Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79174 |
| ensemblid | ENSG00000184164.15 |
| hgncid | 28150 |
| symbol | CRELD2 |
| name | cysteine rich with EGF like domains 2 |
| refseq_nuc | NM_024324.5 |
| refseq_prot | NP_077300.3 |
| ensembl_nuc | ENST00000328268.9 |
| ensembl_prot | ENSP00000332223.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 49918634 |
| end | 49927537 |
| strand | + |
| ver | v1.2 |
| region | chr22:49918634-49927537 |
| region5000 | chr22:49913634-49932537 |
| regionname0 | CRELD2_chr22_49918634_49927537 |
| regionname5000 | CRELD2_chr22_49913634_49932537 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 353 | 224 | 37 | 51 | 95 | 11 | 28 | 58 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0002 | 0/0 | 353 | 53 | 35 | 4 | 10 | 0 | 4 | 8 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0003 | 0/0 | 353 | 26 | 0 | 6 | 15 | 0 | 5 | 12 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0004 | 0/0 | 353 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0005 | 0/0 | 353 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0006 | 0/0 | 353 | 3 | 1 | 1 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0007 | 0/0 | 353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0008 | 0/0 | 353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0009 | 0/0 | 353 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0010 | 0/0 | 353 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0011 | 0/0 | 353 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(348): Show |
chr22 | 49913634 | 49932537 |
| a0012 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | MRLPR others(331): Show |
chr22 | 49913634 | 49932537 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1059 | 178 | 16 | 48 | 80 | 9 | 23 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0003 | 0/0 | 1059 | 35 | 14 | 3 | 11 | 2 | 5 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0007 | 0/0 | 1059 | 5 | 5 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0011 | 0/0 | 1059 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0016 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0018 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0021 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0001c0027 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0002c0002 | 0/0 | 1059 | 39 | 25 | 3 | 8 | 0 | 3 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0002c0005 | 0/0 | 1059 | 8 | 7 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0002c0009 | 0/0 | 1059 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0002c0012 | 0/0 | 1059 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0002c0014 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0002c0015 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0003c0004 | 0/0 | 1059 | 25 | 0 | 6 | 14 | 0 | 5 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0003c0017 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0004c0006 | 0/0 | 1059 | 7 | 6 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0004c0013 | 0/0 | 1059 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0005c0008 | 0/0 | 1059 | 3 | 0 | 1 | 0 | 2 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0006c0010 | 0/0 | 1059 | 2 | 1 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0006c0025 | 0/0 | 1059 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0007c0019 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0008c0024 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0009c0020 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0010c0026 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0011c0023 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 | ||
| a0012c0022 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | ATGCG others(1054): Show |
chr22 | 49913634 | 49932537 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1428 | 175 | 16 | 48 | 79 | 9 | 21 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0001t0006 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0001t0008 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0001t0011 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0003t0002 | 0/0 | 1428 | 35 | 14 | 3 | 11 | 2 | 5 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0007t0002 | 0/0 | 1428 | 5 | 5 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0011t0001 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0016t0002 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0018t0002 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0021t0001 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0001c0027t0001 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0002t0001 | 0/0 | 1428 | 29 | 20 | 2 | 6 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0002t0003 | 0/0 | 1428 | 6 | 1 | 1 | 2 | 0 | 2 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0002t0005 | 0/0 | 1428 | 4 | 4 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0005t0002 | 0/0 | 1428 | 7 | 6 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0005t0005 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0009t0001 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0012t0001 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0014t0002 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0002c0015t0002 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0003c0004t0002 | 0/0 | 1428 | 23 | 0 | 5 | 14 | 0 | 4 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0003c0004t0007 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0003c0004t0009 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0003c0017t0002 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0004c0006t0002 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0004c0006t0004 | 0/0 | 1429 | 5 | 4 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1424): Show |
chr22 | 49913634 | 49932537 |
| a0004c0006t0010 | 0/0 | 1429 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1424): Show |
chr22 | 49913634 | 49932537 |
| a0004c0013t0002 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0005c0008t0002 | 0/0 | 1428 | 3 | 0 | 1 | 0 | 2 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0006c0010t0001 | 0/0 | 1428 | 2 | 1 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0006c0025t0001 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0007c0019t0001 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0008c0024t0001 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0009c0020t0001 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0010c0026t0001 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0011c0023t0001 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| a0012c0022t0001 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | GGGGC others(1423): Show |
chr22 | 49913634 | 49932537 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 64 | 10 | 16 | 25 | 6 | 6 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 0 | 9 | 0 | 4 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0004 | 0/0 | 9 | 1 | 4 | 4 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0001t0011g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0007t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0007t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0007t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0007t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0007t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0011t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0011t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0016t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0018t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0021t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0001c0027t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0009 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0002t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0005t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0005t0002g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0005t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0005t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0005t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0009t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0012t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0012t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0014t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0002c0015t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0003 | 0/0 | 10 | 0 | 4 | 4 | 0 | 2 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0004t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0003c0017t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0006t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0006t0004g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0006t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0006t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0006t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0013t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0004c0013t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0005c0008t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0005c0008t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0005c0008t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0006c0010t0001g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0006c0025t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0007c0019t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0008c0024t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0009c0020t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0010c0026t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0011c0023t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| a0012c0022t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0159 | EUR | GBR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00140 | hp2 | a0001 | c0003 | t0002 | g0160 | EUR | GBR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00323 | hp2 | a0005 | c0008 | t0002 | g0155 | EUR | FIN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00423 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00438 | hp1 | a0003 | c0004 | t0002 | g0032 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00597 | hp1 | a0003 | c0004 | t0002 | g0032 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00609 | hp1 | a0001 | c0011 | t0001 | g0086 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00642 | hp2 | a0003 | c0004 | t0002 | g0114 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01069 | hp1 | a0006 | c0025 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01074 | hp2 | a0001 | c0003 | t0002 | g0036 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01106 | hp1 | a0005 | c0008 | t0002 | g0157 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0119 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | PUR | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01255 | hp1 | a0004 | c0006 | t0004 | g0029 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0102 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01361 | hp1 | a0002 | c0005 | t0002 | g0033 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01433 | hp1 | a0003 | c0004 | t0007 | g0135 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01515 | hp1 | a0005 | c0008 | t0002 | g0156 | EUR | IBS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01516 | hp1 | a0006 | c0010 | t0001 | g0001 | EUR | IBS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01884 | hp2 | a0002 | c0005 | t0002 | g0033 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0120 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01891 | hp2 | a0002 | c0005 | t0002 | g0146 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01952 | hp1 | a0003 | c0004 | t0002 | g0003 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01952 | hp2 | a0003 | c0004 | t0002 | g0003 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01975 | hp2 | a0003 | c0004 | t0002 | g0003 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02040 | hp1 | a0002 | c0002 | t0003 | g0028 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02055 | hp1 | a0001 | c0007 | t0002 | g0131 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02055 | hp2 | a0002 | c0002 | t0005 | g0092 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02056 | hp2 | a0003 | c0004 | t0002 | g0140 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02071 | hp1 | a0001 | c0003 | t0002 | g0152 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02080 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0151 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | CDX | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02451 | hp2 | a0002 | c0015 | t0002 | g0147 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02572 | hp2 | a0001 | c0016 | t0002 | g0115 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0161 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0112 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0116 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02630 | hp2 | a0007 | c0019 | t0001 | g0094 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02723 | hp1 | a0002 | c0005 | t0002 | g0145 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02735 | hp1 | a0001 | c0003 | t0002 | g0035 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02809 | hp1 | a0001 | c0007 | t0002 | g0130 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0118 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02886 | hp1 | a0004 | c0013 | t0002 | g0122 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0128 