Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1990 |
| ensemblid | ENSG00000139610.2 |
| hgncid | 3308 |
| symbol | CELA1 |
| name | chymotrypsin like elastase 1 |
| refseq_nuc | NM_001971.6 |
| refseq_prot | NP_001962.3 |
| ensembl_nuc | ENST00000293636.2 |
| ensembl_prot | ENSP00000293636.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 51328442 |
| end | 51346679 |
| strand | - |
| ver | v1.2 |
| region | chr12:51328442-51346679 |
| region5000 | chr12:51323442-51351679 |
| regionname0 | CELA1_chr12_51328442_51346679 |
| regionname5000 | CELA1_chr12_51323442_51351679 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 18 | 211 | 41 | 40 | 106 | 8 | 16 | 79 | CELA1_chr12_51323442_51351679 | CELA1 | MLRFL others(13): Show |
chr12 | 51323442 | 51351679 |
| a0002 | 1/1 | 258 | 189 | 48 | 34 | 76 | 6 | 23 | 57 | CELA1_chr12_51323442_51351679 | CELA1 | MLVLY others(253): Show |
chr12 | 51323442 | 51351679 |
| a0003 | 0/0 | 258 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | MLVLY others(253): Show |
chr12 | 51323442 | 51351679 |
| a0004 | 0/0 | 258 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | MLVLY others(253): Show |
chr12 | 51323442 | 51351679 |
| a0005 | 0/0 | 258 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | MLVLY others(253): Show |
chr12 | 51323442 | 51351679 |
| a0006 | 0/0 | 258 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | MLVLY others(253): Show |
chr12 | 51323442 | 51351679 |
| a0007 | 0/0 | 258 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | MLVLY others(253): Show |
chr12 | 51323442 | 51351679 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 773 | 76 | 8 | 17 | 49 | 0 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(768): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0003 | 0/0 | 773 | 47 | 14 | 2 | 31 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(768): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0004 | 0/0 | 774 | 42 | 8 | 16 | 4 | 5 | 9 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0005 | 0/0 | 773 | 35 | 6 | 3 | 21 | 3 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(768): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0006 | 0/0 | 773 | 6 | 5 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(768): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0007 | 0/0 | 774 | 3 | 0 | 0 | 0 | 0 | 3 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0009 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0001c0010 | 0/0 | 773 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(768): Show |
chr12 | 51323442 | 51351679 | ||
| a0002c0001 | 1/1 | 774 | 189 | 48 | 34 | 76 | 6 | 23 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0003c0008 | 0/0 | 774 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0004c0011 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0005c0012 | 0/0 | 774 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0006c0013 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 | ||
| a0007c0014 | 0/0 | 774 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | ATGCT others(769): Show |
chr12 | 51323442 | 51351679 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 0/0 | 952 | 76 | 8 | 17 | 49 | 0 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(947): Show |
chr12 | 51323442 | 51351679 |
| a0001c0003t0001 | 0/0 | 952 | 33 | 2 | 0 | 31 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(947): Show |
chr12 | 51323442 | 51351679 |
| a0001c0003t0002 | 0/0 | 952 | 14 | 12 | 2 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(947): Show |
chr12 | 51323442 | 51351679 |
| a0001c0004t0002 | 0/0 | 953 | 42 | 8 | 16 | 4 | 5 | 9 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0001c0005t0001 | 0/0 | 952 | 35 | 6 | 3 | 21 | 3 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(947): Show |
chr12 | 51323442 | 51351679 |
| a0001c0006t0001 | 0/0 | 952 | 6 | 5 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(947): Show |
chr12 | 51323442 | 51351679 |
| a0001c0007t0002 | 0/0 | 953 | 3 | 0 | 0 | 0 | 0 | 3 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0001c0009t0002 | 0/0 | 953 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0001c0010t0002 | 0/0 | 952 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(947): Show |
chr12 | 51323442 | 51351679 |
| a0002c0001t0001 | 0/1 | 953 | 172 | 33 | 34 | 75 | 6 | 23 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0002c0001t0002 | 1/0 | 953 | 17 | 15 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0003c0008t0001 | 0/0 | 953 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0004c0011t0001 | 0/0 | 953 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0005c0012t0001 | 0/0 | 953 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0006c0013t0002 | 0/0 | 953 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| a0007c0014t0001 | 0/0 | 953 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | TTGGT others(948): Show |
chr12 | 51323442 | 51351679 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0004 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0005 | 0/0 | 12 | 0 | 8 | 4 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0013 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0002 | 0/0 | 16 | 0 | 0 | 16 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0012 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0006 | 0/0 | 11 | 3 | 4 | 0 | 3 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0007 | 0/0 | 10 | 0 | 5 | 2 | 0 | 3 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0024 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0004t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0003 | 0/0 | 13 | 3 | 1 | 9 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0005t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0006t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0007t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0007t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0009t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0001c0010t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0001 | 0/0 | 20 | 8 | 5 | 5 | 1 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0008 | 0/0 | 10 | 1 | 1 | 7 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0009 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0010 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0011 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0014 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0019 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0031 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0032 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0002c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0003c0008t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0003c0008t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0004c0011t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0005c0012t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0006c0013t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| a0007c0014t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0001 | EUR | GBR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00099 | hp2 | a0001 | c0004 | t0002 | g0006 | EUR | GBR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0199 | EUR | GBR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00140 | hp2 | a0001 | c0005 | t0001 | g0023 | EUR | GBR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0126 | EUR | FIN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0049 | EUR | FIN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0149 | EUR | FIN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00323 | hp2 | a0002 | c0001 | t0001 | g0148 | EUR | FIN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00423 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00438 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0210 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00597 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | CHS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00639 | hp1 | a0002 | c0001 | t0001 | g0019 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00639 | hp2 | a0001 | c0004 | t0002 | g0007 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00642 | hp1 | a0001 | c0004 | t0002 | g0022 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00733 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00735 | hp2 | a0002 | c0001 | t0001 | g0044 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00738 | hp1 | a0001 | c0004 | t0002 | g0007 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0031 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0043 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01070 | hp1 | a0002 | c0001 | t0001 | g0174 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01070 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01071 | hp1 | a0001 | c0004 | t0002 | g0006 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0008 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01081 | hp1 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01099 | hp2 | a0001 | c0004 | t0002 | g0081 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01106 | hp1 | a0001 | c0005 | t0001 | g0003 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0031 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0046 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0041 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0012 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01168 | hp2 | a0001 | c0005 | t0001 | g0023 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01169 | hp2 | a0002 | c0001 | t0001 | g0154 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01175 | hp1 | a0002 | c0001 | t0001 | g0133 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01175 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01243 | hp1 | a0004 | c0011 | t0001 | g0124 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0198 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0152 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01256 | hp2 | a0001 | c0004 | t0002 | g0074 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01257 | hp1 | a0001 | c0004 | t0002 | g0006 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0019 