Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1397 |
| ensemblid | ENSG00000182809.11 |
| hgncid | 2361 |
| symbol | CRIP2 |
| name | cysteine rich protein 2 |
| refseq_nuc | NM_001312.4 |
| refseq_prot | NP_001303.1 |
| ensembl_nuc | ENST00000329146.9 |
| ensembl_prot | ENSP00000328521.5 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 105474821 |
| end | 105480162 |
| strand | + |
| ver | v1.2 |
| region | chr14:105474821-105480162 |
| region5000 | chr14:105469821-105485162 |
| regionname0 | CRIP2_chr14_105474821_105480162 |
| regionname5000 | CRIP2_chr14_105469821_105485162 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 208 | 314 | 79 | 62 | 122 | 10 | 39 | 82 | CRIP2_chr14_105469821_105485162 | CRIP2 | MASKC others(203): Show |
chr14 | 105469821 | 105485162 |
| a0002 | 0/0 | 208 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | MASKC others(203): Show |
chr14 | 105469821 | 105485162 |
| a0003 | 0/0 | 208 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | MASKC others(203): Show |
chr14 | 105469821 | 105485162 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 624 | 289 | 59 | 58 | 122 | 10 | 38 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 | ||
| a0001c0002 | 0/0 | 624 | 21 | 19 | 2 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 | ||
| a0001c0003 | 0/0 | 624 | 2 | 1 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 | ||
| a0001c0005 | 0/0 | 624 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 | ||
| a0001c0006 | 0/0 | 624 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 | ||
| a0002c0004 | 0/0 | 624 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 | ||
| a0003c0007 | 0/0 | 624 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | ATGGC others(619): Show |
chr14 | 105469821 | 105485162 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1178 | 262 | 42 | 54 | 117 | 10 | 37 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0002 | 0/0 | 1178 | 14 | 13 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0003 | 0/0 | 1178 | 3 | 2 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0004 | 0/0 | 1178 | 3 | 0 | 0 | 3 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0005 | 0/0 | 1216 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1211): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0006 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0007 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0008 | 0/0 | 1178 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0009 | 0/0 | 1178 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0010 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0001t0011 | 0/0 | 1178 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0002t0001 | 0/0 | 1178 | 21 | 19 | 2 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0003t0001 | 0/0 | 1178 | 2 | 1 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0005t0001 | 0/0 | 1178 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0001c0006t0001 | 0/0 | 1178 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0002c0004t0001 | 0/0 | 1178 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| a0003c0007t0001 | 0/0 | 1178 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | GGAGA others(1173): Show |
chr14 | 105469821 | 105485162 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 0 | 13 | 7 | 1 | 2 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0010 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0234 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0007g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0001c0006t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| a0003c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | GBR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | FIN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0022 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01361 | hp1 | a0001 | c0006 | t0001 | g0096 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0058 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0210 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0189 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CDX | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0243 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03688 | hp1 | a0003 | c0007 | t0001 | g0092 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03710 | hp1 | a0001 | c0005 | t0001 | g0202 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03927 | hp1 | a0001 | c0001 | t0011 | g0142 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0208 | EAS | CHB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | YRI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | LWK | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0232 | AFR | YRI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ASW | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | GIH | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | USA | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | USA | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0218 | REF | REF | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0234 | REF | REF | CRIP2_chr14_105469821_105485162 | CRIP2 | chr14 | 105469821 | 105485162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105478773 | C | T | 1 | a0003 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.239C>T | p.Pro80Leu | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 4/8 | 281/1178 | 239/627 | 80/208 | chr14 | 105478773 | |||
| chr14:105479024 | G | A | 1 | a0002 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.383G>A | p.Arg128His | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 5/8 | 425/1178 | 383/627 | 128/208 | chr14 | 105479024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105479001 | C | G | 1 | a0001c0002 | 21 | HG00735.hp2 HG01167.hp2 HG02055.hp1 others(18): Show |
synonymous_variant | LOW | c.360C>G | p.Thr120Thr | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 5/8 | 402/1178 | 360/627 | 120/208 | chr14 | 105479001 | |||
| chr14:105479441 | C | T | 1 | a0001c0003 | 2 | HG00639.hp2 HG02976.hp1 |
synonymous_variant | LOW | c.507C>T | p.Asp169Asp | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 7/8 | 549/1178 | 507/627 | 169/208 | chr14 | 105479441 | |||
| chr14:105479480 | C | T | 1 | a0001c0006 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.546C>T | p.Leu182Leu | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 7/8 | 588/1178 | 546/627 | 182/208 | chr14 | 105479480 | |||
| chr14:105479596 | C | T | 1 | a0001c0005 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.570C>T | p.Thr190Thr | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 612/1178 | 570/627 | 190/208 | chr14 | 105479596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105474836 | G | A | 1 | a0001c0001t0002 | 14 | HG01167.hp1 HG02559.hp1 HG02615.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-27G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/8 | 27 | chr14 | 105474836 | ||||||
| chr14:105479781 | G | A | 1 | a0001c0001t0003 | 3 | HG01243.hp2 HG03098.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*128G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 128 | chr14 | 105479781 | ||||||
