Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10505 |
| ensemblid | ENSG00000135622.13 |
| hgncid | 10734 |
| symbol | SEMA4F |
| name | ssemaphorin 4F |
| refseq_nuc | NM_004263.5 |
| refseq_prot | NP_004254.2 |
| ensembl_nuc | ENST00000357877.7 |
| ensembl_prot | ENSP00000350547.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 74654247 |
| end | 74683841 |
| strand | + |
| ver | v1.2 |
| region | chr2:74654247-74683841 |
| region5000 | chr2:74649247-74688841 |
| regionname0 | SEMA4F_chr2_74654247_74683841 |
| regionname5000 | SEMA4F_chr2_74649247_74688841 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 770 | 282 | 88 | 47 | 123 | 3 | 19 | 91 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0002 | 0/0 | 770 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0003 | 0/0 | 770 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0004 | 0/0 | 687 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(682): Show |
chr2 | 74649247 | 74688841 |
| a0005 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0006 | 0/0 | 770 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPACA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0007 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MSACA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0008 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0009 | 0/0 | 770 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0010 | 0/0 | 770 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0011 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| a0012 | 0/0 | 770 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | MPASA others(765): Show |
chr2 | 74649247 | 74688841 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2310 | 248 | 85 | 44 | 99 | 3 | 15 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0001c0002 | 0/0 | 2310 | 26 | 1 | 1 | 20 | 0 | 4 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0001c0003 | 0/0 | 2310 | 3 | 0 | 0 | 3 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0001c0006 | 0/0 | 2310 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0001c0008 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0001c0009 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0001c0012 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0002c0004 | 0/0 | 2310 | 2 | 0 | 1 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0003c0005 | 0/0 | 2310 | 2 | 0 | 2 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0004c0013 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0004c0015 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0005c0017 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0006c0018 | 0/0 | 2310 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0007c0019 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGTC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0008c0007 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0009c0014 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0010c0016 | 0/0 | 2310 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0011c0011 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 | ||
| a0012c0010 | 0/0 | 2310 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | ATGCC others(2305): Show |
chr2 | 74649247 | 74688841 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6075 | 98 | 12 | 10 | 70 | 1 | 5 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0002 | 1/1 | 6075 | 79 | 13 | 28 | 26 | 2 | 8 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0003 | 0/0 | 6076 | 14 | 14 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6071): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0004 | 0/0 | 6075 | 9 | 9 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0005 | 0/0 | 6075 | 6 | 4 | 1 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0006 | 0/0 | 6075 | 9 | 7 | 2 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0007 | 0/0 | 6075 | 9 | 7 | 2 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0008 | 0/0 | 6074 | 5 | 4 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6069): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0009 | 0/0 | 6074 | 4 | 4 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6069): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0010 | 0/0 | 6075 | 3 | 3 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0011 | 0/0 | 6075 | 3 | 3 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0012 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0013 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0017 | 0/0 | 6074 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6069): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0018 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0019 | 0/0 | 6074 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6069): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0020 | 0/0 | 6076 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6071): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0022 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0023 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0001t0024 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0002t0001 | 0/0 | 6075 | 24 | 0 | 1 | 20 | 0 | 3 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0002t0004 | 0/0 | 6075 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0002t0021 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0003t0001 | 0/0 | 6075 | 3 | 0 | 0 | 3 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0006t0005 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0006t0016 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0008t0014 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0009t0002 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0001c0012t0001 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0002c0004t0002 | 0/0 | 6075 | 2 | 0 | 1 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0003c0005t0001 | 0/0 | 6075 | 2 | 0 | 2 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0004c0013t0005 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0004c0015t0002 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0005c0017t0005 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0006c0018t0004 | 0/0 | 6075 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0007c0019t0015 | 0/0 | 6076 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6071): Show |
chr2 | 74649247 | 74688841 |
| a0008c0007t0001 | 0/0 | 6075 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0009c0014t0003 | 0/0 | 6076 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6071): Show |
chr2 | 74649247 | 74688841 |
| a0010c0016t0002 | 0/0 | 6075 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0011c0011t0001 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| a0012c0010t0001 | 0/0 | 6075 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | GTTTC others(6070): Show |
chr2 | 74649247 | 74688841 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 1 | 0 | 12 | 0 | 3 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0004 | 0/0 | 8 | 2 | 0 | 6 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0001 | 0/0 | 27 | 8 | 11 | 7 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0005 | 0/0 | 7 | 2 | 2 | 2 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0033 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0008g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0009g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0010g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0011g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0017g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0018g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0020g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0022g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0023g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0001t0024g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0003 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0002t0021g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0006t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0006t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0008t0014g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0009t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0001c0012t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0002c0004t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0003c0005t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0004c0013t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0004c0015t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0005c0017t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0006c0018t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0007c0019t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0008c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0009c0014t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0010c0016t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0011c0011t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| a0012c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0134 | EUR | FIN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00438 | hp1 | a0001 | c0001 | t0018 | g0064 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00438 | hp2 | a0001 | c0012 | t0001 | g0084 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00642 | hp2 | a0002 | c0004 | t0002 | g0014 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00673 | hp1 | a0001 | c0001 | t0020 | g0071 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00733 | hp1 | a0003 | c0005 | t0001 | g0037 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00735 | hp1 | a0005 | c0017 | t0005 | g0143 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00735 | hp2 | a0003 | c0005 | t0001 | g0037 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0146 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0158 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0046 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0042 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0080 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01256 | hp2 | a0006 | c0018 | t0004 | g0050 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01884 | hp1 | a0001 | c0001 | t0023 | g0104 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0147 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01928 | hp2 | a0001 | c0009 | t0002 | g0020 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02165 | hp1 | a0001 | c0001 | t0012 | g0116 | EAS | CDX | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02257 | hp2 | a0001 | c0006 | t0005 | g0136 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02615 | hp2 | a0007 | c0019 | t0015 | g0051 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0031 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02717 | hp2 | a0001 | c0001 | t0024 | g0027 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02735 | hp1 | a0001 | c0002 | t0004 | g0059 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0086 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0031 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0157 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0132 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02897 | hp1 | a0008 | c0007 | t0001 | g0040 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0130 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0046 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0138 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0057 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0054 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03453 | hp2 | a0001 | c0002 | t0021 | g0049 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03486 | hp2 | a0004 | c0013 | t0005 | g0140 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0159 | AFR | GWD | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03831 | hp1 | a0001 | c0001 | t0017 | g0144 | SAS | BEB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG04184 | hp2 | a0010 | c0016 | t0002 | g0005 | SAS | BEB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | YRI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | YRI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | YRI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | YRI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18946 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18952 | hp1 | a0011 | c0011 | t0001 | g0004 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19001 | hp1 | a0012 | c0010 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19030 | hp1 | a0001 | c0001 | t0011 | g0123 | AFR | LWK | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | LWK | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | LWK | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19085 | hp2 | a0004 | c0015 | t0002 | g0001 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | YRI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | YRI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20129 | hp1 | a0001 | c0001 | t0022 | g0154 | AFR | ASW | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | ASW | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | TSI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20805 | hp2 | a0002 | c0004 | t0002 | g0014 | EUR | TSI | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | GIH | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01123 | hp1 | a0001 | c0008 | t0014 | g0087 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG03471 | hp2 | a0009 | c0014 | t0003 | g0055 | AFR | MSL | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| HG06807 | hp2 | a0001 | c0006 | t0016 | g0135 | AFR | USA | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | USA | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | USA | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0097 | REF | REF | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0033 | REF | REF | SEMA4F_chr2_74649247_74688841 | SEMA4F | chr2 | 74649247 | 74688841 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74654380 | C | T | 1 | a0007 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.4C>T | p.Pro2Ser | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/14 | 134/6075 | 4/2313 | 2/770 | chr2 | 74654380 | |||
| chr2:74654387 | C | G | 2 | a0006 a0007 |
2 | HG01256.hp2 HG02615.hp2 |
missense_variant | MODERATE | c.11C>G | p.Ser4Cys | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/14 | 141/6075 | 11/2313 | 4/770 | chr2 | 74654387 | |||
| chr2:74656555 | G | A | 1 | a0008 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.167G>A | p.Arg56Gln | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/14 | 297/6075 | 167/2313 | 56/770 | chr2 | 74656555 | |||
| chr2:74656623 | G | A | 1 | a0002 | 2 | HG00642.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.235G>A | p.Val79Ile | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/14 | 365/6075 | 235/2313 | 79/770 | chr2 | 74656623 | |||
| chr2:74673773 | G | A | 1 | a0003 | 2 | HG00733.hp1 HG00735.hp2 |
missense_variant | MODERATE | c.767G>A | p.Arg256Gln | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/14 | 897/6075 | 767/2313 | 256/770 | chr2 | 74673773 | |||
| chr2:74674646 | C | T | 1 | a0005 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.971C>T | p.Pro324Leu | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 8/14 | 1101/6075 | 971/2313 | 324/770 | chr2 | 74674646 | |||
| chr2:74674901 | A | G | 1 | a0010 | 1 | HG04184.hp2 | missense_variant | MODERATE | c.1015A>G | p.Ile339Val | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 9/14 | 1145/6075 | 1015/2313 | 339/770 | chr2 | 74674901 | |||
| chr2:74675222 | G | A | 1 | a0012 | 1 | NA19001.hp1 | missense_variant | MODERATE | c.1210G>A | p.Val404Ile | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 10/14 | 1340/6075 | 1210/2313 | 404/770 | chr2 | 74675222 | |||
| chr2:74679670 | G | A | 1 | a0011 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1774G>A | p.Ala592Thr | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1904/6075 | 1774/2313 | 592/770 | chr2 | 74679670 | |||
| chr2:74679694 | C | T | 1 | a0004 | 1 | NA19085.hp2 | stop_gained | HIGH | c.1798C>T | p.Gln600* | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1928/6075 | 1798/2313 | 600/770 | chr2 | 74679694 | |||
| chr2:74679943 | C | T | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.2047C>T | p.Arg683Cys | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2177/6075 | 2047/2313 | 683/770 | chr2 | 74679943 | |||
| chr2:74679958 | C | T | 1 | a0004 | 1 | HG03486.hp2 | stop_gained | HIGH | c.2062C>T | p.Arg688* | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2192/6075 | 2062/2313 | 688/770 | chr2 | 74679958 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74673461 | G | T | 1 | a0001c0002 | 26 | HG00621.hp1 HG01106.hp2 HG02132.hp2 others(23): Show |
synonymous_variant | LOW | c.555G>T | p.Gly185Gly | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 6/14 | 685/6075 | 555/2313 | 185/770 | chr2 | 74673461 | |||
| chr2:74673500 | G | A | 1 | a0001c0008 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.594G>A | p.Thr198Thr | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 6/14 | 724/6075 | 594/2313 | 198/770 | chr2 | 74673500 | |||
| chr2:74673554 | T | C | 1 | a0001c0009 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.648T>C | p.Asp216Asp | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 6/14 | 778/6075 | 648/2313 | 216/770 | chr2 | 74673554 | |||
| chr2:74674506 | C | T | 1 | a0001c0006 | 2 | HG02257.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.831C>T | p.Leu277Leu | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 8/14 | 961/6075 | 831/2313 | 277/770 | chr2 | 74674506 | |||