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02895 | hp2 | a0001 | c0007 | t0002 | g0129 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02897 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02922 | hp1 | a0002 | c0012 | t0001 | g0088 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02965 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0117 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02976 | hp1 | a0002 | c0005 | t0005 | g0091 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03041 | hp1 | a0002 | c0002 | t0005 | g0093 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03041 | hp2 | a0008 | c0024 | t0001 | g0051 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03098 | hp1 | a0001 | c0007 | t0002 | g0133 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03098 | hp2 | a0009 | c0020 | t0001 | g0048 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ESN | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03209 | hp1 | a0004 | c0006 | t0004 | g0124 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03209 | hp2 | a0002 | c0002 | t0005 | g0026 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03239 | hp1 | a0003 | c0004 | t0002 | g0003 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0153 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03486 | hp2 | a0001 | c0007 | t0002 | g0132 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0163 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0001 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0162 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03540 | hp1 | a0004 | c0013 | t0002 | g0121 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0126 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03688 | hp2 | a0010 | c0026 | t0001 | g0090 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03704 | hp1 | a0003 | c0004 | t0002 | g0003 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03704 | hp2 | a0002 | c0002 | t0003 | g0105 | SAS | PJL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0054 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03927 | hp2 | a0003 | c0004 | t0002 | g0143 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03942 | hp1 | a0002 | c0014 | t0002 | g0148 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG04204 | hp2 | a0003 | c0004 | t0009 | g0141 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG04228 | hp1 | a0002 | c0002 | t0003 | g0103 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG04228 | hp2 | a0003 | c0004 | t0002 | g0113 | SAS | STU | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18522 | hp1 | a0001 | c0003 | t0002 | g0127 | AFR | YRI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18612 | hp2 | a0001 | c0003 | t0002 | g0150 | EAS | CHB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | YRI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0031 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18941 | hp1 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18947 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18952 | hp1 | a0003 | c0004 | t0002 | g0137 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18961 | hp2 | a0001 | c0021 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18967 | hp2 | a0003 | c0004 | t0002 | g0136 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0035 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18974 | hp1 | a0003 | c0004 | t0002 | g0139 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18976 | hp1 | a0001 | c0003 | t0002 | g0149 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18976 | hp2 | a0011 | c0023 | t0001 | g0078 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18980 | hp2 | a0003 | c0004 | t0002 | g0031 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18989 | hp1 | a0003 | c0004 | t0002 | g0142 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18990 | hp1 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18994 | hp1 | a0003 | c0017 | t0002 | g0138 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19007 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19012 | hp1 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19012 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19030 | hp1 | a0002 | c0012 | t0001 | g0089 | AFR | LWK | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19030 | hp2 | a0004 | c0006 | t0010 | g0125 | AFR | LWK | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | LWK | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19043 | hp2 | a0002 | c0005 | t0002 | g0018 | AFR | LWK | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19057 | hp1 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19065 | hp1 | a0001 | c0011 | t0001 | g0077 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19065 | hp2 | a0003 | c0004 | t0002 | g0003 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19067 | hp1 | a0001 | c0027 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19070 | hp2 | a0002 | c0009 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19084 | hp1 | a0012 | c0022 | t0001 | g0044 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19086 | hp2 | a0003 | c0004 | t0002 | g0144 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19088 | hp2 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | YRI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0158 | AFR | YRI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0008 | AFR | ASW | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20129 | hp2 | a0004 | c0006 | t0002 | g0123 | AFR | ASW | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01123 | hp1 | a0003 | c0004 | t0002 | g0003 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02486 | hp1 | a0002 | c0002 | t0005 | g0026 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02486 | hp2 | a0002 | c0005 | t0002 | g0018 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02559 | hp1 | a0006 | c0010 | t0001 | g0001 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03471 | hp1 | a0004 | c0006 | t0004 | g0030 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG03471 | hp2 | a0004 | c0006 | t0004 | g0029 | AFR | MSL | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG06807 | hp1 | a0001 | c0018 | t0002 | g0134 | AFR | USA | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| HG06807 | hp2 | a0002 | c0005 | t0002 | g0018 | AFR | USA | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA20300 | hp2 | a0004 | c0006 | t0004 | g0030 | AFR | USA | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0036 | AFR | LWK | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0050 | REF | REF | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CRELD2_chr22_49913634_49932537 | CRELD2 | chr22 | 49913634 | 49932537 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49918806 | C | T | 1 | a0004 | 9 | HG01255.hp1 HG02886.hp1 HG03209.hp1 others(6): Show |
missense_variant | MODERATE | c.37C>T | p.Pro13Ser | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 173/1428 | 37/1062 | 13/353 | chr22 | 49918806 | |||
| chr22:49919804 | C | T | 1 | a0010 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.287C>T | p.Ala96Val | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 3/10 | 423/1428 | 287/1062 | 96/353 | chr22 | 49919804 | |||
| chr22:49921693 | C | T | 1 | a0008 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.524C>T | p.Pro175Leu | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 660/1428 | 524/1062 | 175/353 | chr22 | 49921693 | |||
| chr22:49921713 | G | A | 1 | a0002 | 2 | NA18941.hp1 NA19070.hp2 |
missense_variant | MODERATE | c.544G>A | p.Asp182Asn | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 680/1428 | 544/1062 | 182/353 | chr22 | 49921713 | |||
| chr22:49921715 | C | A | 3 | a0002 a0007 a0010 |
53 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(50): Show |
missense_variant | MODERATE | c.546C>A | p.Asp182Glu | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 682/1428 | 546/1062 | 182/353 | chr22 | 49921715 | |||
| chr22:49921734 | C | G | 1 | a0005 | 3 | HG00323.hp2 HG01106.hp1 HG01515.hp1 |
missense_variant | MODERATE | c.565C>G | p.Arg189Gly | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 701/1428 | 565/1062 | 189/353 | chr22 | 49921734 | |||
| chr22:49923254 | G | A | 1 | a0007 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.709G>A | p.Glu237Lys | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/10 | 845/1428 | 709/1062 | 237/353 | chr22 | 49923254 | |||
| chr22:49923258 | C | T | 1 | a0010 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.713C>T | p.Pro238Leu | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/10 | 849/1428 | 713/1062 | 238/353 | chr22 | 49923258 | |||
| chr22:49924395 | G | A | 1 | a0009 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.808G>A | p.Gly270Ser | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/10 | 944/1428 | 808/1062 | 270/353 | chr22 | 49924395 | |||
| chr22:49924412 | A | C | 1 | a0011 | 1 | NA18976.hp2 | missense_variant | MODERATE | c.825A>C | p.Lys275Asn | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/10 | 961/1428 | 825/1062 | 275/353 | chr22 | 49924412 | |||
| chr22:49924413 | G | C | 1 | a0006 | 3 | HG01069.hp1 HG01516.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.826G>C | p.Glu276Gln | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/10 | 962/1428 | 826/1062 | 276/353 | chr22 | 49924413 | |||
| chr22:49925431 | T | G | 1 | a0003 | 26 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(23): Show |
missense_variant | MODERATE | c.883T>G | p.Ser295Ala | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/10 | 1019/1428 | 883/1062 | 295/353 | chr22 | 49925431 | |||
| chr22:49925522 | A | G | 1 | a0003 | 26 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(23): Show |
missense_variant | MODERATE | c.974A>G | p.Glu325Gly | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/10 | 1110/1428 | 974/1062 | 325/353 | chr22 | 49925522 | |||
| chr22:49925555 | C | G | 1 | a0012 | 1 | NA19084.hp1 | missense_variant&splice_region_variant | MODERATE | c.1007C>G | p.Ala336Gly | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/10 | 1143/1428 | 1007/1062 | 336/353 | chr22 | 49925555 | |||
| chr22:49925557 | G | T | 1 | a0012 | 1 | NA19084.hp1 | stop_gained&splice_region_variant | HIGH | c.1009G>T | p.Glu337* | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/10 | 1145/1428 | 1009/1062 | 337/353 | chr22 | 49925557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49918829 | C | T | 1 | a0001c0027 | 1 | NA19067.hp1 | synonymous_variant | LOW | c.60C>T | p.Pro20Pro | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 196/1428 | 60/1062 | 20/353 | chr22 | 49918829 | |||
| chr22:49919790 | T | C | 12 | a0001c0003 a0001c0007 a0001c0016 others(9): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
synonymous_variant | LOW | c.273T>C | p.Asn91Asn | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 3/10 | 409/1428 | 273/1062 | 91/353 | chr22 | 49919790 | |||
| chr22:49920162 | C | T | 1 | a0002c0012 | 2 | HG02922.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.330C>T | p.Ser110Ser | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/10 | 466/1428 | 330/1062 | 110/353 | chr22 | 49920162 | |||
| chr22:49921655 | C | T | 1 | a0001c0007 | 5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.486C>T | p.Gly162Gly | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 622/1428 | 486/1062 | 162/353 | chr22 | 49921655 | |||
| chr22:49921658 | C | T | 1 | a0006c0025 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.489C>T | p.Asp163Asp | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 625/1428 | 489/1062 | 163/353 | chr22 | 49921658 | |||
| chr22:49921706 | C | T | 1 | a0001c0018 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.537C>T | p.Asp179Asp | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/10 | 673/1428 | 537/1062 | 179/353 | chr22 | 49921706 | |||
| chr22:49923253 | C | T | 1 | a0002c0015 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.708C>T | p.Ala236Ala | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/10 | 844/1428 | 708/1062 | 236/353 | chr22 | 49923253 | |||
| chr22:49923277 | G | A | 1 | a0001c0016 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.732G>A | p.Ala244Ala | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/10 | 868/1428 | 732/1062 | 244/353 | chr22 | 49923277 | |||
| chr22:49924442 | C | T | 1 | a0001c0011 | 2 | HG00609.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.855C>T | p.His285His | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/10 | 991/1428 | 855/1062 | 285/353 | chr22 | 49924442 | |||
| chr22:49925526 | G | A | 1 | a0001c0021 | 1 | NA18961.hp2 | synonymous_variant | LOW | c.978G>A | p.Thr326Thr | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/10 | 1114/1428 | 978/1062 | 326/353 | chr22 | 49925526 | |||
| chr22:49925556 | T | C | 1 | a0012c0022 | 1 | NA19084.hp1 | splice_region_variant&synonymous_variant | LOW | c.1008T>C | p.Ala336Ala | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/10 | 1144/1428 | 1008/1062 | 336/353 | chr22 | 49925556 | |||
| chr22:49927295 | C | T | 6 | a0001c0003 a0001c0007 a0001c0018 others(3): Show |
52 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(49): Show |
synonymous_variant | LOW | c.1050C>T | p.Arg350Arg | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 10/10 | 1186/1428 | 1050/1062 | 350/353 | chr22 | 49927295 | |||
