Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55731 |
| ensemblid | ENSG00000173065.14 |
| hgncid | 25563 |
| symbol | FAM222B |
| name | family with sequence similarity 222 member B |
| refseq_nuc | NM_001077498.3 |
| refseq_prot | NP_001070966.1 |
| ensembl_nuc | ENST00000581407.6 |
| ensembl_prot | ENSP00000462419.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 28755980 |
| end | 28842790 |
| strand | - |
| ver | v1.2 |
| region | chr17:28755980-28842790 |
| region5000 | chr17:28750980-28847790 |
| regionname0 | FAM222B_chr17_28755980_28842790 |
| regionname5000 | FAM222B_chr17_28750980_28847790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 562 | 269 | 72 | 57 | 97 | 6 | 35 | 79 | FAM222B_chr17_28750980_28847790 | FAM222B | MLACL others(557): Show |
chr17 | 28750980 | 28847790 |
| a0002 | 0/0 | 562 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | MLACL others(557): Show |
chr17 | 28750980 | 28847790 |
| a0003 | 0/0 | 562 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | MLACL others(557): Show |
chr17 | 28750980 | 28847790 |
| a0004 | 0/0 | 562 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | MLACL others(557): Show |
chr17 | 28750980 | 28847790 |
| a0005 | 0/0 | 562 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | MLACL others(557): Show |
chr17 | 28750980 | 28847790 |
| a0006 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | MLACL others(557): Show |
chr17 | 28750980 | 28847790 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1686 | 182 | 57 | 40 | 56 | 4 | 24 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0001c0002 | 0/1 | 1686 | 84 | 14 | 15 | 41 | 2 | 11 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0001c0006 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0001c0007 | 0/0 | 1686 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0001c0010 | 0/0 | 1686 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0002c0003 | 0/0 | 1686 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0003c0004 | 0/0 | 1686 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0004c0008 | 0/0 | 1686 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0005c0009 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 | ||
| a0006c0005 | 0/0 | 1686 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | ATGCT others(1681): Show |
chr17 | 28750980 | 28847790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4128 | 125 | 30 | 33 | 39 | 4 | 18 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0004 | 0/0 | 4135 | 22 | 12 | 2 | 7 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4130): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0005 | 0/0 | 4129 | 11 | 2 | 3 | 6 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4124): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0007 | 0/0 | 4130 | 2 | 1 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4125): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0008 | 0/0 | 4129 | 2 | 0 | 1 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4124): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0009 | 0/0 | 4128 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0010 | 0/0 | 4128 | 2 | 0 | 0 | 0 | 0 | 2 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0011 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0012 | 0/0 | 4135 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4130): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0013 | 0/0 | 4135 | 2 | 2 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4130): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0014 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4126): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0015 | 0/0 | 4129 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4124): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0016 | 0/0 | 4129 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4124): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0017 | 0/0 | 4128 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0018 | 0/0 | 4128 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0019 | 0/0 | 4128 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0020 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0021 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0023 | 0/0 | 4136 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0026 | 0/0 | 4135 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4130): Show |
chr17 | 28750980 | 28847790 |
| a0001c0001t0027 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4137): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0002 | 0/1 | 4136 | 53 | 13 | 10 | 19 | 1 | 9 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0003 | 0/0 | 4136 | 22 | 0 | 3 | 16 | 1 | 2 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0004 | 0/0 | 4135 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4130): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0006 | 0/0 | 4137 | 4 | 0 | 0 | 4 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4132): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0022 | 0/0 | 4137 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4132): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0024 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0002t0025 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0006t0001 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0001c0007t0002 | 0/0 | 4136 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0001c0010t0001 | 0/0 | 4128 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0002c0003t0001 | 0/0 | 4128 | 2 | 1 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0003c0004t0001 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0003c0004t0005 | 0/0 | 4129 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4124): Show |
chr17 | 28750980 | 28847790 |
| a0004c0008t0003 | 0/0 | 4136 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| a0005c0009t0011 | 0/0 | 4128 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4123): Show |
chr17 | 28750980 | 28847790 |
| a0006c0005t0003 | 0/0 | 4136 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | AGTCC others(4131): Show |
chr17 | 28750980 | 28847790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0011g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0016g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0017g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0018g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0019g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0021g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0023g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0026g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0001t0027g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0004g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0022g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0024g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0002t0025g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0007t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0001c0010t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0002c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0003c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0004c0008t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0005c0009t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| a0006c0005t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0213 | EUR | GBR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | CHS | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00738 | hp1 | a0001 | c0010 | t0001 | g0098 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0099 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0165 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01074 | hp1 | a0001 | c0002 | t0025 | g0201 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0237 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0164 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01168 | hp2 | a0001 | c0002 | t0004 | g0197 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01243 | hp2 | a0002 | c0003 | t0001 | g0125 | AMR | PUR | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0202 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01433 | hp2 | a0001 | c0007 | t0002 | g0208 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0167 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0079 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02055 | hp1 | a0001 | c0001 | t0023 | g0249 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02055 | hp2 | a0003 | c0004 | t0005 | g0027 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0184 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0163 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0190 | EAS | CDX | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0211 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0166 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0223 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0228 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0274 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0033 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0147 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0245 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02683 | hp2 | a0004 | c0008 | t0003 | g0173 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0148 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0262 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0028 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0068 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03041 | hp1 | a0001 | c0001 | t0027 | g0276 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0102 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03195 | hp2 | a0001 | c0006 | t0001 | g0088 | AFR | ESN | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0205 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03239 | hp1 | a0001 | c0001 | t0017 | g0100 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0004 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0066 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03492 | hp1 | a0001 | c0001 | t0010 | g0067 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0161 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03540 | hp1 | a0001 | c0001 | t0013 | g0261 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03579 | hp1 | a0001 | c0001 | t0021 | g0270 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0236 | SAS | STU | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0214 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03710 | hp1 | a0001 | c0001 | t0016 | g0082 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03831 | hp2 | a0001 | c0002 | t0003 | g0219 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0178 | EAS | CHB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18947 | hp1 | a0001 | c0002 | t0006 | g0194 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18948 | hp2 | a0001 | c0002 | t0006 | g0206 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18961 | hp2 | a0001 | c0002 | t0022 | g0177 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0117 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18967 | hp1 | a0001 | c0002 | t0006 | g0172 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0216 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0183 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18974 | hp1 | a0001 | c0002 | t0024 | g0168 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19000 | hp2 | a0006 | c0005 | t0003 | g0192 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | LWK | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | LWK | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19066 | hp1 | a0001 | c0001 | t0019 | g0049 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19066 | hp2 | a0001 | c0001 | t0026 | g0266 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19086 | hp1 | a0001 | c0002 | t0006 | g0200 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19086 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0119 | AFR | ASW | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0209 | AFR | ASW | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0231 | EUR | TSI | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | GIH | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0271 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0193 | AFR | MSL | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| HG06807 | hp2 | a0005 | c0009 | t0011 | g0003 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0269 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | USA | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0229 | REF | REF | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | FAM222B_chr17_28750980_28847790 | FAM222B | chr17 | 28750980 | 28847790 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28758335 | C | T | 1 | a0003 | 2 | HG02055.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1624G>A | p.Gly542Ser | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1773/4128 | 1624/1689 | 542/562 | chr17 | 28758335 | |||
| chr17:28758379 | C | T | 1 | a0002 | 2 | HG01243.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1580G>A | p.Arg527Gln | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1729/4128 | 1580/1689 | 527/562 | chr17 | 28758379 | |||
| chr17:28758980 | T | C | 1 | a0004 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.979A>G | p.Met327Val | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1128/4128 | 979/1689 | 327/562 | chr17 | 28758980 | |||
| chr17:28759115 | T | C | 1 | a0005 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.844A>G | p.Ile282Val | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 993/4128 | 844/1689 | 282/562 | chr17 | 28759115 | |||
| chr17:28759600 | C | T | 1 | a0006 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.359G>A | p.Arg120Gln | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 508/4128 | 359/1689 | 120/562 | chr17 | 28759600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28758546 | A | G | 4 | a0001c0002 a0001c0007 a0004c0008 others(1): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
synonymous_variant | LOW | c.1413T>C | p.Leu471Leu | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1562/4128 | 1413/1689 | 471/562 | chr17 | 28758546 | |||
| chr17:28758810 | C | T | 1 | a0001c0006 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1149G>A | p.Thr383Thr | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1298/4128 | 1149/1689 | 383/562 | chr17 | 28758810 | |||
| chr17:28758957 | G | A | 1 | a0001c0007 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1002C>T | p.Thr334Thr | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1151/4128 | 1002/1689 | 334/562 | chr17 | 28758957 | |||
| chr17:28759182 | G | A | 1 | a0001c0010 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.777C>T | p.His259His | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 926/4128 | 777/1689 | 259/562 | chr17 | 28759182 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28756090 | T | C | 1 | a0001c0001t0018 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2180A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 2180 | chr17 | 28756090 | ||||||
| chr17:28756140 | G | C | 1 | a0001c0002t0024 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2130C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 2130 | chr17 | 28756140 | ||||||
| chr17:28756537 | G | A | 1 | a0001c0001t0015 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1733 | chr17 | 28756537 | ||||||
| chr17:28756570 | C | T | 2 | a0001c0001t0016 a0001c0001t0017 |
2 | HG03239.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1700 | chr17 | 28756570 | ||||||
| chr17:28756695 | T | C | 1 | a0001c0001t0009 | 2 | HG02622.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1575A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1575 | chr17 | 28756695 | ||||||
| chr17:28757041 | T | G | 1 | a0001c0002t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1229 | chr17 | 28757041 | ||||||
| chr17:28757207 | T | G | 1 | a0001c0001t0013 | 2 | HG02965.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1063A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1063 | chr17 | 28757207 | ||||||
| chr17:28757270 | C | A | 1 | a0001c0001t0019 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 1000 | chr17 | 28757270 | ||||||
| chr17:28757318 | C | T | 1 | a0001c0001t0026 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 952 | chr17 | 28757318 | ||||||
| chr17:28757346 | T | C | 3 | a0001c0002t0003 a0004c0008t0003 a0006c0005t0003 |
24 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*924A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 924 | chr17 | 28757346 | ||||||
| chr17:28757376 | A | AT | 11 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0016 others(8): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*893dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 893 | chr17 | 28757376 | ||||||
| chr17:28757376 | A | ATT | 2 | a0001c0001t0014 a0001c0002t0006 |
5 | HG02615.hp2 NA18947.hp1 NA18948.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*893dupAA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 893 | chr17 | 28757376 | ||||||
| chr17:28757391 | G | A | 1 | a0001c0001t0010 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 879 | chr17 | 28757391 | ||||||
| chr17:28757514 | G | T | 2 | a0001c0001t0012 a0001c0001t0021 |
3 | HG02109.hp1 HG03579.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*756C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 756 | chr17 | 28757514 | ||||||
| chr17:28757602 | T | A | 2 | a0001c0001t0011 a0005c0009t0011 |
2 | HG03453.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*668A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 668 | chr17 | 28757602 | ||||||
| chr17:28757788 | G | A | 1 | a0001c0001t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 482 | chr17 | 28757788 | ||||||
| chr17:28757854 | A | AG | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(5): Show |
19 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*415dupC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 3/3 | 415 | chr17 | 28757854 | ||||||
| chr17:28842719 | T | TGCCGCCC | 16 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0013 others(13): Show |
115 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-85_-79dupGGGCGGC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/3 | 76053 | chr17 | 28842719 | ||||||
| chr17:28842719 | T | TGCCGCCC others(7): Show |
1 | a0001c0001t0027 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92_-79dupGGGCGGCG others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/3 | 76053 | chr17 | 28842719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:28760200 | A | C | 1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.83-324T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760200 | |||||||
| chr17:28760247 | C | A | 1 | a0001c0001t0001g0019 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.83-371G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760247 | |||||||
| chr17:28760362 | G | T | 1 | a0001c0001t0020g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-486C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760362 | |||||||
| chr17:28760587 | G | GA | 88 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0002t0002g0160 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.83-712dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760587 | |||||||
| chr17:28760734 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.83-858C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760734 | |||||||
| chr17:28760911 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.83-1035G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28760911 | |||||||
| chr17:28761117 | G | A | 1 | a0001c0001t0004g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.83-1241C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761117 | |||||||
| chr17:28761298 | G | A | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.83-1422C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761298 | |||||||
| chr17:28761418 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.83-1542G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761418 | |||||||
| chr17:28761488 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83-1612G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761488 | |||||||
| chr17:28761583 | T | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.83-1707A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761583 | |||||||
| chr17:28761608 | C | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.83-1732G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761608 | |||||||
| chr17:28761610 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0083 a0001c0001t0007g0070 |
3 | NA18950.hp2 NA18959.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.83-1734G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761610 | |||||||
| chr17:28761805 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0019g0049 |
2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.83-1929T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761805 | |||||||
| chr17:28761891 | C | T | 2 | a0001c0001t0004g0258 a0001c0001t0004g0259 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.83-2015G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28761891 | |||||||
| chr17:28762231 | G | T | 3 | a0001c0001t0004g0253 a0001c0001t0013g0261 a0001c0001t0013g0262 |
3 | HG02965.hp1 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.83-2355C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762231 | |||||||
| chr17:28762238 | C | A | 1 | a0001c0001t0005g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.83-2362G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762238 | |||||||
| chr17:28762394 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.83-2518C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762394 | |||||||
| chr17:28762403 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.83-2527C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762403 | |||||||
| chr17:28762442 | A | G | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0036 others(1): Show |
4 | HG02602.hp2 HG02698.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-2566T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762442 | |||||||
| chr17:28762626 | CA | C | 203 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.83-2751delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762626 | |||||||
| chr17:28762626 | CAA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(12): Show |
15 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-2752_83-2751del others(2): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762626 | |||||||
| chr17:28762839 | C | G | 6 | a0001c0002t0002g0180 a0001c0002t0002g0196 a0001c0002t0002g0218 others(3): Show |
6 | NA18950.hp1 NA18961.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2963G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762839 | |||||||
| chr17:28762861 | C | T | 6 | a0001c0002t0002g0180 a0001c0002t0002g0196 a0001c0002t0002g0218 others(3): Show |
6 | NA18950.hp1 NA18961.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2985G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762861 | |||||||
| chr17:28762937 | CA | C | 6 | a0001c0001t0004g0256 a0001c0001t0013g0262 a0001c0001t0020g0054 others(3): Show |
6 | HG01168.hp2 HG02135.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-3062delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28762937 | |||||||
| chr17:28763212 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.83-3336G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763212 | |||||||
| chr17:28763307 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0093 a0001c0001t0001g0101 |
3 | HG03041.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.82+3279A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763307 | |||||||
| chr17:28763406 | C | T | 1 | a0001c0001t0016g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.82+3180G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763406 | |||||||
| chr17:28763723 | C | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.82+2863G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28763723 | |||||||
| chr17:28764135 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.82+2451T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764135 | |||||||
| chr17:28764255 | G | C | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82+2331C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764255 | |||||||
| chr17:28764271 | C | CA | 89 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0048 others(86): Show |
89 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.82+2314dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | |||||||
| chr17:28764271 | C | CAA | 12 | a0001c0001t0001g0113 a0001c0002t0002g0178 a0001c0002t0002g0185 others(9): Show |
12 | HG01884.hp1 HG02015.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.82+2313_82+2314dup others(2): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | |||||||
| chr17:28764271 | CA | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(19): Show |
22 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.82+2314delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | |||||||
| chr17:28764271 | CAA | C | 28 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(25): Show |
28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.82+2313_82+2314del others(2): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764271 | |||||||
| chr17:28764294 | A | G | 1 | a0001c0001t0004g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.82+2292T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764294 | |||||||
| chr17:28764350 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82+2236C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764350 | |||||||
| chr17:28764377 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82+2209C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764377 | |||||||
| chr17:28764468 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.82+2118C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764468 | |||||||
| chr17:28764815 | G | A | 3 | a0001c0002t0002g0207 a0001c0002t0002g0237 a0001c0002t0002g0245 |
3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82+1771C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764815 | |||||||
| chr17:28764933 | G | A | 6 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0093 others(3): Show |
6 | HG02647.hp2 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+1653C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28764933 | |||||||
| chr17:28765183 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.82+1403C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765183 | |||||||
| chr17:28765307 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.82+1279C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765307 | |||||||
| chr17:28765592 | G | A | 1 | a0001c0001t0007g0070 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.82+994C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765592 | |||||||
| chr17:28765685 | G | C | 2 | a0001c0001t0004g0267 a0001c0001t0026g0266 |
2 | NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.82+901C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765685 | |||||||
| chr17:28765776 | G | C | 30 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(27): Show |
30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.82+810C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765776 | |||||||
| chr17:28765924 | A | G | 4 | a0001c0002t0002g0180 a0001c0002t0002g0196 a0001c0002t0006g0200 others(1): Show |