| chr2:74675239 | G | C | 1 | a0001c0003 | 3 | NA18946.hp2 NA18956.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.1227G>C | p.Arg409Arg | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 10/14 | 1357/6075 | 1227/2313 | 409/770 | chr2 | 74675239 | |||
| chr2:74680053 | C | G | 1 | a0001c0012 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.2157C>G | p.Pro719Pro | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2287/6075 | 2157/2313 | 719/770 | chr2 | 74680053 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74654338 | C | G | 1 | a0001c0001t0024 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/14 | 39 | chr2 | 74654338 | ||||||
| chr2:74680566 | C | T | 1 | a0001c0001t0023 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 357 | chr2 | 74680566 | ||||||
| chr2:74680837 | A | G | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
206 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*628A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 628 | chr2 | 74680837 | ||||||
| chr2:74680915 | T | C | 1 | a0001c0001t0012 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*706T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 706 | chr2 | 74680915 | ||||||
| chr2:74681172 | C | T | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
185 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*963C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 963 | chr2 | 74681172 | ||||||
| chr2:74681555 | T | C | 1 | a0001c0001t0018 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1346 | chr2 | 74681555 | ||||||
| chr2:74681674 | C | A | 3 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0023 |
11 | HG01192.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1465C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1465 | chr2 | 74681674 | ||||||
| chr2:74681676 | A | G | 2 | a0001c0001t0007 a0001c0001t0022 |
10 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1467A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1467 | chr2 | 74681676 | ||||||
| chr2:74681871 | A | G | 2 | a0001c0001t0008 a0001c0001t0017 |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1662A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1662 | chr2 | 74681871 | ||||||
| chr2:74681930 | C | T | 1 | a0001c0002t0021 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1721 | chr2 | 74681930 | ||||||
| chr2:74682110 | C | T | 2 | a0001c0001t0007 a0001c0001t0022 |
10 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1901C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 1901 | chr2 | 74682110 | ||||||
| chr2:74682302 | G | T | 1 | a0001c0001t0017 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2093 | chr2 | 74682302 | ||||||
| chr2:74682372 | C | T | 1 | a0001c0008t0014 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2163C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2163 | chr2 | 74682372 | ||||||
| chr2:74682415 | C | CA | 4 | a0001c0001t0003 a0001c0001t0020 a0007c0019t0015 others(1): Show |
17 | HG00673.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2222dupA | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2223 | INFO_REALIGN_3_PRIME | chr2 | 74682415 | |||||
| chr2:74682415 | CA | C | 3 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0019 |
7 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2222delA | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2222 | INFO_REALIGN_3_PRIME | chr2 | 74682415 | |||||
| chr2:74682555 | G | A | 1 | a0001c0001t0013 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2346G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2346 | chr2 | 74682555 | ||||||
| chr2:74682638 | T | C | 12 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0018 others(9): Show |
137 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2429T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2429 | chr2 | 74682638 | ||||||
| chr2:74683035 | GC | G | 1 | a0001c0001t0009 | 4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2830delC | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2830 | INFO_REALIGN_3_PRIME | chr2 | 74683035 | |||||
| chr2:74683150 | G | A | 1 | a0001c0006t0016 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2941G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 2941 | chr2 | 74683150 | ||||||
| chr2:74683439 | C | T | 1 | a0001c0001t0009 | 4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3230C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 3230 | chr2 | 74683439 | ||||||
| chr2:74683576 | G | T | 1 | a0001c0001t0007 | 9 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3367G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 3367 | chr2 | 74683576 | ||||||
| chr2:74683628 | C | T | 1 | a0001c0001t0011 | 3 | HG03209.hp1 NA19030.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3419C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 3419 | chr2 | 74683628 | ||||||
| chr2:74683740 | G | C | 1 | a0001c0001t0010 | 3 | HG02717.hp1 HG02818.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3531G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 14/14 | 3531 | chr2 | 74683740 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:74654535 | G | T | 8 | a0001c0001t0007g0046 a0001c0001t0007g0047 a0001c0001t0007g0155 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.145+14G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74654535 | |||||||
| chr2:74654580 | C | T | 3 | a0001c0001t0003g0151 a0001c0001t0003g0152 a0001c0001t0003g0153 |
3 | HG02145.hp2 HG02886.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.145+59C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74654580 | |||||||
| chr2:74654646 | C | A | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.145+125C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74654646 | |||||||
| chr2:74654705 | T | G | 1 | a0001c0002t0021g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.145+184T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74654705 | |||||||
| chr2:74654739 | G | C | 2 | a0006c0018t0004g0050 a0007c0019t0015g0051 |
2 | HG01256.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.145+218G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74654739 | |||||||
| chr2:74654978 | C | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG01261.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.145+457C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74654978 | |||||||
| chr2:74655067 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.145+546C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655067 | |||||||
| chr2:74655112 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.145+591T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655112 | |||||||
| chr2:74655414 | T | G | 1 | a0001c0001t0022g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.145+893T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655414 | |||||||
| chr2:74655580 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.146-954G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655580 | |||||||
| chr2:74655595 | T | A | 10 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(7): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.146-939T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655595 | |||||||
| chr2:74655931 | T | G | 1 | a0001c0001t0001g0018 | 2 | NA18959.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.146-603T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655931 | |||||||
| chr2:74655998 | A | G | 28 | a0001c0001t0002g0145 a0001c0001t0003g0009 a0001c0001t0003g0010 others(25): Show |
39 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.146-536A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74655998 | |||||||
| chr2:74656012 | A | AT | 8 | a0001c0001t0002g0134 a0001c0001t0004g0133 a0001c0001t0006g0042 others(5): Show |
10 | HG00323.hp2 HG01192.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.146-508dupT | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 74656012 | ||||||
| chr2:74656026 | T | G | 1 | a0001c0001t0002g0058 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.146-508T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74656026 | |||||||
| chr2:74656034 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.146-500A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74656034 | |||||||
| chr2:74656134 | A | G | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.146-400A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74656134 | |||||||
| chr2:74656200 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0058 a0001c0002t0004g0059 |
4 | HG00639.hp1 HG01071.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-334G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74656200 | |||||||