| chr14:105479793 | C | CGGGCAGA others(31): Show |
1 | a0001c0001t0005 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141_*178dupGGGCAG others(32): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 179 | INFO_REALIGN_3_PRIME | chr14 | 105479793 | |||||
| chr14:105479923 | G | A | 1 | a0001c0001t0004 | 3 | HG02027.hp1 NA18747.hp1 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*270G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 270 | chr14 | 105479923 | ||||||
| chr14:105479942 | G | T | 1 | a0001c0001t0011 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*289G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 289 | chr14 | 105479942 | ||||||
| chr14:105479946 | C | T | 1 | a0001c0001t0010 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 293 | chr14 | 105479946 | ||||||
| chr14:105480006 | C | T | 1 | a0001c0001t0009 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*353C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 353 | chr14 | 105480006 | ||||||
| chr14:105480007 | G | A | 1 | a0001c0001t0006 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 354 | chr14 | 105480007 | ||||||
| chr14:105480029 | C | T | 1 | a0001c0001t0008 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*376C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 376 | chr14 | 105480029 | ||||||
| chr14:105480068 | C | T | 1 | a0001c0001t0007 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 8/8 | 415 | chr14 | 105480068 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105474918 | C | CCGCTCCC others(33): Show |
1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.43+15_43+54dupGCTC others(36): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105474918 | ||||||
| chr14:105474937 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.43+32T>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105474937 | |||||||
| chr14:105475035 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.43+130G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475035 | |||||||
| chr14:105475040 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+135C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475040 | |||||||
| chr14:105475157 | G | A | 1 | a0001c0003t0001g0022 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.43+252G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475157 | |||||||
| chr14:105475275 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+370C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475275 | |||||||
| chr14:105475316 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.43+411T>C | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475316 | |||||||
| chr14:105475323 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.43+418C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475323 | |||||||
| chr14:105475422 | CTG | C | 17 | a0001c0002t0001g0008 a0001c0002t0001g0024 a0001c0002t0001g0025 others(14): Show |
19 | HG00735.hp2 HG01167.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.43+519_43+520delGT | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105475422 | ||||||
| chr14:105475429 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.43+524G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475429 | |||||||
| chr14:105475457 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+552C>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475457 | |||||||
| chr14:105475474 | TCCCGACG others(33): Show |
T | 1 | a0001c0001t0001g0040 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.43+570_43+609delCC others(38): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475474 | |||||||
| chr14:105475847 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0041 |
3 | HG03491.hp1 HG03492.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.43+942G>C | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105475847 | |||||||
| chr14:105476005 | C | G | 1 | a0001c0001t0001g0251 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.43+1100C>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476005 | |||||||
| chr14:105476010 | C | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG00741.hp2 HG01123.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+1105C>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476010 | |||||||
| chr14:105476021 | GACCGGAT others(33): Show |
G | 1 | a0001c0001t0001g0246 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.43+1117_43+1156del others(40): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476021 | |||||||
| chr14:105476098 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.43+1193A>C | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476098 | |||||||
| chr14:105476119 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.43+1214C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476119 | |||||||
| chr14:105476323 | C | T | 1 | a0001c0001t0007g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43+1418C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476323 | |||||||
| chr14:105476423 | AACCCAGG others(11): Show |
A | 1 | a0001c0001t0001g0242 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.43+1519_43+1536del others(18): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476423 | |||||||
| chr14:105476494 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0003t0001g0022 others(1): Show |
4 | HG00639.hp2 HG02976.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+1589G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476494 | |||||||
| chr14:105476714 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.44-1552C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476714 | |||||||
| chr14:105476793 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.44-1473C>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476793 | |||||||
| chr14:105476889 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG01257.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.44-1377C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476889 | |||||||
| chr14:105476935 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.44-1331G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476935 | |||||||
| chr14:105476940 | ACCCTTGG others(13): Show |
A | 1 | a0001c0001t0001g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.44-1325_44-1306del others(20): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105476940 | |||||||
| chr14:105477022 | TGCTGAGA others(12): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.44-1243_44-1225del others(19): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477022 | |||||||
| chr14:105477024 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.44-1242C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477024 | |||||||
| chr14:105477095 | G | GGTGGGCC others(10): Show |
1 | a0001c0002t0001g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.44-1169_44-1153dup others(17): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477095 | ||||||
| chr14:105477243 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.44-1023A>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477243 | |||||||
| chr14:105477261 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.44-1005G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477261 | |||||||