4 | NA18961.hp2 NA18966.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+662T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28765924 | |||||||
| chr17:28766052 | G | GAT | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.82+532_82+533dupAT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766052 | |||||||
| chr17:28766116 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.82+470C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766116 | |||||||
| chr17:28766180 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82+406G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766180 | |||||||
| chr17:28766367 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.82+219A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766367 | |||||||
| chr17:28766452 | C | T | 2 | a0001c0001t0004g0255 a0001c0001t0004g0257 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.82+134G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766452 | |||||||
| chr17:28766457 | T | TA | 8 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0007g0070 others(5): Show |
8 | HG01081.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+128dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766457 | |||||||
| chr17:28766457 | TA | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0005g0057 others(4): Show |
7 | HG01070.hp2 HG01099.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+128delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766457 | |||||||
| chr17:28766503 | C | T | 2 | a0001c0001t0004g0258 a0001c0001t0004g0259 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.82+83G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766503 | |||||||
| chr17:28766524 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(220): Show |
223 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.82+62C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 2/2 | chr17 | 28766524 | |||||||
| chr17:28766762 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-55C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28766762 | |||||||
| chr17:28766844 | G | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-137C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28766844 | |||||||
| chr17:28767014 | G | A | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40-307C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767014 | |||||||
| chr17:28767062 | G | GT | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-356dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767062 | |||||||
| chr17:28767349 | G | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 |
3 | HG01346.hp1 HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-40-642C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767349 | |||||||
| chr17:28767401 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-40-694C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767401 | |||||||
| chr17:28767477 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-770G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767477 | |||||||
| chr17:28767778 | A | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-1071T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767778 | |||||||
| chr17:28767788 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0122 |
2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-40-1081T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767788 | |||||||
| chr17:28767880 | A | G | 3 | a0001c0002t0002g0222 a0001c0002t0002g0226 a0001c0002t0002g0227 |
3 | NA18962.hp1 NA18986.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-40-1173T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28767880 | |||||||
| chr17:28768467 | G | A | 81 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(78): Show |
81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-1760C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768467 | |||||||
| chr17:28768536 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0034 |
2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-40-1829T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768536 | |||||||
| chr17:28768602 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-40-1895G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768602 | |||||||
| chr17:28768615 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0084 |
3 | HG02135.hp2 NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-40-1908A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768615 | |||||||
| chr17:28768810 | C | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-2103G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768810 | |||||||
| chr17:28768811 | G | A | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-40-2104C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768811 | |||||||
| chr17:28768836 | C | CA | 13 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0149 others(10): Show |
13 | HG00438.hp1 HG01175.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-40-2130dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768836 | |||||||
| chr17:28768836 | CA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
119 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-40-2130delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768836 | |||||||
| chr17:28768838 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-2131T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28768838 | |||||||
| chr17:28769160 | C | T | 2 | a0001c0002t0002g0220 a0001c0002t0004g0205 |
2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-40-2453G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769160 | |||||||
| chr17:28769174 | C | CT | 136 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0013 others(133): Show |
136 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.-40-2468dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769174 | |||||||
| chr17:28769174 | C | CTT | 41 | a0001c0001t0001g0046 a0001c0001t0001g0055 a0001c0001t0001g0064 others(38): Show |
41 | HG00408.hp2 HG00621.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.-40-2469_-40-2468d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769174 | |||||||
| chr17:28769185 | T | C | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40-2478A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769185 | |||||||
| chr17:28769268 | T | C | 2 | a0001c0002t0002g0160 a0001c0002t0002g0161 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-2561A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769268 | |||||||
| chr17:28769399 | T | C | 1 | a0001c0002t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-40-2692A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769399 | |||||||
| chr17:28769432 | C | A | 1 | a0002c0003t0001g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-40-2725G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769432 | |||||||
| chr17:28769433 | G | A | 1 | a0001c0002t0003g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-40-2726C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769433 | |||||||
| chr17:28769586 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-2879G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769586 | |||||||
| chr17:28769698 | A | T | 1 | a0001c0001t0026g0266 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-40-2991T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769698 | |||||||
| chr17:28769711 | G | A | 3 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0026g0266 |
3 | NA18943.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-40-3004C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769711 | |||||||
| chr17:28769772 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0005g0139 |
3 | HG00642.hp1 HG01192.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-40-3065G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28769772 | |||||||
| chr17:28770352 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-40-3645G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770352 | |||||||
| chr17:28770365 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-40-3658A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770365 | |||||||
| chr17:28770446 | A | C | 1 | a0001c0001t0001g0134 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-40-3739T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770446 | |||||||
| chr17:28770531 | C | G | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-40-3824G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770531 | |||||||
| chr17:28770570 | TA | T | 84 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(81): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-40-3864delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770570 | |||||||
| chr17:28770571 | A | AT | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0064 others(2): Show |
5 | HG01109.hp2 HG02602.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-3865dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770571 | |||||||
| chr17:28770571 | A | T | 2 | a0001c0002t0002g0170 a0001c0002t0002g0187 |
2 | HG00642.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.-40-3864T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770571 | |||||||
| chr17:28770593 | CAG | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-3888_-40-3887d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770593 | |||||||
| chr17:28770640 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-3933C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770640 | |||||||
| chr17:28770663 | T | G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0059 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-3956A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770663 | |||||||
| chr17:28770683 | G | A | 1 | a0001c0002t0002g0188 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-40-3976C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770683 | |||||||
| chr17:28770871 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0122 |
2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-40-4164T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770871 | |||||||
| chr17:28770892 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0056 |
2 | HG01109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-40-4185A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770892 | |||||||
| chr17:28770914 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-40-4207A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770914 | |||||||
| chr17:28770940 | T | TTA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-4235_-40-4234d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770940 | |||||||
| chr17:28770940 | TTA | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0141 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-40-4235_-40-4234d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770940 | |||||||
| chr17:28770952 | A | G | 2 | a0001c0001t0001g0052 a0001c0002t0003g0167 |
2 | HG01496.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-40-4245T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28770952 | |||||||
| chr17:28771006 | A | T | 88 | a0001c0001t0001g0022 a0001c0001t0015g0079 a0001c0002t0002g0160 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-40-4299T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771006 | |||||||
| chr17:28771013 | CT | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0043 others(19): Show |
22 | HG00738.hp1 HG01123.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-40-4307delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771013 | |||||||
| chr17:28771072 | C | T | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-4365G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771072 | |||||||
| chr17:28771120 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-40-4413T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771120 | |||||||
| chr17:28771126 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-40-4419T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771126 | |||||||
| chr17:28771637 | T | C | 1 | a0001c0002t0003g0219 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-40-4930A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771637 | |||||||
| chr17:28771656 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-40-4949C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771656 | |||||||
| chr17:28771675 | C | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-4968G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28771675 | |||||||
| chr17:28772043 | C | A | 81 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(78): Show |
81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-5336G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772043 | |||||||
| chr17:28772098 | T | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-5391A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772098 | |||||||
| chr17:28772132 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0122 |
2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-40-5425G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772132 | |||||||
| chr17:28772202 | A | G | 1 | a0001c0002t0002g0202 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-40-5495T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772202 | |||||||
| chr17:28772295 | C | T | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-5588G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772295 | |||||||
| chr17:28772423 | C | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-5716G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772423 | |||||||
| chr17:28772495 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-40-5788G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772495 | |||||||
| chr17:28772560 | T | TA | 82 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(79): Show |
82 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-40-5854dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772560 | |||||||
| chr17:28772560 | TA | T | 84 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(81): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-40-5854delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772560 | |||||||
| chr17:28772571 | T | C | 2 | a0001c0002t0002g0225 a0001c0002t0025g0201 |
2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-40-5864A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772571 | |||||||
| chr17:28772573 | C | A | 2 | a0001c0002t0002g0225 a0001c0002t0025g0201 |
2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-40-5866G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772573 | |||||||
| chr17:28772573 | C | CA | 84 | a0001c0001t0001g0072 a0001c0001t0001g0135 a0001c0002t0002g0160 others(81): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-40-5867dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772573 | |||||||
| chr17:28772573 | CA | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.-40-5867delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28772573 | |||||||
| chr17:28773035 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-40-6328C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773035 | |||||||
| chr17:28773134 | C | T | 81 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(78): Show |
81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-6427G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773134 | |||||||
| chr17:28773479 | C | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-40-6772G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | |||||||
| chr17:28773479 | C | CA | 85 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(82): Show |
85 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-40-6773dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | |||||||
| chr17:28773479 | C | CAA | 12 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0047 others(9): Show |
12 | HG00438.hp2 HG01192.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-6774_-40-6773d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | |||||||
| chr17:28773479 | CA | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0035 others(9): Show |
12 | HG01168.hp2 HG02647.hp2 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-6773delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | |||||||
| chr17:28773479 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0062 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-40-6782_-40-6773d others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773479 | |||||||
| chr17:28773534 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-40-6827G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773534 | |||||||
| chr17:28773656 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-40-6949C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773656 | |||||||
| chr17:28773749 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-7042C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773749 | |||||||
| chr17:28773777 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-7070C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773777 | |||||||
| chr17:28773906 | T | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-7199A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28773906 | |||||||
| chr17:28774146 | C | CT | 95 | a0001c0001t0004g0248 a0001c0001t0004g0250 a0001c0001t0004g0251 others(92): Show |
95 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-40-7440dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774146 | |||||||
| chr17:28774233 | C | T | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-40-7526G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774233 | |||||||
| chr17:28774385 | C | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-7678G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774385 | |||||||
| chr17:28774738 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-40-8031G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774738 | |||||||
| chr17:28774954 | T | TTAAA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(5): Show |
8 | HG01346.hp1 HG02258.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-8251_-40-8248d others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774954 | |||||||
| chr17:28774957 | A | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-8250T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28774957 | |||||||
| chr17:28775003 | A | AT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(163): Show |
166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.-40-8297dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775003 | |||||||
| chr17:28775003 | A | ATT | 92 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0023 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.-40-8298_-40-8297d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775003 | |||||||
| chr17:28775003 | A | ATTT | 11 | a0001c0002t0002g0179 a0001c0002t0002g0198 a0001c0002t0002g0202 others(8): Show |
11 | HG01346.hp2 HG02132.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40-8299_-40-8297d others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775003 | |||||||
| chr17:28775147 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-8440A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775147 | |||||||
| chr17:28775229 | C | G | 30 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(27): Show |
30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-40-8522G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775229 | |||||||
| chr17:28775274 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-40-8567G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775274 | |||||||
| chr17:28775275 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-40-8568C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775275 | |||||||
| chr17:28775282 | C | G | 1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-40-8575G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775282 | |||||||
| chr17:28775461 | C | CA | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0136 others(4): Show |
7 | HG02055.hp2 HG02602.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-8755dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775461 | |||||||
| chr17:28775461 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-40-8755delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775461 | |||||||
| chr17:28775475 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40-8768T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775475 | |||||||
| chr17:28775602 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(127): Show |
130 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-40-8895T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28775602 | |||||||
| chr17:28776080 | A | G | 1 | a0003c0004t0005g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-40-9373T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776080 | |||||||
| chr17:28776325 | G | A | 2 | a0001c0001t0004g0258 a0001c0001t0004g0259 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-40-9618C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776325 | |||||||
| chr17:28776375 | C | CA | 101 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(98): Show |
101 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-40-9669dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776375 | |||||||
| chr17:28776375 | C | CAA | 34 | a0001c0001t0001g0060 a0001c0001t0004g0259 a0001c0001t0004g0274 others(31): Show |
34 | HG00544.hp2 HG00642.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-40-9670_-40-9669d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776375 | |||||||
| chr17:28776375 | C | CAAA | 7 | a0001c0002t0002g0230 a0001c0002t0002g0232 a0001c0002t0002g0233 others(4): Show |
7 | HG02135.hp1 NA18952.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-9671_-40-9669d others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776375 | |||||||
| chr17:28776442 | C | A | 2 | a0001c0002t0002g0174 a0001c0007t0002g0208 |
2 | HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40-9735G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776442 | |||||||
| chr17:28776452 | C | CT | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(52): Show |
55 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-40-9746dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776452 | |||||||
| chr17:28776452 | C | CTT | 5 | a0001c0001t0001g0043 a0001c0001t0001g0149 a0001c0001t0001g0152 others(2): Show |
5 | HG01361.hp1 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-9747_-40-9746d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776452 | |||||||
| chr17:28776452 | CT | C | 88 | a0001c0001t0001g0021 a0001c0001t0004g0162 a0001c0001t0004g0247 others(85): Show |
88 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-40-9746delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776452 | |||||||
| chr17:28776629 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-9922T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28776629 | |||||||
| chr17:28777225 | C | T | 1 | a0001c0002t0003g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-40-10518G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28777225 | |||||||
| chr17:28777522 | A | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-10815T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28777522 | |||||||
| chr17:28777782 | C | CT | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-11076dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28777782 | |||||||
| chr17:28778007 | C | CT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-40-11301dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778007 | |||||||
| chr17:28778007 | CT | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0072 others(4): Show |
7 | HG00099.hp1 HG02015.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-11301delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778007 | |||||||
| chr17:28778028 | T | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-11321A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778028 | |||||||
| chr17:28778050 | A | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-11343T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778050 | |||||||
| chr17:28778206 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-40-11499A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778206 | |||||||
| chr17:28778343 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-40-11636C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778343 | |||||||
| chr17:28778501 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-11794G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778501 | |||||||
| chr17:28778507 | C | T | 2 | a0001c0002t0002g0225 a0001c0002t0025g0201 |
2 | HG01074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-40-11800G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778507 | |||||||
| chr17:28778662 | C | A | 81 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(78): Show |
81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-11955G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778662 | |||||||
| chr17:28778662 | CCTAG | C | 3 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0221 |
3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-11959_-40-1195 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778662 | |||||||
| chr17:28778670 | A | AT | 13 | a0001c0002t0002g0164 a0001c0002t0002g0169 a0001c0002t0002g0170 others(10): Show |
13 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-40-11964dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778670 | |||||||
| chr17:28778670 | A | T | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-11963T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778670 | |||||||
| chr17:28778677 | T | TGTG | 3 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0221 |
3 | HG03490.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-11971_-40-1197 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778677 | |||||||
| chr17:28778679 | T | G | 7 | a0001c0001t0001g0115 a0001c0001t0001g0134 a0001c0001t0001g0154 others(4): Show |
7 | HG01069.hp2 HG03017.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-11972A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778679 | |||||||
| chr17:28778680 | TG | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0002t0002g0166 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-40-11974delC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778680 | |||||||
| chr17:28778680 | TGTG | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0114 |
3 | NA18951.hp2 NA18952.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-40-11976_-40-1197 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778680 | |||||||
| chr17:28778681 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
133 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-40-11974C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778681 | |||||||
| chr17:28778683 | G | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0077 a0001c0001t0001g0144 others(8): Show |
11 | HG01168.hp2 HG02135.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-40-11976C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778683 | |||||||
| chr17:28778685 | G | T | 2 | a0001c0001t0001g0144 a0001c0002t0002g0224 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-40-11978C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778685 | |||||||
| chr17:28778695 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0004g0248 a0001c0001t0013g0261 others(1): Show |
4 | HG02258.hp2 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-11988C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778695 | |||||||
| chr17:28778695 | G | GTATATAT others(7): Show |