| chr2:74656382 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.146-152T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 1/13 | chr2 | 74656382 | |||||||
| chr2:74656791 | C | T | 8 | a0001c0001t0007g0046 a0001c0001t0007g0047 a0001c0001t0007g0155 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.297+106C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74656791 | |||||||
| chr2:74656824 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.297+139T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74656824 | |||||||
| chr2:74656826 | G | C | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+141G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74656826 | |||||||
| chr2:74656844 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.297+159T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74656844 | |||||||
| chr2:74656979 | T | C | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.297+294T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74656979 | |||||||
| chr2:74657022 | A | G | 3 | a0001c0003t0001g0126 a0001c0003t0001g0127 a0001c0003t0001g0128 |
3 | NA18946.hp2 NA18956.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.297+337A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657022 | |||||||
| chr2:74657184 | G | A | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.298-381G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657184 | |||||||
| chr2:74657302 | A | T | 9 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(6): Show |
16 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.298-263A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657302 | |||||||
| chr2:74657318 | T | C | 9 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(6): Show |
9 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-247T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657318 | |||||||
| chr2:74657350 | T | C | 1 | a0001c0006t0016g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.298-215T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657350 | |||||||
| chr2:74657422 | C | A | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.298-143C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657422 | |||||||
| chr2:74657484 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0134 |
3 | HG00323.hp2 HG01496.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.298-81A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 2/13 | chr2 | 74657484 | |||||||
| chr2:74657643 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0008c0007t0001g0040 |
3 | HG02630.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.357+19C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657643 | |||||||
| chr2:74657778 | T | C | 5 | a0001c0001t0002g0145 a0001c0001t0008g0016 a0001c0001t0008g0146 others(2): Show |
7 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.358-75T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657778 | |||||||
| chr2:74657797 | T | G | 1 | a0001c0001t0002g0062 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.358-56T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657797 | |||||||
| chr2:74657808 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.358-45C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657808 | |||||||
| chr2:74657809 | G | A | 3 | a0001c0001t0002g0020 a0001c0001t0002g0063 a0001c0009t0002g0020 |
3 | HG01346.hp1 HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.358-44G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657809 | |||||||
| chr2:74657819 | C | T | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.358-34C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657819 | |||||||
| chr2:74657838 | G | A | 1 | a0001c0001t0017g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.358-15G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 3/13 | chr2 | 74657838 | |||||||
| chr2:74657963 | T | G | 28 | a0001c0001t0002g0145 a0001c0001t0003g0009 a0001c0001t0003g0010 others(25): Show |
39 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.456+12T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74657963 | |||||||
| chr2:74657965 | T | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0021 others(3): Show |
15 | HG00438.hp1 HG00544.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.456+14T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74657965 | |||||||
| chr2:74657968 | G | T | 10 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(7): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.456+17G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74657968 | |||||||
| chr2:74658017 | G | T | 1 | a0005c0017t0005g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.456+66G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658017 | |||||||
| chr2:74658022 | A | G | 1 | a0005c0017t0005g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.456+71A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658022 | |||||||
| chr2:74658260 | G | A | 1 | a0001c0001t0002g0022 | 2 | NA18940.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.456+309G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658260 | |||||||
| chr2:74658316 | C | T | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.456+365C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658316 | |||||||
| chr2:74658481 | T | C | 10 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(7): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.456+530T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658481 | |||||||
| chr2:74658509 | A | G | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.456+558A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658509 | |||||||
| chr2:74658538 | A | G | 10 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(7): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.456+587A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658538 | |||||||
| chr2:74658650 | G | A | 28 | a0001c0001t0002g0145 a0001c0001t0003g0009 a0001c0001t0003g0010 others(25): Show |
39 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.456+699G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658650 | |||||||
| chr2:74658720 | T | C | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+769T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658720 | |||||||
| chr2:74658797 | C | T | 1 | a0001c0001t0011g0123 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.456+846C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658797 | |||||||
| chr2:74658904 | C | G | 2 | a0001c0001t0002g0039 a0001c0001t0002g0122 |
3 | HG01123.hp2 HG01192.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.456+953C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74658904 | |||||||
| chr2:74659679 | C | T | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+1728C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74659679 | |||||||
| chr2:74659781 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0121 |
3 | NA18941.hp1 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.456+1830C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74659781 | |||||||
| chr2:74659796 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.456+1845T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74659796 | |||||||
| chr2:74659959 | T | C | 1 | a0001c0002t0001g0068 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.456+2008T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74659959 | |||||||
| chr2:74660036 | C | G | 7 | a0001c0001t0007g0046 a0001c0001t0007g0047 a0001c0001t0007g0155 others(4): Show |
9 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.456+2085C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660036 | |||||||
| chr2:74660048 | A | T | 7 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(4): Show |
7 | HG00735.hp1 HG01243.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.456+2097A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660048 | |||||||
| chr2:74660376 | A | G | 2 | a0001c0001t0001g0012 a0003c0005t0001g0037 |
6 | HG00733.hp1 HG00735.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-2356A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660376 | |||||||
| chr2:74660483 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.457-2249C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660483 | |||||||
| chr2:74660484 | A | G | 1 | a0001c0001t0013g0054 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.457-2248A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660484 | |||||||
| chr2:74660506 | G | A | 2 | a0001c0001t0007g0155 a0001c0001t0007g0156 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.457-2226G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660506 | |||||||
| chr2:74660631 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.457-2101G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660631 | |||||||
