Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4340 |
| ensemblid | ENSG00000204655.12 |
| hgncid | 7197 |
| symbol | MOG |
| name | myelin oligodendrocyte glycoprotein |
| refseq_nuc | NM_206809.4 |
| refseq_prot | NP_996532.2 |
| ensembl_nuc | ENST00000376917.8 |
| ensembl_prot | ENSP00000366115.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 29657092 |
| end | 29672365 |
| strand | + |
| ver | v1.2 |
| region | chr6:29657092-29672365 |
| region5000 | chr6:29652092-29677365 |
| regionname0 | MOG_chr6_29657092_29672365 |
| regionname5000 | MOG_chr6_29652092_29677365 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 247 | 310 | 59 | 54 | 148 | 12 | 36 | 111 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0002 | 0/0 | 247 | 78 | 14 | 13 | 48 | 1 | 2 | 38 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0003 | 0/0 | 246 | 29 | 19 | 5 | 3 | 1 | 1 | 3 | MOG_chr6_29652092_29677365 | MOG | MASLS others(241): Show |
chr6 | 29652092 | 29677365 |
| a0004 | 0/0 | 247 | 15 | 0 | 6 | 0 | 0 | 9 | 0 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0005 | 0/0 | 247 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0006 | 0/0 | 247 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0007 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0008 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| a0009 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | MASLS others(242): Show |
chr6 | 29652092 | 29677365 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 741 | 291 | 55 | 44 | 145 | 10 | 36 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0001c0004 | 0/0 | 741 | 17 | 4 | 9 | 3 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0001c0007 | 0/0 | 741 | 2 | 0 | 1 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0002c0002 | 0/0 | 741 | 78 | 14 | 13 | 48 | 1 | 2 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0003c0003 | 0/0 | 738 | 29 | 19 | 5 | 3 | 1 | 1 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(733): Show |
chr6 | 29652092 | 29677365 | ||
| a0004c0005 | 0/0 | 741 | 14 | 0 | 6 | 0 | 0 | 8 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0004c0011 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0005c0006 | 0/0 | 741 | 3 | 0 | 3 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0006c0012 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0007c0010 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0008c0008 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 | ||
| a0009c0009 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | ATGGC others(736): Show |
chr6 | 29652092 | 29677365 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2038 | 27 | 3 | 0 | 21 | 0 | 3 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0002 | 0/0 | 2042 | 38 | 1 | 0 | 33 | 0 | 4 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0003 | 0/0 | 2046 | 62 | 5 | 7 | 41 | 1 | 8 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0004 | 0/0 | 2042 | 30 | 7 | 7 | 12 | 3 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0005 | 0/1 | 2050 | 29 | 4 | 7 | 10 | 2 | 5 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2045): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0006 | 0/0 | 2042 | 25 | 0 | 3 | 17 | 0 | 5 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0007 | 0/0 | 2034 | 15 | 13 | 0 | 0 | 1 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2029): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0008 | 0/0 | 2046 | 12 | 0 | 4 | 4 | 2 | 2 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0010 | 0/0 | 2046 | 9 | 3 | 5 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0011 | 0/0 | 2030 | 9 | 6 | 1 | 0 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2025): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0014 | 0/0 | 2046 | 5 | 0 | 2 | 0 | 0 | 3 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0017 | 0/0 | 2026 | 5 | 4 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2021): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0019 | 0/0 | 2046 | 4 | 0 | 3 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0020 | 0/0 | 2034 | 4 | 0 | 2 | 1 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2029): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0021 | 0/0 | 2038 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0022 | 0/0 | 2046 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0024 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0025 | 0/0 | 2042 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0026 | 0/0 | 2050 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2045): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0027 | 0/0 | 2050 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2045): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0029 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0030 | 0/0 | 2054 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2049): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0031 | 0/0 | 2030 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2025): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0032 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2029): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0033 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0035 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0036 | 0/0 | 2038 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0037 | 0/0 | 2042 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0001t0038 | 0/0 | 2026 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2021): Show |
chr6 | 29652092 | 29677365 |
| a0001c0004t0001 | 0/0 | 2038 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0001c0004t0012 | 0/0 | 2038 | 9 | 1 | 6 | 1 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0001c0004t0013 | 0/0 | 2042 | 5 | 2 | 3 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0004t0034 | 0/0 | 2042 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0001c0007t0007 | 0/0 | 2034 | 2 | 0 | 1 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2029): Show |
chr6 | 29652092 | 29677365 |
| a0002c0002t0001 | 0/0 | 2038 | 44 | 14 | 9 | 19 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0002c0002t0002 | 0/0 | 2042 | 28 | 0 | 3 | 24 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0002c0002t0003 | 0/0 | 2046 | 4 | 0 | 0 | 4 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0002c0002t0005 | 0/0 | 2050 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2045): Show |
chr6 | 29652092 | 29677365 |
| a0002c0002t0028 | 0/0 | 2038 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0003c0003t0002 | 0/0 | 2039 | 3 | 3 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2034): Show |
chr6 | 29652092 | 29677365 |
| a0003c0003t0009 | 0/0 | 2043 | 10 | 5 | 0 | 3 | 1 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2038): Show |
chr6 | 29652092 | 29677365 |
| a0003c0003t0015 | 0/0 | 2047 | 6 | 5 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2042): Show |
chr6 | 29652092 | 29677365 |
| a0003c0003t0016 | 0/0 | 2039 | 5 | 2 | 3 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2034): Show |
chr6 | 29652092 | 29677365 |
| a0003c0003t0018 | 0/0 | 2022 | 4 | 3 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2017): Show |
chr6 | 29652092 | 29677365 |
| a0003c0003t0023 | 0/0 | 2039 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2034): Show |
chr6 | 29652092 | 29677365 |
| a0004c0005t0004 | 0/0 | 2042 | 10 | 0 | 5 | 0 | 0 | 5 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0004c0005t0006 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0004c0005t0014 | 0/0 | 2046 | 2 | 0 | 0 | 0 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0004c0005t0021 | 0/0 | 2038 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0004c0011t0002 | 0/0 | 2042 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0005c0006t0013 | 0/0 | 2042 | 3 | 0 | 3 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| a0006c0012t0021 | 0/0 | 2038 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0007c0010t0001 | 0/0 | 2038 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2033): Show |
chr6 | 29652092 | 29677365 |
| a0008c0008t0003 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2041): Show |
chr6 | 29652092 | 29677365 |
| a0009c0009t0002 | 0/0 | 2042 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | AGCAC others(2037): Show |
chr6 | 29652092 | 29677365 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 19 | 2 | 0 | 15 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0004 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0023 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0001 | 0/0 | 24 | 2 | 4 | 17 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0004 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0005 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0015 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0024 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0001 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0016 | 0/0 | 4 | 1 | 0 | 0 | 1 | 2 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0006 | 0/0 | 15 | 0 | 2 | 10 | 0 | 3 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0010 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0008g0005 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0008g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0010g0013 | 0/0 | 6 | 2 | 3 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0010g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0011g0017 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0014g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0014g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0014g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0014g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0017g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0017g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0017g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0019g0012 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0020g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0020g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0020g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0021g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0021g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0022g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0024g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0025g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0026g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0027g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0029g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0030g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0031g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0032g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0033g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0035g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0036g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0037g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0001t0038g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0012g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0012g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0012g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0012g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0012g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0013g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0013g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0004t0034g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0007t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0001c0007t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0002 | 0/0 | 25 | 9 | 4 | 11 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0021 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0022 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0005g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0002c0002t0028g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0009g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0015g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0015g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0015g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0016g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0016g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0016g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0018g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0018g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0018g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0003c0003t0023g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0004g0014 