Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 375190 |
| ensemblid | ENSG00000219626.9 |
| hgncid | 24736 |
| symbol | FAM228B |
| name | family with sequence similarity 228 member B |
| refseq_nuc | NM_001145710.2 |
| refseq_prot | NP_001139182.1 |
| ensembl_nuc | ENST00000615575.5 |
| ensembl_prot | ENSP00000482482.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 24123469 |
| end | 24169638 |
| strand | + |
| ver | v1.2 |
| region | chr2:24123469-24169638 |
| region5000 | chr2:24118469-24174638 |
| regionname0 | FAM228B_chr2_24123469_24169638 |
| regionname5000 | FAM228B_chr2_24118469_24174638 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 324 | 242 | 68 | 49 | 93 | 7 | 24 | 72 | FAM228B_chr2_24118469_24174638 | FAM228B | MKNVD others(319): Show |
chr2 | 24118469 | 24174638 |
| a0002 | 0/1 | 324 | 27 | 8 | 5 | 6 | 2 | 5 | 4 | FAM228B_chr2_24118469_24174638 | FAM228B | MKNVD others(319): Show |
chr2 | 24118469 | 24174638 |
| a0003 | 0/0 | 319 | 20 | 2 | 3 | 11 | 3 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | MKNVD others(314): Show |
chr2 | 24118469 | 24174638 |
| a0004 | 0/0 | 324 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | MKNVD others(319): Show |
chr2 | 24118469 | 24174638 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 972 | 141 | 21 | 36 | 67 | 4 | 13 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0002 | 0/0 | 972 | 47 | 12 | 8 | 18 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0003 | 1/0 | 972 | 33 | 27 | 3 | 1 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0006 | 0/0 | 972 | 15 | 4 | 2 | 6 | 0 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0008 | 0/0 | 972 | 3 | 3 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0010 | 0/0 | 972 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0011 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0001c0014 | 0/0 | 972 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0002c0005 | 0/1 | 972 | 16 | 8 | 0 | 5 | 1 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0002c0007 | 0/0 | 972 | 9 | 0 | 4 | 1 | 1 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0002c0009 | 0/0 | 972 | 2 | 0 | 1 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 | ||
| a0003c0004 | 0/0 | 971 | 19 | 2 | 3 | 10 | 3 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(966): Show |
chr2 | 24118469 | 24174638 | ||
| a0003c0013 | 0/0 | 971 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(966): Show |
chr2 | 24118469 | 24174638 | ||
| a0004c0012 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | ATGAA others(967): Show |
chr2 | 24118469 | 24174638 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1369 | 139 | 21 | 36 | 66 | 4 | 12 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0001t0004 | 0/0 | 1369 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0001t0005 | 0/0 | 1379 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1374): Show |
chr2 | 24118469 | 24174638 |
| a0001c0002t0001 | 0/0 | 1369 | 47 | 12 | 8 | 18 | 1 | 8 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0003t0001 | 1/0 | 1369 | 33 | 27 | 3 | 1 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0006t0001 | 0/0 | 1369 | 14 | 3 | 2 | 6 | 0 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0006t0003 | 0/0 | 1369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0008t0001 | 0/0 | 1369 | 3 | 3 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0010t0001 | 0/0 | 1369 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0011t0001 | 0/0 | 1369 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0001c0014t0001 | 0/0 | 1369 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0002c0005t0001 | 0/1 | 1369 | 16 | 8 | 0 | 5 | 1 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0002c0007t0001 | 0/0 | 1369 | 9 | 0 | 4 | 1 | 1 | 3 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0002c0009t0001 | 0/0 | 1369 | 2 | 0 | 1 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| a0003c0004t0001 | 0/0 | 1368 | 19 | 2 | 3 | 10 | 3 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1363): Show |
chr2 | 24118469 | 24174638 |
| a0003c0013t0002 | 0/0 | 1368 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1363): Show |
chr2 | 24118469 | 24174638 |
| a0004c0012t0001 | 0/0 | 1369 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | GGACT others(1364): Show |
chr2 | 24118469 | 24174638 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0006t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0008t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0008t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0010t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0011t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0001c0014t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0028 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0005t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0009t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0002c0009t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0003c0013t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| a0004c0012t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00099 | hp2 | a0002 | c0005 | t0001 | g0025 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0102 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00323 | hp2 | a0003 | c0004 | t0001 | g0107 | EUR | FIN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0105 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01069 | hp1 | a0003 | c0004 | t0001 | g0103 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01069 | hp2 | a0002 | c0007 | t0001 | g0019 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01071 | hp1 | a0002 | c0007 | t0001 | g0020 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01074 | hp2 | a0002 | c0009 | t0001 | g0040 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0104 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0064 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01175 | hp2 | a0004 | c0012 | t0001 | g0201 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0227 | AMR | PUR | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01255 | hp2 | a0001 | c0006 | t0001 | g0270 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01256 | hp2 | a0002 | c0007 | t0001 | g0021 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0206 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01361 | hp1 | a0001 | c0006 | t0001 | g0003 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01496 | hp2 | a0002 | c0007 | t0001 | g0018 | AMR | CLM | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01516 | hp2 | a0001 | c0014 | t0001 | g0266 | EUR | IBS | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01891 | hp1 | a0001 | c0006 | t0001 | g0260 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0090 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01934 | hp2 | a0001 | c0003 | t0001 | g0088 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02040 | hp2 | a0002 | c0005 | t0001 | g0014 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0240 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02055 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02071 | hp1 | a0002 | c0005 | t0001 | g0015 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02071 | hp2 | a0003 | c0004 | t0001 | g0110 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02080 | hp1 | a0003 | c0013 | t0002 | g0063 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | KHV | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0238 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | CDX | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0236 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02257 | hp2 | a0001 | c0003 | t0001 | g0131 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02258 | hp2 | a0002 | c0005 | t0001 | g0024 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02602 | hp2 | a0001 | c0006 | t0001 | g0214 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02615 | hp1 | a0002 | c0005 | t0001 | g0035 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0160 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02630 | hp2 | a0003 | c0004 | t0001 | g0114 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0161 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02717 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02922 | hp2 | a0002 | c0005 | t0001 | g0012 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0208 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03041 | hp1 | a0001 | c0008 | t0001 | g0158 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0034 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0252 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0209 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0269 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03239 | hp1 | a0003 | c0004 | t0001 | g0097 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03453 | hp2 | a0001 | c0011 | t0001 | g0258 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03486 | hp2 | a0002 | c0005 | t0001 | g0038 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03492 | hp1 | a0002 | c0007 | t0001 | g0026 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03516 | hp1 | a0001 | c0006 | t0001 | g0261 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0087 | AFR | ESN | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0207 | AFR | GWD | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03579 | hp2 | a0002 | c0005 | t0001 | g0022 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03669 | hp2 | a0002 | c0007 | t0001 | g0032 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03710 | hp2 | a0002 | c0007 | t0001 | g0017 | SAS | PJL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03927 | hp1 | a0002 | c0005 | t0001 | g0037 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03942 | hp1 | a0002 | c0009 | t0001 | g0027 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03942 | hp2 | a0001 | c0006 | t0001 | g0003 | SAS | BEB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG04204 | hp2 | a0001 | c0006 | t0001 | g0003 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0264 | SAS | STU | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18906 | hp2 | a0001 | c0008 | t0001 | g0159 | AFR | YRI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18943 | hp2 | a0003 | c0004 | t0001 | g0109 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18949 | hp1 | a0001 | c0006 | t0001 | g0267 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0190 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18956 | hp1 | a0003 | c0004 | t0001 | g0112 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18963 | hp2 | a0001 | c0006 | t0001 | g0268 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18968 | hp2 | a0001 | c0010 | t0001 | g0138 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18972 | hp2 | a0003 | c0004 | t0001 | g0113 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18980 | hp1 | a0001 | c0006 | t0001 | g0263 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18981 | hp2 | a0001 | c0006 | t0001 | g0265 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18985 | hp1 | a0001 | c0006 | t0001 | g0262 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18993 | hp2 | a0003 | c0004 | t0001 | g0093 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18995 | hp2 | a0002 | c0005 | t0001 | g0031 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18999 | hp2 | a0002 | c0007 | t0001 | g0036 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19001 | hp2 | a0003 | c0004 | t0001 | g0101 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19004 | hp2 | a0001 | c0006 | t0001 | g0271 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19011 | hp2 | a0003 | c0004 | t0001 | g0096 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19043 | hp1 | a0003 | c0004 | t0001 | g0106 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19043 | hp2 | a0001 | c0006 | t0003 | g0075 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19057 | hp2 | a0003 | c0004 | t0001 | g0095 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19074 | hp1 | a0002 | c0005 | t0001 | g0029 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19079 | hp2 | a0003 | c0004 | t0001 | g0094 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19083 | hp1 | a0002 | c0005 | t0001 | g0016 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0005 | AFR | ASW | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0274 | AFR | ASW | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0171 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20752 | hp2 | a0003 | c0004 | t0001 | g0091 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0142 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20805 | hp2 | a0002 | c0007 | t0001 | g0030 | EUR | TSI | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | GIH | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | GIH | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0039 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02559 | hp1 | a0001 | c0008 | t0001 | g0234 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | MSL | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG06807 | hp1 | a0001 | c0003 | t0001 | g0251 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0084 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0156 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| homoSapiens | chm13v2 | a0002 | c0005 | t0001 | g0028 | REF | REF | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0092 | REF | REF | FAM228B_chr2_24118469_24174638 | FAM228B | chr2 | 24118469 | 24174638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:24135131 | G | C | 1 | a0002 | 26 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
missense_variant | MODERATE | c.112G>C | p.Glu38Gln | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/11 | 209/1369 | 112/975 | 38/324 | chr2 | 24135131 | |||
| chr2:24164308 | GC | G | 1 | a0003 | 20 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(17): Show |
frameshift_variant | HIGH | c.907delC | p.Gln303fs | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/11 | 1004/1369 | 907/975 | 303/324 | INFO_REALIGN_3_PRIME | chr2 | 24164308 | ||
| chr2:24167638 | C | T | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.944C>T | p.Pro315Leu | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/11 | 1041/1369 | 944/975 | 315/324 | chr2 | 24167638 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:24137912 | C | T | 1 | a0001c0014 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.172C>T | p.Leu58Leu | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/11 | 269/1369 | 172/975 | 58/324 | chr2 | 24137912 | |||
| chr2:24139381 | T | C | 1 | a0001c0010 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.372T>C | p.Phe124Phe | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/11 | 469/1369 | 372/975 | 124/324 | chr2 | 24139381 | |||
| chr2:24146786 | A | C | 1 | a0001c0008 | 3 | HG02559.hp1 HG03041.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.480A>C | p.Ala160Ala | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 6/11 | 577/1369 | 480/975 | 160/324 | chr2 | 24146786 | |||