| chr14:105477312 | C | T | 1 | a0001c0001t0007g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-954C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477312 | |||||||
| chr14:105477342 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.44-924G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477342 | |||||||
| chr14:105477603 | T | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0003t0001g0022 others(1): Show |
4 | HG00639.hp2 HG02976.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-663T>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477603 | |||||||
| chr14:105477662 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.44-604G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477662 | |||||||
| chr14:105477668 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0241 |
3 | HG02109.hp1 HG02559.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.44-598G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477668 | |||||||
| chr14:105477670 | C | CGG | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0241 |
3 | HG02109.hp1 HG02559.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.44-596_44-595insGG | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477670 | |||||||
| chr14:105477671 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0241 |
3 | HG02109.hp1 HG02559.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.44-595A>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477671 | |||||||
| chr14:105477679 | G | GTGGGGAA others(1493): Show |
1 | a0001c0001t0001g0041 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.44-587_44-586insTG others(1498): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477679 | |||||||
| chr14:105477679 | G | GTGGGGAA others(1321): Show |
1 | a0001c0001t0001g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.44-587_44-586insTG others(1326): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477679 | |||||||
| chr14:105477680 | G | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.44-586G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477680 | |||||||
| chr14:105477692 | T | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.44-574T>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477692 | |||||||
| chr14:105477698 | TC | T | 35 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0220 others(32): Show |
41 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.44-567delC | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477698 | |||||||
| chr14:105477699 | C | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.44-567C>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477699 | |||||||
| chr14:105477700 | T | G | 35 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0220 others(32): Show |
41 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.44-566T>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477700 | |||||||
| chr14:105477702 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.44-564A>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477702 | |||||||
| chr14:105477719 | G | GGGGAAGC others(2569): Show |
1 | a0001c0001t0001g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2574): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2115): Show |
1 | a0001c0001t0001g0238 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2120): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3189): Show |
1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3194): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2388): Show |
1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2393): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1723): Show |
1 | a0001c0001t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1728): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(905): Show |
1 | a0001c0001t0001g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(910): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1758): Show |
1 | a0001c0002t0001g0024 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1763): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1869): Show |
1 | a0001c0002t0001g0025 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1874): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2716): Show |
1 | a0001c0001t0001g0235 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2721): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(4634): Show |
1 | a0001c0001t0001g0220 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(4639): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(4250): Show |
1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(4255): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1713): Show |
1 | a0001c0001t0001g0222 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1718): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(5525): Show |
1 | a0001c0001t0001g0223 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(5530): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2208): Show |
1 | a0001c0002t0001g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2213): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2805): Show |
1 | a0001c0001t0002g0224 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2810): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2543): Show |
1 | a0001c0001t0002g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2548): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2525): Show |
1 | a0001c0001t0002g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2530): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2540): Show |
1 | a0001c0001t0002g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2545): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2543): Show |
1 | a0001c0001t0002g0228 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2548): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2543): Show |
1 | a0001c0001t0002g0229 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2548): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1584): Show |
1 | a0001c0001t0002g0230 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1589): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2909): Show |
1 | a0001c0001t0002g0231 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2914): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2543): Show |
1 | a0001c0001t0002g0005 | 5 | HG02615.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2548): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2267): Show |
1 | a0001c0002t0001g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2272): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2175): Show |
1 | a0001c0002t0001g0028 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2180): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2225): Show |
1 | a0001c0002t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2230): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2227): Show |
1 | a0001c0002t0001g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2232): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2227): Show |
2 | a0001c0002t0001g0008 a0001c0002t0001g0031 |