| chr22:49927302 | C | T | 1 | a0003c0017 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.1057C>T | p.Leu353Leu | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 10/10 | 1193/1428 | 1057/1062 | 353/353 | chr22 | 49927302 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49918642 | G | T | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 128 | chr22 | 49918642 | ||||||
| chr22:49918645 | G | A | 1 | a0001c0001t0006 | 1 | HG02155.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 125 | chr22 | 49918645 | ||||||
| chr22:49918655 | A | G | 1 | a0004c0006t0010 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 115 | chr22 | 49918655 | ||||||
| chr22:49918697 | C | G | 1 | a0003c0004t0009 | 1 | HG04204.hp2 | 5_prime_UTR_variant | MODIFIER | c.-73C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 73 | chr22 | 49918697 | ||||||
| chr22:49918734 | G | A | 16 | a0001c0003t0002 a0001c0007t0002 a0001c0016t0002 others(13): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 36 | chr22 | 49918734 | ||||||
| chr22:49918759 | C | G | 2 | a0002c0002t0005 a0002c0005t0005 |
5 | HG02055.hp2 HG02486.hp1 HG02976.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-11C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/10 | 11 | chr22 | 49918759 | ||||||
| chr22:49927375 | G | A | 1 | a0001c0001t0008 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 10/10 | 68 | chr22 | 49927375 | ||||||
| chr22:49927396 | C | T | 1 | a0003c0004t0007 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 10/10 | 89 | chr22 | 49927396 | ||||||
| chr22:49927415 | C | G | 1 | a0002c0002t0003 | 6 | HG01256.hp1 HG02040.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*108C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 10/10 | 108 | chr22 | 49927415 | ||||||
| chr22:49927417 | C | CT | 2 | a0004c0006t0004 a0004c0006t0010 |
6 | HG01255.hp1 HG03209.hp1 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*111dupT | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 10/10 | 112 | INFO_REALIGN_3_PRIME | chr22 | 49927417 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:49918982 | A | G | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+84A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49918982 | |||||||
| chr22:49919002 | T | TTCGGGGT others(16): Show |
3 | a0001c0003t0002g0161 a0001c0003t0002g0162 a0001c0003t0002g0163 |
3 | HG02602.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.129+104_129+105ins others(23): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919002 | |||||||
| chr22:49919003 | C | T | 22 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(19): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+105C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919003 | |||||||
| chr22:49919011 | C | G | 25 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(22): Show |
34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.129+113C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919011 | |||||||
| chr22:49919015 | T | C | 22 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(19): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+117T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919015 | |||||||
| chr22:49919020 | C | G | 22 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(19): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+122C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919020 | |||||||
| chr22:49919024 | A | G | 22 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(19): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+126A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919024 | |||||||
| chr22:49919025 | T | C | 22 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(19): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+127T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919025 | |||||||
| chr22:49919026 | T | C | 22 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(19): Show |
31 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.129+128T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919026 | |||||||
| chr22:49919026 | T | TCGGGGTC others(16): Show |
28 | a0001c0003t0002g0008 a0001c0003t0002g0116 a0001c0003t0002g0117 others(25): Show |
34 | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.129+132_129+133ins others(23): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 49919026 | ||||||
| chr22:49919026 | T | TCGGGGTC others(16): Show |
13 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(10): Show |
24 | HG00438.hp1 HG00597.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.129+132_129+133ins others(23): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 49919026 | ||||||
| chr22:49919031 | A | G | 95 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(92): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.129+133A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919031 | |||||||
| chr22:49919039 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0024 others(15): Show |
34 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.129+141C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919039 | |||||||
| chr22:49919153 | ACCCTCGA others(10): Show |
A | 61 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(58): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.130-73_130-57delTC others(15): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 49919153 | ||||||
| chr22:49919154 | CCCTCGAC others(9): Show |
C | 2 | a0003c0004t0002g0143 a0003c0004t0002g0144 |
2 | HG03927.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.130-73_130-58delTC others(14): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 49919154 | ||||||
| chr22:49919221 | T | C | 22 | a0001c0016t0002g0115 a0002c0005t0002g0018 a0002c0005t0002g0033 others(19): Show |
36 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.130-9T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 1/9 | chr22 | 49919221 | |||||||
| chr22:49919331 | C | T | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.212+19C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919331 | |||||||
| chr22:49919366 | T | C | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.212+54T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919366 | |||||||
| chr22:49919434 | C | T | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.212+122C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919434 | |||||||
| chr22:49919476 | C | T | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.212+164C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919476 | |||||||
| chr22:49919531 | G | A | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.213-199G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919531 | |||||||
| chr22:49919551 | G | C | 2 | a0001c0003t0002g0149 a0001c0003t0002g0150 |
2 | NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.213-179G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919551 | |||||||
| chr22:49919557 | C | T | 1 | a0002c0002t0003g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.213-173C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919557 | |||||||
| chr22:49919571 | G | A | 15 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(12): Show |
26 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.213-159G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919571 | |||||||
| chr22:49919581 | C | G | 1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.213-149C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919581 | |||||||
| chr22:49919587 | TC | T | 14 | a0002c0002t0001g0017 a0002c0002t0001g0101 a0002c0002t0001g0104 others(11): Show |
17 | HG01109.hp2 HG01256.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.213-139delC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 49919587 | ||||||
| chr22:49919710 | G | C | 81 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(78): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.213-20G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919710 | |||||||
| chr22:49919711 | G | A | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.213-19G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 2/9 | chr22 | 49919711 | |||||||
| chr22:49920051 | T | C | 2 | a0002c0012t0001g0088 a0002c0012t0001g0089 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.324-105T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 3/9 | chr22 | 49920051 | |||||||
| chr22:49920079 | A | G | 41 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(38): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.324-77A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 3/9 | chr22 | 49920079 | |||||||
| chr22:49920376 | G | A | 4 | a0001c0003t0002g0116 a0001c0003t0002g0117 a0001c0003t0002g0118 others(1): Show |
4 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+129G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920376 | |||||||
| chr22:49920420 | C | A | 13 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(10): Show |
24 | HG00438.hp1 HG00597.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+173C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920420 | |||||||
| chr22:49920424 | G | A | 1 | a0001c0003t0002g0120 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.415+177G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920424 | |||||||
| chr22:49920426 | C | T | 41 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(38): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.415+179C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920426 | |||||||
| chr22:49920502 | C | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0072 a0001c0001t0001g0073 |
4 | HG02129.hp1 NA18990.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+255C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920502 | |||||||
| chr22:49920570 | G | A | 1 | a0001c0016t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+323G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920570 | |||||||
| chr22:49920599 | G | A | 4 | a0002c0005t0002g0018 a0002c0005t0002g0033 a0002c0005t0002g0145 others(1): Show |
7 | HG01361.hp1 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.415+352G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920599 | |||||||
| chr22:49920623 | G | A | 1 | a0001c0003t0002g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415+376G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920623 | |||||||
| chr22:49920641 | G | C | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.415+394G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920641 | |||||||
| chr22:49920668 | G | A | 40 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(37): Show |
52 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.415+421G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920668 | |||||||
| chr22:49920698 | A | G | 94 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(91): Show |
132 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.415+451A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920698 | |||||||
| chr22:49920870 | G | A | 1 | a0001c0003t0002g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.415+623G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920870 | |||||||
| chr22:49920916 | C | T | 8 | a0002c0002t0001g0009 a0002c0002t0001g0015 a0002c0002t0001g0016 others(5): Show |
16 | HG02040.hp2 HG02257.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.415+669C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920916 | |||||||
| chr22:49920925 | C | T | 57 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(54): Show |
80 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.416-660C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49920925 | |||||||
| chr22:49921057 | G | A | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.416-528G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921057 | |||||||
| chr22:49921063 | T | TCCACACG | 22 | a0001c0016t0002g0115 a0002c0005t0002g0018 a0002c0005t0002g0033 others(19): Show |
36 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.416-505_416-499dup others(7): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 49921063 | ||||||
| chr22:49921068 | A | G | 1 | a0002c0002t0001g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.416-517A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921068 | |||||||
| chr22:49921069 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.416-516C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921069 | |||||||
| chr22:49921161 | C | T | 22 | a0001c0016t0002g0115 a0002c0005t0002g0018 a0002c0005t0002g0033 others(19): Show |
36 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.416-424C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921161 | |||||||
| chr22:49921232 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.416-353A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921232 | |||||||
| chr22:49921279 | G | C | 63 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(60): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.416-306G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921279 | |||||||
| chr22:49921322 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0024 |
5 | HG00423.hp2 HG01934.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-263G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921322 | |||||||
| chr22:49921333 | G | C | 2 | a0002c0012t0001g0088 a0002c0012t0001g0089 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.416-252G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921333 | |||||||
| chr22:49921478 | G | A | 1 | a0001c0003t0002g0152 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.416-107G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921478 | |||||||
