Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2165 |
| ensemblid | ENSG00000143278.5 |
| hgncid | 3534 |
| symbol | F13B |
| name | coagulation factor XIII B chain |
| refseq_nuc | NM_001994.3 |
| refseq_prot | NP_001985.2 |
| ensembl_nuc | ENST00000367412.2 |
| ensembl_prot | ENSP00000356382.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 197038741 |
| end | 197067260 |
| strand | - |
| ver | v1.2 |
| region | chr1:197038741-197067260 |
| region5000 | chr1:197033741-197072260 |
| regionname0 | F13B_chr1_197038741_197067260 |
| regionname5000 | F13B_chr1_197033741_197072260 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 661 | 264 | 33 | 48 | 142 | 11 | 30 | 111 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0002 | 1/1 | 661 | 62 | 49 | 5 | 0 | 1 | 5 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0003 | 0/0 | 661 | 7 | 1 | 0 | 6 | 0 | 0 | 4 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0004 | 0/0 | 661 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0005 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0006 | 0/0 | 661 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0007 | 0/0 | 661 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0008 | 0/0 | 661 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0009 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| a0010 | 0/0 | 661 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | MRLKN others(656): Show |
chr1 | 197033741 | 197072260 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1983 | 189 | 21 | 33 | 111 | 7 | 17 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0001c0002 | 0/0 | 1983 | 71 | 12 | 15 | 28 | 3 | 13 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0001c0007 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0001c0008 | 0/0 | 1983 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0001c0012 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0001c0013 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0002c0003 | 1/1 | 1983 | 59 | 46 | 5 | 0 | 1 | 5 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0002c0006 | 0/0 | 1983 | 3 | 3 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0003c0004 | 0/0 | 1983 | 6 | 0 | 0 | 6 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0003c0014 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0004c0005 | 0/0 | 1983 | 3 | 3 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0005c0017 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0006c0009 | 0/0 | 1983 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0007c0011 | 0/0 | 1983 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0008c0015 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0009c0010 | 0/0 | 1983 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 | ||
| a0010c0016 | 0/0 | 1983 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | ATGAG others(1978): Show |
chr1 | 197033741 | 197072260 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2660 | 188 | 21 | 33 | 110 | 7 | 17 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0001t0007 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0002t0001 | 0/0 | 2660 | 7 | 7 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0002t0002 | 0/0 | 2660 | 63 | 5 | 15 | 27 | 3 | 13 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0002t0005 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0007t0001 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0008t0002 | 0/0 | 2660 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0012t0001 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0001c0013t0001 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0002c0003t0001 | 1/1 | 2660 | 58 | 45 | 5 | 0 | 1 | 5 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0002c0003t0006 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0002c0006t0001 | 0/0 | 2660 | 3 | 3 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0003c0004t0003 | 0/0 | 2660 | 6 | 0 | 0 | 6 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0003c0014t0004 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0004c0005t0004 | 0/0 | 2660 | 3 | 3 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0005c0017t0001 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0006c0009t0002 | 0/0 | 2660 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0007c0011t0001 | 0/0 | 2660 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0008c0015t0001 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0009c0010t0001 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| a0010c0016t0001 | 0/0 | 2660 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | AGAAT others(2655): Show |
chr1 | 197033741 | 197072260 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 41 | 1 | 5 | 30 | 0 | 5 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0003 | 0/0 | 20 | 1 | 6 | 8 | 1 | 4 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0002 | 0/0 | 26 | 4 | 7 | 8 | 1 | 6 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0005 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0007t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0008t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0012t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0001c0013t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0004 | 1/0 | 14 | 9 | 3 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0008 | 0/0 | 6 | 2 | 1 | 0 | 1 | 2 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0003t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0006t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0002c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0003c0004t0003g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0003c0014t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0004c0005t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0004c0005t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0005c0017t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0006c0009t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0007c0011t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0008c0015t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0009c0010t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| a0010c0016t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0024 | EUR | FIN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00323 | hp2 | a0001 | c0008 | t0002 | g0060 | EUR | FIN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00408 | hp1 | a0005 | c0017 | t0001 | g0155 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0076 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01071 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0056 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01358 | hp2 | a0006 | c0009 | t0002 | g0063 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01891 | hp1 | a0002 | c0003 | t0001 | g0043 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0057 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0125 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02145 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0165 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02523 | hp2 | a0003 | c0004 | t0003 | g0009 | EAS | KHV | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02572 | hp1 | a0002 | c0003 | t0001 | g0008 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0048 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0041 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0008 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02717 | hp2 | a0002 | c0003 | t0001 | g0012 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0054 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0022 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02735 | hp2 | a0007 | c0011 | t0001 | g0104 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02809 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02818 | hp2 | a0004 | c0005 | t0004 | g0032 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02895 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02896 | hp2 | a0002 | c0006 | t0001 | g0033 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02897 | hp1 | a0002 | c0006 | t0001 | g0033 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0050 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02965 | hp1 | a0002 | c0006 | t0001 | g0128 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02965 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02976 | hp1 | a0004 | c0005 | t0004 | g0032 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02976 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03041 | hp2 | a0004 | c0005 | t0004 | g0126 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0023 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0012 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0051 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0055 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03486 | hp2 | a0003 | c0014 | t0004 | g0042 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0004 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03540 | hp2 | a0008 | c0015 | t0001 | g0053 | AFR | GWD | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0016 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03688 | hp2 | a0002 | c0003 | t0001 | g0008 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03710 | hp1 | a0002 | c0003 | t0001 | g0052 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0064 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0059 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0014 | AFR | YRI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | YRI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18612 | hp1 | a0003 | c0004 | t0003 | g0009 | EAS | CHB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18906 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | YRI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18906 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | YRI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18940 | hp1 | a0001 | c0002 | t0005 | g0074 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18945 | hp2 | a0003 | c0004 | t0003 | g0009 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18969 | hp1 | a0003 | c0004 | t0003 | g0009 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18978 | hp1 | a0009 | c0010 | t0001 | g0082 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19005 | hp2 | a0001 | c0013 | t0001 | g0154 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19006 | hp2 | a0003 | c0004 | t0003 | g0009 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19043 | hp1 | a0010 | c0016 | t0001 | g0127 | AFR | LWK | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | LWK | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19065 | hp2 | a0001 | c0007 | t0001 | g0079 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19072 | hp2 | a0003 | c0004 | t0003 | g0009 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19088 | hp2 | a0001 | c0012 | t0001 | g0151 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19089 | hp2 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | YRI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0022 | AFR | ASW | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ASW | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0008 | EUR | TSI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0069 | EUR | TSI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02109 | hp1 | a0002 | c0003 | t0001 | g0012 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0044 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03471 | hp1 | a0002 | c0003 | t0006 | g0046 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0004 | AFR | MSL | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0049 | AFR | USA | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | USA | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | LWK | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0040 | REF | REF | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0001 | g0004 | REF | REF | F13B_chr1_197033741_197072260 | F13B | chr1 | 197033741 | 197072260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:197039403 | G | A | 1 | a0007 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.1961C>T | p.Ser654Phe | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 1998/2660 | 1961/1986 | 654/661 | chr1 | 197039403 | |||
| chr1:197040539 | T | A | 1 | a0008 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1935A>T | p.Arg645Ser | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/12 | 1972/2660 | 1935/1986 | 645/661 | chr1 | 197040539 | |||
| chr1:197050728 | A | C | 2 | a0003 a0004 |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
missense_variant | MODERATE | c.1707T>G | p.Asp569Glu | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/12 | 1744/2660 | 1707/1986 | 569/661 | chr1 | 197050728 | |||
| chr1:197050849 | A | G | 1 | a0004 | 3 | HG02818.hp2 HG02976.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.1586T>C | p.Leu529Pro | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/12 | 1623/2660 | 1586/1986 | 529/661 | chr1 | 197050849 | |||
| chr1:197055756 | C | T | 1 | a0009 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.1313G>A | p.Arg438His | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/12 | 1350/2660 | 1313/1986 | 438/661 | chr1 | 197055756 | |||
| chr1:197055771 | C | T | 1 | a0010 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1298G>A | p.Gly433Glu | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/12 | 1335/2660 | 1298/1986 | 433/661 | chr1 | 197055771 | |||
| chr1:197057135 | T | C | 1 | a0004 | 3 | HG02818.hp2 HG02976.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.1049A>G | p.His350Arg | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 7/12 | 1086/2660 | 1049/1986 | 350/661 | chr1 | 197057135 | |||
| chr1:197057159 | A | G | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.1025T>C | p.Ile342Thr | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 7/12 | 1062/2660 | 1025/1986 | 342/661 | chr1 | 197057159 | |||
| chr1:197061891 | C | T | 6 | a0001 a0004 a0005 others(3): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
missense_variant | MODERATE | c.344G>A | p.Arg115His | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/12 | 381/2660 | 344/1986 | 115/661 | chr1 | 197061891 | |||
| chr1:197062965 | T | C | 1 | a0005 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.157A>G | p.Lys53Glu | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/12 | 194/2660 | 157/1986 | 53/661 | chr1 | 197062965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:197040668 | A | G | 7 | a0001c0001 a0001c0007 a0001c0012 others(4): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
synonymous_variant | LOW | c.1806T>C | p.Asn602Asn | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/12 | 1843/2660 | 1806/1986 | 602/661 | chr1 | 197040668 | |||
| chr1:197050791 | T | C | 1 | a0001c0012 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.1644A>G | p.Ser548Ser | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/12 | 1681/2660 | 1644/1986 | 548/661 | chr1 | 197050791 | |||
| chr1:197057095 | T | G | 1 | a0003c0004 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
synonymous_variant | LOW | c.1089A>C | p.Ala363Ala | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 7/12 | 1126/2660 | 1089/1986 | 363/661 | chr1 | 197057095 | |||
| chr1:197060517 | T | C | 1 | a0001c0013 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.654A>G | p.Leu218Leu | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/12 | 691/2660 | 654/1986 | 218/661 | chr1 | 197060517 | |||
| chr1:197060957 | C | T | 1 | a0001c0008 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.570G>A | p.Lys190Lys | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 4/12 | 607/2660 | 570/1986 | 190/661 | chr1 | 197060957 | |||
| chr1:197061071 | T | C | 14 | a0001c0001 a0001c0002 a0001c0007 others(11): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
synonymous_variant | LOW | c.456A>G | p.Thr152Thr | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 4/12 | 493/2660 | 456/1986 | 152/661 | chr1 | 197061071 | |||
| chr1:197061863 | G | T | 1 | a0001c0007 | 1 | NA19065.hp2 | synonymous_variant | LOW | c.372C>A | p.Thr124Thr | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/12 | 409/2660 | 372/1986 | 124/661 | chr1 | 197061863 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:197038803 | A | T | 1 | a0001c0001t0007 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 575 | chr1 | 197038803 | ||||||
| chr1:197039026 | A | T | 1 | a0001c0001t0007 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*352T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 352 | chr1 | 197039026 | ||||||