4 | HG02622.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2232): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2156): Show |
1 | a0001c0002t0001g0032 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2161): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3066): Show |
1 | a0001c0002t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3071): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2780): Show |
1 | a0001c0002t0001g0039 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2785): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2174): Show |
1 | a0001c0002t0001g0034 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2179): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2209): Show |
1 | a0001c0002t0001g0035 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2214): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2209): Show |
1 | a0001c0002t0001g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2214): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2360): Show |
1 | a0001c0002t0001g0037 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2365): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2229): Show |
1 | a0001c0002t0001g0038 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2234): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1747): Show |
1 | a0001c0001t0010g0232 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1752): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1009): Show |
1 | a0001c0001t0002g0233 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1014): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1435): Show |
1 | a0001c0001t0001g0072 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1440): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3893): Show |
1 | a0001c0001t0007g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3898): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3248): Show |
1 | a0001c0001t0001g0051 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3253): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3159): Show |
1 | a0001c0001t0003g0052 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3164): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3225): Show |
1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3230): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3205): Show |
1 | a0001c0001t0001g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3210): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3355): Show |
1 | a0001c0001t0001g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3360): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3337): Show |
1 | a0001c0001t0001g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3342): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3203): Show |
1 | a0001c0001t0001g0057 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3208): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2940): Show |
1 | a0001c0001t0003g0021 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2945): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3166): Show |
1 | a0002c0004t0001g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3171): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3405): Show |
1 | a0001c0001t0001g0237 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3410): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3232): Show |
1 | a0001c0001t0001g0059 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3237): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3193): Show |
1 | a0001c0001t0001g0244 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3198): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3224): Show |
1 | a0001c0001t0001g0060 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3229): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3204): Show |
1 | a0001c0001t0001g0061 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3209): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3223): Show |
1 | a0001c0001t0001g0062 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3228): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3534): Show |
1 | a0001c0001t0001g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3539): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2374): Show |
1 | a0001c0002t0001g0012 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2379): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2358): Show |
1 | a0001c0001t0001g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2363): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2354): Show |
1 | a0001c0001t0001g0065 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2359): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3265): Show |
1 | a0001c0001t0001g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3270): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3266): Show |
1 | a0001c0001t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3271): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3287): Show |
1 | a0001c0001t0001g0068 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3292): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2410): Show |
1 | a0001c0001t0001g0069 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2415): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3237): Show |
1 | a0001c0001t0003g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3242): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(795): Show |
1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(800): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(808): Show |
1 | a0001c0001t0001g0041 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(813): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2717): Show |
1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2722): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2497): Show |
1 | a0001c0001t0001g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2502): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1438): Show |
1 | a0001c0001t0001g0075 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1443): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1696): Show |
1 | a0001c0001t0001g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1701): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1497): Show |
1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1502): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2607): Show |
1 | a0001c0001t0001g0077 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2612): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2567): Show |
1 | a0001c0001t0001g0246 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2572): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2648): Show |
1 | a0001c0001t0001g0078 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2653): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1451): Show |
1 | a0001c0001t0001g0079 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1456): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2714): Show |
1 | a0001c0001t0001g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2719): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2733): Show |