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0006g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0014g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0005t0021g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0004c0011t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0005c0006t0013g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0006c0012t0021g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0007c0010t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0008c0008t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| a0009c0009t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | GBR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | GBR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00140 | hp1 | a0003 | c0003 | t0009 | g0049 | EUR | GBR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0016 | EUR | GBR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0022 | EUR | FIN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00280 | hp2 | a0001 | c0004 | t0012 | g0028 | EUR | FIN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00423 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00558 | hp1 | a0002 | c0002 | t0005 | g0008 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00597 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | CHS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00639 | hp1 | a0001 | c0004 | t0013 | g0007 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0013 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00642 | hp2 | a0003 | c0003 | t0016 | g0180 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00733 | hp1 | a0001 | c0001 | t0010 | g0027 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00733 | hp2 | a0001 | c0001 | t0014 | g0046 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00735 | hp1 | a0004 | c0005 | t0004 | g0151 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00735 | hp2 | a0003 | c0003 | t0018 | g0175 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00738 | hp1 | a0004 | c0005 | t0004 | g0014 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01069 | hp1 | a0001 | c0004 | t0012 | g0127 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0069 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01070 | hp2 | a0001 | c0004 | t0012 | g0041 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01071 | hp1 | a0001 | c0004 | t0012 | g0007 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01071 | hp2 | a0001 | c0004 | t0012 | g0041 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01081 | hp1 | a0001 | c0007 | t0007 | g0083 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01081 | hp2 | a0003 | c0003 | t0016 | g0177 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01106 | hp2 | a0003 | c0003 | t0016 | g0049 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0013 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01109 | hp2 | a0004 | c0005 | t0004 | g0030 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01168 | hp1 | a0001 | c0001 | t0020 | g0007 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01169 | hp1 | a0001 | c0001 | t0020 | g0007 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01175 | hp1 | a0005 | c0006 | t0013 | g0007 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01175 | hp2 | a0001 | c0004 | t0013 | g0040 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01192 | hp2 | a0003 | c0003 | t0015 | g0019 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01243 | hp2 | a0001 | c0001 | t0017 | g0164 | AMR | PUR | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0013 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01255 | hp2 | a0001 | c0001 | t0037 | g0080 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01257 | hp1 | a0002 | c0002 | t0028 | g0002 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01257 | hp2 | a0005 | c0006 | t0013 | g0007 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01258 | hp2 | a0005 | c0006 | t0013 | g0007 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01261 | hp1 | a0001 | c0004 | t0012 | g0007 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01346 | hp1 | a0001 | c0004 | t0012 | g0028 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01358 | hp1 | a0001 | c0004 | t0013 | g0182 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0143 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01361 | hp2 | a0006 | c0012 | t0021 | g0156 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0015 | EUR | IBS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0005 | EUR | IBS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0015 | EUR | IBS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0001 | EUR | IBS | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01943 | hp1 | a0001 | c0001 | t0027 | g0012 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01978 | hp1 | a0004 | c0005 | t0021 | g0030 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01978 | hp2 | a0004 | c0005 | t0004 | g0014 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0099 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01993 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02004 | hp2 | a0001 | c0001 | t0019 | g0012 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02015 | hp2 | a0001 | c0004 | t0012 | g0125 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0113 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02055 | hp1 | a0003 | c0003 | t0009 | g0050 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0090 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02071 | hp2 | a0001 | c0001 | t0029 | g0070 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02083 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02132 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02132 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02145 | hp1 | a0003 | c0003 | t0018 | g0048 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02145 | hp2 | a0001 | c0001 | t0030 | g0138 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02148 | hp1 | a0001 | c0001 | t0019 | g0012 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02148 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CDX | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | CDX | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02273 | hp1 | a0001 | c0001 | t0019 | g0012 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0038 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0081 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02293 | hp2 | a0004 | c0005 | t0004 | g0030 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02451 | hp2 | a0003 | c0003 | t0015 | g0034 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02523 | hp2 | a0007 | c0010 | t0001 | g0047 | EAS | KHV | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02572 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02602 | hp2 | a0004 | c0005 | t0004 | g0014 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02615 | hp1 | a0003 | c0003 | t0009 | g0034 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0082 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0168 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02647 | hp1 | a0003 | c0003 | t0016 | g0178 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0121 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02698 | hp2 | a0003 | c0003 | t0009 | g0181 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02717 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02717 | hp2 | a0001 | c0001 | t0031 | g0171 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02723 | hp2 | a0003 | c0003 | t0018 | g0048 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0006 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0045 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02738 | hp2 | a0001 | c0001 | t0014 | g0146 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02809 | hp1 | a0003 | c0003 | t0009 | g0033 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02886 | hp2 | a0003 | c0003 | t0015 | g0033 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02897 | hp1 | a0003 | c0003 | t0015 | g0179 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02976 | hp1 | a0001 | c0004 | t0012 | g0007 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0006 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03041 | hp1 | a0001 | c0001 | t0021 | g0140 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03098 | hp2 | a0001 | c0001 | t0017 | g0166 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0039 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03225 | hp1 | a0001 | c0001 | t0021 | g0005 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03225 | hp2 | a0001 | c0001 | t0038 | g0122 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03239 | hp2 | a0004 | c0011 | t0002 | g0011 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0047 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03490 | hp1 | a0004 | c0005 | t0014 | g0044 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0161 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0162 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03492 | hp1 | a0004 | c0005 | t0014 | g0044 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ESN | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03540 | hp1 | a0003 | c0003 | t0023 | g0173 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03540 | hp2 | a0003 | c0003 | t0002 | g0004 | AFR | GWD | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03579 | hp1 | a0003 | c0003 | t0018 | g0174 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03579 | hp2 | a0003 | c0003 | t0009 | g0034 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0057 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03654 | hp2 | a0001 | c0001 | t0014 | g0045 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03669 | hp2 | a0004 | c0005 | t0004 | g0014 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03688 | hp1 | a0004 | c0005 | t0004 | g0014 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03704 | hp2 | a0004 | c0005 | t0006 | g0149 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | PJL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0117 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03831 | hp2 | a0004 | c0005 | t0004 | g0145 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0084 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03927 | hp2 | a0004 | c0005 | t0004 | g0014 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0056 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04115 | hp1 | a0001 | c0001 | t0024 | g0115 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0116 | SAS | BEB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04199 | hp1 | a0001 | c0001 | t0020 | g0165 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0061 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0006 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | STU | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | YRI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | CHB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | CHB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | YRI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | YRI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18952 | hp2 | a0003 | c0003 | t0009 | g0019 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18954 | hp1 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0095 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18963 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18965 | hp2 | a0003 | c0003 | t0009 | g0019 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18975 | hp1 | a0001 | c0001 | t0019 | g0012 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18978 | hp2 | a0001 | c0001 | t0020 | g0040 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18982 | hp2 | a0008 | c0008 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18993 | hp2 | a0001 | c0001 | t0022 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18997 | hp1 | a0001 | c0001 | t0035 | g0029 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19001 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19005 | hp2 | a0009 | c0009 | t0002 | g0104 