| chr22:49921504 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.416-81T>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921504 | |||||||
| chr22:49921580 | T | C | 38 | a0002c0002t0001g0009 a0002c0002t0001g0015 a0002c0002t0001g0016 others(35): Show |
53 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(50): Show |
splice_region_variant&intron_variant | LOW | c.416-5T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 4/9 | chr22 | 49921580 | |||||||
| chr22:49921765 | C | T | 28 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(25): Show |
34 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(31): Show |
splice_region_variant&intron_variant | LOW | c.592+4C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49921765 | |||||||
| chr22:49921773 | G | A | 1 | a0002c0002t0001g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592+12G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49921773 | |||||||
| chr22:49921830 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA18941.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.592+69T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49921830 | |||||||
| chr22:49921859 | C | CT | 42 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(39): Show |
55 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.592+101dupT | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr22 | 49921859 | ||||||
| chr22:49921878 | A | G | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.592+117A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49921878 | |||||||
| chr22:49921889 | A | G | 24 | a0002c0002t0001g0009 a0002c0002t0001g0015 a0002c0002t0001g0016 others(21): Show |
35 | HG00741.hp1 HG01255.hp1 HG02040.hp2 others(32): Show |
intron_variant | MODIFIER | c.592+128A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49921889 | |||||||
| chr22:49921979 | G | A | 19 | a0001c0003t0002g0010 a0001c0003t0002g0034 a0001c0003t0002g0035 others(16): Show |
25 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.592+218G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49921979 | |||||||
| chr22:49922002 | C | G | 1 | a0002c0002t0001g0027 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.592+241C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922002 | |||||||
| chr22:49922008 | C | T | 6 | a0002c0002t0001g0017 a0002c0002t0001g0106 a0002c0002t0001g0107 others(3): Show |
8 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+247C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922008 | |||||||
| chr22:49922074 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG00733.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.592+313G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922074 | |||||||
| chr22:49922090 | C | T | 1 | a0001c0011t0001g0086 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.592+329C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922090 | |||||||
| chr22:49922102 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.592+341A>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922102 | |||||||
| chr22:49922256 | TAGTCAGG others(31): Show |
T | 19 | a0001c0001t0001g0006 a0002c0002t0001g0015 a0002c0002t0001g0097 others(16): Show |
36 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.593-327_593-290del others(38): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr22 | 49922256 | ||||||
| chr22:49922276 | G | T | 41 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(38): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.593-336G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922276 | |||||||
| chr22:49922280 | C | G | 41 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(38): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.593-332C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922280 | |||||||
| chr22:49922287 | CCCTCAGC others(31): Show |
C | 22 | a0001c0007t0002g0129 a0001c0007t0002g0130 a0001c0007t0002g0131 others(19): Show |
32 | HG00741.hp1 HG01361.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.593-321_593-284del others(38): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr22 | 49922287 | ||||||
| chr22:49922304 | C | T | 56 | a0001c0001t0001g0070 a0001c0003t0002g0008 a0001c0003t0002g0010 others(53): Show |
71 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.593-308C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922304 | |||||||
| chr22:49922325 | G | C | 32 | a0001c0001t0001g0070 a0002c0002t0001g0017 a0002c0002t0001g0095 others(29): Show |
46 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.593-287G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922325 | |||||||
| chr22:49922367 | C | T | 14 | a0001c0003t0002g0008 a0001c0003t0002g0120 a0001c0003t0002g0126 others(11): Show |
20 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.593-245C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922367 | |||||||
| chr22:49922547 | G | A | 1 | a0002c0012t0001g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.593-65G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 5/9 | chr22 | 49922547 | |||||||
| chr22:49922721 | C | T | 42 | a0001c0001t0001g0070 a0002c0002t0001g0017 a0002c0002t0001g0095 others(39): Show |
58 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.688+14C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922721 | |||||||
| chr22:49922726 | G | A | 50 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(47): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.688+19G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922726 | |||||||
| chr22:49922746 | G | GAGGCGTG others(51): Show |
1 | a0002c0002t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.688+86_688+87insAT others(56): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922746 | ||||||
| chr22:49922746 | G | GAGGCGTG others(80): Show |
3 | a0002c0002t0001g0104 a0002c0002t0003g0028 a0002c0002t0003g0105 |
4 | HG02040.hp1 HG03139.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+86_688+87insAT others(85): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922746 | ||||||
| chr22:49922746 | G | GAGGCGTG others(109): Show |
9 | a0002c0002t0001g0017 a0002c0002t0001g0101 a0002c0002t0001g0106 others(6): Show |
11 | HG01256.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.688+86_688+87insAT others(114): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922746 | ||||||
| chr22:49922746 | G | GAGGCGTG others(138): Show |
1 | a0002c0002t0003g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.688+86_688+87insAT others(143): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922746 | ||||||
| chr22:49922751 | G | A | 2 | a0001c0001t0001g0038 a0002c0012t0001g0088 |
2 | HG02738.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.688+44G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922751 | |||||||
| chr22:49922765 | A | ATGGGGGC others(24): Show |
1 | a0002c0005t0002g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.688+88_688+89insGT others(29): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922765 | ||||||
| chr22:49922780 | G | A | 1 | a0002c0002t0001g0096 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.688+73G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922780 | |||||||
| chr22:49922781 | T | TGGGGGGT others(81): Show |
2 | a0001c0001t0001g0070 a0002c0002t0001g0111 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.688+86_688+87insAT others(86): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922781 | ||||||
| chr22:49922788 | T | G | 1 | a0002c0002t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.688+81T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922788 | |||||||
| chr22:49922788 | T | TGTGAGAT others(51): Show |
1 | a0007c0019t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.688+86_688+87insAT others(56): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922788 | ||||||
| chr22:49922796 | A | G | 98 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0070 others(95): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.688+89A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922796 | |||||||
| chr22:49922811 | A | AG | 6 | a0001c0001t0001g0022 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
7 | HG00597.hp2 HG00621.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.688+110dupG | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922811 | ||||||
| chr22:49922823 | A | G | 76 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(73): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.688+116A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922823 | |||||||
| chr22:49922834 | G | A | 6 | a0002c0005t0002g0018 a0002c0005t0002g0033 a0002c0005t0002g0145 others(3): Show |
9 | HG01361.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.688+127G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922834 | |||||||
| chr22:49922840 | TGGG | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0066 |
5 | HG00099.hp2 HG00323.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+136_688+138del others(3): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922840 | ||||||
| chr22:49922845 | G | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.688+138G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922845 | |||||||
| chr22:49922846 | C | T | 1 | a0001c0007t0002g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.688+139C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922846 | |||||||
| chr22:49922854 | GT | G | 72 | a0001c0001t0001g0075 a0001c0003t0002g0008 a0001c0003t0002g0010 others(69): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.688+148delT | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922854 | |||||||
| chr22:49922855 | T | G | 4 | a0001c0001t0001g0076 a0002c0002t0001g0100 a0003c0004t0009g0141 others(1): Show |
4 | HG03139.hp1 HG04204.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+148T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922855 | |||||||
| chr22:49922858 | GGCT | G | 4 | a0001c0001t0001g0076 a0002c0002t0001g0100 a0003c0004t0009g0141 others(1): Show |
4 | HG03139.hp1 HG04204.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+152_688+154del others(3): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922858 | |||||||
| chr22:49922860 | C | T | 71 | a0001c0001t0001g0075 a0001c0003t0002g0008 a0001c0003t0002g0010 others(68): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.688+153C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922860 | |||||||
| chr22:49922861 | T | G | 72 | a0001c0001t0001g0075 a0001c0003t0002g0008 a0001c0003t0002g0010 others(69): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.688+154T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922861 | |||||||
| chr22:49922864 | G | A | 72 | a0001c0001t0001g0075 a0001c0003t0002g0008 a0001c0003t0002g0010 others(69): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.688+157G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922864 | |||||||
| chr22:49922864 | G | T | 4 | a0001c0001t0001g0076 a0002c0002t0001g0100 a0003c0004t0009g0141 others(1): Show |
4 | HG03139.hp1 HG04204.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+157G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922864 | |||||||
| chr22:49922866 | G | A | 4 | a0001c0001t0001g0076 a0002c0002t0001g0100 a0003c0004t0009g0141 others(1): Show |
4 | HG03139.hp1 HG04204.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+159G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922866 | |||||||
| chr22:49922867 | T | G | 4 | a0001c0001t0001g0076 a0002c0002t0001g0100 a0003c0004t0009g0141 others(1): Show |
4 | HG03139.hp1 HG04204.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.688+160T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922867 | |||||||
| chr22:49922867 | TGTG | T | 72 | a0001c0001t0001g0075 a0001c0003t0002g0008 a0001c0003t0002g0010 others(69): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.688+162_688+164del others(3): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922867 | ||||||
| chr22:49922876 | C | G | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0002c0002t0001g0009 others(10): Show |
20 | HG00741.hp1 HG02040.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.688+169C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922876 | |||||||
| chr22:49922883 | TGTGG | T | 61 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(58): Show |
87 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.688+178_688+181del others(4): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922883 | ||||||
| chr22:49922883 | TGTGGGGG others(8): Show |
T | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0002c0002t0001g0009 others(10): Show |
20 | HG00741.hp1 HG02040.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.688+183_688+197del others(15): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922883 | ||||||
| chr22:49922885 | T | G | 1 | a0001c0007t0002g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.688+178T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922885 | |||||||
| chr22:49922891 | A | G | 62 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(59): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.688+184A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922891 | |||||||
| chr22:49922894 | A | G | 62 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(59): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.688+187A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922894 | |||||||
| chr22:49922900 | T | G | 1 | a0001c0003t0002g0149 | 1 | NA18976.hp1 | intron_variant | MODIFIER | c.688+193T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922900 | |||||||