1 | a0001c0001t0001g0081 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2738): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2734): Show |
1 | a0001c0001t0001g0082 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2739): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2569): Show |
1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2574): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2549): Show |
1 | a0001c0001t0001g0084 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2554): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2604): Show |
1 | a0001c0001t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2609): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2551): Show |
1 | a0001c0001t0001g0086 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2556): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2533): Show |
1 | a0001c0001t0001g0087 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2538): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2975): Show |
1 | a0001c0001t0001g0088 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2980): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2533): Show |
1 | a0001c0001t0001g0089 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2538): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2551): Show |
1 | a0001c0001t0001g0090 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2556): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2551): Show |
1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2556): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2750): Show |
1 | a0003c0007t0001g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2755): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2511): Show |
1 | a0001c0001t0001g0093 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2516): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2545): Show |
1 | a0001c0001t0004g0094 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2550): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2485): Show |
1 | a0001c0001t0001g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2490): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2758): Show |
1 | a0001c0006t0001g0096 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2763): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3672): Show |
1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3677): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2622): Show |
1 | a0001c0001t0001g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2627): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2624): Show |
1 | a0001c0001t0001g0098 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2629): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2549): Show |
1 | a0001c0001t0001g0099 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2554): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2624): Show |
1 | a0001c0001t0001g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2629): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2547): Show |
1 | a0001c0001t0004g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2552): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2547): Show |
1 | a0001c0001t0001g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2552): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2548): Show |
1 | a0001c0001t0001g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2553): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2531): Show |
1 | a0001c0001t0001g0104 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2536): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2547): Show |
1 | a0001c0001t0001g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2552): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2547): Show |
1 | a0001c0001t0001g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2552): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2548): Show |
1 | a0001c0001t0001g0107 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2553): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1599): Show |
1 | a0001c0001t0001g0108 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1604): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2513): Show |
1 | a0001c0001t0001g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2518): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2515): Show |
1 | a0001c0001t0001g0110 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2520): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2719): Show |
1 | a0001c0001t0001g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2724): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2189): Show |
1 | a0001c0001t0001g0112 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2194): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2289): Show |
1 | a0001c0001t0001g0113 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2294): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2000): Show |
1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2005): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2272): Show |
1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2277): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2308): Show |
1 | a0001c0001t0001g0116 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2313): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1996): Show |
1 | a0001c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2001): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2189): Show |
1 | a0001c0001t0001g0118 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2194): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2306): Show |
1 | a0001c0001t0001g0119 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2311): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1997): Show |
1 | a0001c0001t0001g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2002): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2034): Show |
1 | a0001c0001t0001g0121 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2039): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2016): Show |
1 | a0001c0001t0001g0122 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2021): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2309): Show |
1 | a0001c0001t0001g0011 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2314): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1924): Show |
1 | a0001c0001t0001g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1929): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2016): Show |
1 | a0001c0001t0001g0013 | 2 | NA19066.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2021): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2016): Show |
1 | a0001c0001t0001g0003 | 5 | HG00642.hp1 HG00738.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2021): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2176): Show |
1 | a0001c0001t0001g0124 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2181): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1998): Show |
1 | a0001c0001t0001g0014 | 2 | NA18952.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2003): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2289): Show |