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19030 | hp1 | a0001 | c0004 | t0034 | g0126 | AFR | LWK | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0098 | AFR | LWK | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | LWK | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19043 | hp2 | a0001 | c0001 | t0025 | g0027 | AFR | LWK | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19057 | hp2 | a0003 | c0003 | t0009 | g0176 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19059 | hp1 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19070 | hp2 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19075 | hp2 | a0001 | c0001 | t0022 | g0064 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19081 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19090 | hp2 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19091 | hp1 | a0001 | c0001 | t0033 | g0005 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | YRI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | YRI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0118 | AFR | ASW | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20129 | hp2 | a0003 | c0003 | t0016 | g0019 | AFR | ASW | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20752 | hp1 | a0001 | c0001 | t0008 | g0005 | EUR | TSI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20752 | hp2 | a0001 | c0007 | t0007 | g0036 | EUR | TSI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0046 | EUR | TSI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20805 | hp2 | a0001 | c0001 | t0010 | g0013 | EUR | TSI | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0160 | SAS | GIH | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0075 | SAS | GIH | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0153 | AMR | CLM | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02109 | hp1 | a0003 | c0003 | t0002 | g0004 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02486 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG02559 | hp2 | a0001 | c0004 | t0013 | g0007 | AFR | ACB | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03471 | hp1 | a0003 | c0003 | t0015 | g0033 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0042 | AFR | MSL | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG06807 | hp1 | a0003 | c0003 | t0009 | g0050 | AFR | USA | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | USA | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20300 | hp1 | a0003 | c0003 | t0015 | g0019 | AFR | USA | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA20300 | hp2 | a0001 | c0004 | t0013 | g0028 | AFR | USA | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA21309 | hp1 | a0001 | c0001 | t0032 | g0147 | AFR | LWK | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| NA21309 | hp2 | a0001 | c0001 | t0036 | g0172 | AFR | LWK | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0062 | REF | REF | MOG_chr6_29652092_29677365 | MOG | chr6 | 29652092 | 29677365 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:29657255 | TTCC | T | 1 | a0003 | 29 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
disruptive_inframe_deletion | MODERATE | c.65_67delTCC | p.Leu22del | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/8 | 183/2042 | 65/744 | 22/247 | INFO_REALIGN_3_PRIME | chr6 | 29657255 | ||
| chr6:29659441 | C | G | 1 | a0006 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.211C>G | p.Pro71Ala | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/8 | 329/2042 | 211/744 | 71/247 | chr6 | 29659441 | |||
| chr6:29659445 | C | A | 1 | a0004 | 14 | HG00735.hp1 HG00738.hp1 HG01109.hp2 others(11): Show |
missense_variant | MODERATE | c.215C>A | p.Pro72His | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/8 | 333/2042 | 215/744 | 72/247 | chr6 | 29659445 | |||
| chr6:29659445 | C | T | 1 | a0004 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.215C>T | p.Pro72Leu | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/8 | 333/2042 | 215/744 | 72/247 | chr6 | 29659445 | |||
| chr6:29659513 | C | G | 1 | a0007 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.283C>G | p.Arg95Gly | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/8 | 401/2042 | 283/744 | 95/247 | chr6 | 29659513 | |||
| chr6:29659619 | G | A | 1 | a0008 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.389G>A | p.Arg130Gln | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/8 | 507/2042 | 389/744 | 130/247 | chr6 | 29659619 | |||
| chr6:29666220 | A | T | 1 | a0009 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.505A>T | p.Ile169Phe | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/8 | 623/2042 | 505/744 | 169/247 | chr6 | 29666220 | |||
| chr6:29666226 | G | C | 3 | a0002 a0007 a0009 |
80 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
missense_variant | MODERATE | c.511G>C | p.Val171Leu | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/8 | 629/2042 | 511/744 | 171/247 | chr6 | 29666226 | |||
| chr6:29666235 | A | G | 8 | a0001 a0002 a0003 others(5): Show |
435 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(432): Show |
missense_variant | MODERATE | c.520A>G | p.Ile174Val | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/8 | 638/2042 | 520/744 | 174/247 | chr6 | 29666235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:29657224 | A | G | 10 | a0001c0001 a0001c0007 a0002c0002 others(7): Show |
418 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(415): Show |
synonymous_variant | LOW | c.15A>G | p.Ser5Ser | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/8 | 133/2042 | 15/744 | 5/247 | chr6 | 29657224 | |||
| chr6:29659536 | A | G | 1 | a0001c0007 | 2 | HG01081.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.306A>G | p.Lys102Lys | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/8 | 424/2042 | 306/744 | 102/247 | chr6 | 29659536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:29657117 | T | C | 5 | a0003c0003t0009 a0003c0003t0015 a0003c0003t0016 others(2): Show |
26 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-93T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/8 | 93 | chr6 | 29657117 | ||||||
| chr6:29671240 | C | T | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 55 | chr6 | 29671240 | ||||||
| chr6:29671301 | C | G | 1 | a0001c0001t0022 | 2 | NA18993.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 116 | chr6 | 29671301 | ||||||
| chr6:29671511 | G | A | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 326 | chr6 | 29671511 | ||||||
| chr6:29671636 | A | G | 2 | a0001c0001t0036 a0001c0001t0037 |
2 | HG01255.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 451 | chr6 | 29671636 | ||||||
| chr6:29671639 | G | A | 3 | a0001c0001t0010 a0001c0001t0025 a0001c0001t0026 |
11 | HG00642.hp1 HG00733.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 454 | chr6 | 29671639 | ||||||
| chr6:29671867 | T | C | 2 | a0001c0001t0019 a0001c0001t0027 |
5 | HG01943.hp1 HG02004.hp2 HG02148.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*682T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 682 | chr6 | 29671867 | ||||||
| chr6:29671999 | C | T | 1 | a0001c0001t0008 | 12 | HG00609.hp2 HG00639.hp2 HG01123.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*814C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 814 | chr6 | 29671999 | ||||||
| chr6:29672011 | G | A | 1 | a0001c0001t0036 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 826 | chr6 | 29672011 | ||||||
| chr6:29672020 | G | A | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 835 | chr6 | 29672020 | ||||||
| chr6:29672047 | G | T | 1 | a0001c0001t0035 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*862G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 862 | chr6 | 29672047 | ||||||
| chr6:29672054 | C | T | 1 | a0001c0004t0034 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*869C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 869 | chr6 | 29672054 | ||||||
| chr6:29672063 | C | T | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*878C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 878 | chr6 | 29672063 | ||||||
| chr6:29672073 | G | A | 1 | a0002c0002t0028 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*888G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 888 | chr6 | 29672073 | ||||||
| chr6:29672085 | A | G | 14 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0014 others(11): Show |
72 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*900A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 900 | chr6 | 29672085 | ||||||
| chr6:29672209 | A | T | 2 | a0001c0001t0006 a0004c0005t0006 |
26 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1024A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1024 | chr6 | 29672209 | ||||||
| chr6:29672244 | T | C | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(47): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
3_prime_UTR_variant | MODIFIER | c.*1059T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1059 | chr6 | 29672244 | ||||||
| chr6:29672253 | A | G | 1 | a0001c0001t0033 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1068 | chr6 | 29672253 | ||||||
| chr6:29672261 | C | T | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1076C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1076 | chr6 | 29672261 | ||||||
| chr6:29672262 | G | A | 12 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0014 others(9): Show |
67 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1077G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1077 | chr6 | 29672262 | ||||||
| chr6:29672289 | A | AAAAT | 10 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(7): Show |
111 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1148_*1151dupTAAA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1152 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672289 | A | AAAATAAA others(1): Show |
5 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(2): Show |
37 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1144_*1151dupTAAA others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1152 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672289 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0030 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1140_*1151dupTAAA others(8): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1152 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672289 | AAAAT | A | 10 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0036 others(7): Show |
89 | HG00280.hp2 HG00621.hp1 HG01069.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1148_*1151delTAAA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1148 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672289 | AAAATAAA others(1): Show |
A | 4 | a0001c0001t0007 a0001c0001t0020 a0001c0001t0032 others(1): Show |
22 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1144_*1151delTAAA others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1144 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672289 | AAAATAAA others(5): Show |
A | 2 | a0001c0001t0011 a0001c0001t0031 |
10 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1140_*1151delTAAA others(8): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1140 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672289 | AAAATAAA others(9): Show |
A | 2 | a0001c0001t0017 a0001c0001t0038 |
6 | HG01243.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1136_*1151delTAAA others(12): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1136 | INFO_REALIGN_3_PRIME | chr6 | 29672289 | |||||
| chr6:29672317 | TAAATAAA others(10): Show |
T | 1 | a0003c0003t0018 | 4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1136_*1152delTAAA others(13): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1136 | INFO_REALIGN_3_PRIME | chr6 | 29672317 | |||||
| chr6:29672321 | TAAATAAA others(6): Show |
T | 1 | a0003c0003t0023 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140_*1152delTAAA others(9): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1140 | INFO_REALIGN_3_PRIME | chr6 | 29672321 | |||||
| chr6:29672321 | TAAATAAA others(8): Show |
T | 1 | a0001c0001t0006 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143_*1157delATAA others(11): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1143 | INFO_REALIGN_3_PRIME | chr6 | 29672321 | |||||
| chr6:29672325 | TAAATAAA others(4): Show |
T | 2 | a0001c0001t0006 a0004c0005t0006 |