| chr22:49922900 | T | TG | 57 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(54): Show |
83 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.688+197dupG | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922900 | ||||||
| chr22:49922900 | TGGGGCGT others(21): Show |
T | 3 | a0001c0001t0001g0040 a0002c0012t0001g0088 a0002c0012t0001g0089 |
3 | HG02922.hp1 NA18968.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.688+214_688+241del others(28): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922900 | ||||||
| chr22:49922901 | G | A | 2 | a0001c0011t0001g0077 a0001c0011t0001g0086 |
2 | HG00609.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.688+194G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922901 | |||||||
| chr22:49922905 | C | G | 62 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(59): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.688+198C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922905 | |||||||
| chr22:49922906 | G | T | 14 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0007t0002g0132 others(11): Show |
21 | HG00741.hp1 HG02040.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+199G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922906 | |||||||
| chr22:49922909 | A | G | 14 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0007t0002g0132 others(11): Show |
21 | HG00741.hp1 HG02040.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+202A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922909 | |||||||
| chr22:49922914 | TG | T | 59 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(56): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.688+212delG | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922914 | ||||||
| chr22:49922915 | GGGGGCGT others(5): Show |
G | 14 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0007t0002g0132 others(11): Show |
21 | HG00741.hp1 HG02040.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.688+213_688+224del others(12): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922915 | ||||||
| chr22:49922920 | C | G | 3 | a0001c0003t0002g0149 a0003c0004t0002g0140 a0003c0004t0009g0141 |
3 | HG02056.hp2 HG04204.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.688+213C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922920 | |||||||
| chr22:49922921 | G | T | 59 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(56): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.688+214G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922921 | |||||||
| chr22:49922924 | A | G | 59 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(56): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.688+217A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922924 | |||||||
| chr22:49922924 | A | T | 3 | a0001c0003t0002g0149 a0003c0004t0002g0140 a0003c0004t0009g0141 |
3 | HG02056.hp2 HG04204.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.688+217A>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922924 | |||||||
| chr22:49922926 | GT | G | 3 | a0001c0003t0002g0149 a0003c0004t0002g0140 a0003c0004t0009g0141 |
3 | HG02056.hp2 HG04204.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.688+220delT | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922926 | |||||||
| chr22:49922927 | T | TGTG | 59 | a0001c0003t0002g0008 a0001c0003t0002g0010 a0001c0003t0002g0034 others(56): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.688+221_688+222ins others(3): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 49922927 | ||||||
| chr22:49922949 | A | G | 76 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(73): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.688+242A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922949 | |||||||
| chr22:49922995 | G | A | 1 | a0010c0026t0001g0090 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.689-239G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49922995 | |||||||
| chr22:49923064 | G | C | 3 | a0002c0012t0001g0088 a0002c0012t0001g0089 a0010c0026t0001g0090 |
3 | HG02922.hp1 HG03688.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.689-170G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923064 | |||||||
| chr22:49923111 | G | C | 1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.689-123G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923111 | |||||||
| chr22:49923112 | C | G | 1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.689-122C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923112 | |||||||
| chr22:49923118 | T | G | 1 | a0002c0002t0001g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.689-116T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923118 | |||||||
| chr22:49923149 | G | A | 15 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(12): Show |
26 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.689-85G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923149 | |||||||
| chr22:49923187 | T | C | 80 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(77): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.689-47T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923187 | |||||||
| chr22:49923188 | G | A | 1 | a0001c0003t0002g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.689-46G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 6/9 | chr22 | 49923188 | |||||||
| chr22:49923336 | T | TCTGCACT others(7): Show |
75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.772+24_772+37dupAC others(12): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 49923336 | ||||||
| chr22:49923401 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.772+84T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923401 | |||||||
| chr22:49923497 | A | G | 15 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(12): Show |
26 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.772+180A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923497 | |||||||
| chr22:49923539 | C | T | 76 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(73): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.772+222C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923539 | |||||||
| chr22:49923558 | CACTGCTC others(26): Show |
C | 1 | a0001c0001t0001g0065 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.772+242_772+274del others(33): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923558 | |||||||
| chr22:49923572 | C | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0081 |
2 | HG00438.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.772+255C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923572 | |||||||
| chr22:49923584 | C | T | 3 | a0001c0001t0001g0080 a0002c0002t0001g0015 a0002c0002t0001g0097 |
5 | HG02559.hp2 HG02717.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.772+267C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923584 | |||||||
| chr22:49923648 | C | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0023 others(64): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.772+331C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923648 | |||||||
| chr22:49923682 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.772+365G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923682 | |||||||
| chr22:49923698 | C | T | 27 | a0002c0005t0002g0018 a0002c0005t0002g0033 a0002c0005t0002g0145 others(24): Show |
43 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.772+381C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923698 | |||||||
| chr22:49923753 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.772+436G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923753 | |||||||
| chr22:49923761 | A | AAT | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.772+444_772+445ins others(2): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923761 | |||||||
| chr22:49923762 | C | CTG | 21 | a0001c0001t0001g0070 a0001c0016t0002g0115 a0002c0002t0001g0017 others(18): Show |
24 | HG01109.hp2 HG01256.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.772+446_772+447ins others(2): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 49923762 | ||||||
| chr22:49923762 | C | G | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.772+445C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923762 | |||||||
| chr22:49923770 | C | T | 3 | a0001c0003t0002g0036 a0001c0003t0002g0159 a0001c0003t0002g0160 |
4 | HG00099.hp1 HG00140.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.772+453C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923770 | |||||||
| chr22:49923888 | C | G | 1 | a0002c0002t0001g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.773-472C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923888 | |||||||
| chr22:49923921 | G | A | 48 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(45): Show |
65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.773-439G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49923921 | |||||||
| chr22:49924028 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.773-332G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924028 | |||||||
| chr22:49924039 | G | A | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.773-321G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924039 | |||||||
| chr22:49924049 | G | T | 1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.773-311G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924049 | |||||||
| chr22:49924066 | A | G | 48 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(45): Show |
65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.773-294A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924066 | |||||||
| chr22:49924155 | A | G | 63 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(60): Show |
91 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.773-205A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924155 | |||||||
| chr22:49924177 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.773-183T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924177 | |||||||
| chr22:49924203 | T | G | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.773-157T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924203 | |||||||
| chr22:49924209 | G | A | 47 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(44): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.773-151G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924209 | |||||||
| chr22:49924226 | C | A | 1 | a0004c0006t0004g0029 | 2 | HG01255.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.773-134C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924226 | |||||||
| chr22:49924300 | G | T | 2 | a0001c0003t0002g0149 a0001c0003t0002g0150 |
2 | NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.773-60G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924300 | |||||||
| chr22:49924341 | C | T | 47 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(44): Show |
64 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.773-19C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 7/9 | chr22 | 49924341 | |||||||
| chr22:49924551 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.868+96T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924551 | |||||||
| chr22:49924664 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+209T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924664 | |||||||
| chr22:49924723 | C | T | 1 | a0001c0003t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.868+268C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924723 | |||||||
| chr22:49924752 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.868+297G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924752 | |||||||
| chr22:49924764 | G | C | 1 | a0001c0016t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.868+309G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924764 | |||||||
| chr22:49924774 | T | G | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+319T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924774 | |||||||
| chr22:49924797 | C | T | 1 | a0004c0013t0002g0122 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.868+342C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924797 | |||||||
| chr22:49924858 | C | T | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+403C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924858 | |||||||
| chr22:49924861 | C | G | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+406C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924861 | |||||||
| chr22:49924862 | A | G | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+407A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924862 | |||||||
| chr22:49924866 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+411T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924866 | |||||||
| chr22:49924870 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.868+415T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924870 | |||||||
| chr22:49924914 | G | A | 1 | a0002c0005t0002g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.868+459G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924914 | |||||||
| chr22:49924917 | G | A | 1 | a0003c0004t0007g0135 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.868+462G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924917 | |||||||
| chr22:49924957 | C | A | 1 | a0002c0015t0002g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.869-460C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924957 | |||||||
| chr22:49924973 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 others(77): Show |