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0019 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01258 | hp2 | a0001 | c0004 | t0002 | g0025 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01261 | hp1 | a0001 | c0004 | t0002 | g0022 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0030 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01346 | hp2 | a0001 | c0006 | t0001 | g0018 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01361 | hp2 | a0001 | c0009 | t0002 | g0073 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01433 | hp1 | a0005 | c0012 | t0001 | g0153 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01433 | hp2 | a0001 | c0004 | t0002 | g0007 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0010 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0007 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01515 | hp1 | a0001 | c0005 | t0001 | g0057 | EUR | IBS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01515 | hp2 | a0001 | c0004 | t0002 | g0006 | EUR | IBS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01516 | hp1 | a0001 | c0004 | t0002 | g0024 | EUR | IBS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01516 | hp2 | a0001 | c0004 | t0002 | g0022 | EUR | IBS | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01884 | hp1 | a0002 | c0001 | t0002 | g0159 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0010 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01978 | hp1 | a0001 | c0004 | t0002 | g0025 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0104 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0170 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01993 | hp2 | a0001 | c0004 | t0002 | g0082 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0142 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0146 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02040 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02055 | hp1 | a0002 | c0001 | t0001 | g0130 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02055 | hp2 | a0002 | c0001 | t0002 | g0162 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02056 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0200 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02129 | hp2 | a0001 | c0005 | t0001 | g0061 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02132 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0014 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02145 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0010 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | CDX | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | CDX | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02165 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | CDX | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02165 | hp2 | a0001 | c0004 | t0002 | g0007 | EAS | CDX | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0177 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02258 | hp1 | a0002 | c0001 | t0002 | g0047 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02258 | hp2 | a0001 | c0003 | t0002 | g0037 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02280 | hp1 | a0002 | c0001 | t0002 | g0020 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0054 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0001 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02451 | hp1 | a0002 | c0001 | t0001 | g0123 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02451 | hp2 | a0002 | c0001 | t0001 | g0141 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02572 | hp1 | a0002 | c0001 | t0002 | g0161 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02602 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02615 | hp1 | a0001 | c0004 | t0002 | g0006 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02615 | hp2 | a0001 | c0004 | t0002 | g0036 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02630 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0172 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02647 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02647 | hp2 | a0006 | c0013 | t0002 | g0187 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0031 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02683 | hp2 | a0001 | c0004 | t0002 | g0072 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02717 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0006 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02723 | hp2 | a0002 | c0001 | t0002 | g0184 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02735 | hp1 | a0001 | c0007 | t0002 | g0034 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02735 | hp2 | a0002 | c0001 | t0001 | g0173 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0066 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02809 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0003 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02818 | hp2 | a0002 | c0001 | t0001 | g0157 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0156 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0038 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0014 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02897 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0139 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02965 | hp1 | a0002 | c0001 | t0002 | g0020 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02965 | hp2 | a0002 | c0001 | t0002 | g0163 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0058 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0063 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02976 | hp1 | a0001 | c0004 | t0002 | g0071 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02976 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0176 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03017 | hp2 | a0002 | c0001 | t0001 | g0019 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0036 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0077 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03130 | hp1 | a0003 | c0008 | t0001 | g0189 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03130 | hp2 | a0001 | c0004 | t0002 | g0024 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0080 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03139 | hp2 | a0002 | c0001 | t0002 | g0045 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03195 | hp1 | a0002 | c0001 | t0002 | g0047 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0097 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03209 | hp1 | a0002 | c0001 | t0002 | g0183 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0003 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0155 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03225 | hp2 | a0002 | c0001 | t0001 | g0195 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03239 | hp1 | a0002 | c0001 | t0001 | g0192 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03239 | hp2 | a0001 | c0004 | t0002 | g0007 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03453 | hp1 | a0002 | c0001 | t0002 | g0160 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0046 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03486 | hp2 | a0002 | c0001 | t0002 | g0020 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03490 | hp1 | a0001 | c0004 | t0002 | g0033 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0175 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03491 | hp1 | a0002 | c0001 | t0001 | g0150 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0009 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03492 | hp1 | a0001 | c0004 | t0002 | g0033 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0131 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0037 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03516 | hp2 | a0002 | c0001 | t0001 | g0144 | AFR | ESN | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0136 | AFR | GWD | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0132 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03669 | hp2 | a0001 | c0004 | t0002 | g0007 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03688 | hp1 | a0007 | c0014 | t0001 | g0196 | SAS | STU | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0201 | SAS | STU | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0180 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0053 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0134 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03710 | hp2 | a0001 | c0007 | t0002 | g0070 | SAS | PJL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0181 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03831 | hp2 | a0001 | c0005 | t0001 | g0062 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03834 | hp1 | a0001 | c0007 | t0002 | g0034 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0135 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0140 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03927 | hp2 | a0001 | c0004 | t0002 | g0025 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0178 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0194 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0147 | SAS | STU | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG04115 | hp2 | a0001 | c0004 | t0002 | g0007 | SAS | STU | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG04184 | hp1 | a0001 | c0004 | t0002 | g0035 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0106 | SAS | BEB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0009 | SAS | STU | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0166 | SAS | STU | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | YRI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18522 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | YRI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | CHB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0113 | EAS | CHB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0202 | EAS | CHB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0076 | AFR | YRI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18906 