1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-11989_-40-1198 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778695 | |||||||
| chr17:28778697 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(44): Show |
47 | HG00408.hp1 HG00642.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.-40-11990C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778697 | |||||||
| chr17:28778697 | GTA | G | 34 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0023 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.-40-11992_-40-1199 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778697 | |||||||
| chr17:28778699 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0114 others(2): Show |
5 | HG01074.hp2 HG03195.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-11992T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778699 | |||||||
| chr17:28778717 | A | T | 1 | a0001c0002t0002g0228 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-40-12010T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778717 | |||||||
| chr17:28778718 | TA | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0133 a0001c0001t0001g0134 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-12012delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778718 | |||||||
| chr17:28778719 | A | ATATATAT others(16): Show |
1 | a0001c0002t0003g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(18): Show |
1 | a0001c0002t0003g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(27): Show |
1 | a0001c0002t0006g0200 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(31): Show |
1 | a0001c0002t0002g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(42): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(27): Show |
1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(21): Show |
2 | a0001c0002t0002g0171 a0001c0002t0003g0240 |
2 | NA19085.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(25): Show |
2 | a0001c0002t0002g0234 a0001c0002t0003g0181 |
2 | NA18946.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(36): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(27): Show |
2 | a0001c0002t0002g0224 a0001c0002t0025g0201 |
2 | HG01074.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(19): Show |
2 | a0001c0002t0002g0238 a0001c0002t0003g0186 |
2 | NA18960.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(20): Show |
1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(21): Show |
5 | a0001c0002t0002g0163 a0001c0002t0002g0175 a0001c0002t0002g0188 others(2): Show |
5 | HG00544.hp2 HG02148.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(22): Show |
1 | a0001c0002t0022g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(25): Show |
2 | a0001c0002t0002g0160 a0001c0002t0002g0161 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(36): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(26): Show |
4 | a0001c0002t0002g0185 a0001c0002t0002g0207 a0001c0002t0002g0218 others(1): Show |
4 | HG02015.hp1 NA18971.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(37): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0166 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(28): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(19): Show |
4 | a0001c0002t0002g0231 a0001c0002t0003g0183 a0001c0002t0003g0184 others(1): Show |
4 | HG02132.hp1 NA18953.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(21): Show |
6 | a0001c0002t0002g0210 a0001c0002t0002g0232 a0001c0002t0003g0189 others(3): Show |
6 | HG00140.hp2 HG00408.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(22): Show |
1 | a0001c0002t0002g0180 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(35): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(27): Show |
1 | a0001c0002t0002g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(19): Show |
5 | a0001c0002t0002g0202 a0001c0002t0002g0211 a0001c0002t0002g0221 others(2): Show |
5 | HG01346.hp2 HG02273.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(20): Show |
4 | a0001c0002t0002g0196 a0001c0002t0002g0215 a0001c0002t0002g0230 others(1): Show |
4 | NA18943.hp1 NA18947.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(21): Show |
3 | a0001c0002t0002g0217 a0001c0002t0002g0225 a0006c0005t0003g0192 |
3 | HG04184.hp1 NA19000.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(22): Show |
1 | a0001c0002t0004g0197 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(15): Show |
2 | a0001c0002t0002g0179 a0001c0002t0006g0206 |
2 | HG03710.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(26): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(17): Show |
3 | a0001c0002t0002g0227 a0001c0002t0003g0219 a0004c0008t0003g0173 |
3 | HG02683.hp2 HG03831.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(28): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(19): Show |
5 | a0001c0002t0002g0222 a0001c0002t0002g0226 a0001c0002t0002g0233 others(2): Show |
5 | NA18952.hp1 NA18978.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(21): Show |
1 | a0001c0007t0002g0208 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(19): Show |
3 | a0001c0002t0002g0187 a0001c0002t0002g0220 a0001c0002t0002g0246 |
3 | HG01884.hp1 HG03139.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(18): Show |
1 | a0001c0002t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(23): Show |
1 | a0001c0002t0002g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(34): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(9): Show |
2 | a0001c0002t0002g0169 a0001c0002t0002g0170 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(16): Show |
1 | a0001c0002t0003g0195 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(4): Show |
1 | a0001c0002t0003g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-40-12013_-40-1201 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | ATATATAT others(7): Show |
2 | a0001c0002t0003g0182 a0001c0002t0003g0243 |
2 | HG02135.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-40-12013_-40-1201 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | A | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0029 others(9): Show |
12 | HG01109.hp1 HG01361.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-12012T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | AT | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0039 others(15): Show |
18 | HG00438.hp2 HG01168.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.-40-12013delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | ATT | A | 48 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(45): Show |
48 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-40-12014_-40-1201 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778719 | ATTT | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0080 a0001c0001t0005g0073 others(3): Show |
6 | HG01496.hp1 HG02055.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-12015_-40-1201 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778719 | |||||||
| chr17:28778720 | T | TA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0149 others(2): Show |
5 | HG01891.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-12014_-40-1201 others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778720 | |||||||
| chr17:28778720 | T | TATA | 5 | a0001c0001t0001g0010 a0001c0001t0004g0267 a0001c0001t0004g0268 others(2): Show |
5 | HG02970.hp1 HG06807.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-12014_-40-1201 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778720 | |||||||
| chr17:28778720 | T | TATATATA others(16): Show |
1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40-12014_-40-1201 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778720 | |||||||
| chr17:28778721 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0090 others(11): Show |
14 | HG00621.hp2 HG01934.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-12014A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778721 | |||||||
| chr17:28778722 | T | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(13): Show |
16 | HG00438.hp2 HG01168.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-40-12015A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778722 | |||||||
| chr17:28778723 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0071 others(11): Show |
14 | HG00642.hp1 HG01934.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40-12016A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778723 | |||||||
| chr17:28778724 | T | A | 3 | a0001c0001t0001g0113 a0001c0001t0014g0033 a0003c0004t0001g0028 |
3 | HG02615.hp2 HG02970.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-40-12017A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778724 | |||||||
| chr17:28778876 | C | T | 3 | a0001c0001t0004g0260 a0001c0001t0004g0263 a0001c0001t0004g0272 |
3 | NA18947.hp2 NA19054.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-40-12169G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778876 | |||||||
| chr17:28778896 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-12189C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778896 | |||||||
| chr17:28778898 | T | G | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40-12191A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778898 | |||||||
| chr17:28778923 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-12216C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28778923 | |||||||
| chr17:28779148 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-40-12441G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779148 | |||||||
| chr17:28779327 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-12620A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779327 | |||||||
| chr17:28779623 | C | T | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-40-12916G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779623 | |||||||
| chr17:28779743 | T | G | 9 | a0001c0001t0004g0260 a0001c0001t0004g0263 a0001c0001t0004g0264 others(6): Show |
9 | HG00408.hp1 HG02602.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40-13036A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779743 | |||||||
| chr17:28779751 | A | AAAAT | 87 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0086 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-13048_-40-1304 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | |||||||
| chr17:28779751 | A | AAAATAAA others(1): Show |
15 | a0001c0001t0001g0140 a0001c0001t0004g0267 a0001c0001t0004g0268 others(12): Show |
15 | HG01070.hp2 HG01168.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40-13052_-40-1304 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | |||||||
| chr17:28779751 | A | AAAATAAA others(5): Show |
2 | a0001c0002t0002g0166 a0001c0002t0022g0177 |
2 | HG02293.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-40-13056_-40-1304 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | |||||||
| chr17:28779751 | A | AATCAATA others(3): Show |
1 | a0001c0002t0003g0223 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-40-13045_-40-1304 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | |||||||
| chr17:28779751 | AAAATAAA others(5): Show |
A | 5 | a0001c0001t0005g0102 a0001c0001t0012g0269 a0001c0001t0012g0271 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-13056_-40-1304 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | |||||||
| chr17:28779751 | AAAATAAA others(9): Show |
A | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-13060_-40-1304 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779751 | |||||||
| chr17:28779795 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-40-13088C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779795 | |||||||
| chr17:28779800 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-40-13093A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779800 | |||||||
| chr17:28779854 | C | G | 117 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(114): Show |
117 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-40-13147G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779854 | |||||||
| chr17:28779884 | C | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-13177G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779884 | |||||||
| chr17:28779975 | CT | C | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-13269delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28779975 | |||||||
| chr17:28780007 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-40-13300C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780007 | |||||||
| chr17:28780099 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-40-13392C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780099 | |||||||
| chr17:28780191 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0005g0073 |
2 | NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-40-13484G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780191 | |||||||
| chr17:28780192 | G | A | 2 | a0003c0004t0001g0028 a0003c0004t0005g0027 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-40-13485C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780192 | |||||||
| chr17:28780197 | C | T | 2 | a0001c0001t0011g0004 a0005c0009t0011g0003 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-40-13490G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780197 | |||||||
| chr17:28780257 | G | T | 1 | a0001c0002t0004g0197 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-40-13550C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780257 | |||||||
| chr17:28780338 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-13631G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780338 | |||||||
| chr17:28780362 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-40-13655A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780362 | |||||||
| chr17:28780427 | T | A | 2 | a0001c0002t0002g0179 a0001c0002t0002g0236 |
2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-40-13720A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780427 | |||||||
| chr17:28780538 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-40-13831C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780538 | |||||||
| chr17:28780832 | A | C | 1 | a0001c0001t0005g0057 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-40-14125T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780832 | |||||||
| chr17:28780841 | C | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-14134G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28780841 | |||||||
| chr17:28781114 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-14407G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781114 | |||||||
| chr17:28781301 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-40-14594T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781301 | |||||||
| chr17:28781329 | T | C | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-40-14622A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781329 | |||||||
| chr17:28781368 | A | AAT | 12 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0043 others(9): Show |
12 | HG02015.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-14663_-40-1466 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781368 | |||||||
| chr17:28781498 | A | G | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-14791T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781498 | |||||||
| chr17:28781627 | C | A | 4 | a0001c0002t0003g0176 a0001c0002t0003g0189 a0001c0002t0003g0190 others(1): Show |
4 | HG00408.hp2 HG02015.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-14920G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781627 | |||||||
| chr17:28781810 | G | A | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-15103C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28781810 | |||||||
| chr17:28782035 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-40-15328T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782035 | |||||||
| chr17:28782512 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-15805T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782512 | |||||||
| chr17:28782861 | G | C | 1 | a0001c0001t0005g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-40-16154C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782861 | |||||||
| chr17:28782934 | G | A | 1 | a0001c0002t0002g0196 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-40-16227C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782934 | |||||||
| chr17:28782995 | G | A | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-40-16288C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28782995 | |||||||
| chr17:28783006 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-16299A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783006 | |||||||
| chr17:28783137 | C | CA | 19 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0077 others(16): Show |
19 | HG01106.hp2 HG01361.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-40-16431dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783137 | |||||||
| chr17:28783377 | G | A | 1 | a0001c0001t0017g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-40-16670C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783377 | |||||||
| chr17:28783499 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0059 others(2): Show |
5 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-16792G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783499 | |||||||
| chr17:28783508 | CATGAG | C | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-16806_-40-1680 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783508 | |||||||
| chr17:28783924 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-40-17217T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28783924 | |||||||
| chr17:28784046 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0020g0054 |
3 | HG02976.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-40-17339G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784046 | |||||||
| chr17:28784068 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-17361T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784068 | |||||||
| chr17:28784093 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-17386T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784093 | |||||||
| chr17:28784199 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-40-17492G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784199 | |||||||
| chr17:28784242 | G | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-17535C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784242 | |||||||
| chr17:28784321 | A | T | 1 | a0001c0001t0013g0262 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-40-17614T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784321 | |||||||
| chr17:28784444 | T | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-17737A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784444 | |||||||
| chr17:28784491 | T | TA | 40 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0020 others(37): Show |
40 | HG00099.hp2 HG00438.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.-40-17785dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAA | 25 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0029 others(22): Show |
25 | HG00733.hp2 HG00738.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.-40-17786_-40-1778 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0056 a0001c0001t0001g0146 others(3): Show |
6 | HG00408.hp1 HG01109.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-17787_-40-1778 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA | 8 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0118 others(5): Show |
8 | HG00099.hp1 HG00642.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-17791_-40-1778 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA others(3): Show |
2 | a0001c0001t0001g0038 a0001c0001t0007g0104 |
2 | HG03486.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.-40-17794_-40-1778 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-40-17796_-40-1778 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA others(7): Show |
1 | a0001c0010t0001g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-40-17798_-40-1778 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA others(8): Show |
1 | a0001c0001t0004g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-40-17799_-40-1778 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA others(11): Show |
1 | a0001c0001t0001g0069 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-40-17802_-40-1778 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | T | TAAAAAAA others(16): Show |
1 | a0001c0001t0001g0048 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-40-17807_-40-1778 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAA | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(3): Show |
6 | HG01358.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-17790_-40-1778 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(1): Show |
T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(3): Show |
6 | HG00544.hp1 HG00621.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-17792_-40-1778 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(3): Show |
T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0061 a0001c0001t0001g0078 others(2): Show |
5 | HG02155.hp1 HG02280.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-17794_-40-1778 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-40-17795_-40-1778 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0144 |
2 | HG01123.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-40-17796_-40-1778 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(6): Show |
T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0090 a0001c0001t0001g0093 others(7): Show |
10 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-17797_-40-1778 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(7): Show |
T | 13 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0105 others(10): Show |
13 | HG01243.hp1 HG01256.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-40-17798_-40-1778 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0154 a0001c0001t0013g0261 |
3 | HG01069.hp2 HG02602.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-40-17799_-40-1778 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(9): Show |
T | 1 | a0001c0002t0002g0228 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-40-17800_-40-1778 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(10): Show |
T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0065 a0001c0001t0001g0086 |
3 | HG01192.hp1 HG02015.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-40-17801_-40-1778 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(11): Show |
T | 6 | a0001c0001t0001g0005 a0001c0002t0002g0202 a0001c0002t0002g0211 others(3): Show |
6 | HG01346.hp2 HG01952.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-17802_-40-1778 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(12): Show |
T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0005g0024 others(74): Show |
77 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-40-17803_-40-1778 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(13): Show |
T | 7 | a0001c0001t0001g0077 a0001c0002t0002g0174 a0001c0002t0002g0185 others(4): Show |
7 | HG01168.hp2 HG01884.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-17804_-40-1778 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784491 | TAAAAAAA others(17): Show |
T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0083 |
2 | NA18950.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-40-17808_-40-1778 others(28): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784491 | |||||||
| chr17:28784536 | A | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-17829T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784536 | |||||||
| chr17:28784614 | G | A | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-40-17907C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784614 | |||||||
| chr17:28784626 | C | T | 2 | a0001c0002t0002g0178 a0001c0002t0002g0185 |
2 | NA18612.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-40-17919G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784626 | |||||||
| chr17:28784916 | AT | A | 7 | a0001c0001t0001g0144 a0001c0001t0004g0259 a0001c0002t0002g0193 others(4): Show |
7 | HG01081.hp1 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-18210delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784916 | |||||||
| chr17:28784982 | C | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-18275G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28784982 | |||||||
| chr17:28785150 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-40-18443G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785150 | |||||||
| chr17:28785197 | C | CT | 81 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(78): Show |
81 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-40-18491dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785197 | |||||||
| chr17:28785198 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-40-18491A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785198 | |||||||
| chr17:28785522 | T | G | 2 | a0001c0002t0002g0169 a0001c0002t0002g0170 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-40-18815A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785522 | |||||||
| chr17:28785537 | GGAT | G | 4 | a0001c0002t0002g0180 a0001c0002t0002g0196 a0001c0002t0006g0200 others(1): Show |
4 | NA18961.hp2 NA18966.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-18833_-40-1883 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785537 | |||||||
| chr17:28785701 | AT | A | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0002t0002g0187 others(4): Show |
7 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-18995delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785701 | |||||||
| chr17:28785734 | C | T | 4 | a0001c0002t0003g0181 a0001c0002t0003g0182 a0001c0002t0003g0183 others(1): Show |
4 | HG02132.hp1 HG02135.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-19027G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28785734 | |||||||
| chr17:28786018 | G | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-19311C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786018 | |||||||
| chr17:28786200 | T | A | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-40-19493A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786200 | |||||||
| chr17:28786489 | C | T | 1 | a0001c0001t0020g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-40-19782G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786489 | |||||||
| chr17:28786613 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-40-19906G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786613 | |||||||
| chr17:28786708 | G | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-20001C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786708 | |||||||
| chr17:28786769 | T | C | 1 | a0001c0001t0005g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-40-20062A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786769 | |||||||
| chr17:28786792 | C | T | 1 | a0001c0002t0003g0184 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-40-20085G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786792 | |||||||
| chr17:28786802 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0084 |
3 | HG02135.hp2 NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-40-20095A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786802 | |||||||
| chr17:28786865 | C | T | 1 | a0001c0002t0002g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-40-20158G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786865 | |||||||
| chr17:28786894 | AT | A | 45 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(42): Show |