| chr1:197039027 | T | A | 1 | a0001c0001t0007 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*351A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 351 | chr1 | 197039027 | ||||||
| chr1:197039069 | A | G | 1 | a0002c0003t0006 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 309 | chr1 | 197039069 | ||||||
| chr1:197039235 | C | T | 6 | a0001c0002t0002 a0001c0002t0005 a0001c0008t0002 others(3): Show |
70 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 143 | chr1 | 197039235 | ||||||
| chr1:197039289 | C | G | 3 | a0003c0004t0003 a0003c0014t0004 a0004c0005t0004 |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*89G>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 89 | chr1 | 197039289 | ||||||
| chr1:197039289 | C | T | 1 | a0001c0002t0005 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 12/12 | 89 | chr1 | 197039289 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:197039467 | A | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1953-56T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039467 | |||||||
| chr1:197039540 | T | A | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1953-129A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039540 | |||||||
| chr1:197039582 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1953-171G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039582 | |||||||
| chr1:197039606 | T | C | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1953-195A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039606 | |||||||
| chr1:197039645 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0137 |
3 | HG02280.hp1 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1953-234A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039645 | |||||||
| chr1:197039651 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1953-240C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039651 | |||||||
| chr1:197039749 | A | G | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1953-338T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039749 | |||||||
| chr1:197039787 | G | A | 1 | a0002c0003t0001g0047 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1953-376C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039787 | |||||||
| chr1:197039932 | T | C | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1953-521A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039932 | |||||||
| chr1:197039937 | T | A | 2 | a0004c0005t0004g0032 a0004c0005t0004g0126 |
3 | HG02818.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1953-526A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197039937 | |||||||
| chr1:197040049 | G | A | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1952+473C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040049 | |||||||
| chr1:197040255 | G | A | 1 | a0003c0014t0004g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1952+267C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040255 | |||||||
| chr1:197040312 | G | C | 1 | a0002c0003t0001g0048 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1952+210C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040312 | |||||||
| chr1:197040378 | G | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1952+144C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040378 | |||||||
| chr1:197040442 | A | T | 1 | a0001c0001t0001g0029 | 2 | HG00609.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1952+80T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040442 | |||||||
| chr1:197040483 | C | A | 1 | a0001c0001t0007g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1952+39G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040483 | |||||||
| chr1:197040501 | C | CA | 2 | a0001c0002t0002g0026 a0003c0004t0003g0009 |
8 | HG02523.hp2 HG04199.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.1952+20dupT | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 11/11 | chr1 | 197040501 | |||||||
| chr1:197041118 | GAAAGTTC others(4): Show |
G | 1 | a0001c0001t0007g0133 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1739-394_1739-384d others(13): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041118 | |||||||
| chr1:197041126 | A | T | 2 | a0001c0002t0001g0165 a0008c0015t0001g0053 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1739-391T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041126 | |||||||
| chr1:197041345 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1739-610C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041345 | |||||||
| chr1:197041399 | G | A | 1 | a0010c0016t0001g0127 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1739-664C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041399 | |||||||
| chr1:197041401 | T | A | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1739-666A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041401 | |||||||
| chr1:197041467 | G | A | 1 | a0001c0002t0002g0024 | 2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.1739-732C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041467 | |||||||
| chr1:197041468 | G | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1739-733C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041468 | |||||||
| chr1:197041607 | GC | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(139): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1739-873delG | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041607 | |||||||
| chr1:197041665 | C | T | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1739-930G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041665 | |||||||
| chr1:197041756 | A | G | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1739-1021T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041756 | |||||||
| chr1:197041936 | C | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1739-1201G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041936 | |||||||
| chr1:197041986 | G | A | 1 | a0001c0002t0002g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1739-1251C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197041986 | |||||||
| chr1:197042082 | G | A | 1 | a0006c0009t0002g0063 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1739-1347C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042082 | |||||||
| chr1:197042176 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0097 |
3 | HG01952.hp1 NA18988.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1739-1441G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042176 | |||||||
| chr1:197042296 | T | C | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-1561A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042296 | |||||||
| chr1:197042447 | T | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1739-1712A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042447 | |||||||
| chr1:197042506 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1739-1771T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042506 | |||||||
| chr1:197042580 | A | C | 2 | a0002c0006t0001g0033 a0002c0006t0001g0128 |
3 | HG02896.hp2 HG02897.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1739-1845T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042580 | |||||||
| chr1:197042649 | T | A | 4 | a0002c0003t0001g0014 a0002c0003t0001g0021 a0002c0003t0001g0022 others(1): Show |
8 | HG02258.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1739-1914A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042649 | |||||||
| chr1:197042655 | C | CA | 16 | a0001c0001t0001g0034 a0001c0001t0001g0093 a0001c0001t0001g0096 others(13): Show |
23 | HG01175.hp1 HG01884.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.1739-1921dupT | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042655 | |||||||
| chr1:197042728 | G | GAAGAATC others(283): Show |
1 | a0001c0001t0001g0136 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1739-1994_1739-199 others(294): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(284): Show |
1 | a0001c0001t0001g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1739-1994_1739-199 others(295): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(267): Show |
1 | a0001c0001t0001g0036 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(278): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(278): Show |
4 | a0001c0001t0001g0037 a0001c0001t0001g0156 a0001c0001t0001g0160 others(1): Show |
5 | HG01099.hp1 NA18977.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(289): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(279): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(31): Show |