23 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1147_*1157delATAA others(7): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1147 | INFO_REALIGN_3_PRIME | chr6 | 29672325 | |||||
| chr6:29672325 | TAAATAAA others(5): Show |
T | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1143_*1154delATAA others(8): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1143 | INFO_REALIGN_3_PRIME | chr6 | 29672325 | |||||
| chr6:29672337 | A | T | 1 | a0001c0001t0029 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1152A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1152 | chr6 | 29672337 | ||||||
| chr6:29672340 | T | A | 1 | a0001c0001t0029 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 8/8 | 1155 | chr6 | 29672340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:29657305 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG03927.hp1 | splice_region_variant&intron_variant | LOW | c.88+8A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657305 | |||||||
| chr6:29657347 | G | T | 1 | a0001c0004t0013g0182 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.88+50G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657347 | |||||||
| chr6:29657350 | A | G | 16 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0034 others(13): Show |
21 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.88+53A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657350 | |||||||
| chr6:29657418 | A | G | 20 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0034 others(17): Show |
26 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+121A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657418 | |||||||
| chr6:29657450 | G | A | 16 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0034 others(13): Show |
21 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.88+153G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657450 | |||||||
| chr6:29657552 | C | T | 1 | a0001c0001t0036g0172 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88+255C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657552 | |||||||
| chr6:29657647 | C | A | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+350C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657647 | |||||||
| chr6:29657663 | CT | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0120 others(114): Show |
247 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.88+387delT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29657663 | ||||||
| chr6:29657663 | CTT | C | 77 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0086 others(74): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.88+386_88+387delTT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29657663 | ||||||
| chr6:29657663 | CTTTTT | C | 8 | a0001c0001t0006g0006 a0001c0001t0006g0025 a0001c0001t0006g0052 others(5): Show |
24 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.88+383_88+387delTT others(3): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29657663 | ||||||
| chr6:29657675 | T | C | 1 | a0001c0001t0003g0051 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.88+378T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657675 | |||||||
| chr6:29657695 | A | G | 3 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 |
4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+398A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657695 | |||||||
| chr6:29657755 | C | T | 1 | a0002c0002t0001g0091 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.88+458C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657755 | |||||||
| chr6:29657761 | A | G | 56 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(53): Show |
94 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.88+464A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657761 | |||||||
| chr6:29657765 | TCCCAAAG others(8): Show |
T | 1 | a0002c0002t0002g0169 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.88+469_88+483delCC others(13): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657765 | |||||||
| chr6:29657784 | T | C | 21 | a0001c0001t0021g0140 a0003c0003t0009g0019 a0003c0003t0009g0033 others(18): Show |
27 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.88+487T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657784 | |||||||
| chr6:29657789 | G | A | 1 | a0001c0001t0004g0141 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+492G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657789 | |||||||
| chr6:29657834 | G | A | 1 | a0001c0001t0004g0142 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.88+537G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657834 | |||||||
| chr6:29657874 | AC | A | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+579delC | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29657874 | ||||||
| chr6:29657920 | C | T | 6 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0011g0017 others(3): Show |
11 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+623C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29657920 | |||||||
| chr6:29658143 | T | A | 1 | a0001c0001t0014g0143 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.88+846T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658143 | |||||||
| chr6:29658377 | AAAAC | A | 17 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0089 others(14): Show |
34 | HG02109.hp1 HG02602.hp1 HG02698.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-939_89-936delAC others(2): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29658377 | ||||||
| chr6:29658544 | T | C | 41 | a0001c0001t0003g0038 a0001c0001t0003g0093 a0001c0001t0005g0038 others(38): Show |
85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.89-775T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658544 | |||||||
| chr6:29658599 | T | C | 16 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0089 others(13): Show |
33 | HG02109.hp1 HG02698.hp1 HG02723.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-720T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658599 | |||||||
| chr6:29658628 | G | A | 16 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0034 others(13): Show |
21 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-691G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658628 | |||||||
| chr6:29658723 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.89-596G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658723 | |||||||
| chr6:29658723 | G | GGCAGATG others(55): Show |
1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.89-595_89-534dupGC others(60): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29658723 | ||||||
| chr6:29658805 | G | A | 1 | a0001c0001t0003g0093 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.89-514G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658805 | |||||||
| chr6:29658846 | G | C | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.89-473G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658846 | |||||||
| chr6:29658971 | A | G | 16 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0034 others(13): Show |
21 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-348A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658971 | |||||||
| chr6:29658975 | G | A | 5 | a0001c0001t0002g0032 a0001c0001t0003g0032 a0001c0001t0003g0160 others(2): Show |
5 | HG00099.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-344G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29658975 | |||||||
| chr6:29659060 | C | T | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-259C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659060 | |||||||
| chr6:29659101 | C | G | 1 | a0001c0001t0031g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.89-218C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659101 | |||||||
| chr6:29659107 | C | T | 1 | a0001c0001t0003g0087 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.89-212C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659107 | |||||||
| chr6:29659140 | G | A | 20 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0034 others(17): Show |
26 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.89-179G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659140 | |||||||
| chr6:29659151 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.89-168A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659151 | |||||||
| chr6:29659153 | G | GGAA | 6 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0011g0017 others(3): Show |
11 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-150_89-148dupGA others(1): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 29659153 | ||||||
| chr6:29659172 | C | G | 34 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0002g0032 others(31): Show |
63 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.89-147C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659172 | |||||||
| chr6:29659274 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.89-45G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 1/7 | chr6 | 29659274 | |||||||
| chr6:29659696 | A | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0007g0010 others(8): Show |
18 | HG01081.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.436+30A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29659696 | |||||||
| chr6:29659914 | C | T | 2 | a0001c0001t0036g0172 a0001c0001t0037g0080 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.436+248C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29659914 | |||||||
| chr6:29660148 | T | G | 3 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 |
4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+482T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660148 | |||||||
| chr6:29660253 | G | A | 5 | a0001c0001t0010g0013 a0001c0001t0010g0027 a0001c0001t0010g0078 others(2): Show |
11 | HG00642.hp1 HG00733.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.436+587G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660253 | |||||||
| chr6:29660260 | G | A | 57 | a0001c0001t0001g0065 a0001c0001t0001g0163 a0001c0001t0002g0001 others(54): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.436+594G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660260 | |||||||
| chr6:29660273 | G | A | 2 | a0001c0001t0011g0116 a0001c0001t0011g0117 |
2 | HG03831.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.436+607G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660273 | |||||||
| chr6:29660317 | C | T | 48 | a0001c0001t0001g0065 a0001c0001t0001g0163 a0001c0001t0002g0001 others(45): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.436+651C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660317 | |||||||
| chr6:29660365 | C | CA | 23 | a0001c0001t0001g0065 a0001c0001t0001g0119 a0001c0001t0001g0120 others(20): Show |
30 | HG00642.hp1 HG00733.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.436+715dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660365 | ||||||
| chr6:29660365 | CAAA | C | 8 | a0003c0003t0009g0034 a0003c0003t0009g0050 a0003c0003t0009g0181 others(5): Show |
10 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+713_436+715del others(3): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660365 | ||||||
| chr6:29660371 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.436+705A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660371 | |||||||
| chr6:29660382 | T | G | 3 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 |
4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+716T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660382 | |||||||
| chr6:29660420 | A | G | 3 | a0001c0001t0017g0039 a0001c0001t0017g0121 a0001c0001t0038g0122 |
4 | HG02572.hp1 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+754A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660420 | |||||||
| chr6:29660456 | G | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(33): Show |
68 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.436+790G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660456 | |||||||
| chr6:29660525 | G | A | 30 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0002g0032 others(27): Show |
58 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.436+859G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660525 | |||||||
| chr6:29660529 | C | CA | 35 | a0001c0001t0001g0123 a0001c0001t0002g0011 a0001c0001t0002g0129 others(32): Show |
46 | HG00438.hp1 HG00544.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.436+879dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660529 | ||||||
