001c0001t0001g0028 a0001c0001t0001g0074 a0001c0001t0001g0082 others(25): Show |
29 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.196-1805dupC | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850103 | |||||||
| chr6:49850110 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.196-1811T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850110 | |||||||
| chr6:49850123 | G | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.196-1824C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850123 | |||||||
| chr6:49850194 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.195+1807T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850194 | |||||||
| chr6:49850232 | A | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+1769T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850232 | |||||||
| chr6:49850269 | A | G | 2 | a0002c0003t0004g0056 a0002c0003t0004g0057 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.195+1732T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850269 | |||||||
| chr6:49850389 | C | T | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+1612G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850389 | |||||||
| chr6:49850426 | C | T | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.195+1575G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850426 | |||||||
| chr6:49850494 | C | G | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.195+1507G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850494 | |||||||
| chr6:49850696 | T | C | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.195+1305A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850696 | |||||||
| chr6:49850742 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0076 others(3): Show |
7 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.195+1259C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850742 | |||||||
| chr6:49850783 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.195+1218C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850783 | |||||||
| chr6:49850814 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.195+1187A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850814 | |||||||
| chr6:49850957 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.195+1044A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49850957 | |||||||
| chr6:49851162 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.195+839A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851162 | |||||||
| chr6:49851270 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.195+731A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851270 | |||||||
| chr6:49851284 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.195+717C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851284 | |||||||
| chr6:49851362 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.195+639G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851362 | |||||||
| chr6:49851382 | C | T | 2 | a0001c0004t0002g0055 a0001c0004t0002g0229 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.195+619G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851382 | |||||||
| chr6:49851704 | C | T | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.195+297G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851704 | |||||||
| chr6:49851944 | T | A | 1 | a0001c0001t0001g0094 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.195+57A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851944 | |||||||
| chr6:49851959 | A | G | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.195+42T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 3/7 | chr6 | 49851959 | |||||||
| chr6:49852437 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.67-308T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852437 | |||||||
| chr6:49852492 | C | A | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-363G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852492 | |||||||
| chr6:49852546 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-417G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852546 | |||||||
| chr6:49852585 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67-456T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852585 | |||||||
| chr6:49852759 | T | C | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67-630A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852759 | |||||||
| chr6:49852845 | TTTG | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0197 a0001c0001t0001g0199 |
3 | HG01361.hp1 HG01361.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.67-719_67-717delCA others(1): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852845 | |||||||
| chr6:49852846 | T | TTG | 30 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0094 others(27): Show |
36 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.67-719_67-718dupCA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | T | TTGTG | 11 | a0001c0001t0001g0083 a0001c0001t0001g0122 a0001c0001t0001g0144 others(8): Show |
11 | HG00323.hp1 HG01934.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-721_67-718dupCA others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | T | TTGTGTG | 6 | a0001c0001t0001g0030 a0001c0001t0002g0023 a0001c0001t0002g0066 others(3): Show |
8 | HG01255.hp1 HG02683.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-723_67-718dupCA others(4): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | T | TTGTGTGT others(1): Show |
4 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0072 others(1): Show |
4 | HG00741.hp2 HG02602.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-725_67-718dupCA others(6): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0002g0073 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67-729_67-718dupCA others(10): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | TTG | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(46): Show |
84 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.67-719_67-718delCA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | TTGTG | T | 19 | a0001c0001t0001g0034 a0001c0001t0001g0091 a0001c0001t0001g0092 others(16): Show |
20 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-721_67-718delCA others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | TTGTGTG | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0102 others(12): Show |
28 | HG00642.hp2 HG00733.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.67-723_67-718delCA others(4): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | TTGTGTGT others(1): Show |
T | 4 | a0002c0003t0004g0022 a0002c0003t0004g0054 a0002c0003t0004g0056 others(1): Show |
5 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-725_67-718delCA others(6): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49852846 | TTGTGTGT others(5): Show |
T | 1 | a0002c0003t0004g0053 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67-729_67-718delCA others(10): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49852846 | |||||||
| chr6:49853246 | C | T | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-1117G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49853246 | |||||||
| chr6:49853303 | C | A | 2 | a0001c0001t0007g0012 a0001c0001t0007g0044 |
4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1174G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49853303 | |||||||
| chr6:49853537 | A | T | 1 | a0001c0001t0002g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.67-1408T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49853537 | |||||||
| chr6:49853668 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.67-1539A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49853668 | |||||||
| chr6:49854035 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.67-1906T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854035 | |||||||
| chr6:49854044 | C | T | 21 | a0001c0001t0001g0210 a0001c0001t0001g0249 a0001c0001t0002g0020 others(18): Show |