1 | a0001c0001t0001g0239 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2294): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2016): Show |
1 | a0001c0001t0001g0015 | 2 | HG01074.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2021): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2290): Show |
1 | a0001c0001t0001g0240 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2295): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(908): Show |
1 | a0001c0001t0001g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(913): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2017): Show |
1 | a0001c0001t0001g0126 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2022): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2246): Show |
1 | a0001c0001t0001g0127 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2251): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2533): Show |
1 | a0001c0001t0001g0128 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2538): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2117): Show |
1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2122): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2601): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2606): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2515): Show |
1 | a0001c0001t0001g0132 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2520): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1979): Show |
1 | a0001c0001t0001g0133 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1984): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2698): Show |
1 | a0001c0001t0001g0134 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2703): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2697): Show |
1 | a0001c0001t0001g0247 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2702): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2699): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0248 |
2 | HG02145.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2704): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2717): Show |
1 | a0001c0001t0001g0249 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2722): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2717): Show |
1 | a0001c0001t0001g0250 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2722): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2737): Show |
1 | a0001c0001t0001g0135 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2742): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1813): Show |
1 | a0001c0001t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1818): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2717): Show |
1 | a0001c0001t0001g0016 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(2722): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2873): Show |
1 | a0001c0001t0001g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2878): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2699): Show |
1 | a0001c0001t0001g0241 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2704): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2740): Show |
1 | a0001c0001t0001g0047 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2745): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2513): Show |
1 | a0001c0001t0001g0138 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2518): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2832): Show |
1 | a0001c0001t0001g0048 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2837): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3263): Show |
1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3268): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2031): Show |
1 | a0001c0001t0001g0251 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2036): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1830): Show |
1 | a0001c0001t0001g0139 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1835): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1945): Show |
1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1950): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1998): Show |
1 | a0001c0001t0001g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2003): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2036): Show |
1 | a0001c0001t0011g0142 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2041): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2018): Show |
1 | a0001c0001t0001g0143 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2023): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2463): Show |
1 | a0001c0001t0001g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2468): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1998): Show |
1 | a0001c0001t0001g0020 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2003): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1951): Show |
1 | a0001c0001t0001g0145 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1956): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1998): Show |
1 | a0001c0001t0001g0146 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2003): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2739): Show |
1 | a0001c0001t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2744): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2061): Show |
1 | a0001c0001t0001g0044 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2066): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2532): Show |
1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2537): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1461): Show |
1 | a0001c0001t0001g0148 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1466): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1489): Show |
1 | a0001c0001t0001g0149 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1494): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1510): Show |
1 | a0001c0001t0001g0040 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1515): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0242 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1851): Show |
1 | a0001c0001t0001g0150 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1856): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1375): Show |
1 | a0001c0001t0001g0151 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1380): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1643): Show |
1 | a0001c0001t0001g0152 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1648): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1998): Show |
1 | a0001c0001t0001g0153 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2003): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1453): Show |
1 | a0001c0001t0001g0017 | 2 | HG01074.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1458): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2732): Show |
1 | a0001c0001t0001g0216 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2737): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1471): Show |
1 | a0001c0001t0001g0154 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1476): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1471): Show |