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | YRI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18940 | hp2 | a0001 | c0005 | t0001 | g0052 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18941 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18942 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18943 | hp1 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18944 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18947 | hp1 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18948 | hp2 | a0002 | c0001 | t0001 | g0171 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18949 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18951 | hp1 | a0001 | c0005 | t0001 | g0051 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0206 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18961 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0186 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18963 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18964 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0205 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0191 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18973 | hp2 | a0001 | c0004 | t0002 | g0035 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18978 | hp2 | a0001 | c0005 | t0001 | g0056 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18979 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0193 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0208 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18988 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18990 | hp2 | a0001 | c0004 | t0002 | g0024 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18991 | hp1 | a0001 | c0005 | t0001 | g0050 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18992 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18992 | hp2 | a0002 | c0001 | t0001 | g0143 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0207 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18994 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18995 | hp2 | a0001 | c0005 | t0001 | g0059 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18997 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18997 | hp2 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0041 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19003 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19007 | hp2 | a0001 | c0010 | t0002 | g0075 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0168 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19011 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19012 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19012 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19030 | hp1 | a0003 | c0008 | t0001 | g0188 | AFR | LWK | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0060 | AFR | LWK | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19043 | hp1 | a0001 | c0003 | t0002 | g0079 | AFR | LWK | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19043 | hp2 | a0002 | c0001 | t0002 | g0020 | AFR | LWK | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19058 | hp2 | a0002 | c0001 | t0001 | g0203 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19060 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0008 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19063 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19063 | hp2 | a0001 | c0005 | t0001 | g0055 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0204 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19065 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19077 | hp2 | a0002 | c0001 | t0001 | g0167 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19078 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19084 | hp2 | a0002 | c0001 | t0002 | g0129 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19087 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19088 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19090 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0069 | AFR | YRI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA19240 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | YRI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0043 | AFR | ASW | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0014 | AFR | ASW | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0032 | EUR | TSI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20805 | hp2 | a0001 | c0004 | t0002 | g0006 | EUR | TSI | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0008 | SAS | GIH | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0013 | SAS | GIH | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01123 | hp1 | a0001 | c0005 | t0001 | g0023 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0007 | AMR | CLM | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0064 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02559 | hp1 | a0002 | c0001 | t0001 | g0158 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0078 | AFR | ACB | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03471 | hp1 | a0002 | c0001 | t0001 | g0001 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG03471 | hp2 | a0002 | c0001 | t0001 | g0001 | AFR | MSL | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG06807 | hp1 | a0002 | c0001 | t0002 | g0045 | AFR | USA | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | USA | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | USA | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| NA20300 | hp2 | a0001 | c0004 | t0002 | g0006 | AFR | USA | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0211 | REF | REF | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0002 | g0164 | REF | REF | CELA1_chr12_51323442_51351679 | CELA1 | chr12 | 51323442 | 51351679 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51329715 | T | C | 2 | a0001 a0003 |
43 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(40): Show |
missense_variant | MODERATE | c.728A>G | p.Gln243Arg | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/8 | 769/953 | 728/777 | 243/258 | chr12 | 51329715 | |||
| chr12:51329814 | A | AG | 1 | a0001 | 46 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
frameshift_variant | HIGH | c.628dupC | p.Leu210fs | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/8 | 669/953 | 628/777 | 210/258 | chr12 | 51329814 | |||
| chr12:51339948 | G | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.521C>T | p.Ala174Val | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/8 | 562/953 | 521/777 | 174/258 | chr12 | 51339948 | |||
| chr12:51341360 | C | T | 1 | a0001 | 3 | HG02735.hp1 HG03710.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.347G>A | p.Arg116His | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/8 | 388/953 | 347/777 | 116/258 | chr12 | 51341360 | |||
| chr12:51343778 | T | C | 1 | a0001 | 47 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(44): Show |
missense_variant | MODERATE | c.175A>G | p.Met59Val | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/8 | 216/953 | 175/777 | 59/258 | chr12 | 51343778 | |||
| chr12:51343823 | G | A | 3 | a0001 a0003 a0006 |
120 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(117): Show |
missense_variant | MODERATE | c.130C>T | p.Arg44Trp | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/8 | 171/953 | 130/777 | 44/258 | chr12 | 51343823 | |||
| chr12:51345841 | C | T | 1 | a0004 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.53G>A | p.Arg18His | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/8 | 94/953 | 53/777 | 18/258 | chr12 | 51345841 | |||
| chr12:51345856 | G | A | 1 | a0007 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.38C>T | p.Pro13Leu | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/8 | 79/953 | 38/777 | 13/258 | chr12 | 51345856 | |||
| chr12:51345864 | C | G | 1 | a0001 | 35 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
missense_variant | MODERATE | c.30G>C | p.Gln10His | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/8 | 71/953 | 30/777 | 10/258 | chr12 | 51345864 | |||
| chr12:51346625 | T | G | 1 | a0001 | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
missense_variant&splice_region_variant | MODERATE | c.14A>C | p.Tyr5Ser | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/8 | 55/953 | 14/777 | 5/258 | chr12 | 51346625 | |||
| chr12:51346626 | A | G | 1 | a0001 | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
missense_variant | MODERATE | c.13T>C | p.Tyr5His | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/8 | 54/953 | 13/777 | 5/258 | chr12 | 51346626 | |||
| chr12:51346628 | AG | A | 1 | a0001 | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
frameshift_variant | HIGH | c.10delC | p.Leu4fs | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/8 | 51/953 | 10/777 | 4/258 | chr12 | 51346628 | |||
| chr12:51346631 | A | C | 1 | a0001 | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
missense_variant | MODERATE | c.8T>G | p.Val3Gly | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/8 | 49/953 | 8/777 | 3/258 | chr12 | 51346631 | |||
| chr12:51346632 | C | G | 1 | a0001 | 211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
missense_variant | MODERATE | c.7G>C | p.Val3Leu | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/8 | 48/953 | 7/777 | 3/258 | chr12 | 51346632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51329684 | A | G | 1 | a0001c0009 | 1 | HG01361.hp2 | splice_region_variant&synonymous_variant | LOW | c.759T>C | p.Asn253Asn | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/8 | 800/953 | 759/777 | 253/258 | chr12 | 51329684 | |||
| chr12:51339950 | G | A | 5 | a0001c0002 a0001c0005 a0001c0006 others(2): Show |
120 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(117): Show |
synonymous_variant | LOW | c.519C>T | p.Tyr173Tyr | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/8 | 560/953 | 519/777 | 173/258 | chr12 | 51339950 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51328527 | C | T | 8 | a0001c0003t0001 a0001c0005t0001 a0001c0006t0001 others(5): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*50G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 8/8 | 50 | chr12 | 51328527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:51328625 | G | GT | 22 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(19): Show |