| chr6:29660562 | G | GCA | 15 | a0001c0001t0007g0082 a0001c0001t0010g0013 a0001c0001t0010g0027 others(12): Show |
23 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.436+922_436+923dup others(2): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660562 | ||||||
| chr6:29660562 | G | GCACA | 6 | a0001c0001t0010g0078 a0001c0001t0024g0115 a0001c0001t0026g0118 others(3): Show |
6 | HG00642.hp2 HG01081.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+920_436+923dup others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660562 | ||||||
| chr6:29660562 | G | GCACACA | 3 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 |
4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+918_436+923dup others(6): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660562 | ||||||
| chr6:29660562 | GCA | G | 85 | a0001c0001t0001g0065 a0001c0001t0001g0163 a0001c0001t0002g0001 others(82): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.436+922_436+923del others(2): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660562 | ||||||
| chr6:29660564 | A | G | 5 | a0001c0001t0003g0088 a0001c0001t0005g0061 a0001c0001t0005g0069 others(2): Show |
5 | HG00544.hp1 HG01070.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+898A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660564 | |||||||
| chr6:29660566 | A | G | 45 | a0001c0001t0001g0065 a0001c0001t0001g0163 a0001c0001t0002g0001 others(42): Show |
95 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.436+900A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660566 | |||||||
| chr6:29660568 | A | G | 6 | a0001c0001t0002g0077 a0001c0001t0003g0009 a0001c0001t0003g0066 others(3): Show |
13 | HG02056.hp2 NA18939.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.436+902A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660568 | |||||||
| chr6:29660587 | C | CAA | 5 | a0003c0003t0009g0034 a0003c0003t0009g0050 a0003c0003t0015g0034 others(2): Show |
7 | HG02055.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+922_436+923ins others(2): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660587 | ||||||
| chr6:29660588 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+922A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660588 | |||||||
| chr6:29660590 | C | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0170 |
7 | HG01074.hp1 HG01099.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+924C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660590 | |||||||
| chr6:29660599 | G | T | 1 | a0003c0003t0009g0181 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.436+933G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660599 | |||||||
| chr6:29660660 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0065 others(209): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.436+994T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660660 | |||||||
| chr6:29660707 | CT | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0065 others(197): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(395): Show |
intron_variant | MODIFIER | c.436+1052delT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660707 | ||||||
| chr6:29660709 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1043T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660709 | |||||||
| chr6:29660713 | T | C | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+1047T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660713 | |||||||
| chr6:29660733 | C | CTT | 8 | a0003c0003t0009g0034 a0003c0003t0009g0050 a0003c0003t0009g0181 others(5): Show |
10 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+1077_436+1078d others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29660733 | ||||||
| chr6:29660834 | G | A | 1 | a0001c0001t0014g0143 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.436+1168G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660834 | |||||||
| chr6:29660840 | C | A | 1 | a0001c0001t0017g0121 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.436+1174C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660840 | |||||||
| chr6:29660843 | A | G | 178 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0086 others(175): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.436+1177A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660843 | |||||||
| chr6:29660911 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1245G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660911 | |||||||
| chr6:29660912 | T | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1246T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660912 | |||||||
| chr6:29660921 | T | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+1255T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660921 | |||||||
| chr6:29660955 | C | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0007g0010 others(8): Show |
18 | HG01081.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.436+1289C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660955 | |||||||
| chr6:29660963 | C | A | 28 | a0001c0001t0003g0038 a0001c0001t0003g0093 a0001c0001t0005g0038 others(25): Show |
60 | HG00280.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.436+1297C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660963 | |||||||
| chr6:29660966 | C | T | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.436+1300C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29660966 | |||||||
| chr6:29661001 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.436+1335G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661001 | |||||||
| chr6:29661005 | G | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0007g0010 others(8): Show |
18 | HG01081.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.436+1339G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661005 | |||||||
| chr6:29661008 | C | T | 1 | a0003c0003t0018g0048 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.436+1342C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661008 | |||||||
| chr6:29661106 | C | G | 46 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(43): Show |
81 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.436+1440C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661106 | |||||||
| chr6:29661107 | G | T | 1 | a0002c0002t0001g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.436+1441G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661107 | |||||||
| chr6:29661410 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1744C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661410 | |||||||
| chr6:29661412 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1746A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661412 | |||||||
| chr6:29661452 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1786T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661452 | |||||||
| chr6:29661453 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1787C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661453 | |||||||
| chr6:29661456 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1790C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661456 | |||||||
| chr6:29661457 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1791T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661457 | |||||||
| chr6:29661460 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1794C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661460 | |||||||
| chr6:29661502 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1836A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661502 | |||||||
| chr6:29661541 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1875C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661541 | |||||||
| chr6:29661567 | T | C | 48 | a0001c0001t0001g0065 a0001c0001t0001g0163 a0001c0001t0002g0001 others(45): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.436+1901T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661567 | |||||||
| chr6:29661572 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1906A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661572 | |||||||
| chr6:29661578 | T | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1912T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661578 | |||||||
| chr6:29661580 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+1914G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661580 | |||||||
| chr6:29661595 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.436+1929T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661595 | |||||||
| chr6:29661664 | C | T | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.436+1998C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661664 | |||||||
| chr6:29661688 | C | G | 1 | a0001c0001t0031g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.436+2022C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661688 | |||||||
| chr6:29661771 | G | A | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+2105G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661771 | |||||||
| chr6:29661784 | C | T | 1 | a0001c0001t0006g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.436+2118C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661784 | |||||||
| chr6:29661798 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2132A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661798 | |||||||
| chr6:29661816 | C | CA | 5 | a0001c0001t0004g0144 a0001c0001t0004g0150 a0001c0001t0014g0045 others(2): Show |
6 | HG01175.hp2 HG02738.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+2172dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29661816 | ||||||
| chr6:29661816 | CA | C | 17 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0002g0072 others(14): Show |
20 | HG00140.hp1 HG01106.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.436+2172delA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29661816 | ||||||
| chr6:29661816 | CAA | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0065 others(131): Show |
297 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.436+2171_436+2172d others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29661816 | ||||||
| chr6:29661816 | CAAA | C | 12 | a0001c0001t0001g0086 a0001c0001t0002g0032 a0001c0001t0002g0077 others(9): Show |
12 | HG00099.hp1 HG01255.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.436+2170_436+2172d others(5): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29661816 | ||||||
| chr6:29661825 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2159A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661825 | |||||||
| chr6:29661830 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2164A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661830 | |||||||
| chr6:29661840 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2174A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661840 | |||||||
| chr6:29661878 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2212C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661878 | |||||||
| chr6:29661882 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2216G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661882 | |||||||
| chr6:29661929 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2263C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661929 | |||||||
| chr6:29661933 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2267C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661933 | |||||||
| chr6:29661943 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2277T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661943 | |||||||
| chr6:29661954 | G | A | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.436+2288G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661954 | |||||||
| chr6:29661997 | T | C | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.436+2331T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661997 | |||||||
| chr6:29661999 | G | A | 3 | a0001c0001t0017g0039 a0001c0001t0017g0121 a0001c0001t0038g0122 |
4 | HG02572.hp1 HG02647.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2333G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29661999 | |||||||
| chr6:29662002 | C | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2336C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662002 | |||||||
| chr6:29662005 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2339G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662005 | |||||||