32 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.67-1915G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854044 | |||||||
| chr6:49854157 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.67-2028C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854157 | |||||||
| chr6:49854405 | G | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-2276C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854405 | |||||||
| chr6:49854430 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67-2301G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854430 | |||||||
| chr6:49854806 | A | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+2529T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854806 | |||||||
| chr6:49854813 | T | C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
32 | HG00621.hp2 HG01167.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.66+2522A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854813 | |||||||
| chr6:49854889 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+2446T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854889 | |||||||
| chr6:49854963 | G | A | 45 | a0001c0001t0001g0210 a0001c0001t0001g0232 a0001c0001t0001g0233 others(42): Show |
67 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.66+2372C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49854963 | |||||||
| chr6:49855115 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.66+2220G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855115 | |||||||
| chr6:49855216 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.66+2119A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855216 | |||||||
| chr6:49855283 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.66+2052C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855283 | |||||||
| chr6:49855309 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.66+2026T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855309 | |||||||
| chr6:49855394 | ACT | A | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.66+1939_66+1940del others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855394 | |||||||
| chr6:49855399 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.66+1936C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855399 | |||||||
| chr6:49855442 | A | AT | 15 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0002g0021 others(12): Show |
24 | HG00140.hp1 HG00642.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.66+1892dupA | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855442 | |||||||
| chr6:49855442 | A | ATT | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1891_66+1892dup others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855442 | |||||||
| chr6:49855501 | C | G | 1 | a0001c0001t0002g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.66+1834G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855501 | |||||||
| chr6:49855535 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.66+1800G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855535 | |||||||
| chr6:49855699 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.66+1636A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855699 | |||||||
| chr6:49855742 | C | T | 22 | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0037 others(19): Show |
33 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+1593G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49855742 | |||||||
| chr6:49856101 | G | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
112 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.66+1234C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856101 | |||||||
| chr6:49856110 | A | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0172 others(9): Show |
18 | HG00280.hp2 HG00597.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.66+1225T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856110 | |||||||
| chr6:49856125 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.66+1210G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856125 | |||||||
| chr6:49856274 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(98): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.66+1061T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856274 | |||||||
| chr6:49856445 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.66+890G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856445 | |||||||
| chr6:49856561 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.66+774G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856561 | |||||||
| chr6:49856633 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+702G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856633 | |||||||
| chr6:49856764 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.66+571G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856764 | |||||||
| chr6:49856914 | G | A | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.66+421C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856914 | |||||||
| chr6:49856995 | T | C | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+340A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 2/7 | chr6 | 49856995 | |||||||
| chr6:49857534 | G | T | 1 | a0001c0001t0001g0046 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-2-132C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857534 | |||||||
| chr6:49857564 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-2-162T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857564 | |||||||
| chr6:49857607 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-205T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857607 | |||||||
| chr6:49857628 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-2-226C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857628 | |||||||
| chr6:49857651 | T | C | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-249A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857651 | |||||||
| chr6:49857766 | T | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18982.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-2-364A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857766 | |||||||
| chr6:49857812 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-410A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857812 | |||||||
| chr6:49857894 | C | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-492G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857894 | |||||||
| chr6:49857896 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0169 |
2 | NA18956.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-2-494C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857896 | |||||||
| chr6:49857964 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-2-562C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857964 | |||||||
| chr6:49857998 | G | A | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-596C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49857998 | |||||||
| chr6:49858053 | A | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-2-651T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858053 | |||||||
| chr6:49858058 | G | A | 1 | a0001c0004t0002g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-2-656C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858058 | |||||||
| chr6:49858196 | G | C | 2 | a0001c0001t0007g0012 a0001c0001t0007g0044 |
4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-794C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858196 | |||||||
| chr6:49858293 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-891T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858293 | |||||||
| chr6:49858314 | C | A | 2 | a0001c0001t0007g0012 a0001c0001t0007g0044 |
4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-912G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858314 | |||||||
| chr6:49858323 | ACCATCTG | A | 1 | a0001c0001t0002g0020 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-928_-2-922delCA others(5): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858323 | |||||||