| chr2:24146804 | C | T | 10 | a0001c0001 a0001c0002 a0001c0006 others(7): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
synonymous_variant | LOW | c.498C>T | p.Asn166Asn | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 6/11 | 595/1369 | 498/975 | 166/324 | chr2 | 24146804 | |||
| chr2:24161512 | G | A | 1 | a0001c0011 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.693G>A | p.Lys231Lys | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/11 | 790/1369 | 693/975 | 231/324 | chr2 | 24161512 | |||
| chr2:24161554 | T | C | 7 | a0001c0001 a0001c0002 a0001c0010 others(4): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
synonymous_variant | LOW | c.735T>C | p.Pro245Pro | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/11 | 832/1369 | 735/975 | 245/324 | chr2 | 24161554 | |||
| chr2:24167648 | G | A | 4 | a0001c0001 a0001c0010 a0002c0007 others(1): Show |
152 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
synonymous_variant | LOW | c.954G>A | p.Gly318Gly | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/11 | 1051/1369 | 954/975 | 318/324 | chr2 | 24167648 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:24169375 | A | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1706 | chr2 | 24169375 | ||||||
| chr2:24169386 | T | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*45T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1717 | chr2 | 24169386 | ||||||
| chr2:24169405 | T | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*64T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1736 | chr2 | 24169405 | ||||||
| chr2:24169412 | A | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1743 | chr2 | 24169412 | ||||||
| chr2:24169416 | A | T | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1747 | chr2 | 24169416 | ||||||
| chr2:24169418 | G | C | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1749 | chr2 | 24169418 | ||||||
| chr2:24169419 | C | T | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1750 | chr2 | 24169419 | ||||||
| chr2:24169421 | G | GTGGATTG others(3): Show |
1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80_*81insTGGATTGG others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1753 | chr2 | 24169421 | ||||||
| chr2:24169437 | T | C | 1 | a0003c0013t0002 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1768 | chr2 | 24169437 | ||||||
| chr2:24169442 | T | G | 1 | a0001c0001t0005 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1773 | chr2 | 24169442 | ||||||
| chr2:24169516 | G | A | 1 | a0001c0006t0003 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1847 | chr2 | 24169516 | ||||||
| chr2:24169608 | C | T | 1 | a0001c0001t0004 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*267C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 11/11 | 1939 | chr2 | 24169608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:24123601 | C | T | 1 | a0001c0002t0001g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+68C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123601 | |||||||
| chr2:24123648 | C | A | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-33+115C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123648 | |||||||
| chr2:24123824 | A | G | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.-33+291A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123824 | |||||||
| chr2:24123842 | C | G | 1 | a0001c0001t0001g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-33+309C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123842 | |||||||
| chr2:24123882 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-33+349C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24123882 | |||||||
| chr2:24124055 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-32-275C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24124055 | |||||||
| chr2:24124093 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-32-237C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24124093 | |||||||
| chr2:24124223 | A | C | 42 | a0001c0001t0001g0033 a0001c0001t0001g0259 a0001c0001t0005g0264 others(39): Show |
44 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.-32-107A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 1/10 | chr2 | 24124223 | |||||||
| chr2:24125063 | A | T | 3 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0011t0001g0258 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.99+603A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125063 | |||||||
| chr2:24125163 | G | A | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+703G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125163 | |||||||
| chr2:24125226 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.99+766G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125226 | |||||||
| chr2:24125384 | A | C | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+924A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125384 | |||||||
| chr2:24125439 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.99+979A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125439 | |||||||
| chr2:24125494 | G | A | 8 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | HG01071.hp2 HG01192.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1034G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125494 | |||||||
| chr2:24125512 | C | T | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.99+1052C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125512 | |||||||
| chr2:24125654 | G | A | 1 | a0001c0002t0001g0256 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.99+1194G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125654 | |||||||
| chr2:24125921 | A | C | 11 | a0001c0001t0005g0264 a0001c0006t0001g0003 a0001c0006t0001g0262 others(8): Show |
13 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1461A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24125921 | |||||||
| chr2:24126046 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+1586A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126046 | |||||||
| chr2:24126157 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+1697A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126157 | |||||||
| chr2:24126348 | G | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.99+1888G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126348 | |||||||
| chr2:24126592 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.99+2132A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126592 | |||||||
| chr2:24126612 | C | CT | 13 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(10): Show |
13 | HG01099.hp2 HG01169.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2168dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24126612 | ||||||
| chr2:24126612 | CT | C | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.99+2168delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24126612 | ||||||
| chr2:24126663 | C | T | 1 | a0002c0009t0001g0040 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.99+2203C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126663 | |||||||
| chr2:24126666 | A | G | 1 | a0001c0002t0001g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+2206A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126666 | |||||||
| chr2:24126726 | T | C | 8 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(5): Show |
12 | NA18612.hp2 NA18945.hp1 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+2266T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126726 | |||||||
| chr2:24126809 | TAGAG | T | 151 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
159 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.99+2352_99+2355del others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24126809 | ||||||
| chr2:24126827 | C | T | 3 | a0001c0001t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+2367C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126827 | |||||||
| chr2:24126870 | C | T | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+2410C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126870 | |||||||
| chr2:24126975 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99+2515A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24126975 | |||||||
| chr2:24127699 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(37): Show |
45 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.99+3239A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127699 | |||||||
| chr2:24127740 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.99+3280C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127740 | |||||||
| chr2:24127755 | C | T | 1 | a0001c0003t0001g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+3295C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127755 | |||||||
| chr2:24127854 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+3394G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127854 | |||||||
| chr2:24127931 | G | A | 1 | a0002c0005t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.99+3471G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24127931 | |||||||
| chr2:24128037 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(79): Show |
89 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.99+3577A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128037 | |||||||
| chr2:24128139 | T | C | 27 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(24): Show |
27 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+3679T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128139 | |||||||
| chr2:24128210 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0116 others(12): Show |
17 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+3750G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128210 | |||||||
| chr2:24128237 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0273 others(28): Show |
36 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+3777G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128237 | |||||||
| chr2:24128271 | T | G | 31 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0273 others(28): Show |
36 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+3811T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128271 | |||||||
| chr2:24128456 | A | C | 1 | a0002c0005t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+3996A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128456 | |||||||
| chr2:24128614 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.99+4154G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128614 | |||||||
| chr2:24128668 | G | A | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+4208G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128668 | |||||||
| chr2:24128700 | C | CTT | 27 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(24): Show |
27 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+4249_99+4250dup others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24128700 | ||||||
| chr2:24128722 | C | T | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+4262C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128722 | |||||||
| chr2:24128889 | A | G | 1 | a0001c0006t0001g0261 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.99+4429A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128889 | |||||||
| chr2:24128921 | AT | A | 33 | a0001c0001t0001g0033 a0001c0002t0001g0256 a0001c0002t0001g0257 others(30): Show |
33 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.99+4474delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24128921 | ||||||
| chr2:24128973 | C | T | 1 | a0001c0002t0001g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.99+4513C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24128973 | |||||||
| chr2:24129085 | G | A | 8 | a0001c0003t0001g0005 a0001c0003t0001g0084 a0001c0003t0001g0085 others(5): Show |
9 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+4625G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129085 | |||||||
| chr2:24129306 | CT | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0130 others(26): Show |
34 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+4862delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24129306 | ||||||
| chr2:24129398 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+4938A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129398 | |||||||
| chr2:24129474 | G | A | 1 | a0001c0003t0001g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+5014G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129474 | |||||||
| chr2:24129528 | A | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.99+5068A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129528 | |||||||
| chr2:24129564 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.99+5104A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129564 | |||||||
| chr2:24129737 | G | C | 1 | a0001c0003t0001g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+5277G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129737 | |||||||
| chr2:24129954 | A | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-5165A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129954 | |||||||
| chr2:24129955 | C | CT | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-5164_100-5163i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24129955 | |||||||
| chr2:24130040 | G | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-5079G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130040 | |||||||
| chr2:24130124 | C | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(36): Show |
44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-4995C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130124 | |||||||
| chr2:24130193 | C | G | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-4926C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130193 | |||||||
| chr2:24130254 | A | C | 5 | a0001c0002t0001g0235 a0001c0002t0001g0236 a0001c0002t0001g0237 others(2): Show |
5 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-4865A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130254 | |||||||
| chr2:24130342 | C | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-4777C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130342 | |||||||
| chr2:24130433 | G | A | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-4686G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130433 | |||||||
| chr2:24130436 | A | T | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-4683A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130436 | |||||||
| chr2:24130627 | C | G | 1 | a0001c0008t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-4492C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130627 | |||||||
| chr2:24130675 | T | C | 1 | a0003c0004t0001g0091 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.100-4444T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130675 | |||||||
| chr2:24130818 | C | T | 1 | a0001c0003t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-4301C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130818 | |||||||
| chr2:24130976 | G | A | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-4143G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24130976 | |||||||