45 | HG01070.hp1 HG01071.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.-40-20188delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | |||||||
| chr17:28786894 | ATT | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(73): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.-40-20189_-40-2018 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | |||||||
| chr17:28786894 | ATTT | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0072 others(5): Show |
8 | HG02258.hp2 HG02647.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-20190_-40-2018 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | |||||||
| chr17:28786894 | ATTTT | A | 77 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(74): Show |
77 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.-40-20191_-40-2018 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | |||||||
| chr17:28786894 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0035 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-40-20197_-40-2018 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786894 | |||||||
| chr17:28786943 | C | T | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40-20236G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786943 | |||||||
| chr17:28786953 | GGAGTGCA others(13): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-40-20266_-40-2024 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28786953 | |||||||
| chr17:28787056 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-40-20349A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787056 | |||||||
| chr17:28787144 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(127): Show |
130 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.-40-20437T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787144 | |||||||
| chr17:28787466 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-40-20759C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787466 | |||||||
| chr17:28787474 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-20767T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787474 | |||||||
| chr17:28787568 | G | GC | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-20862dupG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787568 | |||||||
| chr17:28787582 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(246): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-40-20875C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787582 | |||||||
| chr17:28787741 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40-21034G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787741 | |||||||
| chr17:28787826 | C | CT | 6 | a0001c0001t0001g0047 a0001c0001t0001g0064 a0001c0001t0001g0083 others(3): Show |
6 | HG00099.hp2 HG03831.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-21120dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | |||||||
| chr17:28787826 | C | CTTTTT | 33 | a0001c0001t0004g0162 a0001c0001t0004g0250 a0001c0001t0004g0252 others(30): Show |
33 | HG00408.hp1 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-40-21124_-40-2112 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | |||||||
| chr17:28787826 | C | CTTTTTT | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(81): Show |
84 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-40-21125_-40-2112 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | |||||||
| chr17:28787826 | C | CTTTTTTT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0011g0004 others(4): Show |
7 | HG00544.hp2 HG01109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-21126_-40-2112 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28787826 | |||||||
| chr17:28788551 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0065 |
2 | HG02015.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-40-21844A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788551 | |||||||
| chr17:28788828 | G | A | 1 | a0001c0002t0002g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-40-22121C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788828 | |||||||
| chr17:28788843 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-40-22136T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788843 | |||||||
| chr17:28788867 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-40-22160C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788867 | |||||||
| chr17:28788871 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-40-22164T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28788871 | |||||||
| chr17:28789079 | C | CA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0016 others(28): Show |
31 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-40-22373dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | |||||||
| chr17:28789079 | C | CAA | 7 | a0001c0001t0001g0047 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG02109.hp1 HG02109.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-22374_-40-2237 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | |||||||
| chr17:28789079 | CA | C | 30 | a0001c0001t0001g0089 a0001c0001t0001g0114 a0001c0001t0008g0068 others(27): Show |
30 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.-40-22373delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | |||||||
| chr17:28789079 | CAA | C | 52 | a0001c0002t0002g0163 a0001c0002t0002g0164 a0001c0002t0002g0169 others(49): Show |
52 | HG00544.hp2 HG00642.hp2 HG01081.hp1 others(49): Show |
intron_variant | MODIFIER | c.-40-22374_-40-2237 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789079 | |||||||
| chr17:28789116 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-40-22409G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789116 | |||||||
| chr17:28789198 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-40-22491A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789198 | |||||||
| chr17:28789200 | C | CT | 8 | a0001c0001t0001g0080 a0001c0001t0001g0144 a0001c0001t0007g0104 others(5): Show |
8 | HG01074.hp1 HG01168.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-40-22494dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789200 | |||||||
| chr17:28789200 | CT | C | 15 | a0001c0001t0001g0093 a0001c0001t0001g0152 a0001c0001t0004g0253 others(12): Show |
15 | HG00408.hp1 HG02602.hp1 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.-40-22494delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789200 | |||||||
| chr17:28789430 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0130 |
2 | HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.-40-22723G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789430 | |||||||
| chr17:28789442 | C | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0025 others(3): Show |
6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-22735G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789442 | |||||||
| chr17:28789562 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-40-22855G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789562 | |||||||
| chr17:28789721 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-40-23014G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789721 | |||||||
| chr17:28789954 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-23247G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28789954 | |||||||
| chr17:28790175 | A | G | 1 | a0001c0001t0004g0256 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-40-23468T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790175 | |||||||
| chr17:28790208 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-40-23501A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790208 | |||||||
| chr17:28790288 | G | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(40): Show |
43 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.-40-23581C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790288 | |||||||
| chr17:28790883 | A | AAATTTTT others(18): Show |
1 | a0001c0001t0004g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-40-24177_-40-2417 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790883 | |||||||
| chr17:28790883 | A | AAATTTTT others(20): Show |
1 | a0001c0001t0004g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-40-24177_-40-2417 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790883 | |||||||
| chr17:28790884 | C | CA | 7 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0007g0070 others(4): Show |
7 | HG01074.hp1 HG01081.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CAT | 23 | a0001c0001t0001g0045 a0001c0001t0001g0060 a0001c0001t0001g0075 others(20): Show |
23 | HG00408.hp2 HG01070.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATT | 29 | a0001c0001t0001g0064 a0001c0001t0001g0144 a0001c0001t0004g0250 others(26): Show |
29 | HG00140.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTT | 8 | a0001c0001t0001g0159 a0001c0001t0004g0255 a0001c0001t0004g0257 others(5): Show |
8 | HG01168.hp2 HG01175.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0142 a0001c0001t0004g0267 others(4): Show |
7 | HG01106.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(29): Show |
32 | HG00544.hp2 HG01109.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00544.hp1 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(1): Show |
12 | a0001c0001t0001g0017 a0001c0001t0001g0096 a0001c0001t0001g0128 others(9): Show |
12 | HG00733.hp1 HG01106.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(2): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0132 a0001c0001t0001g0151 others(1): Show |
4 | HG00099.hp2 HG01934.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(13): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(3): Show |
3 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0150 |
3 | HG01109.hp2 HG02257.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(4): Show |
4 | a0001c0001t0001g0149 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG00621.hp1 HG01243.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(5): Show |
4 | a0001c0001t0001g0152 a0001c0001t0009g0147 a0001c0001t0012g0269 others(1): Show |
4 | HG02622.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(6): Show |
3 | a0001c0001t0004g0253 a0001c0001t0005g0053 a0001c0001t0013g0261 |
3 | HG03130.hp1 HG03540.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(7): Show |
3 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0108 |
3 | HG01192.hp1 HG01361.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(8): Show |
3 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0009g0148 |
3 | HG02895.hp2 NA18953.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(9): Show |
2 | a0001c0001t0001g0059 a0001c0001t0004g0247 |
2 | HG01081.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(10): Show |
1 | a0001c0001t0004g0260 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(11): Show |
4 | a0001c0001t0001g0048 a0001c0001t0004g0263 a0001c0001t0004g0272 others(1): Show |
4 | HG02965.hp1 NA18947.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(12): Show |
1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(13): Show |
4 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0077 others(1): Show |
4 | HG01175.hp1 HG02135.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(14): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0085 a0001c0001t0001g0094 others(2): Show |
5 | HG01358.hp1 HG02630.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(25): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(15): Show |
1 | a0001c0001t0001g0025 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(26): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(16): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG00140.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(27): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(18): Show |
2 | a0001c0001t0004g0264 a0001c0001t0005g0143 |
2 | HG00408.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(29): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(19): Show |
3 | a0001c0001t0001g0061 a0001c0001t0001g0076 a0001c0001t0001g0109 |
3 | HG03688.hp1 HG03834.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(30): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(20): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0095 a0001c0010t0001g0098 |
3 | HG00738.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(31): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(21): Show |
2 | a0001c0001t0001g0029 a0001c0001t0001g0074 |
2 | HG02273.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-40-24178_-40-2417 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CATTTTTT others(24): Show |
1 | a0001c0001t0001g0131 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-40-24178_-40-2417 others(35): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18955.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-40-24194_-40-2417 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0001g0129 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-40-24205_-40-2417 others(32): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0001g0126 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-40-24206_-40-2417 others(33): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | C | T | 2 | a0001c0001t0004g0258 a0001c0001t0004g0259 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-40-24177G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | CTT | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0093 others(7): Show |
10 | HG01069.hp2 HG01361.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-24179_-40-2417 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | CTTT | C | 11 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0078 others(8): Show |
11 | HG01074.hp2 HG01099.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40-24180_-40-2417 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-24188_-40-2417 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | CTTTTTTT others(6): Show |
C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0037 others(9): Show |
12 | HG01168.hp1 HG01952.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-24190_-40-2417 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790884 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-24191_-40-2417 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790884 | |||||||
| chr17:28790885 | T | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0140 a0001c0001t0004g0274 others(1): Show |
4 | HG02602.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-24178A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790885 | |||||||
| chr17:28790886 | T | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0097 a0001c0001t0001g0101 others(1): Show |
4 | HG00738.hp2 HG01433.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-24179A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790886 | |||||||
| chr17:28790887 | T | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0093 others(7): Show |
10 | HG01069.hp2 HG01361.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-40-24180A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790887 | |||||||
| chr17:28790888 | T | A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0063 a0001c0001t0001g0078 others(3): Show |
6 | HG01099.hp2 HG01256.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-24181A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790888 | |||||||
| chr17:28790889 | T | A | 2 | a0001c0001t0001g0071 a0001c0001t0004g0162 |
2 | NA18522.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-40-24182A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790889 | |||||||
| chr17:28790890 | T | A | 3 | a0001c0001t0001g0069 a0001c0001t0005g0073 a0001c0006t0001g0088 |
3 | HG02300.hp2 HG03195.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-40-24183A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790890 | |||||||
| chr17:28790891 | T | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0055 others(1): Show |
4 | HG00438.hp2 NA18973.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-24184A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790891 | |||||||
| chr17:28790892 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-24185A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790892 | |||||||
| chr17:28790893 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-40-24186A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790893 | |||||||
| chr17:28790896 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-24189A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790896 | |||||||
| chr17:28790898 | T | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0037 others(9): Show |
12 | HG01168.hp1 HG01952.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-40-24191A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790898 | |||||||
| chr17:28790899 | T | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-24192A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790899 | |||||||
| chr17:28790915 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(9): Show |
12 | HG00733.hp1 HG01109.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-24208A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28790915 | |||||||
| chr17:28791065 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-24358C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791065 | |||||||
| chr17:28791101 | G | A | 24 | a0001c0002t0002g0166 a0001c0002t0003g0165 a0001c0002t0003g0167 others(21): Show |
24 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-24394C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791101 | |||||||
| chr17:28791161 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-40-24454G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791161 | |||||||
| chr17:28791282 | A | G | 1 | a0001c0001t0008g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-40-24575T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791282 | |||||||
| chr17:28791554 | G | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-40-24847C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791554 | |||||||
| chr17:28791558 | GCAAAAAA | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0025 others(3): Show |
6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-24858_-40-2485 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791558 | |||||||
| chr17:28791675 | A | AT | 49 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0044 others(46): Show |
49 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.-40-24969dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | |||||||
| chr17:28791675 | A | ATT | 38 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0164 others(35): Show |
38 | HG00544.hp2 HG01099.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.-40-24970_-40-2496 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | |||||||
| chr17:28791675 | A | ATTT | 6 | a0001c0002t0002g0163 a0001c0002t0002g0169 a0001c0002t0002g0170 others(3): Show |
6 | HG00642.hp2 HG01106.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40-24971_-40-2496 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | |||||||
| chr17:28791675 | AT | A | 34 | a0001c0001t0001g0045 a0001c0001t0001g0072 a0001c0001t0001g0135 others(31): Show |
34 | HG00408.hp1 HG01069.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.-40-24969delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791675 | |||||||
| chr17:28791737 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0060 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-40-25030T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791737 | |||||||
| chr17:28791767 | G | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(240): Show |
243 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.-40-25060C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791767 | |||||||
| chr17:28791861 | T | C | 1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-40-25154A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28791861 | |||||||
| chr17:28792005 | T | C | 30 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(27): Show |
30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-40-25298A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792005 | |||||||
| chr17:28792049 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-25342G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792049 | |||||||
| chr17:28792055 | T | C | 1 | a0001c0002t0003g0189 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-40-25348A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792055 | |||||||
| chr17:28792082 | C | T | 1 | a0001c0002t0002g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-40-25375G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792082 | |||||||
| chr17:28792099 | CAGG | C | 20 | a0001c0002t0002g0171 a0001c0002t0002g0175 a0001c0002t0002g0188 others(17): Show |
20 | HG00544.hp2 HG01346.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.-40-25395_-40-2539 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792099 | |||||||
| chr17:28792215 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-40-25508C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792215 | |||||||
| chr17:28792311 | C | CA | 77 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(74): Show |
77 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-40-25605dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792311 | |||||||
| chr17:28792311 | CA | C | 88 | a0001c0001t0001g0127 a0001c0001t0004g0258 a0001c0001t0014g0033 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-40-25605delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792311 | |||||||
| chr17:28792506 | C | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-25799G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792506 | |||||||
| chr17:28792780 | C | CA | 14 | a0001c0001t0001g0026 a0001c0001t0001g0123 a0001c0001t0001g0149 others(11): Show |
14 | HG01069.hp2 HG01175.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-40-26074dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792780 | |||||||
| chr17:28792780 | CA | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0105 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-40-26074delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792780 | |||||||
| chr17:28792780 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-26085_-40-2607 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792780 | |||||||
| chr17:28792795 | A | G | 79 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(76): Show |
79 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-40-26088T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792795 | |||||||
| chr17:28792838 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-40-26131T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792838 | |||||||
| chr17:28792935 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-40-26228A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28792935 | |||||||
| chr17:28793612 | A | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-26905T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793612 | |||||||
| chr17:28793742 | A | AT | 14 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0040 others(11): Show |
14 | HG01243.hp2 HG01361.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-40-27036dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793742 | |||||||
| chr17:28793742 | AT | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0045 a0001c0001t0001g0051 others(9): Show |
12 | HG01070.hp1 HG02015.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.-40-27036delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793742 | |||||||
| chr17:28793976 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-27269G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793976 | |||||||
| chr17:28793984 | G | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-40-27277C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28793984 | |||||||
| chr17:28794122 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-40-27415T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794122 | |||||||
| chr17:28794222 | CT | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-27516delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794222 | |||||||
| chr17:28794355 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0137 others(2): Show |
5 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-27648C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794355 | |||||||
| chr17:28794376 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-27669A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794376 | |||||||
| chr17:28794381 | G | A | 2 | a0003c0004t0001g0028 a0003c0004t0005g0027 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-40-27674C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794381 | |||||||
| chr17:28794542 | T | G | 2 | a0001c0002t0002g0174 a0001c0007t0002g0208 |
2 | HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-40-27835A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28794542 | |||||||
| chr17:28795039 | G | C | 24 | a0001c0002t0002g0166 a0001c0002t0003g0165 a0001c0002t0003g0167 others(21): Show |
24 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-28332C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795039 | |||||||
| chr17:28795092 | C | A | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-40-28385G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795092 | |||||||
| chr17:28795092 | C | CA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0062 others(3): Show |
6 | HG01361.hp2 HG01891.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-28386dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795092 | |||||||
| chr17:28795135 | A | G | 80 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(77): Show |
80 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-40-28428T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795135 | |||||||
| chr17:28795137 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-40-28430C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795137 | |||||||
| chr17:28795226 | C | A | 1 | a0001c0001t0015g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-40-28519G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795226 | |||||||
| chr17:28795396 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-28689G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795396 | |||||||
| chr17:28795408 | C | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-28701G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795408 | |||||||
| chr17:28795805 | A | T | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-40-29098T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795805 | |||||||
| chr17:28795812 | C | T | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-29105G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795812 | |||||||
| chr17:28795942 | A | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-29235T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28795942 | |||||||
| chr17:28796516 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-40-29809A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796516 | |||||||
| chr17:28796518 | A | C | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-40-29811T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796518 | |||||||
| chr17:28796577 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0020g0054 |
3 | HG02976.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-40-29870G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796577 | |||||||
| chr17:28796660 | T | G | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-40-29953A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796660 | |||||||
| chr17:28796798 | C | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.-40-30091G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796798 | |||||||