67 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(290): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(280): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
7 | HG02647.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(291): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(281): Show |
3 | a0001c0002t0001g0123 a0001c0002t0001g0125 a0001c0002t0001g0164 |
3 | HG02145.hp1 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(292): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(282): Show |
5 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0117 others(2): Show |
5 | HG01256.hp2 HG01358.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(293): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(283): Show |
39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(36): Show |
91 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(294): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(284): Show |
9 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0077 others(6): Show |
13 | HG00423.hp1 HG00741.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(295): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(285): Show |
2 | a0001c0001t0001g0115 a0001c0001t0001g0137 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(296): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042728 | G | GAAGAATC others(286): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0101 |
2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1739-1994_1739-199 others(297): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042728 | |||||||
| chr1:197042765 | G | A | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-2030C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042765 | |||||||
| chr1:197042817 | TA | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0002t0002g0070 others(3): Show |
11 | HG01106.hp2 HG02523.hp2 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1739-2083delT | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042817 | |||||||
| chr1:197042835 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1739-2100G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042835 | |||||||
| chr1:197042838 | T | C | 1 | a0001c0002t0002g0027 | 2 | NA18980.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1739-2103A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042838 | |||||||
| chr1:197042870 | A | T | 3 | a0002c0003t0001g0041 a0002c0003t0001g0056 a0002c0003t0001g0057 |
3 | HG01175.hp2 HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1739-2135T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042870 | |||||||
| chr1:197042949 | C | T | 1 | a0001c0002t0002g0025 | 2 | NA19003.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1739-2214G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042949 | |||||||
| chr1:197042952 | G | A | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-2217C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042952 | |||||||
| chr1:197042980 | C | T | 1 | a0003c0014t0004g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1739-2245G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042980 | |||||||
| chr1:197042981 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(39): Show |
78 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1739-2246C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197042981 | |||||||
| chr1:197043064 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1739-2329A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043064 | |||||||
| chr1:197043221 | C | A | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-2486G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043221 | |||||||
| chr1:197043640 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1739-2905T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043640 | |||||||
| chr1:197043695 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1739-2960T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043695 | |||||||
| chr1:197043735 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1739-3000A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043735 | |||||||
| chr1:197043829 | A | T | 4 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1739-3094T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043829 | |||||||
| chr1:197043832 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0137 |
3 | HG02280.hp1 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1739-3097A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043832 | |||||||
| chr1:197043842 | G | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1739-3107C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197043842 | |||||||
| chr1:197044042 | C | CAT | 3 | a0003c0014t0004g0042 a0004c0005t0004g0032 a0004c0005t0004g0126 |
4 | HG02818.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1739-3309_1739-330 others(6): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044042 | |||||||
| chr1:197044066 | T | G | 7 | a0001c0002t0002g0005 a0001c0002t0002g0065 a0001c0002t0002g0066 others(4): Show |
18 | HG01256.hp1 HG01261.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.1739-3331A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044066 | |||||||
| chr1:197044068 | T | G | 57 | a0001c0001t0001g0011 a0001c0001t0001g0078 a0001c0001t0001g0086 others(54): Show |
120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1739-3333A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044068 | |||||||
| chr1:197044070 | G | T | 1 | a0002c0003t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1739-3335C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044070 | |||||||
| chr1:197044078 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1739-3343C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044078 | |||||||
| chr1:197044264 | G | A | 2 | a0002c0003t0001g0015 a0002c0003t0001g0050 |
4 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1739-3529C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044264 | |||||||
| chr1:197044310 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1739-3575G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044310 | |||||||
| chr1:197044313 | T | A | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1739-3578A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044313 | |||||||
| chr1:197044328 | G | A | 1 | a0002c0003t0001g0052 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1739-3593C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044328 | |||||||
| chr1:197044334 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(139): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1739-3599A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044334 | |||||||
| chr1:197044826 | A | G | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1739-4091T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044826 | |||||||
| chr1:197044912 | GATAA | G | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-4181_1739-417 others(8): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197044912 | |||||||
| chr1:197045007 | C | T | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1739-4272G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045007 | |||||||
| chr1:197045056 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0090 a0001c0001t0001g0106 |
4 | NA18951.hp2 NA18960.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1739-4321C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045056 | |||||||
| chr1:197045162 | C | T | 1 | a0003c0014t0004g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1739-4427G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045162 | |||||||
| chr1:197045641 | T | C | 1 | a0001c0002t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1739-4906A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045641 | |||||||
| chr1:197045749 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1738+4948C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045749 | |||||||
| chr1:197045806 | C | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738+4891G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045806 | |||||||
| chr1:197045818 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1738+4879C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045818 | |||||||
| chr1:197045856 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738+4841G>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045856 | |||||||