1 | a0001c0001t0001g0155 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1476): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1472): Show |
2 | a0001c0001t0001g0009 a0001c0001t0006g0009 |
3 | HG02056.hp2 NA19056.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1477): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1491): Show |
1 | a0001c0001t0001g0156 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1496): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1491): Show |
1 | a0001c0001t0001g0157 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1496): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1472): Show |
1 | a0001c0001t0001g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1477): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1750): Show |
1 | a0001c0001t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1755): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1472): Show |
1 | a0001c0001t0001g0160 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1477): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0161 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1474): Show |
1 | a0001c0001t0001g0162 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1479): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1472): Show |
1 | a0001c0001t0001g0163 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1477): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0165 |
12 | HG00408.hp1 HG02056.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2067): Show |
1 | a0001c0001t0001g0166 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2072): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
2 | a0001c0001t0001g0001 a0001c0001t0008g0001 |
24 | HG00099.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1493): Show |
1 | a0001c0001t0001g0167 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1498): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0018 | 2 | NA18955.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1454): Show |
1 | a0001c0001t0001g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1459): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1472): Show |
1 | a0001c0001t0001g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1477): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0045 |
4 | HG01993.hp1 HG02257.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(3280): Show |
1 | a0001c0001t0001g0171 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(3285): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0172 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1436): Show |
1 | a0001c0001t0001g0173 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1441): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1434): Show |
1 | a0001c0001t0001g0174 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1439): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1436): Show |
1 | a0001c0001t0001g0006 | 4 | HG02129.hp1 HG02135.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1441): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1472): Show |
1 | a0001c0001t0001g0175 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1477): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1437): Show |
1 | a0001c0001t0001g0177 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1442): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0178 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1419): Show |
1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1424): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1527): Show |
1 | a0001c0001t0001g0180 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1532): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0181 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0007 | 4 | HG03834.hp1 NA18942.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1493): Show |
1 | a0001c0001t0001g0182 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1498): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1435): Show |
1 | a0001c0001t0001g0183 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1440): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0245 |
2 | HG02080.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1884): Show |
1 | a0001c0001t0001g0019 | 2 | HG01934.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.44-544_44-543insAA others(1889): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1475): Show |
1 | a0001c0001t0001g0185 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1480): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1488): Show |
1 | a0001c0001t0001g0186 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1493): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1474): Show |
1 | a0001c0001t0001g0188 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1479): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0009g0189 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0190 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0191 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1436): Show |
1 | a0001c0001t0001g0192 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1441): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1662): Show |
1 | a0001c0001t0001g0193 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1667): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1676): Show |
1 | a0001c0001t0001g0194 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1681): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0253 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1474): Show |
1 | a0001c0001t0001g0198 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1479): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0199 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1584): Show |
1 | a0001c0001t0001g0200 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1589): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1473): Show |
1 | a0001c0001t0001g0201 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1478): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2406): Show |
1 | a0001c0005t0001g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2411): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1475): Show |
1 | a0001c0001t0001g0203 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1480): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1455): Show |
1 | a0001c0001t0001g0204 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1460): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1436): Show |
1 | a0001c0001t0001g0205 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1441): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1478): Show |
1 | a0001c0001t0001g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1483): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1361): Show |
1 | a0001c0001t0001g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1366): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2547): Show |
1 | a0001c0001t0004g0208 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2552): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(2853): Show |