| chr6:29662007 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2341A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662007 | |||||||
| chr6:29662077 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2411C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662077 | |||||||
| chr6:29662124 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2458C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662124 | |||||||
| chr6:29662125 | T | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2459T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662125 | |||||||
| chr6:29662184 | A | T | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+2518A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662184 | |||||||
| chr6:29662200 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2534A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662200 | |||||||
| chr6:29662291 | C | A | 7 | a0001c0001t0011g0116 a0001c0001t0011g0117 a0001c0001t0017g0039 others(4): Show |
8 | HG01243.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+2625C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662291 | |||||||
| chr6:29662308 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2642A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662308 | |||||||
| chr6:29662309 | C | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2643C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662309 | |||||||
| chr6:29662373 | A | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.436+2707A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662373 | |||||||
| chr6:29662483 | C | CA | 54 | a0001c0001t0001g0123 a0001c0001t0002g0089 a0001c0001t0004g0005 others(51): Show |
90 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.436+2829dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29662483 | ||||||
| chr6:29662583 | C | T | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.436+2917C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662583 | |||||||
| chr6:29662589 | G | A | 15 | a0001c0001t0004g0005 a0001c0001t0004g0154 a0001c0001t0005g0043 others(12): Show |
18 | HG00642.hp2 HG01081.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.436+2923G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662589 | |||||||
| chr6:29662609 | C | A | 7 | a0001c0001t0011g0116 a0001c0001t0011g0117 a0001c0001t0017g0039 others(4): Show |
8 | HG01243.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+2943C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662609 | |||||||
| chr6:29662869 | A | G | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+3203A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662869 | |||||||
| chr6:29662960 | G | A | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.437-3192G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662960 | |||||||
| chr6:29662971 | T | A | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3181T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662971 | |||||||
| chr6:29662979 | A | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3173A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662979 | |||||||
| chr6:29662980 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3172A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662980 | |||||||
| chr6:29662981 | A | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3171A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662981 | |||||||
| chr6:29662989 | G | C | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3163G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662989 | |||||||
| chr6:29662990 | C | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3162C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662990 | |||||||
| chr6:29662991 | C | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3161C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662991 | |||||||
| chr6:29662995 | C | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3157C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662995 | |||||||
| chr6:29662998 | G | A | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3154G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29662998 | |||||||
| chr6:29663002 | G | A | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.437-3150G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663002 | |||||||
| chr6:29663006 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3146A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663006 | |||||||
| chr6:29663008 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3144A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663008 | |||||||
| chr6:29663011 | T | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-3141T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663011 | |||||||
| chr6:29663011 | T | G | 5 | a0001c0001t0002g0032 a0001c0001t0003g0032 a0001c0001t0003g0160 others(2): Show |
5 | HG00099.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-3141T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663011 | |||||||
| chr6:29663017 | C | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3135C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663017 | |||||||
| chr6:29663019 | C | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3133C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663019 | |||||||
| chr6:29663022 | T | C | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3130T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663022 | |||||||
| chr6:29663033 | C | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3119C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663033 | |||||||
| chr6:29663036 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3116A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663036 | |||||||
| chr6:29663041 | G | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3111G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663041 | |||||||
| chr6:29663047 | A | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3105A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663047 | |||||||
| chr6:29663055 | G | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3097G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663055 | |||||||
| chr6:29663056 | T | C | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3096T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663056 | |||||||
| chr6:29663057 | C | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3095C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663057 | |||||||
| chr6:29663059 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3093A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663059 | |||||||
| chr6:29663063 | A | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3089A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663063 | |||||||
| chr6:29663073 | T | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3079T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663073 | |||||||
| chr6:29663077 | A | G | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3075A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663077 | |||||||
| chr6:29663078 | G | A | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3074G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663078 | |||||||
| chr6:29663079 | C | T | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3073C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663079 | |||||||
| chr6:29663080 | T | C | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3072T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663080 | |||||||
| chr6:29663089 | G | A | 1 | a0006c0012t0021g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.437-3063G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663089 | |||||||
| chr6:29663107 | C | A | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-3045C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663107 | |||||||
| chr6:29663121 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.437-3031A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663121 | |||||||
| chr6:29663200 | A | G | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.437-2952A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663200 | |||||||
| chr6:29663206 | A | G | 2 | a0001c0001t0007g0010 a0001c0001t0007g0081 |
9 | HG01884.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.437-2946A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663206 | |||||||
| chr6:29663249 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2903G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663249 | |||||||
| chr6:29663266 | C | CA | 66 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0119 others(63): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.437-2868dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29663266 | ||||||
| chr6:29663266 | CA | C | 30 | a0001c0001t0004g0018 a0001c0001t0004g0142 a0001c0001t0006g0006 others(27): Show |
58 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.437-2868delA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29663266 | ||||||
| chr6:29663275 | A | C | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2877A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663275 | |||||||
| chr6:29663284 | A | C | 1 | a0002c0002t0002g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.437-2868A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663284 | |||||||
| chr6:29663285 | G | C | 1 | a0002c0002t0002g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.437-2867G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663285 | |||||||
| chr6:29663286 | C | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2866C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663286 | |||||||
| chr6:29663346 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.437-2806C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663346 | |||||||
| chr6:29663447 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2705T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663447 | |||||||
| chr6:29663448 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2704A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663448 | |||||||
| chr6:29663455 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2697T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663455 | |||||||
| chr6:29663514 | T | C | 11 | a0001c0001t0004g0046 a0001c0001t0004g0152 a0001c0001t0014g0045 others(8): Show |
19 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.437-2638T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663514 | |||||||
| chr6:29663584 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2568G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663584 | |||||||
| chr6:29663585 | T | G | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2567T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663585 | |||||||
| chr6:29663586 | G | T | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2566G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663586 | |||||||
| chr6:29663664 | T | A | 1 | a0001c0001t0003g0088 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.437-2488T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663664 | |||||||
| chr6:29663749 | C | A | 1 | a0001c0001t0002g0134 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.437-2403C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663749 | |||||||
| chr6:29663811 | T | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-2341T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663811 | |||||||
| chr6:29663851 | A | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-2301A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663851 | |||||||
| chr6:29663913 | G | A | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-2239G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663913 | |||||||
| chr6:29663967 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0065 others(209): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.437-2185C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29663967 | |||||||
| chr6:29664024 | G | A | 1 | a0001c0001t0029g0070 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.437-2128G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664024 | |||||||
| chr6:29664040 | C | A | 1 | a0002c0002t0001g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.437-2112C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664040 | |||||||
| chr6:29664195 | T | C | 1 | a0001c0004t0013g0182 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.437-1957T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664195 | |||||||