| chr17:28796843 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-40-30136A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796843 | |||||||
| chr17:28796876 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-40-30169A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796876 | |||||||
| chr17:28796994 | C | CT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(90): Show |
93 | HG00140.hp2 HG00408.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.-40-30288dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796994 | |||||||
| chr17:28796994 | C | CTT | 19 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0047 others(16): Show |
19 | HG00544.hp2 HG00642.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-40-30289_-40-3028 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796994 | |||||||
| chr17:28796994 | CT | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0058 others(3): Show |
6 | HG01168.hp1 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-30288delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28796994 | |||||||
| chr17:28797037 | C | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0025 others(3): Show |
6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-30330G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797037 | |||||||
| chr17:28797064 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-30357C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797064 | |||||||
| chr17:28797289 | G | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-30582C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797289 | |||||||
| chr17:28797618 | G | T | 2 | a0001c0001t0001g0051 a0001c0001t0019g0049 |
2 | NA18953.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-40-30911C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797618 | |||||||
| chr17:28797739 | G | T | 1 | a0001c0001t0005g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-40-31032C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797739 | |||||||
| chr17:28797878 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-40-31171A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797878 | |||||||
| chr17:28797897 | C | CA | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-31191dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28797897 | |||||||
| chr17:28798117 | G | C | 1 | a0001c0002t0002g0166 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-40-31410C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798117 | |||||||
| chr17:28798296 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-40-31589G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798296 | |||||||
| chr17:28798449 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-31742T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798449 | |||||||
| chr17:28798639 | C | CT | 86 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(83): Show |
86 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-40-31933dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798639 | |||||||
| chr17:28798640 | T | C | 1 | a0001c0002t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-40-31933A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798640 | |||||||
| chr17:28798658 | G | A | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-40-31951C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798658 | |||||||
| chr17:28798774 | T | A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-32067A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798774 | |||||||
| chr17:28798774 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-40-32067A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798774 | |||||||
| chr17:28798892 | C | G | 1 | a0001c0002t0002g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-40-32185G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798892 | |||||||
| chr17:28798909 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-32202T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798909 | |||||||
| chr17:28798972 | G | GT | 3 | a0001c0002t0002g0166 a0001c0002t0003g0165 a0001c0002t0003g0167 |
3 | HG01070.hp2 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-40-32266dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798972 | |||||||
| chr17:28798972 | G | GTT | 81 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(78): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-40-32267_-40-3226 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798972 | |||||||
| chr17:28798975 | G | T | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-40-32268C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798975 | |||||||
| chr17:28798986 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-40-32279G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28798986 | |||||||
| chr17:28799024 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-32317C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799024 | |||||||
| chr17:28799257 | GC | G | 8 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
8 | HG01243.hp1 HG01934.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-32551delG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799257 | |||||||
| chr17:28799297 | C | CT | 9 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0064 others(6): Show |
9 | HG01261.hp1 HG01891.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40-32591dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799297 | |||||||
| chr17:28799297 | CT | C | 86 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0056 others(83): Show |
86 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-32591delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799297 | |||||||
| chr17:28799392 | G | GGTTCAAG others(727): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0074 others(2): Show |
5 | HG00738.hp1 HG01358.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-33419_-40-3268 others(738): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799392 | |||||||
| chr17:28799471 | T | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-40-32764A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799471 | |||||||
| chr17:28799798 | A | C | 1 | a0001c0002t0002g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-40-33091T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28799798 | |||||||
| chr17:28800034 | C | CT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0052 others(2): Show |
5 | HG00438.hp2 HG04184.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-33328dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800034 | |||||||
| chr17:28800034 | CT | C | 86 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0002t0002g0160 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-33328delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800034 | |||||||
| chr17:28800421 | G | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-33714C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800421 | |||||||
| chr17:28800853 | G | GA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(98): Show |
101 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-40-34147dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800853 | |||||||
| chr17:28800853 | G | GAA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0061 others(7): Show |
10 | HG00438.hp2 HG00544.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-34148_-40-3414 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800853 | |||||||
| chr17:28800853 | GA | G | 15 | a0001c0001t0001g0010 a0001c0001t0004g0250 a0001c0001t0004g0251 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40-34147delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800853 | |||||||
| chr17:28800926 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-40-34219C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800926 | |||||||
| chr17:28800931 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-34224C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28800931 | |||||||
| chr17:28801109 | A | G | 1 | a0001c0002t0003g0243 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-40-34402T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801109 | |||||||
| chr17:28801128 | G | A | 4 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0217 others(1): Show |
4 | HG02647.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-40-34421C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801128 | |||||||
| chr17:28801151 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-34444G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801151 | |||||||
| chr17:28801160 | GA | G | 9 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-40-34454delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801160 | |||||||
| chr17:28801191 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-34484G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801191 | |||||||
| chr17:28801235 | C | T | 5 | a0001c0002t0002g0178 a0001c0002t0002g0185 a0001c0002t0002g0225 others(2): Show |
5 | HG01074.hp1 HG01168.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-34528G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801235 | |||||||
| chr17:28801246 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0059 others(1): Show |
4 | HG00099.hp2 HG01081.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-34539C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801246 | |||||||
| chr17:28801310 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0137 others(2): Show |
5 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-34603C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801310 | |||||||
| chr17:28801316 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-34609A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801316 | |||||||
| chr17:28801385 | C | G | 1 | a0001c0002t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-40-34678G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801385 | |||||||
| chr17:28801433 | G | A | 1 | a0001c0001t0005g0124 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-40-34726C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801433 | |||||||
| chr17:28801451 | C | CA | 24 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0090 others(21): Show |
24 | HG00621.hp1 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-40-34745dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801451 | |||||||
| chr17:28801451 | CA | C | 18 | a0001c0001t0001g0043 a0001c0001t0001g0129 a0001c0001t0001g0155 others(15): Show |
18 | HG00642.hp1 HG01074.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-40-34745delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801451 | |||||||
| chr17:28801451 | CAA | C | 75 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(72): Show |
75 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-40-34746_-40-3474 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801451 | |||||||
| chr17:28801466 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0035 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-40-34759T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801466 | |||||||
| chr17:28801620 | A | G | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-40-34913T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28801620 | |||||||
| chr17:28802007 | CA | C | 86 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-35301delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802007 | |||||||
| chr17:28802096 | C | CT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(124): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-40-35390dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802096 | |||||||
| chr17:28802111 | AAG | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-35406_-40-3540 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802111 | |||||||
| chr17:28802534 | A | T | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-40-35827T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802534 | |||||||
| chr17:28802544 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-35837T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802544 | |||||||
| chr17:28802619 | A | G | 28 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(25): Show |
28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40-35912T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802619 | |||||||
| chr17:28802810 | G | A | 8 | a0001c0002t0002g0175 a0001c0002t0002g0215 a0001c0002t0002g0222 others(5): Show |
8 | NA18943.hp1 NA18947.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-36103C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802810 | |||||||
| chr17:28802886 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-40-36179T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28802886 | |||||||
| chr17:28803018 | T | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-40-36311A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803018 | |||||||
| chr17:28803271 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-36564C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803271 | |||||||
| chr17:28803276 | G | A | 3 | a0001c0002t0002g0166 a0001c0002t0003g0165 a0001c0002t0003g0167 |
3 | HG01070.hp2 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-40-36569C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803276 | |||||||
| chr17:28803287 | C | A | 1 | a0001c0001t0004g0272 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-40-36580G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803287 | |||||||
| chr17:28803502 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-36795C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803502 | |||||||
| chr17:28803557 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-40-36850T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803557 | |||||||
| chr17:28803695 | T | C | 1 | a0001c0001t0005g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-40-36988A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803695 | |||||||
| chr17:28803740 | G | T | 28 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(25): Show |
28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40-37033C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803740 | |||||||
| chr17:28803750 | C | T | 1 | a0001c0001t0005g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-40-37043G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803750 | |||||||
| chr17:28803946 | G | A | 28 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(25): Show |
28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-40-37239C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803946 | |||||||
| chr17:28803973 | C | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-40-37266G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803973 | |||||||
| chr17:28803973 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-37266G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803973 | |||||||
| chr17:28803980 | C | CA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0135 a0001c0001t0005g0102 others(3): Show |
6 | HG01346.hp1 HG02015.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-40-37274dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28803980 | |||||||
| chr17:28804077 | T | C | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-40-37370A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804077 | |||||||
| chr17:28804116 | T | C | 3 | a0001c0001t0012g0269 a0001c0001t0012g0271 a0001c0001t0021g0270 |
3 | HG02109.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-40-37409A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804116 | |||||||
| chr17:28804168 | G | C | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-40-37461C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804168 | |||||||
| chr17:28804339 | AT | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0138 a0001c0001t0001g0141 others(2): Show |
5 | HG01192.hp1 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-37633delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804339 | |||||||
| chr17:28804375 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-40-37668C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804375 | |||||||
| chr17:28804482 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-40-37775C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804482 | |||||||
| chr17:28804586 | G | A | 5 | a0001c0002t0002g0178 a0001c0002t0002g0185 a0001c0002t0002g0225 others(2): Show |
5 | HG01074.hp1 HG01168.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40-37879C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804586 | |||||||
| chr17:28804643 | G | A | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-40-37936C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804643 | |||||||
| chr17:28804765 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-41+37917C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804765 | |||||||
| chr17:28804870 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-41+37812T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804870 | |||||||
| chr17:28804979 | G | A | 2 | a0001c0002t0002g0238 a0001c0002t0002g0239 |
2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+37703C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28804979 | |||||||
| chr17:28805003 | G | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+37679C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805003 | |||||||
| chr17:28805087 | G | A | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+37595C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805087 | |||||||
| chr17:28805140 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0122 |
2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-41+37542A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805140 | |||||||
| chr17:28805182 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-41+37500T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805182 | |||||||
| chr17:28805276 | G | C | 1 | a0001c0002t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-41+37406C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805276 | |||||||
| chr17:28805489 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0074 others(2): Show |
5 | HG00738.hp1 HG01358.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+37193G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805489 | |||||||
| chr17:28805620 | G | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+37062C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805620 | |||||||
| chr17:28805724 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+36958C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805724 | |||||||
| chr17:28805875 | G | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+36807C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28805875 | |||||||
| chr17:28806512 | T | G | 1 | a0001c0001t0005g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+36170A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806512 | |||||||
| chr17:28806557 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-41+36125C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806557 | |||||||
| chr17:28806672 | T | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0156 |
3 | HG01069.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-41+36010A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806672 | |||||||
| chr17:28806826 | T | C | 1 | a0001c0001t0004g0258 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-41+35856A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806826 | |||||||
| chr17:28806891 | A | C | 1 | a0001c0002t0002g0221 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-41+35791T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806891 | |||||||
| chr17:28806936 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0060 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-41+35746T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28806936 | |||||||
| chr17:28807085 | G | A | 2 | a0001c0002t0002g0209 a0001c0002t0002g0224 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-41+35597C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807085 | |||||||
| chr17:28807251 | G | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+35431C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807251 | |||||||
| chr17:28807360 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-41+35322C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807360 | |||||||
| chr17:28807467 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-41+35215G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807467 | |||||||
| chr17:28807693 | T | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0072 |
2 | HG02698.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-41+34989A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807693 | |||||||
| chr17:28807829 | G | T | 4 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+34853C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28807829 | |||||||
| chr17:28808343 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0093 a0001c0001t0001g0101 |
3 | HG03041.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-41+34339A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808343 | |||||||
| chr17:28808708 | T | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+33974A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808708 | |||||||
| chr17:28808813 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-41+33869A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808813 | |||||||
| chr17:28808880 | CAA | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0156 |
3 | HG01069.hp2 HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-41+33800_-41+3380 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808880 | |||||||
| chr17:28808952 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41+33730C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28808952 | |||||||
| chr17:28809082 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-41+33600C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809082 | |||||||
| chr17:28809167 | A | G | 5 | a0001c0001t0001g0086 a0001c0001t0001g0138 a0001c0001t0001g0141 others(2): Show |
5 | HG01192.hp1 HG02258.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+33515T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809167 | |||||||
| chr17:28809211 | C | T | 1 | a0006c0005t0003g0192 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-41+33471G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809211 | |||||||
| chr17:28809296 | A | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02132.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-41+33386T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809296 | |||||||
| chr17:28809352 | C | CA | 13 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0108 others(10): Show |
13 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-41+33329dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809352 | |||||||
| chr17:28809352 | CA | C | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0060 others(6): Show |
9 | HG01071.hp1 HG01081.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+33329delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809352 | |||||||
| chr17:28809674 | A | G | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+33008T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809674 | |||||||
| chr17:28809942 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-41+32740C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809942 | |||||||
| chr17:28809985 | G | GT | 7 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0058 others(4): Show |
7 | HG02148.hp1 HG02615.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+32696dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809985 | |||||||
| chr17:28809985 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-41+32697C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809985 | |||||||
| chr17:28809995 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-41+32687C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28809995 | |||||||
| chr17:28810373 | C | CTGTTTTA others(103): Show |
1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-41+32199_-41+3230 others(114): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28810373 | |||||||
| chr17:28810439 | CTGTTTTA others(15): Show |
C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
241 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.-41+32221_-41+3224 others(26): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28810439 | |||||||
| chr17:28810984 | A | T | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+31698T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28810984 | |||||||
| chr17:28811059 | CA | C | 87 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0014g0033 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+31622delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811059 | |||||||
| chr17:28811229 | A | G | 1 | a0001c0002t0002g0237 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-41+31453T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811229 | |||||||
| chr17:28811465 | C | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+31217G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811465 | |||||||
| chr17:28811786 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-41+30896G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811786 | |||||||
| chr17:28811799 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+30883A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811799 | |||||||
| chr17:28811949 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+30733T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811949 | |||||||
| chr17:28811950 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41+30732C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811950 | |||||||
| chr17:28811952 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+30730C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811952 | |||||||
| chr17:28811982 | A | G | 1 | a0001c0002t0002g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-41+30700T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28811982 | |||||||
| chr17:28812065 | G | GGAAAAAA others(3): Show |
1 | a0001c0001t0001g0075 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-41+30607_-41+3061 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812065 | |||||||
| chr17:28812075 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-41+30607A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812075 | |||||||
| chr17:28812091 | C | T | 2 | a0001c0002t0002g0238 a0001c0002t0002g0239 |
2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+30591G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812091 | |||||||
| chr17:28812314 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-41+30368C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812314 | |||||||
| chr17:28812416 | A | AC | 5 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0008g0099 others(2): Show |
5 | HG00738.hp2 HG01934.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+30265dupG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812416 | |||||||
| chr17:28812593 | A | G | 1 | a0001c0001t0008g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-41+30089T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812593 | |||||||
| chr17:28812621 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0122 |
2 | HG00438.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-41+30061C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812621 | |||||||
| chr17:28812732 | C | T | 28 | a0001c0001t0001g0062 a0001c0001t0004g0247 a0001c0001t0004g0248 others(25): Show |