| chr1:197045888 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1738+4809T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045888 | |||||||
| chr1:197045966 | C | G | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1738+4731G>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197045966 | |||||||
| chr1:197046271 | G | A | 4 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+4426C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046271 | |||||||
| chr1:197046402 | C | T | 1 | a0002c0003t0001g0014 | 3 | HG02258.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1738+4295G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046402 | |||||||
| chr1:197046453 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0141 a0005c0017t0001g0155 |
4 | HG00408.hp1 HG02056.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738+4244T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046453 | |||||||
| chr1:197046598 | A | G | 1 | a0001c0002t0002g0069 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1738+4099T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046598 | |||||||
| chr1:197046668 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(136): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1738+4029T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046668 | |||||||
| chr1:197046683 | A | T | 4 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+4014T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046683 | |||||||
| chr1:197046738 | A | C | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1738+3959T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046738 | |||||||
| chr1:197046793 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1738+3904C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046793 | |||||||
| chr1:197046794 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1738+3903T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046794 | |||||||
| chr1:197046935 | G | A | 1 | a0002c0003t0001g0049 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1738+3762C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046935 | |||||||
| chr1:197046987 | T | C | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738+3710A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197046987 | |||||||
| chr1:197047124 | C | T | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738+3573G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047124 | |||||||
| chr1:197047152 | A | G | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1738+3545T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047152 | |||||||
| chr1:197047310 | C | T | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1738+3387G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047310 | |||||||
| chr1:197047321 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1738+3376G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047321 | |||||||
| chr1:197047351 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1738+3346C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047351 | |||||||
| chr1:197047391 | A | G | 1 | a0001c0002t0002g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1738+3306T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047391 | |||||||
| chr1:197047444 | C | T | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+3253G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047444 | |||||||
| chr1:197047675 | T | C | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+3022A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047675 | |||||||
| chr1:197047830 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1738+2867C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197047830 | |||||||
| chr1:197048050 | G | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738+2647C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048050 | |||||||
| chr1:197048123 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1738+2574G>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048123 | |||||||
| chr1:197048132 | T | TTA | 4 | a0001c0001t0001g0109 a0002c0006t0001g0033 a0002c0006t0001g0128 others(1): Show |
5 | HG01081.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738+2563_1738+256 others(6): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048132 | |||||||
| chr1:197048148 | G | A | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+2549C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048148 | |||||||
| chr1:197048148 | G | GTA | 6 | a0002c0003t0001g0014 a0002c0003t0001g0021 a0002c0003t0001g0022 others(3): Show |
11 | HG02258.hp2 HG02622.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1738+2547_1738+254 others(6): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048148 | |||||||
| chr1:197048161 | C | A | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+2536G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048161 | |||||||
| chr1:197048343 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1738+2354G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048343 | |||||||
| chr1:197048456 | G | C | 4 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+2241C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048456 | |||||||
| chr1:197048511 | C | A | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+2186G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048511 | |||||||
| chr1:197048661 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0148 a0001c0001t0001g0149 |
4 | NA18947.hp1 NA18973.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+2036A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048661 | |||||||
| chr1:197048812 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1738+1885C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048812 | |||||||
| chr1:197048823 | CTT | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1738+1872_1738+187 others(6): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048823 | |||||||
| chr1:197048831 | AAGT | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1738+1863_1738+186 others(7): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048831 | |||||||
| chr1:197048836 | T | C | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+1861A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048836 | |||||||
| chr1:197048846 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(136): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1738+1851C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197048846 | |||||||
| chr1:197049028 | G | A | 2 | a0001c0002t0001g0165 a0008c0015t0001g0053 |
2 | HG02280.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1738+1669C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049028 | |||||||
| chr1:197049104 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1738+1593A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049104 | |||||||
| chr1:197049118 | T | G | 2 | a0002c0003t0001g0022 a0002c0003t0006g0046 |
3 | HG02723.hp2 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1738+1579A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049118 | |||||||
| chr1:197049151 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738+1546C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049151 | |||||||
| chr1:197049201 | A | C | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+1496T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049201 | |||||||
| chr1:197049241 | A | T | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+1456T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049241 | |||||||
| chr1:197049263 | G | T | 1 | a0001c0002t0002g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1738+1434C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049263 | |||||||
| chr1:197049268 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1738+1429A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049268 | |||||||
| chr1:197049332 | G | A | 1 | a0003c0014t0004g0042 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1738+1365C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049332 | |||||||
| chr1:197049597 | C | A | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1738+1100G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049597 | |||||||
| chr1:197049599 | C | T | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1738+1098G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049599 | |||||||