| chr2:74660655 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0119 a0001c0001t0011g0008 others(1): Show |
7 | HG02109.hp1 HG02280.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.457-2077C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660655 | |||||||
| chr2:74660693 | C | G | 6 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(3): Show |
6 | HG01243.hp2 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-2039C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660693 | |||||||
| chr2:74660803 | G | A | 6 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(3): Show |
6 | HG01243.hp2 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.457-1929G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74660803 | |||||||
| chr2:74661362 | T | C | 1 | a0005c0017t0005g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.457-1370T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661362 | |||||||
| chr2:74661368 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.457-1364C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661368 | |||||||
| chr2:74661481 | A | G | 5 | a0001c0001t0002g0145 a0001c0001t0008g0016 a0001c0001t0008g0146 others(2): Show |
7 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.457-1251A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661481 | |||||||
| chr2:74661535 | G | A | 1 | a0001c0006t0016g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.457-1197G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661535 | |||||||
| chr2:74661656 | G | C | 12 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(9): Show |
19 | HG01256.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.457-1076G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661656 | |||||||
| chr2:74661691 | T | G | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.457-1041T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661691 | |||||||
| chr2:74661726 | A | C | 1 | a0001c0001t0004g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.457-1006A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661726 | |||||||
| chr2:74661858 | T | A | 2 | a0001c0001t0002g0014 a0002c0004t0002g0014 |
3 | HG00642.hp2 HG03490.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.457-874T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74661858 | |||||||
| chr2:74662102 | A | AC | 12 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(9): Show |
19 | HG01256.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.457-629dupC | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 74662102 | ||||||
| chr2:74662307 | A | G | 12 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(9): Show |
19 | HG01256.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.457-425A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74662307 | |||||||
| chr2:74662328 | G | A | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.457-404G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74662328 | |||||||
| chr2:74662541 | G | A | 1 | a0001c0001t0002g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.457-191G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74662541 | |||||||
| chr2:74662585 | T | G | 1 | a0001c0001t0001g0023 | 2 | HG00558.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.457-147T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74662585 | |||||||
| chr2:74662619 | T | G | 1 | a0001c0001t0002g0070 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.457-113T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 4/13 | chr2 | 74662619 | |||||||
| chr2:74662926 | A | G | 1 | a0001c0001t0007g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.550+101A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74662926 | |||||||
| chr2:74663019 | T | G | 8 | a0001c0001t0007g0046 a0001c0001t0007g0047 a0001c0001t0007g0155 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.550+194T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663019 | |||||||
| chr2:74663136 | A | G | 1 | a0001c0001t0012g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.550+311A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663136 | |||||||
| chr2:74663323 | A | C | 2 | a0001c0001t0005g0141 a0001c0001t0005g0142 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.550+498A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663323 | |||||||
| chr2:74663389 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.550+564A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663389 | |||||||
| chr2:74663415 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.550+590A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663415 | |||||||
| chr2:74663449 | G | A | 11 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(8): Show |
18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.550+624G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663449 | |||||||
| chr2:74663563 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA19001.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.550+738C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663563 | |||||||
| chr2:74663725 | G | T | 1 | a0001c0002t0001g0111 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.550+900G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663725 | |||||||
| chr2:74663784 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.550+959C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663784 | |||||||
| chr2:74663895 | T | G | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+1070T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663895 | |||||||
| chr2:74663988 | C | A | 9 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(6): Show |
16 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.550+1163C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663988 | |||||||
| chr2:74663999 | T | C | 3 | a0001c0001t0005g0137 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG01243.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.550+1174T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74663999 | |||||||
| chr2:74664065 | C | G | 1 | a0001c0001t0005g0137 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.550+1240C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74664065 | |||||||
| chr2:74664390 | G | A | 1 | a0001c0001t0020g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.550+1565G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74664390 | |||||||
| chr2:74664439 | T | TGTGCATA others(301): Show |
2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+1628_550+1629i others(310): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74664439 | ||||||
| chr2:74664806 | T | C | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+1981T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74664806 | |||||||
| chr2:74664852 | T | C | 2 | a0001c0002t0001g0072 a0001c0002t0001g0073 |
2 | NA18956.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.550+2027T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74664852 | |||||||
| chr2:74664872 | C | T | 6 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(3): Show |
6 | HG01243.hp2 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+2047C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74664872 | |||||||
| chr2:74664971 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.550+2146G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74664971 | |||||||
| chr2:74665045 | C | A | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550+2220C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665045 | |||||||
| chr2:74665045 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.550+2220C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665045 | |||||||
| chr2:74665091 | T | C | 1 | a0001c0006t0005g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.550+2266T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665091 | |||||||
| chr2:74665228 | C | CT | 11 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0113 others(8): Show |
12 | HG01175.hp2 HG01346.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.550+2422dupT | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74665228 | ||||||
| chr2:74665228 | CT | C | 23 | a0001c0001t0001g0110 a0001c0001t0003g0009 a0001c0001t0003g0010 others(20): Show |
32 | HG00323.hp1 HG00735.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.550+2422delT | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74665228 | ||||||
| chr2:74665232 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0009g0044 a0001c0001t0009g0045 |
5 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.550+2407T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665232 | |||||||
| chr2:74665238 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.550+2413T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665238 | |||||||
| chr2:74665265 | T | C | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.550+2440T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665265 | |||||||