| chr2:24131120 | C | T | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-3999C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131120 | |||||||
| chr2:24131181 | G | C | 1 | a0003c0004t0001g0093 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.100-3938G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131181 | |||||||
| chr2:24131277 | G | C | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-3842G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131277 | |||||||
| chr2:24131351 | C | G | 1 | a0001c0008t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-3768C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131351 | |||||||
| chr2:24131359 | A | G | 1 | a0002c0005t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100-3760A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131359 | |||||||
| chr2:24131420 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.100-3699G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131420 | |||||||
| chr2:24131426 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-3693C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131426 | |||||||
| chr2:24131537 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.100-3582C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131537 | |||||||
| chr2:24131558 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(30): Show |
38 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-3561A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131558 | |||||||
| chr2:24131590 | A | G | 1 | a0001c0003t0001g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100-3529A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24131590 | |||||||
| chr2:24132166 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.100-2953C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132166 | |||||||
| chr2:24132294 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100-2825T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132294 | |||||||
| chr2:24132464 | G | GT | 36 | a0001c0001t0001g0010 a0001c0001t0001g0041 a0001c0001t0001g0081 others(33): Show |
37 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.100-2629dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | ||||||
| chr2:24132464 | G | GTT | 10 | a0001c0001t0001g0068 a0001c0001t0001g0228 a0001c0002t0001g0064 others(7): Show |
10 | HG01168.hp1 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-2630_100-2629d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | ||||||
| chr2:24132464 | G | GTTT | 26 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0273 others(23): Show |
31 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.100-2631_100-2629d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | ||||||
| chr2:24132464 | G | GTTTT | 9 | a0001c0002t0001g0047 a0001c0002t0001g0048 a0001c0002t0001g0061 others(6): Show |
9 | HG00741.hp2 HG02080.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-2632_100-2629d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | ||||||
| chr2:24132464 | GT | G | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(39): Show |
46 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-2629delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | ||||||
| chr2:24132464 | GTTTTTTT others(7): Show |
G | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-2642_100-2629d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 24132464 | ||||||
| chr2:24132492 | G | A | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.100-2627G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132492 | |||||||
| chr2:24132553 | C | T | 1 | a0003c0013t0002g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-2566C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132553 | |||||||
| chr2:24132658 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.100-2461T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132658 | |||||||
| chr2:24132699 | A | G | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-2420A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132699 | |||||||
| chr2:24132875 | G | C | 1 | a0003c0004t0001g0093 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.100-2244G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24132875 | |||||||
| chr2:24133096 | A | G | 1 | a0003c0004t0001g0112 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.100-2023A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133096 | |||||||
| chr2:24133257 | G | A | 3 | a0001c0001t0001g0259 a0001c0006t0001g0260 a0001c0006t0001g0261 |
3 | HG01496.hp1 HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100-1862G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133257 | |||||||
| chr2:24133298 | CT | C | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-1820delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133298 | |||||||
| chr2:24133586 | T | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(36): Show |
44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-1533T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133586 | |||||||
| chr2:24133606 | C | T | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-1513C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133606 | |||||||
| chr2:24133656 | A | G | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-1463A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133656 | |||||||
| chr2:24133858 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-1261G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24133858 | |||||||
| chr2:24134132 | A | G | 1 | a0001c0003t0001g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100-987A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134132 | |||||||
| chr2:24134346 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-773T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134346 | |||||||
| chr2:24134373 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0148 others(8): Show |
13 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-746C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134373 | |||||||
| chr2:24134593 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-526G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134593 | |||||||
| chr2:24134594 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.100-525T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134594 | |||||||
| chr2:24134787 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-332T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134787 | |||||||
| chr2:24134932 | G | A | 1 | a0001c0003t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-187G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134932 | |||||||
| chr2:24134941 | A | G | 1 | a0002c0005t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100-178A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134941 | |||||||
| chr2:24134956 | G | A | 3 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0011t0001g0258 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.100-163G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 2/10 | chr2 | 24134956 | |||||||
| chr2:24135208 | G | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0204 |
2 | HG01346.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.168+21G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135208 | |||||||
| chr2:24135290 | A | C | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168+103A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135290 | |||||||
| chr2:24135474 | C | T | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168+287C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135474 | |||||||
| chr2:24135782 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
136 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.168+595C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135782 | |||||||
| chr2:24135804 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.168+617A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135804 | |||||||
| chr2:24135845 | A | G | 1 | a0001c0008t0001g0234 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+658A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135845 | |||||||
| chr2:24135887 | G | A | 3 | a0001c0001t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.168+700G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135887 | |||||||
| chr2:24135916 | C | T | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168+729C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135916 | |||||||
| chr2:24135917 | A | C | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168+730A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135917 | |||||||
| chr2:24135966 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.168+779A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24135966 | |||||||
| chr2:24135976 | G | GT | 45 | a0001c0001t0001g0041 a0001c0001t0001g0068 a0001c0001t0001g0111 others(42): Show |
47 | HG00438.hp1 HG00438.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.168+807dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24135976 | ||||||
| chr2:24135976 | GT | G | 27 | a0001c0003t0001g0013 a0001c0003t0001g0085 a0002c0005t0001g0012 others(24): Show |
27 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.168+807delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24135976 | ||||||
| chr2:24136048 | C | A | 1 | a0001c0003t0001g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+861C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136048 | |||||||
| chr2:24136053 | C | CT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
132 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.168+892dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | ||||||
| chr2:24136053 | C | CTT | 49 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0123 others(46): Show |
51 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.168+891_168+892dup others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | ||||||
| chr2:24136053 | C | CTTT | 7 | a0001c0006t0001g0261 a0001c0006t0001g0262 a0001c0006t0001g0271 others(4): Show |
7 | HG02486.hp1 HG03516.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+890_168+892dup others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | ||||||
| chr2:24136053 | CT | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0273 a0001c0002t0001g0001 others(22): Show |
30 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.168+892delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 24136053 | ||||||
| chr2:24136092 | C | T | 2 | a0002c0005t0001g0029 a0002c0005t0001g0031 |
2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.168+905C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136092 | |||||||
| chr2:24136551 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.169-1358C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136551 | |||||||
| chr2:24136572 | A | G | 3 | a0001c0001t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.169-1337A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136572 | |||||||
| chr2:24136652 | C | T | 1 | a0001c0001t0004g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-1257C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136652 | |||||||
| chr2:24136755 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.169-1154G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136755 | |||||||
| chr2:24136774 | A | G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG02083.hp1 NA18949.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1135A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136774 | |||||||
| chr2:24136852 | C | T | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.169-1057C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136852 | |||||||
| chr2:24136880 | T | G | 1 | a0001c0003t0001g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169-1029T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136880 | |||||||
| chr2:24136925 | T | C | 1 | a0001c0001t0004g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-984T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24136925 | |||||||
| chr2:24137014 | T | A | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-895T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137014 | |||||||
| chr2:24137054 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169-855T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137054 | |||||||
| chr2:24137158 | G | A | 1 | a0002c0005t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-751G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137158 | |||||||
| chr2:24137321 | T | G | 1 | a0001c0001t0001g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.169-588T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137321 | |||||||
| chr2:24137516 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.169-393G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137516 | |||||||
| chr2:24137641 | C | T | 2 | a0001c0001t0001g0033 a0001c0003t0001g0013 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.169-268C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137641 | |||||||
| chr2:24137859 | C | T | 2 | a0001c0003t0001g0211 a0001c0003t0001g0227 |
2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.169-50C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 3/10 | chr2 | 24137859 | |||||||
| chr2:24138200 | C | G | 1 | a0001c0006t0001g0270 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.360+100C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138200 | |||||||
| chr2:24138441 | A | G | 1 | a0001c0003t0001g0157 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.360+341A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138441 | |||||||
| chr2:24138641 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.360+541A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138641 | |||||||
| chr2:24138689 | C | T | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.360+589C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138689 | |||||||
| chr2:24138945 | C | CA | 44 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(41): Show |
49 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.361-410dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 24138945 | ||||||
| chr2:24138945 | C | CAA | 27 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(24): Show |
27 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.361-411_361-410dup others(2): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 24138945 | ||||||
| chr2:24138945 | CA | C | 21 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0108 others(18): Show |
21 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.361-410delA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 24138945 | ||||||
| chr2:24138947 | A | C | 1 | a0003c0004t0001g0107 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.361-423A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24138947 | |||||||
| chr2:24139037 | C | T | 1 | a0001c0003t0001g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.361-333C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139037 | |||||||
| chr2:24139092 | G | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.361-278G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139092 | |||||||