| chr1:197049620 | G | T | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738+1077C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049620 | |||||||
| chr1:197049621 | G | C | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1738+1076C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049621 | |||||||
| chr1:197049627 | T | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0165 a0008c0015t0001g0053 |
4 | HG02280.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1738+1070A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049627 | |||||||
| chr1:197049655 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1738+1042A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049655 | |||||||
| chr1:197049757 | C | T | 2 | a0001c0002t0002g0065 a0001c0002t0002g0066 |
2 | HG01261.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1738+940G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049757 | |||||||
| chr1:197049883 | A | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0096 |
5 | NA18947.hp2 NA18995.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738+814T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049883 | |||||||
| chr1:197049925 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(136): Show |
279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1738+772A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049925 | |||||||
| chr1:197049959 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1738+738T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049959 | |||||||
| chr1:197049987 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1738+710T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197049987 | |||||||
| chr1:197050134 | A | C | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738+563T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197050134 | |||||||
| chr1:197050167 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0138 |
2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1738+530T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197050167 | |||||||
| chr1:197050347 | C | T | 1 | a0004c0005t0004g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1738+350G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 10/11 | chr1 | 197050347 | |||||||
| chr1:197050892 | G | T | 1 | a0001c0002t0002g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1556-13C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197050892 | |||||||
| chr1:197051034 | T | C | 1 | a0002c0003t0001g0043 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1556-155A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051034 | |||||||
| chr1:197051189 | G | A | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1556-310C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051189 | |||||||
| chr1:197051312 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1556-433C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051312 | |||||||
| chr1:197051380 | G | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0080 others(5): Show |
13 | HG00280.hp2 HG00609.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1556-501C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051380 | |||||||
| chr1:197051528 | T | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(39): Show |
78 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.1556-649A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051528 | |||||||
| chr1:197051610 | T | A | 1 | a0002c0003t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1556-731A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051610 | |||||||
| chr1:197051668 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1556-789A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051668 | |||||||
| chr1:197051685 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1556-806T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051685 | |||||||
| chr1:197051743 | C | T | 1 | a0002c0006t0001g0033 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1556-864G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051743 | |||||||
| chr1:197051759 | C | A | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1555+875G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051759 | |||||||
| chr1:197051903 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1555+731G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197051903 | |||||||
| chr1:197052059 | C | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.1555+575G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052059 | |||||||
| chr1:197052103 | C | T | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1555+531G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052103 | |||||||
| chr1:197052399 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0132 a0001c0001t0001g0134 others(3): Show |
12 | HG00609.hp2 HG02293.hp1 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1555+235G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052399 | |||||||
| chr1:197052413 | C | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1555+221G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052413 | |||||||
| chr1:197052445 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | NA19000.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1555+189C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052445 | |||||||
| chr1:197052463 | C | CCTGCACA others(2): Show |
3 | a0003c0014t0004g0042 a0004c0005t0004g0032 a0004c0005t0004g0126 |
4 | HG02818.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1555+162_1555+170d others(11): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052463 | |||||||
| chr1:197052618 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1555+16T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 9/11 | chr1 | 197052618 | |||||||
| chr1:197052963 | TCTCA | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1355-133_1355-130d others(6): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197052963 | |||||||
| chr1:197053074 | T | C | 1 | a0002c0003t0001g0023 | 2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1355-240A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053074 | |||||||
| chr1:197053163 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1355-329G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053163 | |||||||
| chr1:197053491 | C | T | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1355-657G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053491 | |||||||
| chr1:197053500 | C | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.1355-666G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053500 | |||||||
| chr1:197053579 | A | G | 1 | a0002c0003t0001g0051 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1355-745T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053579 | |||||||
| chr1:197053634 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1355-800G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053634 | |||||||
| chr1:197053638 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1355-804C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053638 | |||||||
| chr1:197053699 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1355-865C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053699 | |||||||
| chr1:197053723 | G | C | 1 | a0001c0002t0002g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1355-889C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053723 | |||||||
| chr1:197053775 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1355-941T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053775 | |||||||
| chr1:197053918 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1355-1084C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053918 | |||||||
| chr1:197053953 | C | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0165 a0008c0015t0001g0053 |
4 | HG02280.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355-1119G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197053953 | |||||||
| chr1:197054026 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(142): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1355-1192A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054026 | |||||||
| chr1:197054056 | G | A | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1355-1222C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054056 | |||||||