1 | a0001c0001t0001g0209 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2858): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGC others(1454): Show |
1 | a0001c0001t0005g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(1459): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGAAGG others(2028): Show |
1 | a0001c0001t0001g0211 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2033): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGGAAG others(3167): Show |
1 | a0001c0001t0001g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.44-543_44-542insAA others(3172): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGGAAG others(3089): Show |
1 | a0001c0003t0001g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.44-543_44-542insAA others(3094): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGGAAG others(3185): Show |
1 | a0001c0003t0001g0022 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.44-543_44-542insAA others(3190): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGGAAG others(2582): Show |
1 | a0001c0001t0001g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44-543_44-542insAA others(2587): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGGAAG others(2495): Show |
1 | a0001c0001t0001g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.44-543_44-542insAA others(2500): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GGGGGAAG others(1436): Show |
1 | a0001c0001t0001g0214 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.44-543_44-542insAA others(1441): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477719 | ||||||
| chr14:105477719 | G | GTGGGGAA others(3150): Show |
1 | a0001c0001t0001g0236 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.44-547_44-546insTG others(3155): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477719 | |||||||
| chr14:105477720 | G | GGGAAGCG others(2031): Show |
1 | a0001c0001t0001g0197 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.44-544_44-543insAA others(2036): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477720 | ||||||
| chr14:105477736 | T | TGGGG | 25 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(22): Show |
26 | HG01069.hp2 HG01168.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.44-528_44-527insGG others(2): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477736 | ||||||
| chr14:105477746 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0050 others(47): Show |
56 | HG00408.hp1 HG00544.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.44-520C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477746 | |||||||
| chr14:105477753 | G | C | 20 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(17): Show |
20 | HG00544.hp1 HG00673.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.44-513G>C | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477753 | |||||||
| chr14:105477805 | GGGGGGAG others(10): Show |
G | 1 | a0001c0001t0007g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.44-448_44-432delCG others(15): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477805 | ||||||
| chr14:105477854 | A | AGGCAGGT others(11): Show |
18 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0054 others(15): Show |
18 | HG01069.hp2 HG01168.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-333_44-316dupTG others(16): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477854 | ||||||
| chr14:105477854 | A | AGGCAGGT others(65): Show |
1 | a0001c0001t0001g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.44-387_44-316dupTG others(70): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477854 | ||||||
| chr14:105477854 | AGGCAGGT others(11): Show |
A | 10 | a0001c0001t0001g0044 a0001c0001t0001g0130 a0001c0001t0001g0212 others(7): Show |
10 | HG02258.hp1 HG02451.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.44-333_44-316delTG others(16): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477854 | ||||||
| chr14:105477854 | AGGCAGGT others(29): Show |
A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0143 others(2): Show |
5 | HG00639.hp2 HG02976.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-351_44-316delTG others(34): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477854 | ||||||
| chr14:105477854 | AGGCAGGT others(47): Show |
A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.44-369_44-316delTG others(52): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 105477854 | ||||||
| chr14:105477933 | TGTTGGAG others(11): Show |
T | 29 | a0001c0001t0001g0219 a0001c0001t0001g0254 a0001c0001t0002g0005 others(26): Show |
35 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.44-332_44-315delGT others(16): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477933 | |||||||
| chr14:105477951 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0031 |
3 | HG03225.hp2 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.44-315C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477951 | |||||||
| chr14:105477953 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.44-313C>G | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105477953 | |||||||
| chr14:105478052 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.44-214G>C | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105478052 | |||||||
| chr14:105478142 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.44-124C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105478142 | |||||||
| chr14:105478234 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.44-32G>C | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105478234 | |||||||
| chr14:105478234 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.44-32G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 1/7 | chr14 | 105478234 | |||||||
| chr14:105478424 | G | T | 1 | a0001c0001t0009g0189 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.139-26G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 2/7 | chr14 | 105478424 | |||||||
| chr14:105478583 | G | T | 12 | a0001c0001t0001g0219 a0001c0001t0002g0005 a0001c0001t0002g0224 others(9): Show |
16 | HG01167.hp1 HG01891.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.196+76G>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 3/7 | chr14 | 105478583 | |||||||
| chr14:105478928 | G | A | 15 | a0001c0002t0001g0008 a0001c0002t0001g0012 a0001c0002t0001g0026 others(12): Show |
18 | HG01167.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.338-51G>A | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 4/7 | chr14 | 105478928 | |||||||
| chr14:105479117 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | splice_region_variant&intron_variant | LOW | c.407-8C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 5/7 | chr14 | 105479117 | |||||||
| chr14:105479316 | TTC | T | 18 | a0001c0002t0001g0008 a0001c0002t0001g0012 a0001c0002t0001g0024 others(15): Show |
21 | HG00735.hp2 HG01167.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.501+99_501+100delC others(1): Show |
CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 105479316 | ||||||
| chr14:105479554 | C | T | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.560-32C>T | CRIP2 | ENSG00000182809.11 | transcript | ENST00000329146.9 | protein_coding | 7/7 | chr14 | 105479554 |