121 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.869-444T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924973 | |||||||
| chr22:49924974 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.869-443A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924974 | |||||||
| chr22:49924988 | G | A | 1 | a0002c0015t0002g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.869-429G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924988 | |||||||
| chr22:49924991 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.869-426C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924991 | |||||||
| chr22:49924992 | G | A | 5 | a0002c0002t0001g0096 a0002c0002t0005g0026 a0002c0002t0005g0092 others(2): Show |
6 | HG00741.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-425G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49924992 | |||||||
| chr22:49925000 | G | A | 3 | a0002c0012t0001g0088 a0002c0012t0001g0089 a0010c0026t0001g0090 |
3 | HG02922.hp1 HG03688.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.869-417G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925000 | |||||||
| chr22:49925017 | G | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.869-400G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925017 | |||||||
| chr22:49925047 | C | T | 15 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(12): Show |
26 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.869-370C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925047 | |||||||
| chr22:49925087 | C | T | 48 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(45): Show |
65 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.869-330C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925087 | |||||||
| chr22:49925093 | C | T | 76 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(73): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.869-324C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925093 | |||||||
| chr22:49925109 | C | T | 13 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0002c0002t0001g0009 others(10): Show |
20 | HG00741.hp1 HG02040.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.869-308C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925109 | |||||||
| chr22:49925110 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.869-307G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925110 | |||||||
| chr22:49925130 | C | CA | 11 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0072 others(8): Show |
17 | HG00741.hp2 HG01109.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.869-271dupA | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 49925130 | ||||||
| chr22:49925130 | CA | C | 9 | a0001c0001t0001g0062 a0002c0012t0001g0088 a0002c0012t0001g0089 others(6): Show |
11 | HG01255.hp1 HG02922.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.869-271delA | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 49925130 | ||||||
| chr22:49925172 | G | T | 1 | a0001c0016t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.869-245G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925172 | |||||||
| chr22:49925186 | C | T | 26 | a0002c0005t0002g0018 a0002c0005t0002g0033 a0002c0005t0002g0145 others(23): Show |
42 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.869-231C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925186 | |||||||
| chr22:49925279 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.869-138T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925279 | |||||||
| chr22:49925298 | C | T | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.869-119C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 8/9 | chr22 | 49925298 | |||||||
| chr22:49925575 | C | T | 2 | a0001c0001t0001g0070 a0002c0002t0001g0111 |
2 | HG01109.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1009+18C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925575 | |||||||
| chr22:49925613 | G | T | 1 | a0002c0002t0001g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1009+56G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925613 | |||||||
| chr22:49925617 | G | C | 1 | a0007c0019t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1009+60G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925617 | |||||||
| chr22:49925646 | A | C | 2 | a0002c0002t0001g0095 a0007c0019t0001g0094 |
2 | HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1009+89A>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925646 | |||||||
| chr22:49925703 | T | C | 75 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(72): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1009+146T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925703 | |||||||
| chr22:49925724 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1009+167G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925724 | |||||||
| chr22:49925725 | C | T | 1 | a0001c0001t0001g0005 | 9 | HG00639.hp1 HG01081.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1009+168C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925725 | |||||||
| chr22:49925726 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1009+169G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925726 | |||||||
| chr22:49925822 | C | G | 1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.1009+265C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925822 | |||||||
| chr22:49925823 | G | C | 1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.1009+266G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925823 | |||||||
| chr22:49925846 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1009+289G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49925846 | |||||||
| chr22:49926053 | G | A | 21 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(18): Show |
34 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.1009+496G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926053 | |||||||
| chr22:49926088 | G | A | 1 | a0002c0002t0003g0028 | 2 | HG02040.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1009+531G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926088 | |||||||
| chr22:49926136 | C | T | 2 | a0002c0012t0001g0088 a0002c0012t0001g0089 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1009+579C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926136 | |||||||
| chr22:49926216 | C | T | 1 | a0001c0016t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1009+659C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926216 | |||||||
| chr22:49926320 | G | A | 1 | a0002c0014t0002g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1009+763G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926320 | |||||||
| chr22:49926321 | C | T | 1 | a0012c0022t0001g0044 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1009+764C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926321 | |||||||
| chr22:49926332 | CCTCACAG others(27): Show |
C | 1 | a0001c0003t0002g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1009+776_1009+809d others(36): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926332 | |||||||
| chr22:49926381 | G | T | 74 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(71): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1009+824G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926381 | |||||||
| chr22:49926457 | A | G | 69 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0003t0002g0008 others(66): Show |
99 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1010-798A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926457 | |||||||
| chr22:49926526 | A | G | 4 | a0004c0006t0004g0029 a0004c0006t0004g0030 a0004c0006t0010g0125 others(1): Show |
6 | HG01255.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-729A>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926526 | |||||||
| chr22:49926531 | C | T | 4 | a0004c0006t0004g0029 a0004c0006t0004g0030 a0004c0006t0010g0125 others(1): Show |
6 | HG01255.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-724C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926531 | |||||||
| chr22:49926561 | A | AC | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0049 others(11): Show |
14 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.1010-689dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926561 | ||||||
| chr22:49926575 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-680C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926575 | |||||||
| chr22:49926579 | G | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-676G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926579 | |||||||
| chr22:49926580 | C | T | 1 | a0001c0016t0002g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1010-675C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926580 | |||||||
| chr22:49926590 | G | C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-665G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926590 | |||||||
| chr22:49926593 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-662C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926593 | |||||||
| chr22:49926595 | G | GCCTCTTG others(484): Show |
1 | a0001c0003t0002g0154 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1010-649_1010-648i others(493): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926595 | ||||||
| chr22:49926604 | C | T | 8 | a0002c0002t0001g0100 a0002c0005t0002g0018 a0002c0005t0002g0033 others(5): Show |
11 | HG01361.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1010-651C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926604 | |||||||
| chr22:49926608 | C | G | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-647C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926608 | |||||||
| chr22:49926611 | T | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-644T>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926611 | |||||||
| chr22:49926611 | T | TC | 20 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0060 others(17): Show |
21 | HG00408.hp1 HG01243.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1010-638dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926611 | ||||||
| chr22:49926614 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-641C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926614 | |||||||
| chr22:49926620 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-635C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926620 | |||||||
| chr22:49926622 | T | C | 4 | a0001c0003t0002g0154 a0001c0003t0002g0161 a0001c0003t0002g0162 others(1): Show |
4 | HG02602.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-633T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926622 | |||||||
| chr22:49926623 | C | CGGTCCCC others(122): Show |
1 | a0001c0003t0002g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1010-608_1010-607i others(131): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926623 | ||||||
| chr22:49926623 | C | CGGTCCCC others(2195): Show |
1 | a0001c0003t0002g0158 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1010-608_1010-607i others(2204): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926623 | ||||||
| chr22:49926623 | C | CGGTCCCC others(123): Show |
1 | a0005c0008t0002g0157 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1010-608_1010-607i others(132): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926623 | ||||||
| chr22:49926623 | C | G | 4 | a0001c0003t0002g0154 a0001c0003t0002g0161 a0001c0003t0002g0162 others(1): Show |
4 | HG02602.hp1 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-632C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926623 | |||||||
| chr22:49926626 | T | TC | 4 | a0001c0001t0001g0064 a0003c0004t0002g0140 a0003c0004t0009g0141 others(1): Show |
4 | HG02056.hp2 HG03491.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-625dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926626 | ||||||
| chr22:49926644 | T | TC | 7 | a0001c0003t0002g0035 a0001c0003t0002g0149 a0001c0003t0002g0150 others(4): Show |
8 | HG00140.hp2 HG02145.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1010-608dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926644 | ||||||
| chr22:49926644 | T | TCCCCCCC others(89): Show |
1 | a0001c0003t0002g0036 | 2 | HG01074.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1010-608_1010-607i others(98): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926644 | ||||||
| chr22:49926644 | T | TCCCCCCC others(21): Show |
1 | a0001c0003t0002g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1010-608_1010-607i others(30): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926644 | ||||||
| chr22:49926648 | A | C | 17 | a0001c0003t0002g0035 a0001c0003t0002g0036 a0001c0003t0002g0149 others(14): Show |
19 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.1010-607A>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926648 | |||||||
| chr22:49926649 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-606C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926649 | |||||||
| chr22:49926655 | T | C | 19 | a0001c0001t0001g0065 a0001c0003t0002g0035 a0001c0003t0002g0036 others(16): Show |
21 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1010-600T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926655 | |||||||
| chr22:49926655 | T | TGGGTCCC others(125): Show |
1 | a0002c0015t0002g0147 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(134): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926655 | ||||||
| chr22:49926655 | T | TGGGTCCC others(127): Show |
1 | a0002c0005t0002g0033 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(136): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926655 | ||||||