43 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.760-32dupA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51328625 | |||||||
| chr12:51328673 | G | A | 1 | a0001c0005t0001g0054 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.760-79C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51328673 | |||||||
| chr12:51328695 | T | C | 8 | a0001c0002t0002g0005 a0001c0002t0002g0039 a0001c0002t0002g0091 others(5): Show |
20 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.760-101A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51328695 | |||||||
| chr12:51328782 | G | A | 3 | a0001c0003t0001g0114 a0001c0003t0001g0115 a0001c0003t0001g0117 |
3 | NA18982.hp1 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.760-188C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51328782 | |||||||
| chr12:51328826 | A | G | 1 | a0002c0001t0002g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.760-232T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51328826 | |||||||
| chr12:51328849 | G | A | 17 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(14): Show |
46 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.760-255C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51328849 | |||||||
| chr12:51329011 | CT | C | 15 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(12): Show |
31 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.760-418delA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329011 | |||||||
| chr12:51329237 | CAGTG | C | 2 | a0002c0001t0001g0042 a0002c0001t0001g0145 |
3 | NA19003.hp2 NA19011.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.759+443_759+446del others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329237 | |||||||
| chr12:51329253 | C | CA | 69 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(66): Show |
144 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.759+430dupT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329253 | |||||||
| chr12:51329253 | CA | C | 12 | a0001c0003t0001g0068 a0001c0003t0001g0069 a0001c0003t0001g0119 others(9): Show |
12 | HG01070.hp1 HG01515.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.759+430delT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329253 | |||||||
| chr12:51329253 | CAA | C | 17 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(14): Show |
38 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.759+429_759+430del others(2): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329253 | |||||||
| chr12:51329344 | C | T | 97 | a0001c0003t0001g0068 a0001c0003t0001g0069 a0002c0001t0001g0001 others(94): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.759+340G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329344 | |||||||
| chr12:51329543 | AAGGAAGG others(47): Show |
A | 1 | a0001c0006t0001g0063 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.759+87_759+140delG others(53): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329543 | |||||||
| chr12:51329546 | G | T | 21 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(18): Show |
42 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.759+138C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 7/7 | chr12 | 51329546 | |||||||
| chr12:51329943 | A | G | 16 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(13): Show |
44 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.610-110T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51329943 | |||||||
| chr12:51329954 | C | T | 2 | a0001c0003t0002g0079 a0001c0003t0002g0080 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.610-121G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51329954 | |||||||
| chr12:51330043 | A | C | 1 | a0002c0001t0001g0138 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.610-210T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330043 | |||||||
| chr12:51330502 | T | C | 17 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(14): Show |
46 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.610-669A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330502 | |||||||
| chr12:51330661 | G | C | 1 | a0002c0001t0001g0180 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.610-828C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330661 | |||||||
| chr12:51330787 | G | A | 1 | a0001c0003t0002g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.610-954C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330787 | |||||||
| chr12:51330863 | G | T | 1 | a0002c0001t0001g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.610-1030C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330863 | |||||||
| chr12:51330894 | C | T | 1 | a0001c0002t0002g0100 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.610-1061G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330894 | |||||||
| chr12:51330969 | C | CA | 44 | a0001c0002t0002g0094 a0001c0002t0002g0102 a0001c0004t0002g0006 others(41): Show |
90 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.610-1137dupT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330969 | |||||||
| chr12:51330969 | CA | C | 24 | a0001c0002t0002g0004 a0001c0002t0002g0084 a0001c0002t0002g0088 others(21): Show |
51 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.610-1137delT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51330969 | |||||||
| chr12:51331017 | G | A | 2 | a0001c0003t0002g0079 a0001c0003t0002g0080 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.610-1184C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331017 | |||||||
| chr12:51331123 | TC | T | 104 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(101): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.610-1291delG | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331123 | |||||||
| chr12:51331161 | G | A | 1 | a0002c0001t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.610-1328C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331161 | |||||||
| chr12:51331273 | C | T | 1 | a0001c0002t0002g0087 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.610-1440G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331273 | |||||||
| chr12:51331351 | T | C | 1 | a0001c0002t0002g0106 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.610-1518A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331351 | |||||||
| chr12:51331573 | G | A | 1 | a0002c0001t0002g0184 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.610-1740C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331573 | |||||||
| chr12:51331641 | G | C | 2 | a0002c0001t0002g0045 a0002c0001t0002g0162 |
3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.610-1808C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331641 | |||||||
| chr12:51331751 | A | G | 47 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(44): Show |
93 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.610-1918T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331751 | |||||||
| chr12:51331847 | A | G | 2 | a0002c0001t0001g0136 a0002c0001t0001g0141 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.610-2014T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331847 | |||||||
| chr12:51331852 | A | G | 17 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(14): Show |
46 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.610-2019T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331852 | |||||||
| chr12:51331875 | T | C | 1 | a0002c0001t0001g0194 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.610-2042A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51331875 | |||||||
| chr12:51332156 | G | A | 1 | a0001c0002t0002g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.610-2323C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332156 | |||||||
| chr12:51332187 | T | A | 1 | a0002c0001t0001g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.610-2354A>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332187 | |||||||
| chr12:51332187 | T | TA | 25 | a0001c0002t0002g0038 a0001c0002t0002g0065 a0001c0003t0001g0116 others(22): Show |
47 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.610-2355dupT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332187 | |||||||
| chr12:51332187 | T | TAA | 31 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(28): Show |
65 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.610-2356_610-2355d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332187 | |||||||
| chr12:51332187 | T | TAAA | 6 | a0001c0002t0002g0026 a0001c0002t0002g0028 a0001c0002t0002g0087 others(3): Show |
10 | HG02071.hp1 HG02155.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.610-2357_610-2355d others(5): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332187 | |||||||
| chr12:51332187 | TA | T | 42 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(39): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.610-2355delT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332187 | |||||||
| chr12:51332271 | A | G | 2 | a0001c0005t0001g0057 a0001c0005t0001g0062 |
2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.610-2438T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332271 | |||||||
| chr12:51332286 | G | A | 207 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(204): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.610-2453C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332286 | |||||||
| chr12:51332393 | C | T | 4 | a0002c0001t0001g0173 a0002c0001t0001g0174 a0002c0001t0001g0178 others(1): Show |
4 | HG01070.hp1 HG02735.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-2560G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332393 | |||||||
| chr12:51332405 | C | CTG | 104 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(101): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.610-2573_610-2572i others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332405 | |||||||
| chr12:51332431 | A | G | 1 | a0001c0006t0001g0063 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610-2598T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332431 | |||||||