| chr2:24139198 | T | G | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | NA18952.hp2 NA19054.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.361-172T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139198 | |||||||
| chr2:24139344 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.361-26T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 4/10 | chr2 | 24139344 | |||||||
| chr2:24139566 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.441+116T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139566 | |||||||
| chr2:24139618 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.441+168A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139618 | |||||||
| chr2:24139658 | T | C | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+208T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139658 | |||||||
| chr2:24139660 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+210G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139660 | |||||||
| chr2:24139666 | T | C | 1 | a0003c0004t0001g0113 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.441+216T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139666 | |||||||
| chr2:24139674 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0195 |
2 | NA18971.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.441+224G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24139674 | |||||||
| chr2:24140052 | T | A | 2 | a0003c0004t0001g0096 a0003c0004t0001g0109 |
2 | NA18943.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.441+602T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24140052 | |||||||
| chr2:24140095 | A | G | 3 | a0001c0001t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.441+645A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24140095 | |||||||
| chr2:24140908 | GC | G | 14 | a0001c0001t0001g0259 a0001c0001t0005g0264 a0001c0006t0001g0003 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.441+1460delC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24140908 | ||||||
| chr2:24141015 | G | T | 2 | a0003c0004t0001g0096 a0003c0004t0001g0109 |
2 | NA18943.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.441+1565G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141015 | |||||||
| chr2:24141068 | A | G | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+1618A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141068 | |||||||
| chr2:24141139 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
161 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.441+1689G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141139 | |||||||
| chr2:24141207 | T | C | 2 | a0001c0001t0001g0033 a0001c0003t0001g0013 |
2 | HG01109.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.441+1757T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141207 | |||||||
| chr2:24141224 | G | A | 3 | a0001c0002t0001g0052 a0001c0002t0001g0062 a0001c0002t0001g0064 |
3 | HG00741.hp2 HG01074.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.441+1774G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141224 | |||||||
| chr2:24141463 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.441+2013C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141463 | |||||||
| chr2:24141534 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.441+2084G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141534 | |||||||
| chr2:24141687 | G | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
88 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.441+2237G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141687 | |||||||
| chr2:24141709 | G | A | 1 | a0003c0004t0001g0097 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.441+2259G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141709 | |||||||
| chr2:24141866 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(36): Show |
44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.441+2416C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141866 | |||||||
| chr2:24141925 | A | G | 28 | a0001c0001t0001g0033 a0001c0003t0001g0013 a0002c0005t0001g0012 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.441+2475A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24141925 | |||||||
| chr2:24142084 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0221 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.441+2634C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142084 | |||||||
| chr2:24142364 | A | G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+2914A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142364 | |||||||
| chr2:24142390 | C | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(36): Show |
44 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.441+2940C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142390 | |||||||
| chr2:24142403 | T | G | 1 | a0001c0002t0001g0171 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.441+2953T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142403 | |||||||
| chr2:24142599 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.441+3149A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24142599 | |||||||
| chr2:24143045 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.441+3595G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143045 | |||||||
| chr2:24143118 | C | T | 28 | a0001c0001t0001g0033 a0001c0002t0001g0080 a0001c0003t0001g0013 others(25): Show |
28 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-3630C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143118 | |||||||
| chr2:24143262 | C | G | 32 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(29): Show |
37 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.442-3486C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143262 | |||||||
| chr2:24143319 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
130 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.442-3429T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143319 | |||||||
| chr2:24143326 | GCC | G | 25 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0146 others(22): Show |
25 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.442-3420_442-3419d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24143326 | ||||||
| chr2:24143328 | C | A | 2 | a0001c0002t0001g0057 a0001c0003t0001g0251 |
2 | HG03688.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.442-3420C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143328 | |||||||
| chr2:24143328 | C | G | 37 | a0001c0001t0001g0059 a0001c0001t0001g0168 a0001c0001t0001g0191 others(34): Show |
41 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.442-3420C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143328 | |||||||
| chr2:24143328 | C | T | 40 | a0001c0001t0001g0135 a0001c0001t0001g0183 a0001c0001t0001g0184 others(37): Show |
41 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.442-3420C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143328 | |||||||
| chr2:24143329 | C | T | 38 | a0001c0001t0001g0059 a0001c0001t0001g0168 a0001c0001t0001g0191 others(35): Show |
42 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.442-3419C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143329 | |||||||
| chr2:24143330 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-3418G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143330 | |||||||
| chr2:24143332 | C | T | 26 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0146 others(23): Show |
26 | HG01074.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-3416C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143332 | |||||||
| chr2:24143341 | C | T | 1 | a0001c0002t0001g0239 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.442-3407C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143341 | |||||||
| chr2:24143384 | T | C | 28 | a0001c0001t0001g0078 a0001c0001t0001g0098 a0001c0001t0001g0099 others(25): Show |
28 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.442-3364T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143384 | |||||||
| chr2:24143394 | T | C | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
103 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.442-3354T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143394 | |||||||
| chr2:24143395 | C | T | 96 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
101 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.442-3353C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143395 | |||||||
| chr2:24143400 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442-3348T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143400 | |||||||
| chr2:24143401 | A | G | 18 | a0001c0001t0001g0033 a0001c0001t0001g0189 a0001c0001t0001g0200 others(15): Show |
18 | HG00099.hp2 HG01109.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-3347A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143401 | |||||||
| chr2:24143474 | A | T | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442-3274A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143474 | |||||||
| chr2:24143523 | A | T | 1 | a0001c0001t0001g0273 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.442-3225A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143523 | |||||||
| chr2:24143643 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0081 |
2 | HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.442-3105G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143643 | |||||||
| chr2:24143746 | TTAA | T | 7 | a0001c0002t0001g0235 a0001c0002t0001g0236 a0001c0002t0001g0237 others(4): Show |
7 | HG01109.hp1 HG01358.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-2998_442-2996d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24143746 | ||||||
| chr2:24143949 | G | T | 15 | a0001c0002t0001g0080 a0002c0005t0001g0012 a0002c0005t0001g0014 others(12): Show |
15 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-2799G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143949 | |||||||
| chr2:24143957 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0223 |
2 | HG01346.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.442-2791A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143957 | |||||||
| chr2:24143959 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(52): Show |
60 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.442-2789G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24143959 | |||||||
| chr2:24143996 | C | CA | 156 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
166 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.442-2735dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24143996 | ||||||
| chr2:24144072 | G | A | 1 | a0001c0011t0001g0258 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442-2676G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144072 | |||||||
| chr2:24144090 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-2658G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144090 | |||||||
| chr2:24144120 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.442-2628T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144120 | |||||||
| chr2:24144162 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.442-2586C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144162 | |||||||
| chr2:24144252 | C | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-2496C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144252 | |||||||
| chr2:24144327 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.442-2421C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144327 | |||||||
| chr2:24144329 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442-2419C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144329 | |||||||
| chr2:24144330 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442-2418G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144330 | |||||||
| chr2:24144335 | G | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.442-2413G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144335 | |||||||
| chr2:24144405 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(54): Show |
62 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.442-2343G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144405 | |||||||
| chr2:24144670 | C | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.442-2078C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144670 | |||||||
| chr2:24144699 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.442-2049C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144699 | |||||||
| chr2:24144783 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0116 a0001c0001t0001g0118 others(7): Show |
10 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-1965T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144783 | |||||||
| chr2:24144958 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-1790C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144958 | |||||||
| chr2:24144959 | G | A | 1 | a0002c0005t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.442-1789G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24144959 | |||||||
| chr2:24145042 | G | C | 1 | a0001c0002t0001g0057 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.442-1706G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145042 | |||||||
| chr2:24145124 | G | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(54): Show |
62 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.442-1624G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145124 | |||||||
| chr2:24145300 | G | A | 6 | a0001c0003t0001g0206 a0001c0003t0001g0207 a0001c0003t0001g0208 others(3): Show |
6 | HG01358.hp1 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1448G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145300 | |||||||
| chr2:24145560 | C | T | 1 | a0002c0007t0001g0021 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.442-1188C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145560 | |||||||
| chr2:24145627 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.442-1121C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145627 | |||||||
| chr2:24145706 | CT | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.442-1025delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 24145706 | ||||||
| chr2:24145728 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.442-1020C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145728 | |||||||
| chr2:24145765 | C | T | 1 | a0001c0003t0001g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-983C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145765 | |||||||
| chr2:24145810 | T | G | 9 | a0001c0003t0001g0005 a0001c0003t0001g0084 a0001c0003t0001g0085 others(6): Show |
10 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-938T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145810 | |||||||
| chr2:24145841 | A | G | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.442-907A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145841 | |||||||
| chr2:24145879 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-869C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145879 | |||||||