| chr22:49926655 | T | TGGGTCCC others(608): Show |
1 | a0001c0003t0002g0034 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1010-572_1010-571i others(617): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926655 | ||||||
| chr22:49926655 | TGGGTCCC others(26): Show |
T | 5 | a0001c0007t0002g0129 a0001c0007t0002g0130 a0001c0007t0002g0131 others(2): Show |
5 | HG02055.hp1 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1010-571_1010-539d others(35): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926655 | ||||||
| chr22:49926655 | TGGGTCCC others(80): Show |
T | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0002c0002t0001g0009 others(4): Show |
14 | HG01255.hp1 HG02040.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1010-538_1010-452d others(89): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926655 | ||||||
| chr22:49926656 | G | C | 1 | a0001c0003t0002g0161 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1010-599G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926656 | |||||||
| chr22:49926656 | G | GGGTCCCC others(116): Show |
1 | a0005c0008t0002g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1010-572_1010-571i others(125): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926656 | ||||||
| chr22:49926657 | G | C | 1 | a0001c0003t0002g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1010-598G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926657 | |||||||
| chr22:49926659 | TCCCCTCT others(47): Show |
T | 8 | a0003c0004t0002g0003 a0003c0004t0002g0031 a0003c0004t0002g0032 others(5): Show |
19 | HG00438.hp1 HG00597.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1010-538_1010-485d others(56): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926659 | ||||||
| chr22:49926668 | G | T | 1 | a0001c0003t0002g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1010-587G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926668 | |||||||
| chr22:49926670 | C | T | 1 | a0001c0003t0002g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1010-585C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926670 | |||||||
| chr22:49926676 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-579C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926676 | |||||||
| chr22:49926677 | T | TC | 29 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(26): Show |
33 | HG00438.hp2 HG00642.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1010-572dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926677 | ||||||
| chr22:49926677 | T | TCCCCCCC others(21): Show |
3 | a0001c0003t0002g0035 a0001c0003t0002g0160 a0001c0003t0002g0162 |
3 | HG00140.hp2 HG02735.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1010-572_1010-571i others(30): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926677 | ||||||
| chr22:49926677 | T | TCCCCCCC others(126): Show |
1 | a0005c0008t0002g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1010-572_1010-571i others(135): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926677 | ||||||
| chr22:49926678 | CCCCCCAC others(79): Show |
C | 4 | a0002c0002t0001g0016 a0002c0002t0001g0096 a0002c0002t0001g0098 others(1): Show |
4 | HG00741.hp1 HG03209.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-571_1010-486d others(88): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926678 | ||||||
| chr22:49926685 | CCCCGGGT others(46): Show |
C | 1 | a0003c0004t0002g0142 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1010-566_1010-514d others(55): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926685 | ||||||
| chr22:49926686 | C | A | 1 | a0001c0001t0001g0004 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1010-569C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926686 | |||||||
| chr22:49926688 | C | T | 5 | a0001c0003t0002g0035 a0001c0003t0002g0160 a0001c0003t0002g0162 others(2): Show |
5 | HG00140.hp2 HG02735.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-567C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926688 | |||||||
| chr22:49926689 | G | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-566G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926689 | |||||||
| chr22:49926689 | G | C | 5 | a0001c0003t0002g0035 a0001c0003t0002g0160 a0001c0003t0002g0162 others(2): Show |
5 | HG00140.hp2 HG02735.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-566G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926689 | |||||||
| chr22:49926690 | G | C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-565G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926690 | |||||||
| chr22:49926692 | TCCCCTCT others(14): Show |
T | 7 | a0001c0003t0002g0116 a0001c0003t0002g0117 a0001c0003t0002g0118 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1010-538_1010-518d others(23): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926692 | ||||||
| chr22:49926695 | CCTCTTGC others(43): Show |
C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-559_1010-510d others(52): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926695 | |||||||
| chr22:49926707 | CCCTCCCC others(46): Show |
C | 1 | a0003c0017t0002g0138 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1010-545_1010-493d others(55): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926707 | ||||||
| chr22:49926711 | CCCCCCCT others(13): Show |
C | 4 | a0001c0007t0002g0129 a0001c0007t0002g0130 a0001c0007t0002g0132 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-537_1010-518d others(22): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926711 | ||||||
| chr22:49926711 | CCCCCCCT others(79): Show |
C | 1 | a0002c0002t0001g0099 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1010-537_1010-452d others(88): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926711 | ||||||
| chr22:49926712 | CCCCCCTC others(12): Show |
C | 1 | a0001c0007t0002g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1010-537_1010-519d others(21): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926712 | ||||||
| chr22:49926713 | C | CACCACCC others(173): Show |
1 | a0001c0003t0002g0008 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1010-542_1010-541i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926713 | |||||||
| chr22:49926713 | C | CCCCACCC others(5): Show |
9 | a0001c0003t0002g0034 a0001c0003t0002g0036 a0001c0003t0002g0154 others(6): Show |
11 | HG00642.hp2 HG01074.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1010-539_1010-538i others(14): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(372): Show |
1 | a0002c0002t0001g0109 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(381): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(138): Show |
1 | a0001c0001t0001g0001 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(147): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(105): Show |
1 | a0002c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(114): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(205): Show |
1 | a0001c0001t0001g0014 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(214): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(99): Show |
2 | a0001c0003t0002g0149 a0001c0003t0002g0150 |
2 | NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(108): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(147): Show |
1 | a0003c0004t0009g0141 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(156): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(39): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0008g0001 |
3 | HG01192.hp2 HG03490.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(48): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(176): Show |
1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(185): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(174): Show |
1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(72): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0066 |
3 | HG00639.hp2 HG02074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(81): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(174): Show |
1 | a0001c0001t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(171): Show |
1 | a0001c0001t0001g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(180): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(105): Show |
4 | a0001c0001t0001g0001 a0001c0003t0002g0153 a0002c0002t0001g0100 others(1): Show |
4 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-539_1010-538i others(114): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(138): Show |
1 | a0001c0001t0001g0002 | 3 | HG02015.hp2 NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(147): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(339): Show |
1 | a0001c0001t0001g0001 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(348): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(239): Show |
1 | a0002c0002t0001g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(248): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(306): Show |
1 | a0002c0002t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(315): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(909): Show |
1 | a0002c0002t0001g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(918): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(173): Show |
1 | a0009c0020t0001g0048 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(139): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0016t0002g0115 others(7): Show |
12 | HG01361.hp1 HG01891.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1010-539_1010-538i others(148): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(172): Show |
1 | a0001c0021t0001g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(181): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(172): Show |
36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(33): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1010-539_1010-538i others(181): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(438): Show |
1 | a0001c0001t0011g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(447): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(205): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0012 |
2 | HG02723.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(214): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(238): Show |
2 | a0001c0001t0001g0001 a0008c0024t0001g0051 |
3 | HG01168.hp2 HG01943.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(247): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(304): Show |
1 | a0007c0019t0001g0094 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(313): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(505): Show |
1 | a0001c0001t0001g0005 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(514): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(205): Show |
1 | a0001c0001t0001g0073 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(214): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(239): Show |
1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(248): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(173): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0020 |
3 | HG00408.hp1 HG02071.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(173): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0049 others(1): Show |
5 | HG00609.hp2 HG02080.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-539_1010-538i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(173): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0068 |
3 | HG00597.hp2 HG00621.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(174): Show |
1 | a0001c0001t0001g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(134): Show |
1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(143): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(209): Show |
1 | a0012c0022t0001g0044 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(218): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(173): Show |
2 | a0001c0001t0001g0001 a0001c0001t0006g0002 |
2 | HG02155.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(174): Show |
1 | a0001c0001t0001g0022 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(175): Show |
1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(184): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(301): Show |
1 | a0002c0002t0005g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(310): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(173): Show |
1 | a0001c0001t0001g0007 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(174): Show |
1 | a0002c0009t0001g0001 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(174): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0057 |
2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(915): Show |
1 | a0001c0001t0001g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(924): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(297): Show |
1 | a0001c0001t0001g0004 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(306): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(264): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0042 |
6 | HG00642.hp1 HG01123.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-539_1010-538i others(273): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(456): Show |
1 | a0001c0001t0001g0004 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1010-539_1010-538i others(465): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(456): Show |
1 | a0001c0001t0001g0001 | 3 | HG02165.hp2 NA18966.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(465): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(423): Show |