| chr12:51332448 | G | C | 2 | a0001c0003t0002g0079 a0001c0003t0002g0080 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.610-2615C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332448 | |||||||
| chr12:51332646 | C | T | 1 | a0002c0001t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.610-2813G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332646 | |||||||
| chr12:51332860 | AAAAC | A | 2 | a0001c0003t0002g0037 a0001c0003t0002g0066 |
3 | HG02258.hp2 HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.610-3031_610-3028d others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332860 | |||||||
| chr12:51332960 | C | T | 2 | a0002c0001t0001g0168 a0002c0001t0001g0169 |
2 | NA19009.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.610-3127G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51332960 | |||||||
| chr12:51333040 | C | T | 17 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(14): Show |
35 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.610-3207G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333040 | |||||||
| chr12:51333050 | C | T | 1 | a0002c0001t0001g0134 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.610-3217G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333050 | |||||||
| chr12:51333079 | A | T | 2 | a0002c0001t0001g0205 a0002c0001t0001g0206 |
2 | NA18953.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.610-3246T>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333079 | |||||||
| chr12:51333090 | C | T | 1 | a0002c0001t0001g0190 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.610-3257G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333090 | |||||||
| chr12:51333096 | A | AT | 96 | a0001c0002t0002g0098 a0001c0003t0001g0068 a0001c0003t0001g0069 others(93): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.610-3264dupA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333096 | |||||||
| chr12:51333317 | C | A | 2 | a0001c0005t0001g0057 a0001c0005t0001g0062 |
2 | HG01515.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.610-3484G>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333317 | |||||||
| chr12:51333405 | G | GT | 44 | a0002c0001t0001g0008 a0002c0001t0001g0009 a0002c0001t0001g0011 others(41): Show |
80 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.610-3573dupA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333405 | |||||||
| chr12:51333405 | G | T | 3 | a0002c0001t0001g0152 a0002c0001t0001g0192 a0002c0001t0001g0204 |
3 | HG01256.hp1 HG03239.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.610-3572C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333405 | |||||||
| chr12:51333405 | GT | G | 101 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(98): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.610-3573delA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333405 | |||||||
| chr12:51333410 | T | G | 1 | a0001c0005t0001g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.610-3577A>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333410 | |||||||
| chr12:51333469 | C | T | 1 | a0002c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.610-3636G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333469 | |||||||
| chr12:51333501 | C | T | 36 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(33): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.610-3668G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333501 | |||||||
| chr12:51333594 | T | C | 18 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(15): Show |
47 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.610-3761A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333594 | |||||||
| chr12:51333638 | C | T | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-3805G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333638 | |||||||
| chr12:51333684 | C | T | 204 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(201): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.610-3851G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333684 | |||||||
| chr12:51333812 | C | T | 202 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(199): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.610-3979G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51333812 | |||||||
| chr12:51334303 | T | C | 9 | a0001c0003t0002g0012 a0001c0003t0002g0037 a0001c0003t0002g0066 others(6): Show |
16 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.610-4470A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334303 | |||||||
| chr12:51334472 | T | C | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-4639A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334472 | |||||||
| chr12:51334561 | G | A | 1 | a0002c0001t0001g0199 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.610-4728C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334561 | |||||||
| chr12:51334567 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.610-4734C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334567 | |||||||
| chr12:51334579 | A | G | 1 | a0001c0003t0002g0077 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.610-4746T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334579 | |||||||
| chr12:51334594 | C | G | 1 | a0002c0001t0001g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.610-4761G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334594 | |||||||
| chr12:51334595 | G | C | 1 | a0002c0001t0001g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.610-4762C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334595 | |||||||
| chr12:51334635 | C | T | 2 | a0001c0003t0002g0079 a0001c0003t0002g0080 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.610-4802G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334635 | |||||||
| chr12:51334680 | T | C | 26 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(23): Show |
49 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.610-4847A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334680 | |||||||
| chr12:51334697 | G | A | 6 | a0002c0001t0001g0021 a0002c0001t0001g0165 a0002c0001t0001g0171 others(3): Show |
9 | NA18939.hp1 NA18940.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.610-4864C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334697 | |||||||
| chr12:51334733 | C | T | 1 | a0001c0002t0002g0097 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.610-4900G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334733 | |||||||
| chr12:51334983 | C | G | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+4877G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51334983 | |||||||
| chr12:51335062 | G | A | 1 | a0001c0005t0001g0055 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.609+4798C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335062 | |||||||
| chr12:51335280 | G | A | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+4580C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335280 | |||||||
| chr12:51335320 | G | C | 3 | a0001c0002t0002g0065 a0001c0003t0001g0068 a0001c0003t0001g0069 |
3 | HG02622.hp2 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.609+4540C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335320 | |||||||
| chr12:51335505 | T | C | 97 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(94): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.609+4355A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335505 | |||||||
| chr12:51335522 | G | GATTA | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+4337_609+4338i others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335522 | |||||||
| chr12:51335543 | C | T | 36 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(33): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.609+4317G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335543 | |||||||
| chr12:51335566 | T | A | 2 | a0001c0003t0001g0068 a0001c0003t0001g0069 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.609+4294A>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335566 | |||||||
| chr12:51335607 | T | C | 1 | a0001c0004t0002g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.609+4253A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335607 | |||||||
| chr12:51335629 | C | CT | 20 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(17): Show |
47 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.609+4230dupA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335629 | |||||||
| chr12:51335629 | CT | C | 18 | a0001c0002t0002g0104 a0001c0003t0001g0002 a0001c0003t0001g0040 others(15): Show |
34 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.609+4230delA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335629 | |||||||
| chr12:51335932 | C | T | 1 | a0001c0004t0002g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.609+3928G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51335932 | |||||||
| chr12:51336517 | C | G | 60 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(57): Show |
120 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.609+3343G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51336517 | |||||||
| chr12:51336704 | G | A | 1 | a0001c0002t0002g0085 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.609+3156C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51336704 | |||||||
| chr12:51336745 | A | G | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+3115T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51336745 | |||||||
| chr12:51337048 | G | A | 2 | a0001c0002t0002g0038 a0001c0002t0002g0092 |
3 | HG02717.hp1 HG02895.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.609+2812C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337048 | |||||||
| chr12:51337143 | C | G | 97 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(94): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.609+2717G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337143 | |||||||
| chr12:51337185 | T | A | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+2675A>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337185 | |||||||
| chr12:51337207 | C | A | 97 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(94): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.609+2653G>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337207 | |||||||