| chr6:49858324 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0249 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-922G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858324 | |||||||
| chr6:49858407 | A | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.-2-1005T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858407 | |||||||
| chr6:49858413 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
112 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-2-1011G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858413 | |||||||
| chr6:49858425 | A | G | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-1023T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858425 | |||||||
| chr6:49858512 | T | C | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1110A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858512 | |||||||
| chr6:49858849 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0096 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-2-1447C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858849 | |||||||
| chr6:49858947 | C | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1545G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49858947 | |||||||
| chr6:49859001 | G | C | 1 | a0001c0001t0002g0125 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-2-1599C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859001 | |||||||
| chr6:49859237 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-2-1835C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859237 | |||||||
| chr6:49859400 | GA | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0249 a0001c0001t0002g0020 others(2): Show |
7 | HG00741.hp2 HG01243.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-1999delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859400 | |||||||
| chr6:49859406 | A | AC | 21 | a0001c0001t0002g0023 a0001c0001t0002g0059 a0001c0001t0002g0060 others(18): Show |
22 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.-2-2005_-2-2004ins others(1): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859406 | |||||||
| chr6:49859415 | G | A | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 |
3 | HG02145.hp1 HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-2-2013C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859415 | |||||||
| chr6:49859442 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-2040C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859442 | |||||||
| chr6:49859544 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-2142A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859544 | |||||||
| chr6:49859573 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-2-2171T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859573 | |||||||
| chr6:49859610 | T | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-2208A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859610 | |||||||
| chr6:49859874 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-2-2472G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859874 | |||||||
| chr6:49859924 | T | C | 1 | a0001c0001t0002g0020 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-2522A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859924 | |||||||
| chr6:49859987 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-2-2585T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49859987 | |||||||
| chr6:49860076 | A | C | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-2-2674T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860076 | |||||||
| chr6:49860266 | C | G | 45 | a0001c0001t0001g0210 a0001c0001t0001g0232 a0001c0001t0001g0233 others(42): Show |
67 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-2-2864G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860266 | |||||||
| chr6:49860351 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-2-2949C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860351 | |||||||
| chr6:49860418 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0074 |
4 | HG00438.hp1 NA18959.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3016T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860418 | |||||||
| chr6:49860432 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.-2-3030A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860432 | |||||||
| chr6:49860490 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.-2-3088T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860490 | |||||||
| chr6:49860659 | C | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0214 |
3 | HG01516.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-2-3257G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860659 | |||||||
| chr6:49860743 | T | G | 22 | a0001c0001t0002g0038 a0001c0001t0003g0004 a0001c0001t0003g0037 others(19): Show |
33 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-2-3341A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860743 | |||||||
| chr6:49860828 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-2-3426A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860828 | |||||||
| chr6:49860834 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(98): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-2-3432T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860834 | |||||||
| chr6:49860857 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-2-3455G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860857 | |||||||
| chr6:49860979 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-2-3577G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49860979 | |||||||
| chr6:49861050 | A | T | 1 | a0001c0001t0001g0167 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-2-3648T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861050 | |||||||
| chr6:49861116 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02027.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-2-3714C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861116 | |||||||
| chr6:49861169 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3767T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861169 | |||||||
| chr6:49861183 | A | G | 1 | a0001c0001t0002g0020 | 3 | HG02451.hp1 HG02559.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-3781T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861183 | |||||||
| chr6:49861207 | A | T | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-3805T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861207 | |||||||
| chr6:49861377 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-2-3975C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861377 | |||||||
| chr6:49861444 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-2-4042G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861444 | |||||||
| chr6:49861562 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-2-4160T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861562 | |||||||
| chr6:49861601 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0249 |
2 | HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-4199G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861601 | |||||||
| chr6:49861621 | C | T | 1 | a0001c0004t0002g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-2-4219G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861621 | |||||||
| chr6:49861633 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-2-4231G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861633 | |||||||
| chr6:49861739 | T | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(246): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.-2-4337A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861739 | |||||||
| chr6:49861769 | T | C | 1 | a0001c0004t0002g0055 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2-4367A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861769 | |||||||
| chr6:49861881 | TA | T | 10 | a0001c0001t0001g0098 a0001c0001t0001g0210 a0001c0001t0001g0249 others(7): Show |