1 | a0001c0001t0001g0004 | 3 | NA18747.hp1 NA18954.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1010-539_1010-538i others(432): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(391): Show |
1 | a0001c0001t0001g0067 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(400): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCACCC others(353): Show |
1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1010-539_1010-538i others(362): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACA others(8): Show |
1 | a0005c0008t0002g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(17): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(177): Show |
1 | a0001c0001t0001g0062 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(186): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(6): Show |
16 | a0001c0003t0002g0008 a0001c0003t0002g0035 a0001c0003t0002g0120 others(13): Show |
18 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1010-538_1010-537i others(15): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(39): Show |
2 | a0001c0003t0002g0160 a0002c0002t0003g0112 |
2 | HG00140.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1010-538_1010-537i others(48): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(330): Show |
1 | a0001c0003t0002g0010 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(339): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(328): Show |
1 | a0001c0003t0002g0010 | 2 | HG00423.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1010-538_1010-537i others(337): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(106): Show |
3 | a0002c0002t0001g0017 a0002c0002t0001g0107 a0002c0002t0003g0028 |
6 | HG02040.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-538_1010-537i others(115): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(139): Show |
2 | a0002c0002t0001g0015 a0002c0002t0001g0097 |
4 | HG02559.hp2 HG02717.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-538_1010-537i others(148): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(330): Show |
1 | a0001c0003t0002g0034 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(339): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(40): Show |
2 | a0001c0001t0001g0001 a0001c0018t0002g0134 |
2 | HG06807.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1010-538_1010-537i others(49): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(140): Show |
1 | a0002c0002t0003g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(149): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(173): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0007 |
3 | HG01496.hp2 HG02145.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1010-538_1010-537i others(182): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(239): Show |
1 | a0001c0001t0001g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(248): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(174): Show |
1 | a0001c0001t0001g0060 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(331): Show |
1 | a0001c0003t0002g0010 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(340): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(141): Show |
1 | a0001c0001t0001g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(150): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(174): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0005 |
2 | HG01981.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1010-538_1010-537i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(174): Show |
1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(183): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(209): Show |
1 | a0001c0001t0001g0083 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(218): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(241): Show |
1 | a0001c0001t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(250): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(175): Show |
1 | a0001c0001t0001g0058 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(184): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCACC others(490): Show |
1 | a0001c0001t0001g0047 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(499): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCCAC others(107): Show |
1 | a0002c0002t0003g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(116): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCCAC others(342): Show |
1 | a0002c0002t0003g0102 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(351): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCCAC others(42): Show |
1 | a0001c0003t0002g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(51): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCCAC others(143): Show |
1 | a0003c0004t0002g0140 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(152): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCCAC others(102): Show |
1 | a0001c0003t0002g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(111): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCGTC others(266): Show |
1 | a0001c0003t0002g0035 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1010-538_1010-537i others(275): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926713 | C | CCCCCGTC others(333): Show |
1 | a0001c0003t0002g0152 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1010-538_1010-537i others(342): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926713 | ||||||
| chr22:49926731 | T | TC | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(17): Show |
21 | HG00323.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.1010-518dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926731 | ||||||
| chr22:49926735 | C | A | 3 | a0001c0001t0001g0037 a0007c0019t0001g0094 a0008c0024t0001g0051 |
3 | HG02572.hp1 HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1010-520C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926735 | |||||||
| chr22:49926742 | C | T | 4 | a0001c0001t0001g0037 a0004c0006t0002g0123 a0007c0019t0001g0094 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-513C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926742 | |||||||
| chr22:49926743 | G | C | 1 | a0004c0006t0002g0123 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1010-512G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926743 | |||||||
| chr22:49926750 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-505C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926750 | |||||||
| chr22:49926751 | T | C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-504T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926751 | |||||||
| chr22:49926755 | G | C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-500G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926755 | |||||||
| chr22:49926757 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-498C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926757 | |||||||
| chr22:49926764 | T | TC | 32 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0055 others(29): Show |
35 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.1010-485dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926764 | ||||||
| chr22:49926776 | G | C | 1 | a0005c0008t0002g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1010-479G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926776 | |||||||
| chr22:49926790 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-465C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926790 | |||||||
| chr22:49926797 | T | TC | 30 | a0001c0001t0001g0047 a0001c0001t0001g0057 a0001c0001t0001g0073 others(27): Show |
44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1010-452dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926797 | ||||||
| chr22:49926810 | G | GGTCCCCT others(20): Show |
1 | a0001c0001t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1010-436_1010-410d others(29): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926810 | ||||||
| chr22:49926813 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-442C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926813 | |||||||
| chr22:49926830 | T | TC | 20 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0040 others(17): Show |
22 | HG00597.hp2 HG00741.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1010-418dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926830 | ||||||
| chr22:49926830 | TC | T | 17 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0002c0002t0001g0009 others(14): Show |
28 | HG01256.hp1 HG02040.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.1010-418delC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926830 | ||||||
| chr22:49926831 | C | CCCCCCCA others(59): Show |
1 | a0002c0002t0003g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1010-418_1010-417i others(68): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926831 | ||||||
| chr22:49926831 | C | CCCCCCCA others(94): Show |
1 | a0002c0002t0001g0108 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1010-418_1010-417i others(103): Show |
CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926831 | ||||||
| chr22:49926837 | C | G | 2 | a0001c0003t0002g0149 a0001c0003t0002g0150 |
2 | NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.1010-418C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926837 | |||||||
| chr22:49926846 | A | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0075 others(63): Show |
94 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1010-409A>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926846 | |||||||
| chr22:49926848 | T | G | 3 | a0001c0003t0002g0149 a0001c0003t0002g0150 a0002c0002t0005g0093 |
3 | HG03041.hp1 NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.1010-407T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926848 | |||||||
| chr22:49926850 | T | C | 3 | a0001c0003t0002g0149 a0001c0003t0002g0150 a0002c0002t0005g0093 |
3 | HG03041.hp1 NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.1010-405T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926850 | |||||||
| chr22:49926857 | T | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-398T>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926857 | |||||||
| chr22:49926857 | T | TC | 18 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0052 others(15): Show |
19 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.1010-391dupC | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr22 | 49926857 | ||||||
| chr22:49926859 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-396C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926859 | |||||||
| chr22:49926869 | T | C | 2 | a0001c0003t0002g0149 a0001c0003t0002g0150 |
2 | NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.1010-386T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926869 | |||||||
| chr22:49926870 | C | G | 2 | a0001c0003t0002g0149 a0001c0003t0002g0150 |
2 | NA18612.hp2 NA18976.hp1 |
intron_variant | MODIFIER | c.1010-385C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926870 | |||||||
| chr22:49926872 | G | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-383G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926872 | |||||||
| chr22:49926882 | G | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-373G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926882 | |||||||
| chr22:49926890 | C | G | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-365C>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926890 | |||||||
| chr22:49926903 | C | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-352C>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926903 | |||||||
| chr22:49926908 | G | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-347G>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926908 | |||||||
| chr22:49926912 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-343C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926912 | |||||||
| chr22:49926916 | T | A | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-339T>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926916 | |||||||
| chr22:49926922 | C | T | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-333C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926922 | |||||||
| chr22:49926923 | T | C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-332T>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926923 | |||||||
| chr22:49926939 | G | C | 1 | a0003c0004t0002g0139 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1010-316G>C | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926939 | |||||||
| chr22:49926958 | C | T | 2 | a0002c0002t0001g0016 a0002c0002t0001g0099 |
4 | HG02040.hp2 NA18940.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-297C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926958 | |||||||
| chr22:49926959 | G | A | 1 | a0003c0004t0002g0137 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1010-296G>A | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926959 | |||||||
| chr22:49926972 | T | G | 1 | a0011c0023t0001g0078 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.1010-283T>G | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49926972 | |||||||
| chr22:49927100 | C | T | 1 | a0002c0005t0002g0033 | 2 | HG01361.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1010-155C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49927100 | |||||||
| chr22:49927158 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1010-97C>T | CRELD2 | ENSG00000184164.15 | transcript | ENST00000328268.9 | protein_coding | 9/9 | chr22 | 49927158 |