Tag | Content |
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EnhancerAtlas ID | HS098-08892 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:133774530-133776490 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:133775941-133775962 | TTCCGTTTTCATTTTCCTTTT | + | 6.3 | Nr2f6(var.2) | MA0728.1 | chr10:133776450-133776465 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_47883 | chr10:133774246-133774742 | Pancreas | SE_47883 | chr10:133774821-133775236 | Pancreas | SE_47883 | chr10:133776060-133776372 | Pancreas |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH10I131960 | chr10 | 133774247 | 133774742 | GH10I131961 | chr10 | 133774987 | 133776470 |
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Enhancer Sequence | AGGGACGGAA GCTGTCCGTG AGCTGGTGAG ACAGCAAGCC AGGAATCCAG CCACAGGTGG 60 GGAGACAATG CAGCTCAAAC TGGTGGAGCT GCAAGGGCCC ACAGACCACC TTCAGACGCT 120 GCCCGCGGCC GACGCTTCCC CAACCCCTGG GAGAGGCCTG GGCCTGGGGG CCTGGCGGGC 180 CCCGCGCTCT TCCCTTGGGT CCCGTCCTCC GAGGGGGCTG CCTGCCAAAG CCAAGTTCAG 240 CAGTCCCCGA CAGTGGGCTT CTCTGCACAG GTGGTGTGCA GGGGTGGGTG GAGTGTAGAC 300 CAGATGTGAG TAAAGGCAGC ACCCCCAGCC CCACAGGGCT GTCACAGCTC AGGCCCTGCA 360 GAGCTGTGGG GTTTGGCTGC TGTGGGTGGC AACCCCTCCT AAGTGCCTGC TGCAGGTGGG 420 CGCTGGGCCA GGGCTTTCCC TACAGCCACC CTGGCCATGG GTCACAGACG CACACACCAC 480 AGCACCCGGC TGGGCACTGG GGTGATACTG GGCTTGGCTT TGAGCTCCGT GCCTCTGTGC 540 CCCATACGCC CCTCAGATCT CTGGTGACAG TGCGGGGCTG CCTACAGGAC ACCCAGGGCT 600 CCTTGATCTT TTAGGAACTG CGGCACCCCC GAAGCTGTGA CAGGTGCAGA GGCGCTGCCG 660 TCCTGGGCCG GGCCTCACCT TCCGCCTTGT GTGCTCTGGC GCCAGCACCC AGTCCCAAGG 720 GCACAGCGGC TGCGACTTGC CTCTGGCCAG GGCAGGTGGT GGTGTCATAC CCAGGACGGG 780 AACCCACACT TGATGTCCTC CAGGGTTTTT TTTTTTTACA TTATCTTAAG GACTGACAGT 840 CTCCCACCCC ATCTGCTCCC ATCTGTCCCT AATTTCATGC GCCTCCGCCT GAGTTCCTGC 900 ACGCATTTCC TGAATAAACA CACCCCTGTG CCAGTCAGAA CCCGCGGGGG TTTTGGAAGT 960 GAGAGCCCAG CAAGGCAGCT GGCCAGGGGG CGGCACTGCC CTCCGGGGAG CACCGGTGCC 1020 CGGGACTCTG CTTCTGAGGC TGGCCTGTAC GATGATTTTG TATAAATATC TCCAATCAGA 1080 ACCTTTTTAG TGTATTTCTT AATATAACAG AAACTGGTGT CTTAAAATAC AAGACTAGCT 1140 GCCCGGTGAT GACACCAAAT CGAGCAGCGG GGCTCGCAGT GGCCAGGATC CCCGACAGTG 1200 GAATGCTGAG GTTAGAACTG AAACCGCGTT TCGTGAAGTC ATCATCACGC ACGGGAAACA 1260 GGTTTGGGGT GAGGGGCGGT CCAGTCCTAA GAAAGCTCTC CAGCTCCACG CGGTCACCTT 1320 CACTCACTCA CCAGATGCAG ATTGCAAAGA GGCGAAACCT GTGATTTCTT TAATAATCAC 1380 AGTCTCCATC TGGTGAGTGG TTAAAGTCAC GTTCCGTTTT CATTTTCCTT TTGGTGGCTG 1440 GGAAATGCTT CTGATAGTAA TAGTTTTCGA TTCTGCAACT CCCATTGTCT TAGGCTCTGT 1500 AGCTCTCCAT TTTCTTCTTA TCCTTGGGAC GTGTCTTGGA CGTTTCTAAC AGGCTGTGTT 1560 CCTGGACCTG AAACTCAGCT GGAGACTGGG TCCCTTGCAG ATTTGCAGGG ACCGTCCATC 1620 GCTGGTGTGT AGATGCAAAA ACAAAACACT GGCACCACCC AGTCAGAACT GGCAGGGGCT 1680 GCCTGCACTG GGCACCAACC CCGCAGATGG CCAGGCCCAG ACCACGTGAC TGCCTGCTGG 1740 GCTCCACCCC CAACCGCAGC CCAGCCAAGG CAGAGAGGTG GCTGCACTTC CGCCGATCAG 1800 AGGTCCAGAT AGAGCTCCGT CTGCTTGCCT TGGAGTTGTT AGAAAATTAT CTTTGGGGCT 1860 AGGCATGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA AGCTGAGGTG GGCGGATCAC 1920 GAGGTCAGGA GTTCAAGACC AGCCTGGCCA TCATAGTGAA 1960
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