28 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.-41+29950G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812732 | |||||||
| chr17:28812770 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-41+29912G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812770 | |||||||
| chr17:28812771 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-41+29911T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812771 | |||||||
| chr17:28812772 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-41+29910G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812772 | |||||||
| chr17:28812794 | A | AC | 21 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0034 others(18): Show |
21 | HG01069.hp2 HG01175.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-41+29887dupG | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812794 | |||||||
| chr17:28812816 | C | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+29866G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812816 | |||||||
| chr17:28812869 | A | G | 2 | a0001c0001t0004g0267 a0001c0001t0026g0266 |
2 | NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-41+29813T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28812869 | |||||||
| chr17:28813022 | C | CGG | 20 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0037 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.-41+29658_-41+2965 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813022 | C | CGGG | 32 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0022 others(29): Show |
32 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.-41+29657_-41+2965 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813022 | C | CGGGG | 26 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(23): Show |
26 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.-41+29656_-41+2965 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813022 | C | CGGGGG | 19 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0041 others(16): Show |
19 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-41+29655_-41+2965 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813022 | C | CGGGGGG | 18 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0042 others(15): Show |
18 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41+29654_-41+2965 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813022 | C | CGGGGGGG others(3): Show |
1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-41+29650_-41+2965 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813022 | C | CGGGGGGG others(4): Show |
1 | a0001c0001t0005g0103 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-41+29649_-41+2965 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813022 | |||||||
| chr17:28813028 | GGGGGGGG others(7): Show |
G | 15 | a0001c0002t0002g0178 a0001c0002t0002g0180 a0001c0002t0002g0202 others(12): Show |
15 | HG01346.hp2 HG01952.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813028 | |||||||
| chr17:28813029 | GGGGGGGG others(6): Show |
G | 35 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(32): Show |
35 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813029 | |||||||
| chr17:28813030 | GGGGGGGG others(5): Show |
G | 25 | a0001c0002t0002g0164 a0001c0002t0002g0166 a0001c0002t0002g0175 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813030 | |||||||
| chr17:28813031 | GGGGGGGG others(4): Show |
G | 7 | a0001c0002t0002g0207 a0001c0002t0002g0217 a0001c0002t0003g0181 others(4): Show |
7 | HG01074.hp1 HG03225.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+29640_-41+2965 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813031 | |||||||
| chr17:28813032 | GGGGGGGG others(3): Show |
G | 3 | a0001c0002t0002g0245 a0001c0002t0003g0213 a0003c0004t0001g0028 |
3 | HG00140.hp2 HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-41+29640_-41+2964 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813032 | |||||||
| chr17:28813040 | G | GGGGGGGG others(4): Show |
1 | a0001c0001t0001g0029 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-41+29641_-41+2964 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813040 | |||||||
| chr17:28813041 | G | GGGGGGGG others(3): Show |
1 | a0001c0001t0015g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-41+29640_-41+2964 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813041 | |||||||
| chr17:28813041 | G | GGGGGGGG others(8): Show |
1 | a0001c0001t0005g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+29640_-41+2964 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813041 | |||||||
| chr17:28813042 | A | G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
34 | HG00738.hp2 HG01175.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.-41+29640T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813042 | |||||||
| chr17:28813044 | G | A | 2 | a0001c0001t0001g0157 a0002c0003t0001g0125 |
2 | HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.-41+29638C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813044 | |||||||
| chr17:28813044 | G | T | 1 | a0001c0002t0002g0211 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-41+29638C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813044 | |||||||
| chr17:28813051 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+29631G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813051 | |||||||
| chr17:28813052 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41+29630C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813052 | |||||||
| chr17:28813053 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41+29629A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813053 | |||||||
| chr17:28813055 | G | A | 88 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+29627C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813055 | |||||||
| chr17:28813068 | G | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-41+29614C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813068 | |||||||
| chr17:28813127 | C | CA | 12 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(9): Show |
12 | HG01123.hp2 HG01192.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+29554dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813127 | |||||||
| chr17:28813127 | CA | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(34): Show |
37 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.-41+29554delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813127 | |||||||
| chr17:28813129 | A | C | 85 | a0001c0001t0001g0059 a0001c0002t0002g0160 a0001c0002t0002g0161 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+29553T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813129 | |||||||
| chr17:28813131 | A | C | 2 | a0001c0002t0002g0225 a0001c0002t0003g0199 |
2 | HG04184.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-41+29551T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813131 | |||||||
| chr17:28813140 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41+29542T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813140 | |||||||
| chr17:28813152 | C | CA | 17 | a0001c0001t0001g0012 a0001c0001t0001g0064 a0001c0001t0001g0080 others(14): Show |
17 | HG01069.hp2 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-41+29529dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813152 | |||||||
| chr17:28813152 | CAA | C | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+29528_-41+2952 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813152 | |||||||
| chr17:28813322 | T | C | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+29360A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813322 | |||||||
| chr17:28813524 | CT | C | 87 | a0001c0001t0004g0267 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+29157delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813524 | |||||||
| chr17:28813535 | G | GT | 9 | a0001c0001t0001g0023 a0001c0001t0001g0046 a0001c0001t0001g0064 others(6): Show |
9 | HG00140.hp1 HG01175.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+29146dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813535 | |||||||
| chr17:28813535 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-41+29147C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813535 | |||||||
| chr17:28813702 | A | AT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(37): Show |
40 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.-41+28979dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813702 | |||||||
| chr17:28813702 | AT | A | 9 | a0001c0001t0001g0118 a0001c0001t0004g0263 a0001c0001t0004g0264 others(6): Show |
9 | HG00408.hp1 HG00438.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-41+28979delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813702 | |||||||
| chr17:28813736 | C | T | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+28946G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813736 | |||||||
| chr17:28813793 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41+28889C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813793 | |||||||
| chr17:28813836 | G | A | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+28846C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28813836 | |||||||
| chr17:28814092 | A | G | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+28590T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814092 | |||||||
| chr17:28814320 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-41+28362G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814320 | |||||||
| chr17:28814321 | G | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+28361C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814321 | |||||||
| chr17:28814455 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-41+28227A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814455 | |||||||
| chr17:28814487 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+28195G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814487 | |||||||
| chr17:28814532 | TAATCTTG others(25): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+28118_-41+2814 others(36): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814532 | |||||||
| chr17:28814724 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27958G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814724 | |||||||
| chr17:28814731 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27951A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814731 | |||||||
| chr17:28814758 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27924A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814758 | |||||||
| chr17:28814770 | C | CT | 26 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0034 others(23): Show |
26 | HG01099.hp2 HG01168.hp2 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.-41+27911dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814770 | |||||||
| chr17:28814770 | C | CTT | 80 | a0001c0001t0004g0272 a0001c0001t0005g0124 a0001c0002t0002g0160 others(77): Show |
80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-41+27910_-41+2791 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814770 | |||||||
| chr17:28814813 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-41+27869T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814813 | |||||||
| chr17:28814842 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27840A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814842 | |||||||
| chr17:28814874 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27808T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814874 | |||||||
| chr17:28814880 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27802A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814880 | |||||||
| chr17:28814881 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27801G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814881 | |||||||
| chr17:28814882 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27800A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814882 | |||||||
| chr17:28814898 | C | T | 8 | a0001c0002t0002g0175 a0001c0002t0002g0215 a0001c0002t0002g0222 others(5): Show |
8 | NA18943.hp1 NA18947.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+27784G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28814898 | |||||||
| chr17:28815026 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-41+27656C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815026 | |||||||
| chr17:28815034 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-41+27648T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815034 | |||||||
| chr17:28815214 | CT | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(122): Show |
125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-41+27467delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815214 | |||||||
| chr17:28815258 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-41+27424C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815258 | |||||||
| chr17:28815275 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27407C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815275 | |||||||
| chr17:28815350 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27332T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815350 | |||||||
| chr17:28815354 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27328G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815354 | |||||||
| chr17:28815447 | C | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0084 |
2 | NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-41+27235G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815447 | |||||||
| chr17:28815458 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27224G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815458 | |||||||
| chr17:28815487 | T | A | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-41+27195A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815487 | |||||||
| chr17:28815488 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27194T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815488 | |||||||
| chr17:28815497 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27185T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815497 | |||||||
| chr17:28815504 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-41+27178C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815504 | |||||||
| chr17:28815510 | G | A | 1 | a0001c0001t0004g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-41+27172C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815510 | |||||||
| chr17:28815547 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27135G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815547 | |||||||
| chr17:28815548 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27134G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815548 | |||||||
| chr17:28815549 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27133T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815549 | |||||||
| chr17:28815550 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27132C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815550 | |||||||
| chr17:28815603 | G | A | 2 | a0001c0002t0002g0174 a0001c0007t0002g0208 |
2 | HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-41+27079C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815603 | |||||||
| chr17:28815655 | T | C | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+27027A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815655 | |||||||
| chr17:28815668 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+27014T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815668 | |||||||
| chr17:28815966 | CA | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0014g0033 others(4): Show |
7 | HG01243.hp2 HG01361.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+26715delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815966 | |||||||
| chr17:28815994 | G | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0130 a0001c0001t0004g0253 others(2): Show |
5 | HG01123.hp2 HG01261.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+26688C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28815994 | |||||||
| chr17:28816023 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26659G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816023 | |||||||
| chr17:28816105 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26577T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816105 | |||||||
| chr17:28816196 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26486C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816196 | |||||||
| chr17:28816215 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26467A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816215 | |||||||
| chr17:28816490 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26192A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816490 | |||||||
| chr17:28816559 | A | T | 2 | a0001c0001t0004g0268 a0001c0001t0014g0033 |
2 | HG02615.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.-41+26123T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816559 | |||||||
| chr17:28816562 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26120T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816562 | |||||||
| chr17:28816588 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26094T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816588 | |||||||
| chr17:28816590 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+26092A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816590 | |||||||
| chr17:28816753 | G | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0025 others(3): Show |
6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+25929C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816753 | |||||||
| chr17:28816757 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25925T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816757 | |||||||
| chr17:28816777 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25905A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816777 | |||||||
| chr17:28816792 | T | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+25890A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816792 | |||||||
| chr17:28816850 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25832A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816850 | |||||||
| chr17:28816874 | A | G | 12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0061 others(9): Show |
12 | HG00738.hp1 HG01123.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+25808T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816874 | |||||||
| chr17:28816889 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25793A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816889 | |||||||
| chr17:28816943 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25739T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816943 | |||||||
| chr17:28816951 | A | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25731T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816951 | |||||||
| chr17:28816952 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25730A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816952 | |||||||
| chr17:28816953 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25729T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28816953 | |||||||
| chr17:28817054 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-41+25628T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817054 | |||||||
| chr17:28817323 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25359C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817323 | |||||||
| chr17:28817324 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25358T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817324 | |||||||
| chr17:28817366 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25316A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817366 | |||||||
| chr17:28817367 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25315G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817367 | |||||||
| chr17:28817376 | G | A | 1 | a0001c0002t0002g0236 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-41+25306C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817376 | |||||||
| chr17:28817411 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-41+25271A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817411 | |||||||
| chr17:28817412 | CA | C | 93 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0095 others(90): Show |
93 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.-41+25269delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817412 | |||||||
| chr17:28817489 | C | G | 1 | a0001c0001t0005g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+25193G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817489 | |||||||
| chr17:28817513 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41+25169C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817513 | |||||||
| chr17:28817514 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41+25168T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817514 | |||||||
| chr17:28817515 | G | T | 1 | a0001c0001t0001g0044 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-41+25167C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817515 | |||||||
| chr17:28817634 | G | A | 3 | a0001c0001t0004g0253 a0001c0001t0013g0261 a0001c0001t0013g0262 |
3 | HG02965.hp1 HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-41+25048C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28817634 | |||||||
| chr17:28818010 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-41+24672T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818010 | |||||||
| chr17:28818057 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+24625G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818057 | |||||||
| chr17:28818106 | T | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+24576A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818106 | |||||||
| chr17:28818185 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0122 others(1): Show |
4 | HG00438.hp2 NA18961.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+24497C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818185 | |||||||
| chr17:28818254 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-41+24428G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818254 | |||||||
| chr17:28818303 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+24379G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818303 | |||||||
| chr17:28818404 | T | G | 1 | a0001c0001t0004g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-41+24278A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818404 | |||||||
| chr17:28818511 | G | C | 1 | a0001c0002t0003g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-41+24171C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818511 | |||||||
| chr17:28818547 | GAATAAAA others(6): Show |
G | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-41+24122_-41+2413 others(17): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818547 | |||||||
| chr17:28818557 | AAAAAATA others(5): Show |
A | 1 | a0001c0001t0001g0017 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-41+24113_-41+2412 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28818557 | |||||||
| chr17:28819337 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-41+23345T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819337 | |||||||
| chr17:28819371 | G | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+23311C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819371 | |||||||
| chr17:28819388 | T | C | 1 | a0001c0002t0006g0200 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-41+23294A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819388 | |||||||
| chr17:28819438 | G | T | 3 | a0001c0002t0003g0186 a0001c0002t0003g0191 a0001c0002t0003g0240 |
3 | NA18953.hp2 NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-41+23244C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819438 | |||||||
| chr17:28819479 | G | C | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+23203C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819479 | |||||||
| chr17:28819670 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0084 |
3 | HG02135.hp2 NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-41+23012T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28819670 | |||||||
| chr17:28820073 | T | G | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+22609A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820073 | |||||||
| chr17:28820122 | C | T | 1 | a0001c0002t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-41+22560G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820122 | |||||||
| chr17:28820189 | T | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+22493A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820189 | |||||||
| chr17:28820230 | T | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+22452A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820230 | |||||||
| chr17:28820438 | G | A | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-41+22244C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820438 | |||||||
| chr17:28820636 | C | CT | 18 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
18 | HG00738.hp1 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-41+22045dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820636 | |||||||
| chr17:28820751 | G | A | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+21931C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820751 | |||||||
| chr17:28820806 | T | A | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0037 others(9): Show |
12 | HG01168.hp1 HG01952.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-41+21876A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820806 | |||||||
| chr17:28820886 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-41+21796G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820886 | |||||||
| chr17:28820950 | C | CT | 6 | a0001c0002t0002g0218 a0001c0002t0002g0224 a0001c0002t0002g0226 others(3): Show |
6 | HG00140.hp2 HG01433.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+21731dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820950 | |||||||
| chr17:28820955 | TA | T | 3 | a0001c0002t0002g0203 a0001c0002t0002g0238 a0001c0002t0003g0243 |
3 | HG02735.hp1 NA18959.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-41+21726delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820955 | |||||||
| chr17:28820956 | A | T | 83 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(80): Show |
83 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-41+21726T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820956 | |||||||
| chr17:28820961 | A | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+21721T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820961 | |||||||
| chr17:28820966 | T | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0140 a0001c0001t0001g0144 others(2): Show |
5 | HG02258.hp1 HG02280.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+21716A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820966 | |||||||
| chr17:28820967 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-41+21715A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28820967 | |||||||
| chr17:28821014 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+21668T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821014 | |||||||
| chr17:28821139 | A | G | 2 | a0001c0002t0003g0199 a0001c0002t0003g0216 |
2 | NA18969.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-41+21543T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821139 | |||||||
| chr17:28821287 | T | C | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-41+21395A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821287 | |||||||