| chr1:197054145 | G | T | 1 | a0002c0003t0001g0014 | 3 | HG02258.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1355-1311C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054145 | |||||||
| chr1:197054281 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1354+1434A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054281 | |||||||
| chr1:197054577 | T | C | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1354+1138A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054577 | |||||||
| chr1:197054589 | T | TATAG | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1354+1125_1354+112 others(8): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054589 | |||||||
| chr1:197054687 | A | G | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1354+1028T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054687 | |||||||
| chr1:197054727 | C | T | 2 | a0002c0003t0001g0015 a0002c0003t0001g0050 |
4 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354+988G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054727 | |||||||
| chr1:197054751 | T | C | 1 | a0002c0003t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1354+964A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197054751 | |||||||
| chr1:197055354 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1354+361A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197055354 | |||||||
| chr1:197055513 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(131): Show |
267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1354+202C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 8/11 | chr1 | 197055513 | |||||||
| chr1:197056535 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1171+478A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 7/11 | chr1 | 197056535 | |||||||
| chr1:197056659 | C | T | 1 | a0002c0003t0001g0054 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1171+354G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 7/11 | chr1 | 197056659 | |||||||
| chr1:197056674 | C | T | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.1171+339G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 7/11 | chr1 | 197056674 | |||||||
| chr1:197057202 | A | G | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.986-4T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 6/11 | chr1 | 197057202 | |||||||
| chr1:197057471 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA19001.hp1 | splice_region_variant&intron_variant | LOW | c.806-6C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057471 | |||||||
| chr1:197057542 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(148): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.806-77T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057542 | |||||||
| chr1:197057662 | T | C | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.806-197A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057662 | |||||||
| chr1:197057716 | T | A | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.806-251A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057716 | |||||||
| chr1:197057751 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.806-286G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057751 | |||||||
| chr1:197057765 | A | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(139): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.806-300T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057765 | |||||||
| chr1:197057904 | C | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0165 a0008c0015t0001g0053 |
4 | HG02280.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.806-439G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057904 | |||||||
| chr1:197057985 | A | T | 6 | a0002c0003t0001g0006 a0002c0003t0001g0015 a0002c0003t0001g0047 others(3): Show |
14 | HG02622.hp1 HG02717.hp1 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.806-520T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197057985 | |||||||
| chr1:197058005 | A | G | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-540T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058005 | |||||||
| chr1:197058090 | C | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.806-625G>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058090 | |||||||
| chr1:197058184 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.806-719A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058184 | |||||||
| chr1:197058476 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(148): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.806-1011T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058476 | |||||||
| chr1:197058492 | A | G | 4 | a0003c0004t0003g0009 a0003c0014t0004g0042 a0004c0005t0004g0032 others(1): Show |
10 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.806-1027T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058492 | |||||||
| chr1:197058581 | T | C | 1 | a0001c0002t0002g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.806-1116A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058581 | |||||||
| chr1:197058619 | C | T | 1 | a0001c0002t0002g0024 | 2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.806-1154G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058619 | |||||||
| chr1:197058872 | C | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
5 | HG00597.hp1 HG02027.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.806-1407G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197058872 | |||||||
| chr1:197059030 | G | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0165 a0008c0015t0001g0053 |
4 | HG02280.hp2 HG03139.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+1336C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059030 | |||||||
| chr1:197059035 | A | C | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.805+1331T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059035 | |||||||
| chr1:197059257 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.805+1109T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059257 | |||||||
| chr1:197059504 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.805+862T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059504 | |||||||
| chr1:197059551 | A | G | 1 | a0001c0002t0002g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.805+815T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059551 | |||||||
| chr1:197059556 | C | T | 1 | a0001c0002t0002g0061 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.805+810G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059556 | |||||||
| chr1:197059579 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.805+787A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059579 | |||||||
| chr1:197059671 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.805+695A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059671 | |||||||
| chr1:197059750 | T | G | 1 | a0002c0003t0001g0054 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.805+616A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197059750 | |||||||
| chr1:197060215 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.805+151C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 5/11 | chr1 | 197060215 | |||||||
| chr1:197060579 | GTTTA | G | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-41_629-38delTA others(2): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 4/11 | chr1 | 197060579 | |||||||
| chr1:197060892 | A | G | 1 | a0001c0001t0001g0017 | 3 | NA18952.hp2 NA18953.hp2 NA19011.hp2 |
splice_region_variant&intron_variant | LOW | c.628+7T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 4/11 | chr1 | 197060892 | |||||||
| chr1:197061107 | CT | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(104): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.452-33delA | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061107 | |||||||
| chr1:197061151 | T | C | 3 | a0003c0004t0003g0009 a0004c0005t0004g0032 a0004c0005t0004g0126 |
9 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-76A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061151 | |||||||
| chr1:197061187 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.452-112T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061187 | |||||||
| chr1:197061319 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.452-244T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061319 | |||||||
| chr1:197061356 | G | T | 4 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-281C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061356 | |||||||