| chr2:24145927 | C | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.442-821C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24145927 | |||||||
| chr2:24146008 | T | G | 18 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(15): Show |
18 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-740T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146008 | |||||||
| chr2:24146104 | A | G | 2 | a0001c0002t0001g0256 a0001c0002t0001g0257 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.442-644A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146104 | |||||||
| chr2:24146149 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.442-599T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146149 | |||||||
| chr2:24146454 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.442-294T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146454 | |||||||
| chr2:24146535 | C | G | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.442-213C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146535 | |||||||
| chr2:24146650 | G | A | 1 | a0001c0006t0001g0270 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.442-98G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 5/10 | chr2 | 24146650 | |||||||
| chr2:24147214 | C | T | 15 | a0001c0002t0001g0080 a0002c0005t0001g0012 a0002c0005t0001g0014 others(12): Show |
15 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+128C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24147214 | |||||||
| chr2:24147780 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0253 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.686+694G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24147780 | |||||||
| chr2:24147916 | C | CT | 6 | a0002c0005t0001g0022 a0002c0005t0001g0023 a0003c0004t0001g0091 others(3): Show |
6 | HG00642.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.686+846dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24147916 | ||||||
| chr2:24147916 | CT | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.686+846delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24147916 | ||||||
| chr2:24148236 | A | T | 1 | a0002c0005t0001g0012 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.686+1150A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24148236 | |||||||
| chr2:24148821 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.686+1735T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24148821 | |||||||
| chr2:24148947 | T | A | 2 | a0001c0003t0001g0005 a0001c0003t0001g0086 |
3 | HG02922.hp1 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.686+1861T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24148947 | |||||||
| chr2:24149055 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.686+1969G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149055 | |||||||
| chr2:24149092 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+2006C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149092 | |||||||
| chr2:24149269 | G | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.686+2183G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149269 | |||||||
| chr2:24149549 | C | G | 2 | a0002c0005t0001g0024 a0002c0005t0001g0025 |
2 | HG00099.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.686+2463C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149549 | |||||||
| chr2:24149579 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
155 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.686+2493C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149579 | |||||||
| chr2:24149651 | T | G | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.686+2565T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149651 | |||||||
| chr2:24149797 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0137 others(33): Show |
41 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.686+2711G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149797 | |||||||
| chr2:24149945 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
170 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.686+2859A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24149945 | |||||||
| chr2:24150083 | G | T | 15 | a0001c0002t0001g0080 a0002c0005t0001g0012 a0002c0005t0001g0014 others(12): Show |
15 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+2997G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150083 | |||||||
| chr2:24150126 | A | AG | 217 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.686+3040_686+3041i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150126 | |||||||
| chr2:24150143 | G | T | 1 | a0003c0004t0001g0104 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.686+3057G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150143 | |||||||
| chr2:24150280 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(52): Show |
60 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.686+3194A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150280 | |||||||
| chr2:24150321 | G | A | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.686+3235G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150321 | |||||||
| chr2:24150627 | A | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0148 others(11): Show |
16 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+3541A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150627 | |||||||
| chr2:24150633 | C | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
149 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.686+3547C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150633 | |||||||
| chr2:24150799 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+3713T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24150799 | |||||||
| chr2:24151260 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0135 a0001c0001t0001g0183 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+4174T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151260 | |||||||
| chr2:24151274 | GTTTTGTT | G | 3 | a0001c0001t0001g0068 a0001c0002t0001g0069 a0001c0002t0001g0070 |
3 | HG02622.hp1 HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.686+4207_686+4213d others(9): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151274 | ||||||
| chr2:24151444 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(54): Show |
62 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.686+4358C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151444 | |||||||
| chr2:24151452 | G | A | 8 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(5): Show |
12 | NA18612.hp2 NA18945.hp1 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.686+4366G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151452 | |||||||
| chr2:24151534 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0273 others(1): Show |
5 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.686+4448C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151534 | |||||||
| chr2:24151567 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.686+4481C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151567 | |||||||
| chr2:24151583 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.686+4497C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151583 | |||||||
| chr2:24151603 | T | G | 15 | a0001c0002t0001g0080 a0002c0005t0001g0012 a0002c0005t0001g0014 others(12): Show |
15 | HG00099.hp2 HG02040.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+4517T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151603 | |||||||
| chr2:24151613 | A | AT | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
214 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.686+4543dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151613 | ||||||
| chr2:24151613 | A | ATT | 14 | a0001c0001t0001g0068 a0001c0001t0001g0081 a0001c0001t0001g0155 others(11): Show |
14 | HG00735.hp2 HG01099.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.686+4542_686+4543d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151613 | ||||||
| chr2:24151613 | A | ATTT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0137 a0001c0001t0001g0273 others(43): Show |
51 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.686+4541_686+4543d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24151613 | ||||||
| chr2:24151687 | C | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+4601C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151687 | |||||||
| chr2:24151733 | A | C | 1 | a0002c0005t0001g0034 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.686+4647A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151733 | |||||||
| chr2:24151768 | C | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(54): Show |
62 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.686+4682C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151768 | |||||||
| chr2:24151859 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
169 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.686+4773T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151859 | |||||||
| chr2:24151961 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0273 others(4): Show |
8 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+4875C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24151961 | |||||||
| chr2:24152004 | G | T | 1 | a0001c0001t0001g0140 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.686+4918G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152004 | |||||||
| chr2:24152022 | C | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0148 others(11): Show |
16 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+4936C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152022 | |||||||
| chr2:24152141 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0137 others(32): Show |
40 | HG00140.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.686+5055T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152141 | |||||||
| chr2:24152160 | C | T | 2 | a0002c0005t0001g0024 a0002c0005t0001g0025 |
2 | HG00099.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.686+5074C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152160 | |||||||
| chr2:24152181 | T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.686+5095T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152181 | |||||||
| chr2:24152360 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0068 others(55): Show |
63 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.686+5274A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152360 | |||||||
| chr2:24152536 | G | GTATTGCC others(16): Show |
1 | a0001c0001t0001g0259 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.686+5451_686+5473d others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24152536 | ||||||
| chr2:24152593 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(152): Show |
166 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.686+5507G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152593 | |||||||
| chr2:24152702 | A | G | 58 | a0001c0001t0001g0098 a0001c0001t0001g0137 a0001c0001t0001g0218 others(55): Show |
62 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.686+5616A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152702 | |||||||
| chr2:24152983 | C | G | 1 | a0001c0001t0001g0011 | 2 | HG00639.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.686+5897C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152983 | |||||||
| chr2:24152984 | T | C | 1 | a0001c0003t0001g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.686+5898T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24152984 | |||||||
| chr2:24153127 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.686+6041C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153127 | |||||||
| chr2:24153135 | G | A | 4 | a0001c0003t0001g0129 a0001c0003t0001g0132 a0001c0003t0001g0160 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+6049G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153135 | |||||||
| chr2:24153264 | G | A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.686+6178G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153264 | |||||||
| chr2:24153309 | C | G | 7 | a0002c0007t0001g0018 a0002c0007t0001g0019 a0002c0007t0001g0020 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.686+6223C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153309 | |||||||
| chr2:24153337 | G | T | 1 | a0001c0003t0001g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.686+6251G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153337 | |||||||
| chr2:24153342 | C | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.686+6256C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153342 | |||||||
| chr2:24153485 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.686+6399G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153485 | |||||||
| chr2:24153515 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.686+6429G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153515 | |||||||
| chr2:24153516 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.686+6430C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153516 | |||||||
| chr2:24153590 | C | T | 6 | a0001c0006t0001g0262 a0001c0006t0001g0263 a0001c0006t0001g0265 others(3): Show |
6 | NA18949.hp1 NA18963.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.686+6504C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153590 | |||||||
| chr2:24153600 | C | T | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+6514C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153600 | |||||||
| chr2:24153761 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(212): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.686+6675T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153761 | |||||||
| chr2:24153780 | T | C | 1 | a0003c0004t0001g0101 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.686+6694T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153780 | |||||||
| chr2:24153789 | T | A | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+6703T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153789 | |||||||
| chr2:24153840 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.686+6754C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153840 | |||||||
| chr2:24153990 | G | A | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+6904G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24153990 | |||||||
| chr2:24154061 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.686+6975C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154061 | |||||||
| chr2:24154127 | C | CA | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.686+7042dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24154127 | ||||||
| chr2:24154145 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0170 |
2 | NA18969.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.686+7059A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154145 | |||||||
| chr2:24154158 | G | C | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+7072G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154158 | |||||||
| chr2:24154222 | A | G | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.686+7136A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154222 | |||||||
| chr2:24154684 | G | T | 2 | a0001c0002t0001g0065 a0001c0002t0001g0072 |