| chr12:51337539 | C | CA | 29 | a0001c0002t0002g0027 a0001c0002t0002g0065 a0001c0002t0002g0090 others(26): Show |
62 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.609+2320dupT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337539 | |||||||
| chr12:51337539 | C | CAA | 135 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(132): Show |
273 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.609+2319_609+2320d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337539 | |||||||
| chr12:51337539 | C | CAAA | 21 | a0001c0002t0002g0016 a0001c0002t0002g0039 a0001c0002t0002g0105 others(18): Show |
26 | HG00621.hp1 HG00621.hp2 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.609+2318_609+2320d others(5): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337539 | |||||||
| chr12:51337539 | CAAA | C | 14 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(11): Show |
30 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.609+2318_609+2320d others(5): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337539 | |||||||
| chr12:51337691 | CA | C | 57 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(54): Show |
114 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.609+2168delT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337691 | |||||||
| chr12:51337880 | C | T | 1 | a0002c0001t0001g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.609+1980G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337880 | |||||||
| chr12:51337920 | A | C | 2 | a0001c0005t0001g0023 a0001c0005t0001g0054 |
4 | HG00140.hp2 HG01123.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+1940T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337920 | |||||||
| chr12:51337923 | A | AAT | 49 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(46): Show |
106 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.609+1935_609+1936d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337923 | |||||||
| chr12:51337923 | A | AATAT | 5 | a0001c0002t0002g0089 a0001c0002t0002g0093 a0001c0002t0002g0094 others(2): Show |
5 | HG00558.hp2 HG02040.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1933_609+1936d others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337923 | |||||||
| chr12:51337938 | G | A | 75 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(72): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.609+1922C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51337938 | |||||||
| chr12:51338060 | G | A | 1 | a0001c0004t0002g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.609+1800C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338060 | |||||||
| chr12:51338130 | C | G | 1 | a0001c0003t0001g0113 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.609+1730G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338130 | |||||||
| chr12:51338184 | G | A | 1 | a0002c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.609+1676C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338184 | |||||||
| chr12:51338255 | T | C | 2 | a0002c0001t0001g0173 a0002c0001t0002g0020 |
2 | HG02735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.609+1605A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338255 | T | TAC | 26 | a0001c0002t0002g0026 a0001c0002t0002g0038 a0001c0002t0002g0090 others(23): Show |
32 | HG00408.hp2 HG00639.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.609+1603_609+1604d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338255 | T | TACAC | 4 | a0001c0004t0002g0007 a0001c0004t0002g0024 a0002c0001t0002g0047 others(1): Show |
5 | HG01433.hp2 HG01496.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1601_609+1604d others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338255 | T | TACACACA others(1): Show |
5 | a0001c0002t0002g0065 a0001c0004t0002g0006 a0001c0004t0002g0022 others(2): Show |
9 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.609+1597_609+1604d others(10): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338255 | T | TACACACA others(3): Show |
3 | a0001c0004t0002g0022 a0001c0004t0002g0036 a0002c0001t0002g0047 |
3 | HG01516.hp2 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.609+1595_609+1604d others(12): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338255 | TAC | T | 2 | a0002c0001t0002g0045 a0002c0001t0002g0162 |
3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.609+1603_609+1604d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338255 | TACACACA others(1): Show |
T | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1597_609+1604d others(10): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338255 | |||||||
| chr12:51338277 | CACACACA others(5): Show |
C | 1 | a0002c0001t0001g0152 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.609+1571_609+1582d others(14): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338277 | |||||||
| chr12:51338287 | C | CACACACA others(1): Show |
2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+1572_609+1573i others(10): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338287 | |||||||
| chr12:51338287 | CAT | C | 56 | a0001c0002t0002g0107 a0002c0001t0001g0001 a0002c0001t0001g0008 others(53): Show |
103 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.609+1571_609+1572d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338287 | |||||||
| chr12:51338289 | T | C | 130 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(127): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.609+1571A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338289 | |||||||
| chr12:51338292 | A | G | 2 | a0002c0001t0001g0192 a0002c0001t0002g0129 |
2 | HG03239.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.609+1568T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338292 | |||||||
| chr12:51338295 | T | C | 52 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
110 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.609+1565A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338295 | |||||||
| chr12:51338298 | G | A | 84 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(81): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.609+1562C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338298 | |||||||
| chr12:51338299 | C | T | 22 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(19): Show |
49 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.609+1561G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338299 | |||||||
| chr12:51338301 | T | C | 42 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(39): Show |
88 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.609+1559A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338301 | |||||||
| chr12:51338302 | A | ACACATAC others(1): Show |
4 | a0001c0003t0001g0040 a0001c0003t0001g0118 a0001c0005t0001g0003 others(1): Show |
5 | HG00597.hp2 HG02970.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+1557_609+1558i others(10): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338302 | |||||||
| chr12:51338302 | A | ACATACG | 8 | a0001c0002t0002g0013 a0001c0002t0002g0016 a0001c0002t0002g0085 others(5): Show |
10 | HG02129.hp2 HG02257.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.609+1557_609+1558i others(8): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338302 | |||||||
| chr12:51338302 | A | ACG | 26 | a0001c0002t0002g0005 a0001c0002t0002g0013 a0001c0002t0002g0027 others(23): Show |
44 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.609+1557_609+1558i others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338302 | |||||||
| chr12:51338302 | A | ATACG | 14 | a0001c0002t0002g0016 a0001c0002t0002g0095 a0001c0002t0002g0096 others(11): Show |
25 | HG00280.hp2 HG00558.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.609+1557_609+1558i others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338302 | |||||||
| chr12:51338302 | A | G | 23 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(20): Show |
50 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.609+1558T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338302 | |||||||
| chr12:51338303 | C | CAT | 3 | a0001c0003t0002g0012 a0001c0003t0002g0083 a0001c0004t0002g0036 |
9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.609+1555_609+1556d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338303 | |||||||
| chr12:51338303 | C | CGCAT | 16 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0024 others(13): Show |
35 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.609+1556_609+1557i others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338303 | |||||||
| chr12:51338303 | CAT | C | 106 | a0001c0003t0001g0068 a0001c0003t0001g0069 a0001c0003t0002g0037 others(103): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.609+1555_609+1556d others(4): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338303 | |||||||
| chr12:51338303 | CATAT | C | 12 | a0001c0002t0002g0026 a0001c0002t0002g0038 a0001c0002t0002g0090 others(9): Show |
18 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.609+1553_609+1556d others(6): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338303 | |||||||
| chr12:51338304 | A | G | 1 | a0001c0002t0002g0107 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.609+1556T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338304 | |||||||
| chr12:51338305 | T | C | 17 | a0001c0002t0002g0107 a0001c0004t0002g0006 a0001c0004t0002g0007 others(14): Show |
36 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.609+1555A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338305 | |||||||
| chr12:51338307 | T | C | 63 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.609+1553A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338307 | |||||||
| chr12:51338309 | T | C | 1 | a0001c0002t0002g0107 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.609+1551A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338309 | |||||||
| chr12:51338406 | C | T | 1 | a0001c0003t0002g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.609+1454G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338406 | |||||||
| chr12:51338409 | T | A | 2 | a0001c0003t0001g0068 a0001c0003t0001g0069 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.609+1451A>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338409 | |||||||