| chr6:29664210 | A | ATT | 8 | a0001c0001t0006g0006 a0001c0001t0006g0052 a0001c0001t0006g0053 others(5): Show |
22 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.437-1940_437-1939d others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29664210 | ||||||
| chr6:29664210 | A | T | 1 | a0001c0001t0002g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.437-1942A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664210 | |||||||
| chr6:29664213 | TA | T | 11 | a0001c0001t0003g0088 a0001c0001t0005g0043 a0001c0001t0005g0139 others(8): Show |
13 | HG00642.hp2 HG01081.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.437-1938delA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664213 | |||||||
| chr6:29664214 | A | AT | 7 | a0001c0001t0005g0159 a0001c0001t0017g0164 a0001c0001t0017g0166 others(4): Show |
8 | HG00735.hp2 HG01243.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-1928dupT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29664214 | ||||||
| chr6:29664214 | A | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0065 others(84): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.437-1938A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664214 | |||||||
| chr6:29664270 | C | T | 1 | a0003c0003t0018g0048 | 2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.437-1882C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664270 | |||||||
| chr6:29664420 | C | T | 1 | a0001c0004t0012g0041 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.437-1732C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664420 | |||||||
| chr6:29664421 | G | A | 9 | a0001c0001t0002g0074 a0001c0001t0003g0016 a0001c0001t0003g0020 others(6): Show |
14 | HG00140.hp2 HG00558.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.437-1731G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664421 | |||||||
| chr6:29664541 | C | T | 41 | a0001c0001t0003g0038 a0001c0001t0003g0093 a0001c0001t0005g0038 others(38): Show |
85 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.437-1611C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664541 | |||||||
| chr6:29664573 | G | A | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-1579G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664573 | |||||||
| chr6:29664594 | A | AC | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-1555dupC | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29664594 | ||||||
| chr6:29664606 | A | AT | 12 | a0001c0001t0001g0123 a0001c0001t0002g0032 a0001c0001t0002g0133 others(9): Show |
12 | HG00099.hp1 HG00140.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-1530dupT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29664606 | ||||||
| chr6:29664606 | AT | A | 58 | a0001c0001t0001g0086 a0001c0001t0002g0130 a0001c0001t0004g0005 others(55): Show |
93 | HG00609.hp2 HG00639.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.437-1530delT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29664606 | ||||||
| chr6:29664649 | G | A | 1 | a0001c0001t0032g0147 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437-1503G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664649 | |||||||
| chr6:29664788 | G | A | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-1364G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664788 | |||||||
| chr6:29664788 | G | C | 10 | a0001c0001t0006g0006 a0001c0001t0006g0025 a0001c0001t0006g0052 others(7): Show |
26 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.437-1364G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664788 | |||||||
| chr6:29664809 | A | G | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-1343A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29664809 | |||||||
| chr6:29665050 | T | G | 3 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 |
4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-1102T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665050 | |||||||
| chr6:29665101 | C | CT | 22 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0002g0089 others(19): Show |
45 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.437-1039dupT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29665101 | ||||||
| chr6:29665141 | G | C | 1 | a0002c0002t0001g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.437-1011G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665141 | |||||||
| chr6:29665143 | C | T | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-1009C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665143 | |||||||
| chr6:29665174 | T | G | 1 | a0003c0003t0023g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.437-978T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665174 | |||||||
| chr6:29665242 | C | A | 143 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0086 others(140): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.437-910C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665242 | |||||||
| chr6:29665264 | T | C | 10 | a0001c0001t0006g0006 a0001c0001t0006g0025 a0001c0001t0006g0052 others(7): Show |
26 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.437-888T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665264 | |||||||
| chr6:29665333 | C | A | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-819C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665333 | |||||||
| chr6:29665444 | T | A | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-708T>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665444 | |||||||
| chr6:29665451 | G | T | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-701G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665451 | |||||||
| chr6:29665536 | A | G | 3 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 |
4 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-616A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665536 | |||||||
| chr6:29665579 | T | C | 1 | a0001c0001t0003g0075 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-573T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665579 | |||||||
| chr6:29665729 | A | AG | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-423_437-422ins others(1): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665729 | |||||||
| chr6:29665730 | C | G | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-422C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665730 | |||||||
| chr6:29665732 | T | C | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-420T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665732 | |||||||
| chr6:29665734 | T | G | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-418T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665734 | |||||||
| chr6:29665736 | T | G | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-416T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665736 | |||||||
| chr6:29665737 | G | GTAAAGGT others(40): Show |
11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-415_437-414ins others(47): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665737 | |||||||
| chr6:29665737 | G | GTAATGGT others(40): Show |
4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-415_437-414ins others(47): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665737 | |||||||
| chr6:29665778 | A | C | 11 | a0002c0002t0002g0008 a0002c0002t0002g0026 a0002c0002t0002g0031 others(8): Show |
23 | HG00438.hp2 HG00558.hp1 NA18612.hp1 others(20): Show |
intron_variant | MODIFIER | c.437-374A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665778 | |||||||
| chr6:29665800 | G | A | 10 | a0001c0001t0006g0006 a0001c0001t0006g0025 a0001c0001t0006g0052 others(7): Show |
26 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.437-352G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665800 | |||||||
| chr6:29665869 | A | G | 5 | a0001c0001t0010g0013 a0001c0001t0010g0027 a0001c0001t0010g0078 others(2): Show |
11 | HG00642.hp1 HG00733.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-283A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665869 | |||||||
| chr6:29665878 | G | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-274G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665878 | |||||||
| chr6:29665897 | G | A | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-255G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665897 | |||||||
| chr6:29665976 | GA | G | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-168delA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 29665976 | ||||||
| chr6:29665998 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0120 others(19): Show |
57 | HG02015.hp1 HG02056.hp1 HG02080.hp2 others(54): Show |
intron_variant | MODIFIER | c.437-154C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 2/7 | chr6 | 29665998 | |||||||
| chr6:29666396 | G | GA | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.550+139dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 29666396 | ||||||
| chr6:29666412 | A | G | 1 | a0003c0003t0016g0178 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.550+147A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666412 | |||||||
| chr6:29666491 | C | G | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.550+226C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666491 | |||||||
| chr6:29666640 | G | A | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.550+375G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666640 | |||||||
| chr6:29666734 | T | C | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.550+469T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666734 | |||||||
| chr6:29666760 | G | T | 2 | a0001c0001t0001g0037 a0001c0001t0007g0037 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.550+495G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666760 | |||||||
| chr6:29666778 | G | A | 1 | a0001c0001t0003g0035 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.550+513G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666778 | |||||||
| chr6:29666840 | A | G | 18 | a0001c0001t0004g0046 a0001c0001t0005g0043 a0001c0001t0005g0139 others(15): Show |
22 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.550+575A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666840 | |||||||
| chr6:29666848 | G | A | 1 | a0001c0001t0006g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.550+583G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666848 | |||||||
| chr6:29666860 | T | C | 10 | a0001c0001t0036g0172 a0001c0001t0037g0080 a0003c0003t0009g0019 others(7): Show |
13 | HG00140.hp1 HG01106.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.550+595T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666860 | |||||||
| chr6:29666874 | T | TA | 3 | a0001c0001t0002g0129 a0002c0002t0001g0100 a0002c0002t0003g0112 |
3 | NA18977.hp1 NA18988.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.550+609_550+610ins others(1): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666874 | |||||||
| chr6:29666939 | C | T | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.550+674C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29666939 | |||||||
| chr6:29667150 | A | G | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-493A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667150 | |||||||
| chr6:29667181 | A | T | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-462A>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667181 | |||||||
| chr6:29667191 | T | C | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-452T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667191 | |||||||
| chr6:29667193 | G | C | 15 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(12): Show |
19 | HG00642.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.551-450G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667193 | |||||||
| chr6:29667195 | C | T | 3 | a0001c0001t0004g0024 a0001c0001t0004g0141 a0001c0001t0004g0144 |
6 | HG00741.hp1 HG01106.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.551-448C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667195 | |||||||
| chr6:29667322 | C | CA | 42 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(39): Show |
75 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.551-318dupA | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 29667322 | ||||||
| chr6:29667404 | G | T | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-239G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667404 | |||||||