2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.687-6822G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154684 | |||||||
| chr2:24154977 | T | G | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-6529T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24154977 | |||||||
| chr2:24155231 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.687-6275C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155231 | |||||||
| chr2:24155237 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.687-6269T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155237 | |||||||
| chr2:24155290 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.687-6216T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155290 | |||||||
| chr2:24155361 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.687-6145A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155361 | |||||||
| chr2:24155504 | C | CAT | 5 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0087 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-5975_687-5974d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155504 | ||||||
| chr2:24155504 | C | CTT | 7 | a0001c0001t0001g0216 a0002c0005t0001g0014 a0002c0005t0001g0015 others(4): Show |
7 | HG02040.hp2 HG02071.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-6002_687-6001i others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | |||||||
| chr2:24155504 | C | CTTATATA others(3): Show |
1 | a0001c0002t0001g0173 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | |||||||
| chr2:24155504 | C | CTTATATA others(5): Show |
1 | a0001c0002t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | |||||||
| chr2:24155504 | C | CTTATATA others(9): Show |
1 | a0002c0005t0001g0025 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | |||||||
| chr2:24155504 | C | CTTATATA others(11): Show |
1 | a0001c0002t0001g0045 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(20): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | |||||||
| chr2:24155504 | C | CTTATATA others(23): Show |
1 | a0002c0005t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.687-6002_687-6001i others(32): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155504 | |||||||
| chr2:24155504 | CATATATA others(5): Show |
C | 1 | a0001c0002t0001g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.687-5985_687-5974d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155504 | ||||||
| chr2:24155505 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
200 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.687-6001A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155505 | |||||||
| chr2:24155517 | A | T | 1 | a0001c0002t0001g0274 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.687-5989A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155517 | |||||||
| chr2:24155521 | ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.687-5983_687-5973d others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155521 | ||||||
| chr2:24155521 | ATATATAT others(5): Show |
A | 1 | a0001c0002t0001g0236 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.687-5983_687-5972d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155521 | ||||||
| chr2:24155521 | ATATATAT others(6): Show |
A | 1 | a0001c0002t0001g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.687-5983_687-5971d others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155521 | ||||||
| chr2:24155523 | ATATATAT others(5): Show |
A | 17 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0098 others(14): Show |
18 | HG00099.hp1 HG00639.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.687-5981_687-5970d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155523 | ||||||
| chr2:24155525 | A | AT | 4 | a0001c0003t0001g0157 a0001c0008t0001g0234 a0003c0004t0001g0094 others(1): Show |
4 | HG02071.hp2 HG02559.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-5980dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | ||||||
| chr2:24155525 | A | T | 1 | a0003c0004t0001g0107 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.687-5981A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155525 | |||||||
| chr2:24155525 | ATATATAT others(4): Show |
A | 8 | a0001c0001t0001g0119 a0001c0001t0001g0144 a0001c0001t0001g0150 others(5): Show |
8 | HG00639.hp1 HG01081.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-5979_687-5969d others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | ||||||
| chr2:24155525 | ATATATAT others(5): Show |
A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
100 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.687-5979_687-5968d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | ||||||
| chr2:24155525 | ATATATAT others(6): Show |
A | 6 | a0001c0001t0001g0128 a0001c0001t0001g0165 a0001c0001t0001g0244 others(3): Show |
6 | HG01255.hp1 HG01516.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-5979_687-5967d others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155525 | ||||||
| chr2:24155527 | A | AT | 11 | a0001c0002t0001g0239 a0001c0003t0001g0131 a0001c0003t0001g0156 others(8): Show |
11 | HG02080.hp1 HG02257.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.687-5978dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | ||||||
| chr2:24155527 | A | T | 12 | a0001c0003t0001g0157 a0001c0003t0001g0240 a0001c0008t0001g0234 others(9): Show |
12 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-5979A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155527 | |||||||
| chr2:24155527 | ATATATTT others(3): Show |
A | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.687-5977_687-5968d others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | ||||||
| chr2:24155527 | ATATATTT others(4): Show |
A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0175 a0001c0001t0001g0255 |
3 | HG00642.hp2 NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.687-5977_687-5967d others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | ||||||
| chr2:24155527 | ATATATTT others(5): Show |
A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0078 others(8): Show |
13 | HG01071.hp2 HG01361.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.687-5977_687-5966d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | ||||||
| chr2:24155527 | ATATATTT others(7): Show |
A | 2 | a0001c0002t0001g0066 a0001c0002t0001g0115 |
2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.687-5977_687-5964d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155527 | ||||||
| chr2:24155529 | A | ATT | 4 | a0001c0003t0001g0005 a0001c0003t0001g0129 a0001c0008t0001g0158 others(1): Show |
4 | HG02897.hp1 HG03041.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-5976_687-5975i others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155529 | ||||||
| chr2:24155529 | A | T | 29 | a0001c0002t0001g0067 a0001c0002t0001g0239 a0001c0003t0001g0131 others(26): Show |
29 | HG00140.hp1 HG00323.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.687-5977A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155529 | |||||||
| chr2:24155529 | ATATTTTT others(5): Show |
A | 1 | a0001c0001t0001g0242 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.687-5975_687-5964d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155529 | ||||||
| chr2:24155529 | ATATTTTT others(8): Show |
A | 1 | a0001c0006t0001g0267 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.687-5975_687-5961d others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155529 | ||||||
| chr2:24155531 | A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0043 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0049 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.687-5974_687-5973i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(8): Show |
2 | a0001c0002t0001g0001 a0001c0002t0001g0074 |
2 | HG02135.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.687-5974_687-5973i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(6): Show |
4 | a0001c0002t0001g0001 a0001c0002t0001g0046 a0001c0002t0001g0047 others(1): Show |
5 | HG02056.hp1 NA18964.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(8): Show |
1 | a0001c0002t0001g0001 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.687-5974_687-5973i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(6): Show |
4 | a0001c0002t0001g0001 a0001c0002t0001g0044 a0001c0002t0001g0048 others(1): Show |
4 | HG01361.hp1 NA18945.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(2): Show |
6 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0054 others(3): Show |
6 | HG00735.hp2 HG01099.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(11): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(3): Show |
2 | a0001c0002t0001g0056 a0001c0002t0001g0070 |
2 | HG01257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.687-5974_687-5973i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATAT others(6): Show |
1 | a0001c0006t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687-5974_687-5973i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATATTT others(3): Show |
1 | a0001c0002t0001g0171 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.687-5974_687-5973i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATATTTTT others(3): Show |
1 | a0001c0006t0001g0265 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.687-5974_687-5973i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | ATT | 6 | a0001c0003t0001g0086 a0001c0003t0001g0088 a0001c0003t0001g0089 others(3): Show |
6 | HG01891.hp2 HG01934.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-5950_687-5949d others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155531 | A | T | 42 | a0001c0002t0001g0045 a0001c0002t0001g0061 a0001c0002t0001g0062 others(39): Show |
42 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.687-5975A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155531 | |||||||
| chr2:24155531 | ATTTTTTT others(3): Show |
A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5958_687-5949d others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24155531 | ||||||
| chr2:24155532 | T | TA | 7 | a0001c0003t0001g0206 a0001c0003t0001g0207 a0001c0003t0001g0209 others(4): Show |
7 | HG01358.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-5974_687-5973i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155532 | |||||||
| chr2:24155533 | T | A | 6 | a0001c0001t0001g0216 a0001c0002t0001g0080 a0001c0003t0001g0208 others(3): Show |
6 | HG02040.hp1 HG02258.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-5973T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155533 | |||||||
| chr2:24155539 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.687-5967T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155539 | |||||||
| chr2:24155541 | T | A | 1 | a0002c0005t0001g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.687-5965T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155541 | |||||||
| chr2:24155542 | T | A | 1 | a0001c0003t0001g0190 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.687-5964T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155542 | |||||||
| chr2:24155543 | T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5963T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155543 | |||||||
| chr2:24155545 | T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5961T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155545 | |||||||
| chr2:24155547 | T | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-5959T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155547 | |||||||
| chr2:24155571 | G | A | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-5935G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155571 | |||||||
| chr2:24155609 | T | C | 19 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(16): Show |
19 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.687-5897T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155609 | |||||||
| chr2:24155735 | T | G | 1 | a0001c0002t0001g0256 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.687-5771T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155735 | |||||||
| chr2:24155740 | C | T | 1 | a0001c0006t0001g0265 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.687-5766C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155740 | |||||||
| chr2:24155752 | G | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0199 a0001c0001t0001g0222 others(2): Show |
5 | HG00438.hp1 HG02080.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-5754G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155752 | |||||||
| chr2:24155924 | T | C | 1 | a0001c0002t0001g0056 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.687-5582T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155924 | |||||||
| chr2:24155930 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.687-5576G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24155930 | |||||||
| chr2:24156055 | G | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.687-5451G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156055 | |||||||
| chr2:24156097 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.687-5409G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156097 | |||||||
| chr2:24156391 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0202 |
2 | NA18955.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.687-5115G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156391 | |||||||
| chr2:24156770 | TTCC | T | 4 | a0002c0005t0001g0022 a0002c0005t0001g0023 a0002c0005t0001g0034 others(1): Show |
4 | HG02717.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-4735_687-4733d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156770 | |||||||
| chr2:24156771 | TCCG | T | 13 | a0001c0001t0001g0216 a0001c0002t0001g0048 a0001c0002t0001g0051 others(10): Show |
13 | HG01099.hp2 HG01433.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.687-4732_687-4730d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156771 | ||||||
| chr2:24156771 | TCCGC | T | 31 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(28): Show |
35 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.687-4732_687-4729d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156771 | ||||||
| chr2:24156771 | TCCGCCC | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(144): Show |
156 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.687-4732_687-4727d others(8): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156771 | ||||||
| chr2:24156774 | G | C | 5 | a0002c0005t0001g0022 a0002c0005t0001g0023 a0002c0005t0001g0034 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-4732G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156774 | |||||||
| chr2:24156774 | G | GC | 14 | a0001c0003t0001g0131 a0001c0003t0001g0161 a0001c0003t0001g0209 others(11): Show |
14 | HG00323.hp2 HG01069.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.687-4719dupC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156774 | ||||||
| chr2:24156774 | GC | G | 15 | a0001c0003t0001g0005 a0001c0003t0001g0084 a0001c0003t0001g0085 others(12): Show |
16 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.687-4719delC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24156774 | ||||||