| chr2:74665279 | G | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0077 |
2 | HG01928.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.550+2454G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665279 | |||||||
| chr2:74665293 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.550+2468A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665293 | |||||||
| chr2:74665375 | G | A | 1 | a0001c0001t0018g0064 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.550+2550G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665375 | |||||||
| chr2:74665480 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG02015.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.550+2655C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665480 | |||||||
| chr2:74665518 | C | T | 4 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+2693C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665518 | |||||||
| chr2:74665551 | T | C | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+2726T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665551 | |||||||
| chr2:74665610 | G | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0122 |
3 | HG01123.hp2 HG01192.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.550+2785G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665610 | |||||||
| chr2:74665630 | A | G | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.550+2805A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665630 | |||||||
| chr2:74665658 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.550+2833T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665658 | |||||||
| chr2:74665661 | A | G | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.550+2836A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665661 | |||||||
| chr2:74665741 | A | G | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.550+2916A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665741 | |||||||
| chr2:74665875 | G | A | 4 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+3050G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665875 | |||||||
| chr2:74665902 | GT | G | 23 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(20): Show |
34 | HG00735.hp1 HG00741.hp2 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.550+3092delT | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74665902 | ||||||
| chr2:74665910 | T | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0125 a0008c0007t0001g0040 |
3 | HG02630.hp1 HG02897.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.550+3085T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665910 | |||||||
| chr2:74665913 | T | G | 2 | a0001c0001t0002g0079 a0001c0001t0006g0080 |
2 | HG01243.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.550+3088T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665913 | |||||||
| chr2:74665914 | T | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(72): Show |
144 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.550+3089T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665914 | |||||||
| chr2:74665940 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.550+3115C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665940 | |||||||
| chr2:74665947 | G | A | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.550+3122G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665947 | |||||||
| chr2:74665993 | C | T | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.550+3168C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74665993 | |||||||
| chr2:74666001 | A | G | 1 | a0001c0001t0002g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.550+3176A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666001 | |||||||
| chr2:74666048 | C | T | 1 | a0001c0001t0007g0047 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.550+3223C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666048 | |||||||
| chr2:74666157 | C | T | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.550+3332C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666157 | |||||||
| chr2:74666172 | C | T | 15 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(12): Show |
19 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.550+3347C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666172 | |||||||
| chr2:74666355 | T | G | 1 | a0001c0001t0002g0076 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.550+3530T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666355 | |||||||
| chr2:74666412 | CT | C | 11 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(8): Show |
18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.550+3600delT | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74666412 | ||||||
| chr2:74666469 | C | T | 1 | a0001c0001t0001g0030 | 2 | NA18985.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.550+3644C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666469 | |||||||
| chr2:74666550 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.550+3725C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666550 | |||||||
| chr2:74666553 | A | T | 1 | a0005c0017t0005g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.550+3728A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666553 | |||||||
| chr2:74666640 | T | A | 6 | a0001c0001t0005g0137 a0001c0001t0005g0138 a0001c0001t0005g0139 others(3): Show |
6 | HG01243.hp2 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+3815T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74666640 | |||||||
| chr2:74667032 | G | A | 1 | a0001c0001t0009g0044 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.550+4207G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74667032 | |||||||
| chr2:74667121 | G | T | 4 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+4296G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74667121 | |||||||
| chr2:74667767 | G | A | 4 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.550+4942G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74667767 | |||||||
| chr2:74667953 | C | T | 1 | a0001c0001t0007g0047 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.550+5128C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74667953 | |||||||
| chr2:74668034 | C | G | 11 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(8): Show |
18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.550+5209C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668034 | |||||||
| chr2:74668075 | A | G | 10 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(7): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.550+5250A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668075 | |||||||
| chr2:74668183 | C | CTT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(112): Show |
198 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.551-5273_551-5272i others(4): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74668183 | ||||||
| chr2:74668221 | T | C | 27 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(24): Show |
38 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.551-5236T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668221 | |||||||
| chr2:74668474 | T | A | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.551-4983T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668474 | |||||||
| chr2:74668475 | A | T | 18 | a0001c0001t0001g0110 a0001c0001t0001g0125 a0001c0001t0003g0009 others(15): Show |
27 | HG00323.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.551-4982A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668475 | |||||||
| chr2:74668613 | G | GT | 7 | a0001c0001t0001g0075 a0001c0001t0001g0093 a0001c0001t0002g0121 others(4): Show |
7 | HG00597.hp2 HG00735.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-4830dupT | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74668613 | ||||||
| chr2:74668671 | C | T | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.551-4786C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668671 | |||||||
| chr2:74668754 | C | T | 3 | a0001c0001t0005g0137 a0001c0001t0005g0141 a0001c0001t0005g0142 |
3 | HG01243.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.551-4703C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668754 | |||||||
| chr2:74668818 | C | T | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-4639C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668818 | |||||||
| chr2:74668872 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.551-4585C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74668872 | |||||||
| chr2:74668929 | C | CA | 35 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0026 others(32): Show |
52 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.551-4504dupA | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74668929 | ||||||