| chr12:51338646 | C | T | 15 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(12): Show |
31 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.609+1214G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338646 | |||||||
| chr12:51338716 | G | A | 95 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(92): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.609+1144C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51338716 | |||||||
| chr12:51339002 | T | C | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.609+858A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339002 | |||||||
| chr12:51339133 | G | A | 2 | a0002c0001t0001g0042 a0002c0001t0001g0145 |
3 | NA19003.hp2 NA19011.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.609+727C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339133 | |||||||
| chr12:51339172 | T | G | 1 | a0002c0001t0001g0157 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.609+688A>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339172 | |||||||
| chr12:51339186 | C | G | 2 | a0001c0003t0001g0068 a0001c0003t0001g0069 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.609+674G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339186 | |||||||
| chr12:51339238 | G | A | 15 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(12): Show |
31 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.609+622C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339238 | |||||||
| chr12:51339279 | G | T | 1 | a0002c0001t0001g0128 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.609+581C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339279 | |||||||
| chr12:51339345 | G | A | 1 | a0001c0004t0002g0036 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.609+515C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339345 | |||||||
| chr12:51339408 | C | T | 1 | a0002c0001t0002g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.609+452G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339408 | |||||||
| chr12:51339483 | G | A | 2 | a0002c0001t0001g0017 a0002c0001t0001g0146 |
6 | HG00408.hp2 HG02027.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+377C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339483 | |||||||
| chr12:51339506 | G | A | 36 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(33): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.609+354C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339506 | |||||||
| chr12:51339563 | C | G | 1 | a0002c0001t0001g0201 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.609+297G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339563 | |||||||
| chr12:51339571 | C | T | 1 | a0002c0001t0001g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.609+289G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339571 | |||||||
| chr12:51339650 | G | A | 14 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0111 others(11): Show |
30 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.609+210C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339650 | |||||||
| chr12:51339779 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.609+81C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 6/7 | chr12 | 51339779 | |||||||
| chr12:51340021 | G | A | 1 | a0002c0001t0001g0044 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.464-16C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340021 | |||||||
| chr12:51340093 | C | T | 2 | a0001c0003t0002g0079 a0001c0003t0002g0080 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.464-88G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340093 | |||||||
| chr12:51340167 | A | C | 95 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(92): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.464-162T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340167 | |||||||
| chr12:51340174 | C | T | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.464-169G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340174 | |||||||
| chr12:51340251 | C | G | 2 | a0002c0001t0002g0045 a0002c0001t0002g0162 |
3 | HG02055.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.464-246G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340251 | |||||||
| chr12:51340273 | G | C | 6 | a0002c0001t0001g0021 a0002c0001t0001g0165 a0002c0001t0001g0171 others(3): Show |
9 | NA18939.hp1 NA18940.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-268C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340273 | |||||||
| chr12:51340322 | G | A | 1 | a0002c0001t0001g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.464-317C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340322 | |||||||
| chr12:51340388 | C | CT | 24 | a0001c0002t0002g0089 a0001c0003t0001g0118 a0001c0003t0001g0121 others(21): Show |
58 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.464-384dupA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340388 | |||||||
| chr12:51340388 | C | CTT | 12 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(9): Show |
28 | HG00408.hp1 HG00438.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.464-385_464-384dup others(2): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340388 | |||||||
| chr12:51340388 | CT | C | 57 | a0001c0002t0002g0065 a0001c0002t0002g0108 a0001c0002t0002g0109 others(54): Show |
95 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.464-384delA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340388 | |||||||
| chr12:51340392 | T | C | 2 | a0001c0003t0002g0079 a0001c0003t0002g0080 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.464-387A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340392 | |||||||
| chr12:51340628 | C | A | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+616G>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340628 | |||||||
| chr12:51340677 | C | T | 1 | a0001c0002t0002g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.463+567G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340677 | |||||||
| chr12:51340741 | C | G | 1 | a0002c0001t0001g0200 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.463+503G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340741 | |||||||
| chr12:51340746 | C | T | 1 | a0001c0002t0002g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.463+498G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340746 | |||||||
| chr12:51340826 | C | T | 1 | a0001c0002t0002g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.463+418G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340826 | |||||||
| chr12:51340843 | A | C | 1 | a0002c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.463+401T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340843 | |||||||
| chr12:51340899 | C | T | 1 | a0002c0001t0001g0166 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.463+345G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340899 | |||||||
| chr12:51340903 | A | T | 3 | a0002c0001t0001g0032 a0002c0001t0001g0198 a0002c0001t0001g0199 |
5 | HG00140.hp1 HG01074.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+341T>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51340903 | |||||||
| chr12:51341238 | A | T | 97 | a0001c0005t0001g0052 a0002c0001t0001g0001 a0002c0001t0001g0008 others(94): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
splice_region_variant&intron_variant | LOW | c.463+6T>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 5/7 | chr12 | 51341238 | |||||||
| chr12:51341471 | C | T | 1 | a0002c0001t0002g0161 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.327-91G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51341471 | |||||||
| chr12:51341535 | G | A | 1 | a0001c0004t0002g0036 | 2 | HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.327-155C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51341535 | |||||||
| chr12:51341585 | T | C | 1 | a0001c0003t0002g0080 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.327-205A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51341585 | |||||||
| chr12:51341773 | G | C | 202 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(199): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.327-393C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51341773 | |||||||
| chr12:51341833 | A | C | 1 | a0001c0002t0002g0087 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.327-453T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51341833 | |||||||
| chr12:51342027 | C | T | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+548G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342027 | |||||||
| chr12:51342055 | T | G | 1 | a0002c0001t0001g0185 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.326+520A>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342055 | |||||||
| chr12:51342102 | C | T | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+473G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342102 | |||||||
| chr12:51342148 | T | G | 3 | a0003c0008t0001g0188 a0003c0008t0001g0189 a0006c0013t0002g0187 |
3 | HG02647.hp2 HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.326+427A>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342148 | |||||||
| chr12:51342162 | G | A | 1 | a0001c0005t0001g0062 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.326+413C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342162 | |||||||
| chr12:51342193 | A | AT | 7 | a0001c0002t0002g0086 a0001c0004t0002g0033 a0002c0001t0001g0041 others(4): Show |
9 | HG01167.hp1 HG03225.hp2 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+381dupA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342193 | |||||||
| chr12:51342193 | AT | A | 17 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(14): Show |
35 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.326+381delA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342193 | |||||||
| chr12:51342221 | G | A | 2 | a0002c0001t0001g0208 a0002c0001t0001g0209 |
2 | NA18944.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.326+354C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 4/7 | chr12 | 51342221 | |||||||
| chr12:51342752 | T | G | 1 | a0002c0001t0001g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.201-52A>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51342752 | |||||||