| chr2:24156776 | C | T | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-4730C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156776 | |||||||
| chr2:24156781 | C | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-4725C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156781 | |||||||
| chr2:24156785 | C | A | 10 | a0001c0003t0001g0005 a0001c0003t0001g0084 a0001c0003t0001g0085 others(7): Show |
11 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.687-4721C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156785 | |||||||
| chr2:24156785 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.687-4721C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156785 | |||||||
| chr2:24156785 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.687-4721C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156785 | |||||||
| chr2:24156787 | C | A | 1 | a0001c0002t0001g0056 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.687-4719C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156787 | |||||||
| chr2:24156818 | T | C | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.687-4688T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24156818 | |||||||
| chr2:24157029 | T | C | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-4477T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157029 | |||||||
| chr2:24157067 | G | A | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.687-4439G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157067 | |||||||
| chr2:24157147 | T | C | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-4359T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157147 | |||||||
| chr2:24157517 | G | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.687-3989G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157517 | |||||||
| chr2:24157737 | CA | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.687-3755delA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24157737 | ||||||
| chr2:24157758 | TC | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.687-3745delC | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24157758 | ||||||
| chr2:24157845 | C | T | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.687-3661C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157845 | |||||||
| chr2:24157874 | T | C | 2 | a0001c0002t0001g0065 a0001c0002t0001g0072 |
2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.687-3632T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157874 | |||||||
| chr2:24157905 | T | G | 19 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(16): Show |
19 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.687-3601T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24157905 | |||||||
| chr2:24158196 | C | CT | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.687-3293dupT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0033 others(24): Show |
30 | HG00642.hp2 HG01109.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.687-3295_687-3293d others(5): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0136 a0001c0001t0001g0154 others(4): Show |
8 | HG00621.hp1 NA18955.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-3296_687-3293d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTT | 24 | a0001c0001t0001g0118 a0001c0002t0001g0050 a0001c0002t0001g0051 others(21): Show |
24 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.687-3298_687-3293d others(8): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT | 8 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(5): Show |
12 | HG03834.hp1 NA18612.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-3299_687-3293d others(9): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(5): Show |
6 | a0001c0003t0001g0131 a0001c0003t0001g0156 a0001c0003t0001g0157 others(3): Show |
6 | HG02257.hp2 HG06807.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-3304_687-3293d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(6): Show |
43 | a0001c0001t0001g0077 a0001c0001t0001g0126 a0001c0001t0001g0134 others(40): Show |
44 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.687-3305_687-3293d others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(7): Show |
84 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(81): Show |
88 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.687-3306_687-3293d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(8): Show |
30 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0082 others(27): Show |
31 | HG00438.hp1 HG00438.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.687-3307_687-3293d others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(9): Show |
5 | a0001c0001t0001g0225 a0001c0001t0001g0232 a0001c0002t0001g0236 others(2): Show |
5 | HG02080.hp2 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-3308_687-3293d others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0001g0083 a0001c0001t0001g0229 a0001c0001t0001g0250 |
3 | HG02602.hp1 HG03471.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.687-3309_687-3293d others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(13): Show |
6 | a0001c0002t0001g0239 a0002c0005t0001g0014 a0002c0005t0001g0016 others(3): Show |
6 | HG02040.hp2 HG02615.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-3293_687-3292i others(22): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(14): Show |
4 | a0002c0005t0001g0015 a0002c0005t0001g0023 a0002c0005t0001g0029 others(1): Show |
4 | HG02071.hp1 HG02717.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-3293_687-3292i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(15): Show |
2 | a0002c0005t0001g0012 a0002c0005t0001g0022 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.687-3293_687-3292i others(24): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(16): Show |
1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.687-3293_687-3292i others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158196 | C | CTTTTTTT others(17): Show |
1 | a0001c0002t0001g0080 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.687-3293_687-3292i others(26): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24158196 | ||||||
| chr2:24158214 | C | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(211): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.687-3292C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158214 | |||||||
| chr2:24158385 | G | A | 1 | a0001c0006t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.687-3121G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158385 | |||||||
| chr2:24158608 | C | A | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.687-2898C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158608 | |||||||
| chr2:24158919 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-2587C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24158919 | |||||||
| chr2:24159015 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-2491G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159015 | |||||||
| chr2:24159051 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-2455C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159051 | |||||||
| chr2:24159160 | C | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
161 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.687-2346C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159160 | |||||||
| chr2:24159524 | A | T | 1 | a0001c0002t0001g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.687-1982A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159524 | |||||||
| chr2:24159595 | C | G | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.687-1911C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159595 | |||||||
| chr2:24159676 | G | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(150): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.687-1830G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159676 | |||||||
| chr2:24159688 | A | G | 2 | a0003c0004t0001g0096 a0003c0004t0001g0109 |
2 | NA18943.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.687-1818A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159688 | |||||||
| chr2:24159809 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-1697C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159809 | |||||||
| chr2:24159811 | C | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.687-1695C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24159811 | |||||||
| chr2:24159989 | AT | A | 11 | a0001c0001t0001g0125 a0001c0001t0001g0181 a0001c0001t0001g0273 others(8): Show |
11 | HG01516.hp1 HG02040.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.687-1500delT | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 24159989 | ||||||
| chr2:24160188 | C | T | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.687-1318C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160188 | |||||||
| chr2:24160189 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(139): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.687-1317C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160189 | |||||||
| chr2:24160190 | G | A | 5 | a0001c0003t0001g0207 a0001c0003t0001g0208 a0001c0003t0001g0209 others(2): Show |
5 | HG02055.hp2 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.687-1316G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160190 | |||||||
| chr2:24160269 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-1237C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24160269 | |||||||
| chr2:24161221 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.687-285A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24161221 | |||||||
| chr2:24161428 | A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.687-78A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 7/10 | chr2 | 24161428 | |||||||
| chr2:24161761 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.794+148T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24161761 | |||||||
| chr2:24161869 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.794+256C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24161869 | |||||||
| chr2:24162275 | T | C | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.794+662T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24162275 | |||||||
| chr2:24162357 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.794+744A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24162357 | |||||||
| chr2:24162978 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.795-1220A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24162978 | |||||||
| chr2:24163160 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.795-1038C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163160 | |||||||
| chr2:24163342 | C | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.795-856C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163342 | |||||||
| chr2:24163686 | G | T | 1 | a0001c0001t0001g0242 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.795-512G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163686 | |||||||
| chr2:24163867 | A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.795-331A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24163867 | |||||||
| chr2:24164055 | C | CA | 47 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(44): Show |
51 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.795-136dupA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 24164055 | ||||||
| chr2:24164101 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.795-97A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 8/10 | chr2 | 24164101 | |||||||
| chr2:24164473 | T | A | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.932+138T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164473 | |||||||
| chr2:24164520 | GGCCCCCT others(22): Show |
G | 2 | a0003c0004t0001g0094 a0003c0004t0001g0095 |
2 | NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.932+200_932+228del others(29): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24164520 | ||||||
| chr2:24164520 | GGCCCCCT others(51): Show |
G | 1 | a0001c0006t0001g0270 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.932+200_932+257del others(58): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24164520 | ||||||
| chr2:24164535 | TCACACGA others(22): Show |
T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(220): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.932+256_932+284del others(29): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24164535 | ||||||
| chr2:24164568 | A | G | 2 | a0001c0002t0001g0066 a0001c0006t0003g0075 |
2 | HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.932+233A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164568 | |||||||
| chr2:24164650 | C | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.932+315C>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164650 | |||||||
| chr2:24164663 | C | T | 48 | a0001c0001t0001g0189 a0001c0002t0001g0001 a0001c0002t0001g0043 others(45): Show |
52 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.932+328C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164663 | |||||||
| chr2:24164704 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.932+369G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164704 | |||||||
| chr2:24164854 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0204 |
2 | HG01346.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.932+519G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164854 | |||||||
| chr2:24164990 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.932+655G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24164990 | |||||||
| chr2:24165113 | T | A | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+778T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165113 | |||||||
| chr2:24165114 | T | C | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+779T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165114 | |||||||
| chr2:24165115 | C | A | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+780C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165115 | |||||||
| chr2:24165123 | A | G | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+788A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165123 | |||||||
| chr2:24165126 | G | C | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+791G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165126 | |||||||
| chr2:24165128 | G | C | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+793G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165128 | |||||||
| chr2:24165129 | A | G | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+794A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165129 | |||||||
| chr2:24165130 | A | T | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+795A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165130 | |||||||
| chr2:24165131 | T | G | 1 | a0001c0002t0001g0046 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.932+796T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165131 | |||||||
| chr2:24165227 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.932+892G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165227 | |||||||