13 | HG00099.hp1 HG00741.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-2-4480delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861881 | |||||||
| chr6:49861900 | ACT | A | 2 | a0001c0001t0007g0012 a0001c0001t0007g0044 |
4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4500_-2-4499del others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861900 | |||||||
| chr6:49861946 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-3+4483T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861946 | |||||||
| chr6:49861989 | T | A | 12 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(9): Show |
21 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-3+4440A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49861989 | |||||||
| chr6:49862030 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-3+4399T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862030 | |||||||
| chr6:49862218 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-3+4211G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862218 | |||||||
| chr6:49862256 | TA | T | 3 | a0001c0001t0005g0129 a0001c0001t0005g0165 a0001c0001t0005g0166 |
3 | NA18946.hp2 NA19001.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-3+4172delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862256 | |||||||
| chr6:49862313 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-3+4116A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862313 | |||||||
| chr6:49862323 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-3+4106T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862323 | |||||||
| chr6:49862385 | C | T | 14 | a0001c0001t0002g0020 a0001c0001t0002g0227 a0001c0002t0001g0007 others(11): Show |
25 | HG00099.hp1 HG00642.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3+4044G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862385 | |||||||
| chr6:49862398 | A | ATAT | 45 | a0001c0001t0001g0210 a0001c0001t0001g0232 a0001c0001t0001g0233 others(42): Show |
67 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.-3+4028_-3+4030dup others(3): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862398 | |||||||
| chr6:49862500 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-3+3929T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862500 | |||||||
| chr6:49862533 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0209 |
2 | NA18956.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-3+3896T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862533 | |||||||
| chr6:49862724 | C | G | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-3+3705G>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862724 | |||||||
| chr6:49862775 | G | T | 1 | a0001c0001t0002g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-3+3654C>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862775 | |||||||
| chr6:49862816 | C | CA | 72 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(69): Show |
113 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-3+3612dupT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862816 | |||||||
| chr6:49862816 | CA | C | 6 | a0001c0001t0001g0142 a0002c0003t0004g0022 a0002c0003t0004g0053 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+3612delT | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862816 | |||||||
| chr6:49862829 | A | G | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+3600T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862829 | |||||||
| chr6:49862881 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-3+3548A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49862881 | |||||||
| chr6:49863075 | A | T | 1 | a0001c0001t0003g0230 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-3+3354T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863075 | |||||||
| chr6:49863214 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-3+3215G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863214 | |||||||
| chr6:49863228 | C | A | 5 | a0002c0003t0004g0022 a0002c0003t0004g0053 a0002c0003t0004g0054 others(2): Show |
6 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+3201G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863228 | |||||||
| chr6:49863289 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-3+3140T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863289 | |||||||
| chr6:49863290 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-3+3139A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863290 | |||||||
| chr6:49863402 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-3+3027G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863402 | |||||||
| chr6:49863531 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-3+2898T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863531 | |||||||
| chr6:49863566 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+2863T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863566 | |||||||
| chr6:49863905 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-3+2524C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863905 | |||||||
| chr6:49863933 | C | T | 2 | a0001c0001t0007g0012 a0001c0001t0007g0044 |
4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+2496G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49863933 | |||||||
| chr6:49864159 | C | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0203 a0001c0001t0001g0204 others(4): Show |
8 | HG00408.hp1 HG00438.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+2270G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864159 | |||||||
| chr6:49864279 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-3+2150A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864279 | |||||||
| chr6:49864384 | C | CTG | 9 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0232 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+2043_-3+2044dup others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | C | CTGTG | 14 | a0001c0001t0002g0023 a0001c0001t0002g0052 a0001c0001t0002g0059 others(11): Show |
15 | HG00280.hp1 HG00621.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3+2041_-3+2044dup others(4): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | C | CTGTGTG | 4 | a0001c0004t0002g0055 a0002c0003t0004g0022 a0002c0003t0004g0056 others(1): Show |
5 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+2039_-3+2044dup others(6): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | C | CTGTGTGT others(3): Show |
2 | a0002c0003t0004g0053 a0002c0003t0004g0054 |
2 | HG01515.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-3+2035_-3+2044dup others(10): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | CTG | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(54): Show |
90 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-3+2043_-3+2044del others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | CTGTG | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-3+2041_-3+2044del others(4): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | CTGTGTG | C | 23 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0209 others(20): Show |
37 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.-3+2039_-3+2044del others(6): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864384 | CTGTGTGT others(1): Show |
C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0219 a0001c0001t0001g0220 others(2): Show |
7 | HG02976.hp1 NA18986.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+2037_-3+2044del others(8): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864384 | |||||||
| chr6:49864426 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-3+2003T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864426 | |||||||
| chr6:49864461 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-3+1968C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864461 | |||||||
| chr6:49864483 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3+1946G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864483 | |||||||