| chr1:197061502 | T | A | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+282A>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061502 | |||||||
| chr1:197061666 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.451+118T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061666 | |||||||
| chr1:197061699 | A | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(54): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.451+85T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061699 | |||||||
| chr1:197061733 | A | G | 3 | a0002c0003t0001g0041 a0002c0003t0001g0056 a0002c0003t0001g0057 |
3 | HG01175.hp2 HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.451+51T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 3/11 | chr1 | 197061733 | |||||||
| chr1:197062417 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.265+440T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/11 | chr1 | 197062417 | |||||||
| chr1:197062453 | A | G | 1 | a0001c0002t0002g0059 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.265+404T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/11 | chr1 | 197062453 | |||||||
| chr1:197062534 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(134): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.265+323A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/11 | chr1 | 197062534 | |||||||
| chr1:197062652 | A | G | 1 | a0001c0001t0001g0019 | 3 | HG01074.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.265+205T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/11 | chr1 | 197062652 | |||||||
| chr1:197062718 | T | C | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+139A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/11 | chr1 | 197062718 | |||||||
| chr1:197062772 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG02132.hp2 NA18949.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.265+85C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 2/11 | chr1 | 197062772 | |||||||
| chr1:197063215 | C | G | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.65-158G>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063215 | |||||||
| chr1:197063215 | C | T | 1 | a0003c0004t0003g0009 | 6 | HG02523.hp2 NA18612.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-158G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063215 | |||||||
| chr1:197063245 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.65-188C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063245 | |||||||
| chr1:197063255 | A | T | 3 | a0003c0004t0003g0009 a0004c0005t0004g0032 a0004c0005t0004g0126 |
9 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.65-198T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063255 | |||||||
| chr1:197063393 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.65-336A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063393 | |||||||
| chr1:197063459 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0077 |
3 | HG00741.hp2 HG01168.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.65-402G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063459 | |||||||
| chr1:197063634 | A | C | 1 | a0002c0003t0001g0014 | 3 | HG02258.hp2 HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.65-577T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063634 | |||||||
| chr1:197063640 | G | A | 1 | a0002c0003t0001g0055 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.65-583C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063640 | |||||||
| chr1:197063773 | T | C | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-716A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063773 | |||||||
| chr1:197063863 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.65-806C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063863 | |||||||
| chr1:197063913 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(134): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.65-856C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063913 | |||||||
| chr1:197063992 | G | C | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-935C>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197063992 | |||||||
| chr1:197064045 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0156 a0001c0001t0001g0157 others(4): Show |
8 | NA18949.hp1 NA18977.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-988A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197064045 | |||||||
| chr1:197064086 | G | T | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-1029C>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197064086 | |||||||
| chr1:197064792 | A | C | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1735T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197064792 | |||||||
| chr1:197064794 | A | C | 1 | a0002c0003t0001g0012 | 4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1737T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197064794 | |||||||
| chr1:197064894 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.65-1837G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197064894 | |||||||
| chr1:197064966 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.65-1909G>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197064966 | |||||||
| chr1:197065410 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64+1750A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065410 | |||||||
| chr1:197065414 | A | T | 3 | a0002c0006t0001g0033 a0002c0006t0001g0128 a0010c0016t0001g0127 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1746T>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065414 | |||||||
| chr1:197065596 | A | G | 3 | a0003c0004t0003g0009 a0004c0005t0004g0032 a0004c0005t0004g0126 |
9 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1564T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065596 | |||||||
| chr1:197065644 | A | G | 4 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0125 others(1): Show |
4 | HG02145.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1516T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065644 | |||||||
| chr1:197065667 | CTGTGAGT others(39): Show |
C | 1 | a0001c0002t0001g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64+1447_64+1492del others(46): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065667 | |||||||
| chr1:197065691 | C | T | 3 | a0003c0004t0003g0009 a0004c0005t0004g0032 a0004c0005t0004g0126 |
9 | HG02523.hp2 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+1469G>A | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065691 | |||||||
| chr1:197065696 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(105): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.64+1464A>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065696 | |||||||
| chr1:197065824 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64+1336C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065824 | |||||||
| chr1:197065990 | GCTTA | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(53): Show |
111 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.64+1166_64+1169del others(4): Show |
F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065990 | |||||||
| chr1:197065995 | C | CT | 25 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0016 others(22): Show |
66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.64+1164dupA | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197065995 | |||||||
| chr1:197066074 | G | A | 2 | a0002c0003t0001g0056 a0002c0003t0001g0057 |
2 | HG01175.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.64+1086C>T | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197066074 | |||||||
| chr1:197066141 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.64+1019T>C | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197066141 | |||||||
| chr1:197066408 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(137): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.64+752A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197066408 | |||||||
| chr1:197066544 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.64+616A>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197066544 | |||||||
| chr1:197067065 | A | C | 1 | a0001c0002t0001g0020 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.64+95T>G | F13B | ENSG00000143278.5 | transcript | ENST00000367412.2 | protein_coding | 1/11 | chr1 | 197067065 |