| chr2:24165304 | GGCCCTAT others(7): Show |
G | 9 | a0001c0003t0001g0005 a0001c0003t0001g0084 a0001c0003t0001g0085 others(6): Show |
10 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.932+971_932+984del others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24165304 | ||||||
| chr2:24165326 | C | T | 9 | a0001c0003t0001g0005 a0001c0003t0001g0084 a0001c0003t0001g0085 others(6): Show |
10 | HG01891.hp2 HG01934.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.932+991C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165326 | |||||||
| chr2:24165398 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.932+1063C>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165398 | |||||||
| chr2:24165499 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.932+1164C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165499 | |||||||
| chr2:24165740 | T | G | 32 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(29): Show |
36 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.932+1405T>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165740 | |||||||
| chr2:24165816 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.932+1481C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165816 | |||||||
| chr2:24165986 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.933-1641G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24165986 | |||||||
| chr2:24166041 | TA | T | 12 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(9): Show |
14 | HG01255.hp2 HG01361.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.933-1572delA | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166041 | ||||||
| chr2:24166050 | A | AATATATA others(3): Show |
3 | a0002c0005t0001g0022 a0002c0005t0001g0023 a0002c0005t0001g0034 |
3 | HG02717.hp2 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.933-1576_933-1575i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166050 | ||||||
| chr2:24166052 | A | AAGAAATA others(9): Show |
1 | a0001c0001t0001g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.933-1574_933-1573i others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AAT | 14 | a0001c0002t0001g0070 a0001c0003t0001g0100 a0001c0003t0001g0131 others(11): Show |
14 | HG01243.hp2 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.933-1574_933-1573i others(4): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AATAT | 7 | a0001c0002t0001g0066 a0001c0003t0001g0129 a0001c0003t0001g0132 others(4): Show |
7 | HG02615.hp2 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.933-1574_933-1573i others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AATATATA others(3): Show |
4 | a0002c0005t0001g0015 a0002c0005t0001g0016 a0002c0005t0001g0029 others(1): Show |
4 | HG02071.hp1 NA18995.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.933-1574_933-1573i others(12): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AATATATA others(5): Show |
1 | a0002c0005t0001g0014 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.933-1574_933-1573i others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AATATATA others(7): Show |
1 | a0002c0005t0001g0037 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.933-1574_933-1573i others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0272 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.933-1574_933-1573i others(22): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166052 | ||||||
| chr2:24166052 | A | AT | 6 | a0001c0003t0001g0084 a0001c0003t0001g0085 a0001c0003t0001g0089 others(3): Show |
6 | HG01516.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.933-1575_933-1574i others(3): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | |||||||
| chr2:24166052 | A | ATATAT | 3 | a0001c0002t0001g0073 a0001c0002t0001g0074 a0001c0002t0001g0173 |
3 | HG02056.hp1 HG02135.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.933-1575_933-1574i others(7): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | |||||||
| chr2:24166052 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.933-1575_933-1574i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | |||||||
| chr2:24166052 | A | T | 10 | a0001c0002t0001g0069 a0001c0003t0001g0207 a0001c0006t0001g0270 others(7): Show |
10 | HG00323.hp2 HG01255.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.933-1575A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166052 | |||||||
| chr2:24166054 | A | AAAAAAAT others(10): Show |
1 | a0001c0001t0001g0254 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.933-1572_933-1571i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAAAATAT others(4): Show |
1 | a0001c0002t0001g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAAAATAT others(8): Show |
12 | a0001c0001t0001g0099 a0001c0001t0001g0116 a0001c0001t0001g0121 others(9): Show |
12 | HG01192.hp2 HG01243.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0127 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAAATATA others(7): Show |
3 | a0001c0001t0001g0118 a0001c0001t0001g0192 a0001c0001t0001g0215 |
3 | HG01978.hp2 NA19068.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.933-1572_933-1571i others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATAATA others(9): Show |
1 | a0001c0001t0001g0145 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.933-1572_933-1571i others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(4): Show |
1 | a0001c0002t0001g0256 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(13): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(6): Show |
17 | a0001c0001t0001g0011 a0001c0001t0001g0068 a0001c0001t0001g0144 others(14): Show |
18 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(15): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(8): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(42): Show |
51 | HG00621.hp1 HG01106.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(10): Show |
15 | a0001c0001t0001g0078 a0001c0001t0001g0120 a0001c0001t0001g0135 others(12): Show |
15 | HG00642.hp2 HG00741.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(12): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0098 a0001c0001t0001g0178 others(6): Show |
9 | HG01099.hp1 HG01169.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(21): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(14): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0246 a0001c0001t0001g0253 |
3 | HG01257.hp1 HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.933-1572_933-1571i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(16): Show |
5 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(2): Show |
5 | HG02109.hp2 HG02647.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-1572_933-1571i others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(18): Show |
2 | a0002c0007t0001g0026 a0002c0007t0001g0030 |
2 | HG03492.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.933-1572_933-1571i others(27): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AAATATAT others(20): Show |
1 | a0002c0007t0001g0018 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.933-1572_933-1571i others(29): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AATATATA others(5): Show |
1 | a0001c0002t0001g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.933-1566_933-1555d others(14): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0187 a0001c0001t0001g0197 |
2 | HG00323.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.933-1568_933-1555d others(16): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AATATATA others(9): Show |
9 | a0001c0001t0001g0108 a0001c0001t0001g0117 a0001c0001t0001g0180 others(6): Show |
9 | HG00099.hp1 HG00621.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.933-1570_933-1555d others(18): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AATATATA others(11): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0175 others(1): Show |
5 | HG01109.hp2 NA18612.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.933-1572_933-1555d others(20): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AATATATA others(13): Show |
2 | a0001c0001t0001g0229 a0001c0011t0001g0258 |
2 | HG03453.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.933-1555_933-1554i others(22): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | AATATATA others(19): Show |
2 | a0002c0007t0001g0019 a0002c0007t0001g0032 |
2 | HG01069.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.933-1555_933-1554i others(28): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166054 | ||||||
| chr2:24166054 | A | ATATAT | 24 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0044 others(21): Show |
28 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.933-1573_933-1572i others(7): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166054 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0059 a0001c0001t0001g0134 |
4 | HG00140.hp2 HG00735.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.933-1573_933-1572i others(17): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166054 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0259 a0001c0001t0001g0273 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.933-1573_933-1572i others(19): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166054 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0220 a0001c0001t0001g0248 |
2 | HG02083.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.933-1573_933-1572i others(23): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166054 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.933-1573_933-1572i others(25): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166054 | A | ATATATAT others(18): Show |
2 | a0002c0007t0001g0017 a0002c0007t0001g0020 |
2 | HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.933-1573_933-1572i others(27): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166054 | A | T | 86 | a0001c0001t0001g0153 a0001c0001t0001g0224 a0001c0001t0001g0272 others(83): Show |
89 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.933-1573A>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166054 | |||||||
| chr2:24166056 | T | A | 1 | a0003c0004t0001g0091 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.933-1571T>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166056 | |||||||
| chr2:24166210 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-1417G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166210 | |||||||
| chr2:24166341 | A | G | 1 | a0001c0006t0001g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.933-1286A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166341 | |||||||
| chr2:24166409 | A | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
37 | HG00621.hp1 HG00642.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.933-1218A>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166409 | |||||||
| chr2:24166496 | G | GTGCT | 35 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(32): Show |
35 | HG00099.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.933-1117_933-1114d others(6): Show |
FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | 24166496 | ||||||
| chr2:24166600 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-1027C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166600 | |||||||
| chr2:24166669 | G | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0079 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.933-958G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166669 | |||||||
| chr2:24166806 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.933-821G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24166806 | |||||||
| chr2:24167214 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-413C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167214 | |||||||
| chr2:24167283 | G | A | 2 | a0001c0002t0001g0256 a0001c0002t0001g0257 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.933-344G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167283 | |||||||
| chr2:24167382 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.933-245G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167382 | |||||||
| chr2:24167424 | G | C | 1 | a0002c0007t0001g0018 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.933-203G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167424 | |||||||
| chr2:24167519 | G | A | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.933-108G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 9/10 | chr2 | 24167519 | |||||||
| chr2:24167780 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.*14+97G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24167780 | |||||||
| chr2:24167787 | A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*14+104A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24167787 | |||||||
| chr2:24167971 | G | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.*14+288G>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24167971 | |||||||
| chr2:24168157 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*14+474C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168157 | |||||||
| chr2:24168260 | A | G | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
161 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.*14+577A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168260 | |||||||
| chr2:24168669 | A | G | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*15-687A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168669 | |||||||
| chr2:24168810 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.*15-546G>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168810 | |||||||
| chr2:24168851 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.*15-505T>C | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168851 | |||||||
| chr2:24168864 | A | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.*15-492A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168864 | |||||||
| chr2:24168878 | C | T | 1 | a0001c0006t0003g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*15-478C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168878 | |||||||
| chr2:24168955 | G | A | 1 | a0002c0005t0001g0023 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*15-401G>A | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24168955 | |||||||
| chr2:24169025 | A | G | 13 | a0001c0006t0001g0003 a0001c0006t0001g0214 a0001c0006t0001g0260 others(10): Show |
15 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.*15-331A>G | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169025 | |||||||
| chr2:24169091 | C | T | 2 | a0001c0002t0001g0054 a0001c0002t0001g0060 |
2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*15-265C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169091 | |||||||
| chr2:24169177 | C | T | 14 | a0001c0002t0001g0080 a0001c0006t0001g0003 a0001c0006t0001g0214 others(11): Show |
16 | HG01255.hp2 HG01361.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.*15-179C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169177 | |||||||
| chr2:24169235 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.*15-121C>T | FAM228B | ENSG00000219626.9 | transcript | ENST00000615575.5 | protein_coding | 10/10 | chr2 | 24169235 |