| chr17:28821532 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-41+21150G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821532 | |||||||
| chr17:28821827 | T | C | 1 | a0001c0001t0005g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-41+20855A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821827 | |||||||
| chr17:28821944 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-41+20738C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28821944 | |||||||
| chr17:28822054 | T | C | 2 | a0001c0002t0002g0163 a0001c0002t0002g0164 |
2 | HG01099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-41+20628A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822054 | |||||||
| chr17:28822123 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-41+20559C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822123 | |||||||
| chr17:28822139 | A | C | 2 | a0001c0001t0010g0066 a0001c0001t0010g0067 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-41+20543T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822139 | |||||||
| chr17:28822169 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-41+20513C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822169 | |||||||
| chr17:28822170 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-41+20512G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822170 | |||||||
| chr17:28822225 | C | T | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-41+20457G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822225 | |||||||
| chr17:28822485 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-41+20197G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822485 | |||||||
| chr17:28822494 | A | G | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+20188T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822494 | |||||||
| chr17:28822541 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+20141C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822541 | |||||||
| chr17:28822541 | G | C | 1 | a0001c0001t0005g0053 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-41+20141C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822541 | |||||||
| chr17:28822657 | C | T | 5 | a0001c0002t0002g0178 a0001c0002t0002g0185 a0001c0002t0002g0225 others(2): Show |
5 | HG01074.hp1 HG01168.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+20025G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822657 | |||||||
| chr17:28822729 | G | A | 80 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(77): Show |
80 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.-41+19953C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822729 | |||||||
| chr17:28822730 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-41+19952C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822730 | |||||||
| chr17:28822737 | A | C | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+19945T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822737 | |||||||
| chr17:28822737 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(8): Show |
11 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+19945T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822737 | |||||||
| chr17:28822802 | C | CA | 21 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0030 others(18): Show |
21 | HG00438.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-41+19879dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | C | CAA | 15 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0040 others(12): Show |
15 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41+19878_-41+1987 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | CA | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0048 others(5): Show |
8 | HG01099.hp2 HG01123.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41+19879delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | CAAAAAAA others(1): Show |
C | 10 | a0001c0002t0002g0164 a0001c0002t0002g0169 a0001c0002t0002g0174 others(7): Show |
10 | HG00140.hp2 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+19872_-41+1987 others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0002t0002g0233 others(3): Show |
6 | HG01069.hp2 HG02683.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41+19871_-41+1987 others(13): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | CAAAAAAA others(3): Show |
C | 42 | a0001c0001t0001g0144 a0001c0002t0002g0160 a0001c0002t0002g0161 others(39): Show |
42 | HG00408.hp2 HG01070.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.-41+19870_-41+1987 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | CAAAAAAA others(4): Show |
C | 10 | a0001c0001t0001g0155 a0001c0002t0002g0178 a0001c0002t0002g0188 others(7): Show |
10 | HG00544.hp2 HG01074.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+19869_-41+1987 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822802 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+19868_-41+1987 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822802 | |||||||
| chr17:28822819 | AAAAAAAA others(12): Show |
A | 2 | a0001c0002t0002g0210 a0001c0002t0002g0224 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-41+19844_-41+1986 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822819 | |||||||
| chr17:28822820 | A | T | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+19862T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822820 | |||||||
| chr17:28822820 | AAAAAAAA others(13): Show |
A | 1 | a0001c0002t0002g0209 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-41+19842_-41+1986 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822820 | |||||||
| chr17:28822821 | AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0002 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-41+19844_-41+1986 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822821 | |||||||
| chr17:28822821 | AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0002g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-41+19842_-41+1986 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822821 | |||||||
| chr17:28822822 | A | T | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+19860T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822822 | |||||||
| chr17:28822822 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0011g0004 |
2 | HG01346.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-41+19842_-41+1985 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822822 | |||||||
| chr17:28822823 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-41+19848_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822823 | |||||||
| chr17:28822823 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0006 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-41+19844_-41+1985 others(19): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822823 | |||||||
| chr17:28822823 | AAAAAAAA others(10): Show |
A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+19842_-41+1985 others(21): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822823 | |||||||
| chr17:28822824 | A | T | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+19858T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822824 | |||||||
| chr17:28822824 | AAAAAAAA others(3): Show |
A | 3 | a0001c0002t0002g0179 a0001c0002t0002g0230 a0001c0002t0002g0236 |
3 | HG03688.hp2 HG03710.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-41+19848_-41+1985 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822824 | |||||||
| chr17:28822824 | AAAAAAAA others(5): Show |
A | 2 | a0001c0002t0002g0241 a0001c0002t0006g0194 |
2 | HG02257.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-41+19846_-41+1985 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822824 | |||||||
| chr17:28822825 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0002t0006g0172 |
3 | HG02895.hp1 HG02896.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-41+19846_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822825 | |||||||
| chr17:28822826 | A | T | 1 | a0001c0002t0002g0231 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-41+19856T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822826 | |||||||
| chr17:28822826 | AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-41+19846_-41+1985 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822826 | |||||||
| chr17:28822828 | A | T | 8 | a0001c0002t0002g0169 a0001c0002t0002g0170 a0001c0002t0002g0231 others(5): Show |
8 | HG00642.hp2 HG01106.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41+19854T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822828 | |||||||
| chr17:28822828 | AAAAAATA others(5): Show |
A | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41+19842_-41+1985 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822828 | |||||||
| chr17:28822828 | AAAAAATA others(13): Show |
A | 1 | a0001c0001t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-41+19834_-41+1985 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822828 | |||||||
| chr17:28822829 | AAAAATAT others(4): Show |
A | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-41+19842_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822829 | |||||||
| chr17:28822829 | AAAAATAT others(12): Show |
A | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-41+19834_-41+1985 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822829 | |||||||
| chr17:28822830 | A | T | 20 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0154 others(17): Show |
20 | HG00642.hp2 HG01069.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.-41+19852T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | |||||||
| chr17:28822830 | AAAATATA others(7): Show |
A | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-41+19838_-41+1985 others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | |||||||
| chr17:28822830 | AAAATATA others(11): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-41+19834_-41+1985 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | |||||||
| chr17:28822830 | AAAATATA others(13): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-41+19832_-41+1985 others(24): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822830 | |||||||
| chr17:28822831 | AAATATAT others(32): Show |
A | 3 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0026g0266 |
3 | NA18943.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-41+19812_-41+1985 others(43): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822831 | |||||||
| chr17:28822832 | A | AAAAATAT others(4): Show |
1 | a0003c0004t0005g0027 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-41+19849_-41+1985 others(15): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822832 | A | AAAATATA others(3): Show |
1 | a0003c0004t0001g0028 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-41+19849_-41+1985 others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822832 | A | ATAT | 4 | a0001c0001t0001g0140 a0001c0001t0013g0262 a0001c0001t0016g0082 others(1): Show |
4 | HG02965.hp1 HG03239.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+19849_-41+1985 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822832 | A | ATATAT | 3 | a0001c0001t0004g0260 a0001c0001t0004g0263 a0001c0001t0004g0264 |
3 | HG00408.hp1 NA18947.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-41+19849_-41+1985 others(9): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822832 | A | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0026 a0001c0001t0001g0089 others(41): Show |
44 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-41+19850T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822832 | AAT | A | 12 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0050 others(9): Show |
12 | HG01070.hp1 HG01081.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+19848_-41+1984 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822832 | AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-41+19832_-41+1984 others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822832 | |||||||
| chr17:28822833 | AT | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0016 others(22): Show |
25 | HG00099.hp2 HG00544.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-41+19848delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822833 | |||||||
| chr17:28822833 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0009g0147 a0001c0001t0009g0148 |
2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-41+19830_-41+1984 others(23): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822833 | |||||||
| chr17:28822834 | T | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-41+19848A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822834 | |||||||
| chr17:28822836 | T | A | 24 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0042 others(21): Show |
24 | HG00099.hp2 HG00738.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-41+19846A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822836 | |||||||
| chr17:28822838 | T | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0059 others(6): Show |
9 | HG01081.hp2 HG02015.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+19844A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822838 | |||||||
| chr17:28822842 | T | TATATATA others(27): Show |
3 | a0001c0001t0004g0255 a0001c0001t0012g0271 a0001c0001t0021g0270 |
3 | HG02109.hp1 HG02109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-41+19839_-41+1984 others(38): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822842 | |||||||
| chr17:28822842 | T | TATATATA others(29): Show |
1 | a0001c0001t0012g0269 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-41+19839_-41+1984 others(40): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822842 | |||||||
| chr17:28822855 | A | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+19827T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822855 | |||||||
| chr17:28822864 | T | C | 33 | a0001c0001t0001g0076 a0001c0001t0001g0086 a0001c0001t0004g0258 others(30): Show |
33 | HG00140.hp2 HG00408.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-41+19818A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822864 | |||||||
| chr17:28822864 | TACACAC | T | 4 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0217 others(1): Show |
4 | HG02647.hp1 NA19030.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+19812_-41+1981 others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822864 | |||||||
| chr17:28822872 | T | C | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+19810A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822872 | |||||||
| chr17:28822882 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+19800A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822882 | |||||||
| chr17:28822905 | A | G | 19 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0093 others(16): Show |
19 | HG01069.hp2 HG01243.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.-41+19777T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822905 | |||||||
| chr17:28822931 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-41+19751C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28822931 | |||||||
| chr17:28823010 | C | G | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+19672G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823010 | |||||||
| chr17:28823048 | T | C | 5 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0137 others(2): Show |
5 | HG01074.hp2 HG01243.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+19634A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823048 | |||||||
| chr17:28823184 | A | C | 1 | a0001c0001t0004g0259 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-41+19498T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823184 | |||||||
| chr17:28823362 | A | AT | 11 | a0001c0001t0001g0041 a0001c0001t0001g0065 a0001c0001t0001g0086 others(8): Show |
11 | HG01168.hp2 HG01192.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+19319dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823362 | |||||||
| chr17:28823362 | A | ATT | 81 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(78): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.-41+19318_-41+1931 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823362 | |||||||
| chr17:28823362 | AT | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0090 others(4): Show |
7 | HG01099.hp2 HG01256.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+19319delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823362 | |||||||
| chr17:28823372 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+19310A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823372 | |||||||
| chr17:28823685 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0035 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-41+18997A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823685 | |||||||
| chr17:28823732 | T | C | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+18950A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823732 | |||||||
| chr17:28823875 | A | AT | 96 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0032 others(93): Show |
96 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-41+18806dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28823875 | |||||||
| chr17:28824114 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-41+18568A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824114 | |||||||
| chr17:28824181 | AT | A | 6 | a0001c0001t0001g0055 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
6 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+18500delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824181 | |||||||
| chr17:28824359 | AT | A | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+18322delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824359 | |||||||
| chr17:28824480 | C | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+18202G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824480 | |||||||
| chr17:28824541 | A | G | 2 | a0001c0001t0004g0258 a0001c0001t0004g0259 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-41+18141T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824541 | |||||||
| chr17:28824834 | G | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+17848C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824834 | |||||||
| chr17:28824873 | C | T | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41+17809G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28824873 | |||||||
| chr17:28825007 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-41+17675C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825007 | |||||||
| chr17:28825015 | T | A | 1 | a0001c0002t0002g0185 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-41+17667A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825015 | |||||||
| chr17:28825161 | A | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0061 others(1): Show |
4 | HG02280.hp2 HG03688.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+17521T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825161 | |||||||
| chr17:28825293 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-41+17389C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825293 | |||||||
| chr17:28825297 | G | A | 4 | a0001c0002t0003g0176 a0001c0002t0003g0189 a0001c0002t0003g0190 others(1): Show |
4 | HG00408.hp2 HG02015.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+17385C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825297 | |||||||
| chr17:28825375 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-41+17307C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825375 | |||||||
| chr17:28825433 | C | CA | 30 | a0001c0001t0001g0026 a0001c0001t0001g0036 a0001c0001t0001g0040 others(27): Show |
30 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-41+17248dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825433 | |||||||
| chr17:28825451 | A | C | 30 | a0001c0001t0001g0154 a0001c0001t0004g0162 a0001c0001t0004g0247 others(27): Show |
30 | HG00408.hp1 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-41+17231T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825451 | |||||||
| chr17:28825652 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+17030A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825652 | |||||||
| chr17:28825666 | T | C | 3 | a0001c0002t0002g0207 a0001c0002t0002g0237 a0001c0002t0002g0245 |
3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+17016A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825666 | |||||||
| chr17:28825761 | T | G | 1 | a0001c0002t0002g0235 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-41+16921A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825761 | |||||||
| chr17:28825836 | C | T | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41+16846G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825836 | |||||||
| chr17:28825851 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
142 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-41+16831A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28825851 | |||||||
| chr17:28826052 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0005g0139 |
2 | HG00642.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-41+16630A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826052 | |||||||
| chr17:28826145 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0018g0117 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-41+16537G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826145 | |||||||
| chr17:28826351 | T | C | 4 | a0001c0001t0001g0086 a0001c0001t0001g0138 a0001c0001t0001g0141 others(1): Show |
4 | HG01192.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+16331A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826351 | |||||||
| chr17:28826522 | C | T | 1 | a0001c0001t0007g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-41+16160G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826522 | |||||||
| chr17:28826535 | G | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+16147C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826535 | |||||||
| chr17:28826586 | C | T | 1 | a0001c0001t0005g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-41+16096G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826586 | |||||||
| chr17:28826681 | C | CA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0064 others(5): Show |
8 | HG01175.hp2 HG01192.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+16000dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826681 | |||||||
| chr17:28826681 | CA | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0035 others(30): Show |
33 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.-41+16000delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826681 | |||||||
| chr17:28826681 | CAA | C | 80 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0002t0002g0160 others(77): Show |
80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.-41+15999_-41+1600 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826681 | |||||||
| chr17:28826986 | T | A | 3 | a0001c0001t0005g0107 a0001c0002t0002g0174 a0001c0006t0001g0088 |
3 | HG00621.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-41+15696A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28826986 | |||||||
| chr17:28827204 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+15478T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28827204 | |||||||
| chr17:28827334 | G | A | 1 | a0001c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-41+15348C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28827334 | |||||||
| chr17:28828039 | C | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(8): Show |
11 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+14643G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828039 | |||||||
| chr17:28828040 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-41+14642A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828040 | |||||||
| chr17:28828095 | A | AT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-41+14586dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828095 | A | ATT | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0084 others(7): Show |
10 | HG00408.hp1 HG01192.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+14585_-41+1458 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828095 | AT | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0035 others(26): Show |
29 | HG01069.hp1 HG01433.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-41+14586delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828095 | ATT | A | 14 | a0001c0002t0002g0187 a0001c0002t0002g0193 a0001c0002t0002g0198 others(11): Show |
14 | HG01884.hp1 HG02683.hp2 HG03225.hp2 others(11): Show |
intron_variant | MODIFIER | c.-41+14585_-41+1458 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828095 | ATTT | A | 63 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(60): Show |
63 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-41+14584_-41+1458 others(7): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828095 | ATTTT | A | 7 | a0001c0002t0002g0171 a0001c0002t0002g0204 a0001c0002t0002g0218 others(4): Show |
7 | HG01168.hp2 HG03017.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+14583_-41+1458 others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828095 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+14575_-41+1458 others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828095 | |||||||
| chr17:28828204 | G | A | 1 | a0001c0002t0002g0198 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-41+14478C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828204 | |||||||
| chr17:28828568 | G | GA | 87 | a0001c0001t0001g0056 a0001c0001t0004g0274 a0001c0001t0005g0102 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+14113dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828568 | |||||||
| chr17:28828574 | A | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 |
3 | HG01346.hp1 HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-41+14108T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828574 | |||||||
| chr17:28828815 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-41+13867A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828815 | |||||||
| chr17:28828846 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0060 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-41+13836T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28828846 | |||||||
| chr17:28829218 | CT | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(263): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-41+13463delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829218 | |||||||
| chr17:28829265 | A | G | 2 | a0001c0002t0002g0207 a0001c0002t0002g0245 |
2 | HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+13417T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829265 | |||||||
| chr17:28829307 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-41+13375G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829307 | |||||||
| chr17:28829357 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-41+13325C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829357 | |||||||
| chr17:28829497 | G | A | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+13185C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829497 | |||||||
| chr17:28829706 | T | C | 8 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+12976A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829706 | |||||||
| chr17:28829848 | A | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+12834T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829848 | |||||||
| chr17:28829875 | A | T | 2 | a0003c0004t0001g0028 a0003c0004t0005g0027 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-41+12807T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28829875 | |||||||