| chr6:29667446 | G | C | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-197G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667446 | |||||||
| chr6:29667449 | A | G | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-194A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667449 | |||||||
| chr6:29667476 | G | C | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-167G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667476 | |||||||
| chr6:29667522 | G | A | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.551-121G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667522 | |||||||
| chr6:29667540 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0120 others(19): Show |
57 | HG02015.hp1 HG02056.hp1 HG02080.hp2 others(54): Show |
intron_variant | MODIFIER | c.551-103C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667540 | |||||||
| chr6:29667633 | T | G | 1 | a0001c0001t0008g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.551-10T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 3/7 | chr6 | 29667633 | |||||||
| chr6:29667731 | G | A | 36 | a0002c0002t0001g0002 a0002c0002t0001g0021 a0002c0002t0001g0047 others(33): Show |
80 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.571+68G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 4/7 | chr6 | 29667731 | |||||||
| chr6:29667740 | C | T | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.571+77C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 4/7 | chr6 | 29667740 | |||||||
| chr6:29667754 | C | G | 6 | a0001c0001t0001g0037 a0001c0001t0007g0036 a0001c0001t0007g0037 others(3): Show |
6 | HG01081.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.571+91C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 4/7 | chr6 | 29667754 | |||||||
| chr6:29667802 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.572-102C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 4/7 | chr6 | 29667802 | |||||||
| chr6:29667965 | T | C | 1 | a0001c0001t0006g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.592+41T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29667965 | |||||||
| chr6:29667993 | G | A | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+69G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29667993 | |||||||
| chr6:29668020 | A | G | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+96A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668020 | |||||||
| chr6:29668151 | T | C | 178 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0086 others(175): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.592+227T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668151 | |||||||
| chr6:29668406 | A | G | 3 | a0001c0001t0011g0017 a0001c0001t0011g0090 a0001c0001t0011g0168 |
7 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+482A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668406 | |||||||
| chr6:29668548 | G | A | 2 | a0001c0001t0036g0172 a0001c0001t0037g0080 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.592+624G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668548 | |||||||
| chr6:29668552 | C | A | 11 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0007g0010 others(8): Show |
18 | HG01081.hp1 HG01884.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.592+628C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668552 | |||||||
| chr6:29668632 | T | G | 35 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(32): Show |
67 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.592+708T>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668632 | |||||||
| chr6:29668649 | G | T | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+725G>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668649 | |||||||
| chr6:29668662 | G | GT | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+739dupT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29668662 | ||||||
| chr6:29668839 | T | C | 1 | a0001c0001t0017g0121 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.592+915T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668839 | |||||||
| chr6:29668851 | G | C | 4 | a0003c0003t0018g0048 a0003c0003t0018g0174 a0003c0003t0018g0175 others(1): Show |
5 | HG00735.hp2 HG02145.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+927G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668851 | |||||||
| chr6:29668929 | C | CT | 10 | a0001c0001t0003g0076 a0001c0001t0004g0142 a0001c0001t0011g0017 others(7): Show |
14 | HG01243.hp1 HG01361.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.592+1020dupT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29668929 | ||||||
| chr6:29668929 | CT | C | 8 | a0001c0001t0001g0124 a0001c0001t0002g0134 a0002c0002t0002g0108 others(5): Show |
9 | HG00735.hp1 HG00735.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.592+1020delT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29668929 | ||||||
| chr6:29668991 | G | A | 1 | a0002c0002t0001g0103 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.592+1067G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668991 | |||||||
| chr6:29668994 | C | T | 1 | a0001c0001t0014g0143 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.592+1070C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29668994 | |||||||
| chr6:29669022 | G | A | 6 | a0004c0005t0004g0014 a0004c0005t0004g0030 a0004c0005t0004g0145 others(3): Show |
13 | HG00735.hp1 HG00738.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+1098G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669022 | |||||||
| chr6:29669045 | T | C | 39 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(36): Show |
72 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.592+1121T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669045 | |||||||
| chr6:29669047 | A | C | 1 | a0009c0009t0002g0104 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.592+1123A>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669047 | |||||||
| chr6:29669128 | C | T | 1 | a0002c0002t0001g0157 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.593-1153C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669128 | |||||||
| chr6:29669184 | G | C | 2 | a0003c0003t0009g0033 a0003c0003t0015g0033 |
3 | HG02809.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.593-1097G>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669184 | |||||||
| chr6:29669206 | C | G | 5 | a0001c0001t0002g0032 a0001c0001t0003g0032 a0001c0001t0003g0160 others(2): Show |
5 | HG00099.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.593-1075C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669206 | |||||||
| chr6:29669284 | A | ATTTC | 5 | a0001c0001t0030g0138 a0003c0003t0018g0048 a0003c0003t0018g0174 others(2): Show |
6 | HG00735.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.593-973_593-970dup others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29669284 | ||||||
| chr6:29669284 | ATTTC | A | 3 | a0001c0001t0011g0017 a0001c0001t0011g0090 a0001c0001t0011g0168 |
7 | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-973_593-970del others(4): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29669284 | ||||||
| chr6:29669284 | ATTTCTTT others(1): Show |
A | 10 | a0001c0001t0006g0006 a0001c0001t0006g0025 a0001c0001t0006g0052 others(7): Show |
26 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-977_593-970del others(8): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29669284 | ||||||
| chr6:29669292 | C | T | 1 | a0001c0001t0014g0045 | 2 | HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.593-989C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669292 | |||||||
| chr6:29669308 | C | CT | 16 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0089 others(13): Show |
33 | HG02109.hp1 HG02698.hp1 HG02723.hp1 others(30): Show |
intron_variant | MODIFIER | c.593-964dupT | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 29669308 | ||||||
| chr6:29669312 | T | C | 1 | a0001c0004t0012g0125 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-969T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669312 | |||||||
| chr6:29669436 | G | A | 1 | a0001c0001t0014g0146 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.593-845G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669436 | |||||||
| chr6:29669540 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0007g0036 a0001c0001t0007g0037 others(3): Show |
6 | HG01081.hp1 HG02109.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-741C>T | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669540 | |||||||
| chr6:29669588 | G | A | 18 | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0007g0010 others(15): Show |
26 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.593-693G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669588 | |||||||
| chr6:29669874 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.593-407G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669874 | |||||||
| chr6:29669933 | C | G | 185 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0086 others(182): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.593-348C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29669933 | |||||||
| chr6:29670016 | G | A | 10 | a0001c0001t0036g0172 a0001c0001t0037g0080 a0003c0003t0009g0019 others(7): Show |
13 | HG00140.hp1 HG01106.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.593-265G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29670016 | |||||||
| chr6:29670066 | G | A | 8 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0049 others(5): Show |
11 | HG00140.hp1 HG01106.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.593-215G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29670066 | |||||||
| chr6:29670082 | T | C | 2 | a0004c0005t0004g0030 a0004c0005t0021g0030 |
3 | HG01109.hp2 HG01978.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.593-199T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 5/7 | chr6 | 29670082 | |||||||
| chr6:29670402 | A | G | 4 | a0001c0001t0002g0023 a0001c0001t0002g0129 a0001c0001t0002g0132 others(1): Show |
7 | NA18950.hp1 NA18952.hp1 NA18962.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.709+5A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670402 | |||||||
| chr6:29670466 | C | A | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.709+69C>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670466 | |||||||
| chr6:29670538 | C | G | 1 | a0001c0001t0031g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.709+141C>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670538 | |||||||
| chr6:29670645 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0093 a0001c0001t0005g0038 others(2): Show |
5 | HG01261.hp2 HG01975.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-56G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670645 | |||||||
| chr6:29670648 | G | A | 11 | a0001c0001t0005g0043 a0001c0001t0005g0139 a0001c0001t0030g0138 others(8): Show |
14 | HG00642.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.710-53G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670648 | |||||||
| chr6:29670657 | A | G | 35 | a0001c0001t0004g0005 a0001c0001t0004g0015 a0001c0001t0004g0018 others(32): Show |
67 | HG00609.hp2 HG00639.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.710-44A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670657 | |||||||
| chr6:29670671 | A | G | 1 | a0001c0004t0034g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.710-30A>G | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670671 | |||||||
| chr6:29670697 | T | C | 4 | a0001c0001t0002g0074 a0001c0001t0003g0016 a0001c0001t0005g0016 others(1): Show |
7 | HG00140.hp2 HG02559.hp1 HG03491.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.710-4T>C | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 6/7 | chr6 | 29670697 | |||||||
| chr6:29670738 | CTGTTA | C | 8 | a0003c0003t0009g0019 a0003c0003t0009g0033 a0003c0003t0009g0049 others(5): Show |
11 | HG00140.hp1 HG01106.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+19_730+23delGT others(3): Show |
MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 29670738 | ||||||
| chr6:29670981 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.731-191G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 7/7 | chr6 | 29670981 | |||||||
| chr6:29671115 | G | A | 1 | a0001c0001t0024g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.731-57G>A | MOG | ENSG00000204655.12 | transcript | ENST00000376917.8 | protein_coding | 7/7 | chr6 | 29671115 |