| chr2:74668929 | C | CAA | 9 | a0001c0001t0002g0094 a0001c0001t0003g0017 a0001c0001t0003g0056 others(6): Show |
12 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.551-4505_551-4504d others(4): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74668929 | ||||||
| chr2:74668929 | CA | C | 8 | a0001c0001t0002g0100 a0001c0001t0004g0034 a0001c0001t0004g0048 others(5): Show |
8 | HG01167.hp1 HG01243.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.551-4504delA | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74668929 | ||||||
| chr2:74668929 | CAA | C | 4 | a0001c0001t0004g0015 a0001c0001t0004g0117 a0001c0001t0004g0133 others(1): Show |
6 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-4505_551-4504d others(4): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74668929 | ||||||
| chr2:74669023 | G | T | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.551-4434G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669023 | |||||||
| chr2:74669178 | C | T | 1 | a0001c0001t0010g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.551-4279C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669178 | |||||||
| chr2:74669512 | G | C | 7 | a0001c0001t0007g0046 a0001c0001t0007g0047 a0001c0001t0007g0155 others(4): Show |
9 | HG01167.hp1 HG01169.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.551-3945G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669512 | |||||||
| chr2:74669585 | A | AAAC | 14 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(11): Show |
21 | HG00735.hp1 HG01243.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.551-3842_551-3840d others(5): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74669585 | ||||||
| chr2:74669585 | AAACAAC | A | 4 | a0001c0001t0001g0085 a0001c0001t0008g0016 a0001c0001t0008g0146 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.551-3845_551-3840d others(8): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74669585 | ||||||
| chr2:74669754 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.551-3703T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669754 | |||||||
| chr2:74669798 | T | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
216 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.551-3659T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669798 | |||||||
| chr2:74669832 | C | T | 12 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(9): Show |
19 | HG01256.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-3625C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669832 | |||||||
| chr2:74669985 | T | A | 1 | a0001c0003t0001g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.551-3472T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74669985 | |||||||
| chr2:74670103 | G | A | 5 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0002g0062 others(2): Show |
7 | HG02040.hp2 HG02523.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.551-3354G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74670103 | |||||||
| chr2:74670218 | C | G | 1 | a0001c0001t0002g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.551-3239C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74670218 | |||||||
| chr2:74670251 | A | C | 11 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(8): Show |
18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.551-3206A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74670251 | |||||||
| chr2:74670346 | C | T | 1 | a0001c0001t0010g0057 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.551-3111C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74670346 | |||||||
| chr2:74670384 | C | T | 10 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(7): Show |
17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.551-3073C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74670384 | |||||||
| chr2:74670984 | CTAGGTCT others(23): Show |
C | 12 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(9): Show |
19 | HG01256.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-2469_551-2440d others(32): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 74670984 | ||||||
| chr2:74670996 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(153): Show |
275 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(272): Show |
intron_variant | MODIFIER | c.551-2461G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74670996 | |||||||
| chr2:74671003 | T | C | 1 | a0001c0001t0022g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.551-2454T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671003 | |||||||
| chr2:74671010 | A | T | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-2447A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671010 | |||||||
| chr2:74671019 | A | C | 1 | a0001c0001t0001g0029 | 2 | NA19010.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.551-2438A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671019 | |||||||
| chr2:74671082 | A | T | 1 | a0001c0002t0001g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.551-2375A>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671082 | |||||||
| chr2:74671083 | T | G | 27 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(24): Show |
38 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.551-2374T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671083 | |||||||
| chr2:74671087 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0122 |
3 | HG01123.hp2 HG01192.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.551-2370C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671087 | |||||||
| chr2:74671152 | T | C | 12 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(9): Show |
19 | HG01256.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-2305T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671152 | |||||||
| chr2:74671297 | A | G | 27 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(24): Show |
38 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.551-2160A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671297 | |||||||
| chr2:74671343 | C | A | 1 | a0001c0002t0001g0082 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.551-2114C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671343 | |||||||
| chr2:74671344 | G | A | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.551-2113G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671344 | |||||||
| chr2:74671467 | C | T | 1 | a0001c0012t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.551-1990C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671467 | |||||||
| chr2:74671513 | A | G | 2 | a0001c0006t0005g0136 a0001c0006t0016g0135 |
2 | HG02257.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.551-1944A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671513 | |||||||
| chr2:74671602 | A | G | 6 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(3): Show |
10 | HG00741.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.551-1855A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671602 | |||||||
| chr2:74671883 | G | A | 24 | a0001c0001t0003g0009 a0001c0001t0003g0151 a0001c0001t0003g0152 others(21): Show |
31 | HG00735.hp1 HG00741.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.551-1574G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671883 | |||||||
| chr2:74671890 | G | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(119): Show |
207 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.551-1567G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671890 | |||||||
| chr2:74671917 | T | G | 1 | a0005c0017t0005g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.551-1540T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671917 | |||||||
| chr2:74671923 | C | T | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-1534C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671923 | |||||||
| chr2:74671932 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.551-1525A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74671932 | |||||||
| chr2:74672128 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.551-1329G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74672128 | |||||||
| chr2:74672232 | G | A | 1 | a0001c0001t0004g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.551-1225G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74672232 | |||||||
| chr2:74672395 | C | T | 2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
4 | HG02257.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.551-1062C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74672395 | |||||||
| chr2:74672466 | C | T | 2 | a0001c0001t0006g0132 a0001c0001t0019g0130 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.551-991C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74672466 | |||||||
| chr2:74672680 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(120): Show |