| chr17:28830161 | C | CT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0115 others(2): Show |
5 | HG01109.hp2 HG04184.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+12520dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830161 | |||||||
| chr17:28830161 | CT | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
138 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.-41+12520delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830161 | |||||||
| chr17:28830161 | CTT | C | 84 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(81): Show |
84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.-41+12519_-41+1252 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830161 | |||||||
| chr17:28830344 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+12338A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830344 | |||||||
| chr17:28830389 | C | A | 1 | a0001c0002t0002g0178 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-41+12293G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830389 | |||||||
| chr17:28830568 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+12114A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830568 | |||||||
| chr17:28830680 | T | C | 1 | a0001c0001t0008g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-41+12002A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830680 | |||||||
| chr17:28830759 | G | A | 5 | a0001c0001t0004g0255 a0001c0001t0012g0269 a0001c0001t0012g0271 others(2): Show |
5 | HG02109.hp1 HG02109.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+11923C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830759 | |||||||
| chr17:28830829 | A | T | 1 | a0001c0001t0023g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-41+11853T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830829 | |||||||
| chr17:28830834 | T | A | 1 | a0001c0002t0002g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-41+11848A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830834 | |||||||
| chr17:28830845 | A | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+11837T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830845 | |||||||
| chr17:28830980 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-41+11702C>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830980 | |||||||
| chr17:28830990 | CT | C | 109 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0022 others(106): Show |
109 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-41+11691delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830990 | |||||||
| chr17:28830990 | CTTTTTTT | C | 69 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(66): Show |
69 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.-41+11685_-41+1169 others(11): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830990 | |||||||
| chr17:28830998 | T | G | 7 | a0001c0002t0002g0166 a0001c0002t0003g0165 a0001c0002t0003g0167 others(4): Show |
7 | HG01070.hp2 HG01496.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41+11684A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830998 | |||||||
| chr17:28830999 | T | G | 79 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(76): Show |
79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-41+11683A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28830999 | |||||||
| chr17:28831004 | T | G | 3 | a0001c0002t0002g0207 a0001c0002t0002g0237 a0001c0002t0002g0245 |
3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+11678A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831004 | |||||||
| chr17:28831014 | G | C | 1 | a0001c0002t0002g0217 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-41+11668C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831014 | |||||||
| chr17:28831169 | A | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+11513T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831169 | |||||||
| chr17:28831205 | A | G | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-41+11477T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831205 | |||||||
| chr17:28831245 | C | T | 1 | a0001c0002t0003g0242 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-41+11437G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831245 | |||||||
| chr17:28831330 | C | T | 2 | a0001c0002t0002g0179 a0001c0002t0002g0236 |
2 | HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-41+11352G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831330 | |||||||
| chr17:28831342 | C | T | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+11340G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831342 | |||||||
| chr17:28831358 | C | CACTGTCT others(2): Show |
3 | a0001c0002t0002g0207 a0001c0002t0002g0237 a0001c0002t0002g0245 |
3 | HG01081.hp1 HG02622.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-41+11315_-41+1132 others(13): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831358 | |||||||
| chr17:28831504 | C | CT | 82 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0048 others(79): Show |
82 | HG00140.hp2 HG00408.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-41+11177dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831504 | |||||||
| chr17:28831504 | C | CTT | 11 | a0001c0002t0002g0160 a0001c0002t0002g0175 a0001c0002t0002g0180 others(8): Show |
11 | HG00544.hp2 HG03225.hp2 HG03490.hp2 others(8): Show |
intron_variant | MODIFIER | c.-41+11176_-41+1117 others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831504 | |||||||
| chr17:28831504 | CT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+11177delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28831504 | |||||||
| chr17:28832043 | AG | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0087 a0001c0001t0005g0139 |
3 | HG00642.hp1 HG01192.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-41+10638delC | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28832043 | |||||||
| chr17:28832497 | C | T | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-41+10185G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28832497 | |||||||
| chr17:28832969 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-41+9713C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28832969 | |||||||
| chr17:28833009 | T | TA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0037 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+9672dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | |||||||
| chr17:28833009 | TA | T | 12 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
12 | HG01070.hp1 HG01261.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.-41+9672delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | |||||||
| chr17:28833009 | TAA | T | 78 | a0001c0002t0002g0161 a0001c0002t0002g0163 a0001c0002t0002g0164 others(75): Show |
78 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-41+9671_-41+9672d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | |||||||
| chr17:28833009 | TAAA | T | 8 | a0001c0002t0002g0160 a0001c0002t0002g0178 a0001c0002t0002g0218 others(5): Show |
8 | HG03490.hp2 HG03491.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-41+9670_-41+9672d others(5): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833009 | |||||||
| chr17:28833240 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+9442A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833240 | |||||||
| chr17:28833301 | T | C | 9 | a0001c0001t0004g0260 a0001c0001t0004g0263 a0001c0001t0004g0264 others(6): Show |
9 | HG00408.hp1 HG02602.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+9381A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833301 | |||||||
| chr17:28833508 | T | C | 2 | a0001c0002t0002g0238 a0001c0002t0002g0239 |
2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+9174A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833508 | |||||||
| chr17:28833612 | C | CA | 15 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(12): Show |
15 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41+9069dupT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | |||||||
| chr17:28833612 | C | CAA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(5): Show |
8 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-41+9068_-41+9069d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | |||||||
| chr17:28833612 | CA | C | 12 | a0001c0001t0004g0162 a0001c0001t0004g0253 a0001c0001t0004g0263 others(9): Show |
12 | HG01884.hp1 HG02965.hp1 HG03130.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+9069delT | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | |||||||
| chr17:28833612 | CAA | C | 79 | a0001c0001t0001g0043 a0001c0002t0002g0160 a0001c0002t0002g0161 others(76): Show |
79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-41+9068_-41+9069d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28833612 | |||||||
| chr17:28834120 | A | G | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+8562T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834120 | |||||||
| chr17:28834269 | T | C | 1 | a0001c0001t0004g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-41+8413A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834269 | |||||||
| chr17:28834383 | ATC | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+8297_-41+8298d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834383 | |||||||
| chr17:28834478 | CT | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+8203delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834478 | |||||||
| chr17:28834700 | T | C | 1 | a0001c0002t0002g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-41+7982A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834700 | |||||||
| chr17:28834798 | C | T | 1 | a0001c0006t0001g0088 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-41+7884G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834798 | |||||||
| chr17:28834854 | A | AT | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0086 others(4): Show |
7 | HG01175.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+7827dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834854 | |||||||
| chr17:28834854 | AT | A | 85 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(82): Show |
85 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-41+7827delA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834854 | |||||||
| chr17:28834868 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-41+7814A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28834868 | |||||||
| chr17:28835024 | T | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | HG00099.hp2 HG00642.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+7658A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTG | 28 | a0001c0001t0001g0019 a0001c0001t0001g0112 a0001c0001t0001g0113 others(25): Show |
28 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.-41+7656_-41+7657d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTG | 17 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0036 others(14): Show |
17 | HG01074.hp2 HG01123.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-41+7654_-41+7657d others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTG | 14 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0026 others(11): Show |
14 | HG00140.hp1 HG01074.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-41+7652_-41+7657d others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTGT others(1): Show |
18 | a0001c0002t0002g0207 a0001c0002t0002g0209 a0001c0002t0002g0210 others(15): Show |
18 | HG00140.hp2 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-41+7650_-41+7657d others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTGT others(3): Show |
5 | a0001c0002t0002g0174 a0001c0002t0002g0175 a0001c0002t0002g0218 others(2): Show |
5 | HG03139.hp1 HG03195.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+7648_-41+7657d others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTGT others(5): Show |
15 | a0001c0002t0002g0163 a0001c0002t0002g0221 a0001c0002t0002g0222 others(12): Show |
15 | HG02148.hp2 HG02293.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.-41+7646_-41+7657d others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTGT others(7): Show |
1 | a0001c0002t0002g0233 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-41+7644_-41+7657d others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTGT others(9): Show |
7 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0164 others(4): Show |
7 | HG01099.hp1 HG03490.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41+7642_-41+7657d others(18): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | T | TTGTGTGT others(11): Show |
1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+7640_-41+7657d others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTG | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(20): Show |
23 | HG00621.hp1 HG01109.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.-41+7656_-41+7657d others(4): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTG | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0086 others(32): Show |
35 | HG00738.hp1 HG00738.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-41+7654_-41+7657d others(6): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTGTG | T | 76 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(73): Show |
76 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.-41+7652_-41+7657d others(8): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTGTGT others(1): Show |
T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(2): Show |
5 | HG02258.hp1 HG02615.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+7650_-41+7657d others(10): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0037 a0001c0002t0022g0177 |
2 | HG02735.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.-41+7648_-41+7657d others(12): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTGTGT others(5): Show |
T | 1 | a0001c0002t0002g0241 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-41+7646_-41+7657d others(14): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0003g0176 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-41+7644_-41+7657d others(16): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835024 | TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+7638_-41+7657d others(22): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835024 | |||||||
| chr17:28835085 | G | A | 1 | a0001c0001t0004g0272 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-41+7597C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835085 | |||||||
| chr17:28835139 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-41+7543C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835139 | |||||||
| chr17:28835162 | A | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01243.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-41+7520T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835162 | |||||||
| chr17:28835277 | C | T | 2 | a0001c0001t0004g0258 a0001c0001t0004g0259 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-41+7405G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835277 | |||||||
| chr17:28835436 | A | G | 30 | a0001c0001t0004g0162 a0001c0001t0004g0247 a0001c0001t0004g0248 others(27): Show |
30 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-41+7246T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835436 | |||||||
| chr17:28835517 | T | G | 1 | a0001c0001t0027g0276 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-41+7165A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835517 | |||||||
| chr17:28835832 | C | T | 1 | a0001c0002t0002g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-41+6850G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835832 | |||||||
| chr17:28835838 | A | AT | 10 | a0001c0001t0001g0036 a0001c0001t0004g0250 a0001c0001t0004g0251 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-41+6843dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835838 | |||||||
| chr17:28835856 | G | C | 1 | a0001c0001t0004g0162 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+6826C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835856 | |||||||
| chr17:28835993 | A | AT | 87 | a0001c0001t0014g0033 a0001c0002t0002g0160 a0001c0002t0002g0161 others(84): Show |
87 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-41+6688dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28835993 | |||||||
| chr17:28836240 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-41+6442C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836240 | |||||||
| chr17:28836277 | C | A | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+6405G>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836277 | |||||||
| chr17:28836279 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0035 |
2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-41+6403G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836279 | |||||||
| chr17:28836329 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+6353C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836329 | |||||||
| chr17:28836415 | G | A | 1 | a0001c0002t0002g0237 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-41+6267C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836415 | |||||||
| chr17:28836615 | G | C | 2 | a0001c0002t0002g0238 a0001c0002t0002g0239 |
2 | NA18960.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-41+6067C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836615 | |||||||
| chr17:28836621 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0141 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-41+6061G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836621 | |||||||
| chr17:28836857 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-41+5825A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836857 | |||||||
| chr17:28836896 | T | G | 1 | a0001c0001t0014g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-41+5786A>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836896 | |||||||
| chr17:28836996 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-41+5686A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28836996 | |||||||
| chr17:28837141 | A | G | 2 | a0001c0001t0011g0004 a0005c0009t0011g0003 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-41+5541T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837141 | |||||||
| chr17:28837199 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-41+5483C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837199 | |||||||
| chr17:28837221 | G | C | 1 | a0001c0001t0005g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-41+5461C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837221 | |||||||
| chr17:28837413 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-41+5269C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837413 | |||||||
| chr17:28837436 | A | T | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+5246T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837436 | |||||||
| chr17:28837440 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(104): Show |
107 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-41+5242T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837440 | |||||||
| chr17:28837444 | T | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0005g0024 others(1): Show |
4 | HG01099.hp2 HG01123.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+5238A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837444 | |||||||
| chr17:28837549 | G | A | 1 | a0001c0002t0003g0240 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-41+5133C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837549 | |||||||
| chr17:28837564 | A | G | 2 | a0001c0001t0004g0247 a0001c0001t0004g0248 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-41+5118T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837564 | |||||||
| chr17:28837646 | G | GT | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0002g0174 others(2): Show |
5 | HG01243.hp1 HG02559.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+5035dupA | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837646 | |||||||
| chr17:28837665 | T | C | 86 | a0001c0002t0002g0160 a0001c0002t0002g0161 a0001c0002t0002g0163 others(83): Show |
86 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-41+5017A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837665 | |||||||
| chr17:28837715 | T | C | 2 | a0001c0002t0002g0169 a0001c0002t0002g0170 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-41+4967A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837715 | |||||||
| chr17:28837748 | A | C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0025 others(3): Show |
6 | HG00140.hp1 HG01099.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+4934T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28837748 | |||||||
| chr17:28838164 | CTGAAGCA others(11): Show |
C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0153 a0001c0001t0001g0154 others(3): Show |
6 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-41+4500_-41+4517d others(20): Show |
FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838164 | |||||||
| chr17:28838371 | G | A | 3 | a0001c0002t0003g0242 a0001c0002t0003g0243 a0001c0002t0003g0244 |
3 | NA18959.hp1 NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-41+4311C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838371 | |||||||
| chr17:28838574 | T | A | 1 | a0001c0002t0002g0245 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-41+4108A>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838574 | |||||||
| chr17:28838648 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-41+4034A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28838648 | |||||||
| chr17:28839122 | G | A | 1 | a0001c0002t0003g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-41+3560C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839122 | |||||||
| chr17:28839123 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-41+3559G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839123 | |||||||
| chr17:28839156 | G | A | 1 | a0001c0001t0005g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-41+3526C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839156 | |||||||
| chr17:28839282 | A | G | 1 | a0001c0002t0002g0171 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-41+3400T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839282 | |||||||
| chr17:28839360 | C | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG00544.hp1 NA18951.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41+3322G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839360 | |||||||
| chr17:28839485 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-41+3197G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839485 | |||||||
| chr17:28839688 | A | T | 2 | a0001c0002t0002g0169 a0001c0002t0002g0170 |
2 | HG00642.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-41+2994T>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28839688 | |||||||
| chr17:28840042 | G | A | 1 | a0001c0001t0004g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-41+2640C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840042 | |||||||
| chr17:28840048 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(8): Show |
11 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-41+2634C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840048 | |||||||
| chr17:28840149 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-41+2533C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840149 | |||||||
| chr17:28840158 | C | G | 1 | a0001c0002t0003g0165 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-41+2524G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840158 | |||||||
| chr17:28840318 | A | C | 1 | a0001c0002t0002g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-41+2364T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840318 | |||||||
| chr17:28840513 | G | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG01069.hp2 HG01256.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41+2169C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840513 | |||||||
| chr17:28840736 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-41+1946G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840736 | |||||||
| chr17:28840748 | G | A | 1 | a0001c0001t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-41+1934C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840748 | |||||||
| chr17:28840792 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-41+1890A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840792 | |||||||
| chr17:28840831 | C | T | 1 | a0001c0002t0024g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-41+1851G>A | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840831 | |||||||
| chr17:28840910 | A | C | 88 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0002g0160 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+1772T>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840910 | |||||||
| chr17:28840955 | C | G | 88 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0002g0160 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+1727G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840955 | |||||||
| chr17:28840960 | C | G | 3 | a0001c0002t0002g0166 a0001c0002t0003g0165 a0001c0002t0003g0167 |
3 | HG01070.hp2 HG01496.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-41+1722G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28840960 | |||||||
| chr17:28841288 | C | G | 2 | a0001c0002t0002g0163 a0001c0002t0002g0164 |
2 | HG01099.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-41+1394G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841288 | |||||||
| chr17:28841309 | T | C | 88 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0002t0002g0160 others(85): Show |
88 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-41+1373A>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841309 | |||||||
| chr17:28841417 | C | G | 1 | a0001c0001t0001g0012 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-41+1265G>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841417 | |||||||
| chr17:28841468 | G | A | 116 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0004g0162 others(113): Show |
116 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.-41+1214C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841468 | |||||||
| chr17:28841942 | G | C | 29 | a0001c0001t0004g0247 a0001c0001t0004g0248 a0001c0001t0004g0250 others(26): Show |
29 | HG00408.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-41+740C>G | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841942 | |||||||
| chr17:28841994 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-41+688T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28841994 | |||||||
| chr17:28842106 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-41+576C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842106 | |||||||
| chr17:28842508 | G | A | 12 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG01069.hp2 HG01243.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.-41+174C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842508 | |||||||
| chr17:28842550 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(7): Show |
10 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-41+132T>C | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842550 | |||||||
| chr17:28842629 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-41+53C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842629 | |||||||
| chr17:28842650 | G | A | 1 | a0001c0002t0002g0275 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-41+32C>T | FAM222B | ENSG00000173065.14 | transcript | ENST00000581407.6 | protein_coding | 1/2 | chr17 | 28842650 |