| chr6:49864686 | T | G | 3 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01928.hp1 HG02129.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-3+1743A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864686 | |||||||
| chr6:49864697 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-3+1732C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864697 | |||||||
| chr6:49864937 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0227 |
4 | HG00741.hp2 HG02451.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+1492C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864937 | |||||||
| chr6:49864954 | G | C | 1 | a0001c0001t0001g0228 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-3+1475C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864954 | |||||||
| chr6:49864957 | A | ATG | 7 | a0001c0002t0001g0007 a0001c0002t0002g0005 a0001c0002t0002g0047 others(4): Show |
15 | HG00642.hp2 HG01069.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+1470_-3+1471dup others(2): Show |
CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49864957 | |||||||
| chr6:49865270 | G | C | 1 | a0001c0004t0002g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-3+1159C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865270 | |||||||
| chr6:49865474 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3+955A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865474 | |||||||
| chr6:49865474 | T | C | 24 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0038 others(21): Show |
35 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3+955A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865474 | |||||||
| chr6:49865713 | C | A | 1 | a0001c0001t0001g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3+716G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865713 | |||||||
| chr6:49865773 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-3+656T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865773 | |||||||
| chr6:49865777 | C | T | 2 | a0001c0001t0007g0012 a0001c0001t0007g0044 |
4 | HG02109.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+652G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865777 | |||||||
| chr6:49865879 | C | T | 1 | a0005c0007t0002g0045 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3+550G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865879 | |||||||
| chr6:49865945 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-3+484A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49865945 | |||||||
| chr6:49866160 | C | T | 1 | a0001c0001t0007g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-3+269G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866160 | |||||||
| chr6:49866268 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
8 | HG02056.hp1 HG03831.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+161A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866268 | |||||||
| chr6:49866328 | T | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+101A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866328 | |||||||
| chr6:49866330 | G | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+99C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866330 | |||||||
| chr6:49866331 | C | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+98G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866331 | |||||||
| chr6:49866332 | A | G | 3 | a0001c0001t0002g0021 a0001c0001t0002g0042 a0001c0001t0002g0043 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+97T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866332 | |||||||
| chr6:49866333 | T | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+96A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866333 | |||||||
| chr6:49866344 | T | G | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+85A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866344 | |||||||
| chr6:49866346 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+83T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866346 | |||||||
| chr6:49866349 | A | G | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+80T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866349 | |||||||
| chr6:49866354 | A | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+75T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866354 | |||||||
| chr6:49866355 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+74T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866355 | |||||||
| chr6:49866357 | A | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+72T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866357 | |||||||
| chr6:49866366 | G | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+63C>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866366 | |||||||
| chr6:49866369 | T | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+60A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866369 | |||||||
| chr6:49866370 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+59T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866370 | |||||||
| chr6:49866373 | C | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+56G>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866373 | |||||||
| chr6:49866374 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+55T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866374 | |||||||
| chr6:49866375 | C | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+54G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866375 | |||||||
| chr6:49866377 | T | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+52A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866377 | |||||||
| chr6:49866384 | C | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+45G>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866384 | |||||||
| chr6:49866386 | T | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+43A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866386 | |||||||
| chr6:49866387 | A | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+42T>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866387 | |||||||
| chr6:49866389 | T | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+40A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866389 | |||||||
| chr6:49866391 | T | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+38A>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866391 | |||||||
| chr6:49866401 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+28T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866401 | |||||||
| chr6:49866410 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+19T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866410 | |||||||
| chr6:49866412 | G | C | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+17C>G | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866412 | |||||||
| chr6:49866415 | A | G | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+14T>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866415 | |||||||
| chr6:49866418 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+11T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866418 | |||||||
| chr6:49866419 | T | G | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-3+10A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866419 | |||||||
| chr6:49866421 | T | G | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.-3+8A>C | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866421 | |||||||
| chr6:49866422 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.-3+7T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866422 | |||||||
| chr6:49866423 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.-3+6T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866423 | |||||||
| chr6:49866425 | T | A | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.-3+4A>T | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866425 | |||||||
| chr6:49866427 | A | T | 1 | a0001c0001t0011g0254 | 1 | HG02165.hp1 | splice_donor_variant&intron_variant | HIGH | c.-3+2T>A | CRISP1 | ENSG00000124812.15 | transcript | ENST00000335847.9 | protein_coding | 1/7 | chr6 | 49866427 |