208 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.551-777T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74672680 | |||||||
| chr2:74673368 | G | A | 57 | a0001c0001t0001g0099 a0001c0001t0002g0001 a0001c0001t0002g0005 others(54): Show |
104 | HG00323.hp2 HG00609.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.551-89G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 5/13 | chr2 | 74673368 | |||||||
| chr2:74673611 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(19): Show |
44 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.670+35G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 6/13 | chr2 | 74673611 | |||||||
| chr2:74674005 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.822+177C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/13 | chr2 | 74674005 | |||||||
| chr2:74674029 | T | G | 1 | a0001c0012t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.822+201T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/13 | chr2 | 74674029 | |||||||
| chr2:74674259 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(71): Show |
144 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.823-239A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/13 | chr2 | 74674259 | |||||||
| chr2:74674355 | C | G | 1 | a0001c0001t0002g0081 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.823-143C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/13 | chr2 | 74674355 | |||||||
| chr2:74674460 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.823-38T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/13 | chr2 | 74674460 | |||||||
| chr2:74674475 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(85): Show |
162 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.823-23C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 7/13 | chr2 | 74674475 | |||||||
| chr2:74674774 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1001+98G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 8/13 | chr2 | 74674774 | |||||||
| chr2:74674831 | A | G | 1 | a0001c0012t0001g0084 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1002-57A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 8/13 | chr2 | 74674831 | |||||||
| chr2:74674875 | C | T | 1 | a0001c0001t0009g0044 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1002-13C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 8/13 | chr2 | 74674875 | |||||||
| chr2:74675101 | A | C | 4 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-61A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 9/13 | chr2 | 74675101 | |||||||
| chr2:74675119 | C | T | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1150-43C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 9/13 | chr2 | 74675119 | |||||||
| chr2:74675463 | G | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0017 others(5): Show |
15 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1373-62G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 10/13 | chr2 | 74675463 | |||||||
| chr2:74675673 | C | A | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1482+39C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 11/13 | chr2 | 74675673 | |||||||
| chr2:74675728 | T | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(22): Show |
54 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1483-21T>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 11/13 | chr2 | 74675728 | |||||||
| chr2:74675745 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(115): Show |
203 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(200): Show |
splice_region_variant&intron_variant | LOW | c.1483-4A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 11/13 | chr2 | 74675745 | |||||||
| chr2:74676044 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0028 others(3): Show |
13 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1643+135C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74676044 | |||||||
| chr2:74676342 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1643+433T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74676342 | |||||||
| chr2:74676698 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
202 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.1643+789C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74676698 | |||||||
| chr2:74676869 | T | C | 1 | a0001c0001t0022g0154 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1643+960T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74676869 | |||||||
| chr2:74676962 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1643+1053C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74676962 | |||||||
| chr2:74676972 | G | C | 1 | a0001c0001t0002g0098 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1643+1063G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74676972 | |||||||
| chr2:74677012 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1643+1103C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677012 | |||||||
| chr2:74677142 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0024g0027 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1643+1233T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677142 | |||||||
| chr2:74677143 | CCA | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0017 |
6 | HG02109.hp2 HG02615.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1643+1236_1643+123 others(6): Show |
SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 74677143 | ||||||
| chr2:74677169 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1643+1260T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677169 | |||||||
| chr2:74677239 | A | G | 1 | a0001c0001t0001g0021 | 2 | NA18946.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1643+1330A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677239 | |||||||
| chr2:74677259 | G | T | 1 | a0001c0001t0023g0104 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1643+1350G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677259 | |||||||
| chr2:74677262 | T | C | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1643+1353T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677262 | |||||||
| chr2:74677444 | A | C | 4 | a0001c0001t0008g0016 a0001c0001t0008g0146 a0001c0001t0008g0147 others(1): Show |
6 | HG00741.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1643+1535A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677444 | |||||||
| chr2:74677932 | A | C | 1 | a0001c0002t0001g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1644-1344A>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677932 | |||||||
| chr2:74677959 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1644-1317A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74677959 | |||||||
| chr2:74678496 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1644-780A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74678496 | |||||||
| chr2:74678585 | G | A | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1644-691G>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74678585 | |||||||
| chr2:74678612 | C | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(118): Show |
206 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.1644-664C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74678612 | |||||||
| chr2:74678897 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0069 |
5 | NA18949.hp2 NA18986.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1644-379A>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74678897 | |||||||
| chr2:74678978 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1644-298G>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74678978 | |||||||
| chr2:74679025 | C | A | 2 | a0001c0001t0005g0138 a0004c0013t0005g0140 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1644-251C>A | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74679025 | |||||||
| chr2:74679073 | C | T | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
202 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.1644-203C>T | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74679073 | |||||||
| chr2:74679082 | G | C | 1 | a0006c0018t0004g0050 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1644-194G>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74679082 | |||||||
| chr2:74679161 | T | C | 1 | a0007c0019t0015g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1644-115T>C | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74679161 | |||||||
| chr2:74679227 | T | G | 1 | a0001c0001t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1644-49T>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 12/13 | chr2 | 74679227 | |||||||
| chr2:74679499 | C | G | 1 | a0001c0001t0002g0053 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1703-100C>G | SEMA4F | ENSG00000135622.13 | transcript | ENST00000357877.7 | protein_coding | 13/13 | chr2 | 74679499 |