| chr12:51342792 | T | A | 4 | a0001c0006t0001g0063 a0002c0001t0001g0030 a0002c0001t0001g0044 others(1): Show |
7 | HG00733.hp2 HG00735.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.201-92A>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51342792 | |||||||
| chr12:51342812 | AT | A | 63 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(60): Show |
124 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.201-113delA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51342812 | |||||||
| chr12:51343129 | A | C | 101 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(98): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.201-429T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51343129 | |||||||
| chr12:51343225 | G | A | 2 | a0003c0008t0001g0188 a0003c0008t0001g0189 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.201-525C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51343225 | |||||||
| chr12:51343258 | G | A | 5 | a0002c0001t0001g0014 a0002c0001t0001g0155 a0002c0001t0001g0156 others(2): Show |
10 | HG02145.hp1 HG02559.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.200+495C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51343258 | |||||||
| chr12:51343655 | G | A | 17 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(14): Show |
35 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.200+98C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51343655 | |||||||
| chr12:51343663 | G | T | 1 | a0001c0003t0001g0068 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.200+90C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51343663 | |||||||
| chr12:51343736 | G | T | 18 | a0001c0004t0002g0006 a0001c0004t0002g0007 a0001c0004t0002g0022 others(15): Show |
47 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.200+17C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 3/7 | chr12 | 51343736 | |||||||
| chr12:51344035 | G | A | 1 | a0002c0001t0001g0158 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-182C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344035 | |||||||
| chr12:51344206 | A | C | 1 | a0002c0001t0002g0159 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100-353T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344206 | |||||||
| chr12:51344257 | C | T | 8 | a0001c0003t0001g0068 a0001c0003t0001g0069 a0001c0003t0002g0037 others(5): Show |
9 | HG02258.hp2 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-404G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344257 | |||||||
| chr12:51344324 | C | G | 8 | a0001c0003t0001g0068 a0001c0003t0001g0069 a0001c0003t0002g0037 others(5): Show |
9 | HG02258.hp2 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-471G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344324 | |||||||
| chr12:51344430 | C | T | 1 | a0001c0004t0002g0033 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.100-577G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344430 | |||||||
| chr12:51344464 | G | A | 17 | a0001c0005t0001g0003 a0001c0005t0001g0015 a0001c0005t0001g0023 others(14): Show |
35 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-611C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344464 | |||||||
| chr12:51344548 | G | A | 4 | a0002c0001t0001g0190 a0002c0001t0001g0191 a0002c0001t0001g0192 others(1): Show |
4 | HG03239.hp1 NA18963.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-695C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344548 | |||||||
| chr12:51344560 | A | C | 20 | a0001c0003t0002g0012 a0001c0003t0002g0083 a0001c0004t0002g0006 others(17): Show |
54 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.100-707T>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344560 | |||||||
| chr12:51344757 | CTTAGGTC others(15): Show |
C | 1 | a0001c0002t0002g0110 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.100-926_100-905del others(22): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344757 | |||||||
| chr12:51344762 | G | A | 1 | a0002c0001t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.100-909C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344762 | |||||||
| chr12:51344843 | G | A | 3 | a0001c0003t0001g0120 a0001c0003t0001g0121 a0001c0003t0001g0122 |
3 | HG00408.hp1 HG00609.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.99+952C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344843 | |||||||
| chr12:51344853 | T | G | 202 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(199): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.99+942A>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344853 | |||||||
| chr12:51344922 | T | C | 4 | a0001c0004t0002g0006 a0001c0004t0002g0022 a0001c0004t0002g0081 others(1): Show |
16 | HG00099.hp2 HG00642.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+873A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51344922 | |||||||
| chr12:51345038 | C | T | 43 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(40): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.99+757G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345038 | |||||||
| chr12:51345093 | C | G | 2 | a0001c0003t0001g0068 a0001c0003t0001g0069 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.99+702G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345093 | |||||||
| chr12:51345125 | CA | C | 74 | a0001c0002t0002g0084 a0001c0003t0001g0068 a0001c0003t0001g0069 others(71): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.99+669delT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345125 | |||||||
| chr12:51345125 | CAA | C | 18 | a0001c0002t0002g0065 a0001c0003t0001g0002 a0001c0003t0001g0040 others(15): Show |
37 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.99+668_99+669delTT | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345125 | |||||||
| chr12:51345390 | G | A | 1 | a0002c0001t0001g0194 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.99+405C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345390 | |||||||
| chr12:51345393 | CGT | C | 2 | a0001c0006t0001g0018 a0001c0006t0001g0064 |
5 | HG01346.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+400_99+401delAC | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345393 | |||||||
| chr12:51345411 | T | C | 2 | a0001c0002t0002g0065 a0002c0001t0001g0195 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.99+384A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345411 | |||||||
| chr12:51345569 | G | T | 1 | a0001c0003t0002g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+226C>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345569 | |||||||
| chr12:51345657 | A | G | 1 | a0002c0001t0001g0126 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.99+138T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345657 | |||||||
| chr12:51345687 | T | C | 43 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0067 others(40): Show |
94 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.99+108A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345687 | |||||||
| chr12:51345737 | A | G | 1 | a0002c0001t0001g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.99+58T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 2/7 | chr12 | 51345737 | |||||||
| chr12:51345948 | C | T | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-71G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51345948 | |||||||
| chr12:51345999 | C | G | 4 | a0001c0005t0001g0015 a0001c0005t0001g0049 a0001c0005t0001g0050 others(1): Show |
8 | HG00280.hp2 NA18942.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.17-122G>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51345999 | |||||||
| chr12:51346203 | C | A | 2 | a0001c0003t0002g0012 a0001c0003t0002g0083 |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.17-326G>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346203 | |||||||
| chr12:51346311 | A | G | 1 | a0001c0003t0001g0111 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.16+312T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346311 | |||||||
| chr12:51346334 | G | A | 15 | a0002c0001t0001g0011 a0002c0001t0001g0032 a0002c0001t0001g0197 others(12): Show |
24 | HG00140.hp1 HG01074.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.16+289C>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346334 | |||||||
| chr12:51346385 | C | A | 36 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(33): Show |
75 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.16+238G>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346385 | |||||||
| chr12:51346483 | T | C | 1 | a0002c0001t0001g0210 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.16+140A>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346483 | |||||||
| chr12:51346496 | G | C | 14 | a0001c0003t0001g0002 a0001c0003t0001g0040 a0001c0003t0001g0111 others(11): Show |
30 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.16+127C>G | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346496 | |||||||
| chr12:51346566 | C | T | 1 | a0001c0004t0002g0022 | 3 | HG00642.hp1 HG01261.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.16+57G>A | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346566 | |||||||
| chr12:51346584 | A | G | 1 | a0002c0001t0001g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.16+39T>C | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346584 | |||||||
| chr12:51346603 | ACTGGACC others(6): Show |
A | 100 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(97): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
splice_region_variant&intron_variant | LOW | c.16+7_16+19delGGATA others(8): Show |
CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346603 | |||||||
| chr12:51346604 | C | A | 104 | a0002c0001t0001g0001 a0002c0001t0001g0008 a0002c0001t0001g0009 others(101): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.16+19G>T | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346604 | |||||||
| chr12:51346618 | CTT | C | 100 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0013 others(97): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(208): Show |
splice_region_variant&intron_variant | LOW | c.16+3_16+4delAA | CELA1 | ENSG00000139610.2 | transcript | ENST00000293636.2 | protein_coding | 1/7 | chr12 | 51346618 |