Tag | Content |
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EnhancerAtlas ID | HS091-35823 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:186755100-186756520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr3:186756450-186756465 | TGTTAATGTTTAACA | - | 6.12 | HNF1B | MA0153.2 | chr3:186756451-186756464 | GTTAATGTTTAAC | - | 6.15 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_10196 | chr3:186756274-186764309 | CD19_Primary | SE_10855 | chr3:186755684-186770377 | CD20 | SE_18374 | chr3:186755865-186764690 | CD4p_CD25-_Il17-_PMAstim_Th | SE_29383 | chr3:186755696-186761364 | Fetal_Intestine_Large | SE_35352 | chr3:186755887-186762896 | HepG2 | SE_50921 | chr3:186756011-186761343 | Sigmoid_Colon | SE_58288 | chr3:186627032-186791622 | Ly1 | SE_59164 | chr3:186703252-186764260 | Ly3 | SE_60441 | chr3:186703232-186762793 | DHL6 | SE_61008 | chr3:186703204-186764166 | HBL1 | SE_62186 | chr3:186703447-186763111 | Toledo | SE_62245 | chr3:186702797-186764702 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I187038 | chr3 | 186755809 | 186763098 |
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Enhancer Sequence | TTAACCATAA CTTTATATGC TTGTTAATTG TGCTTTTTAT TTTGTGATTA GTCTGTTCAT 60 GTTGATTACC TCTTTATTTT GGGAGACTTT TATTATATTA ACCCTTTTTA TATTTTGACT 120 TTTCCTTTTT ATTGTAGTTA CAGTATTTTT CATTGTATAG ATGTTGAAAT TTTCTTGCAA 180 CTGAATGTAT TAAACTTTTC CTTTGCTATT TTCCTACATC GCATCAAAAG AAGAAAGAGC 240 TGACAGGTAT ATATTTATAT TTTTAGCTGT TTTTTGTTGG TTTGTTTAGA GACAGGTTCA 300 CTCTGTCACC TAGGCTGGAG TGCAGTGGCG CTCATAGCTC ACTGCAGCCT CTAACTCCTG 360 GGCTCAAATG ATCCTCCCTC CTCAACCTCC TGAGTAACTG GGACTACAGG CATGCACGCC 420 TGGCTTATTT TTAGCTTTTT AAAATTACAT TTTTATACTT TTGTACATTT TTTCAAAGTC 480 AAAGAATAAT GGATGTACAT TTTAGAAATT TTGGAATATA TGTAAAATTA TAAAAGATGA 540 AAACATCTAT TATTACCATT CTGGGTGTAC TTTTTTCTAG TACTTTTTCC TAGTACTTTT 600 TCACGTTTTT TTAAATGTAT TTTTTTTCTG AATTTGGATA GTGTTTACCG TTTTATAACG 660 TATTTTTTCA GTTACAATTA TACTGATTGA ACTTTCACAT ATTATTAAAT ATTCTTTGAA 720 AATAAATAAT TTTTTGAAAA TCTGTATGAA GTTTATTTCA GGATGGACCT AATTACTCCC 780 TGTTTACCTC CAAGCCAGCA ATTAAACAAC CTGTTCTTCC CAGGTTGGTC CATGGTGGCC 840 GCTTTAGCTT TCTAGCCCAT TCTTATCTGG TGTCAAGTCT ATTTCTTTTT TTTTTTTTTT 900 TTTTTTCTTT TGAGACAGAG TCTCTCTCTG TTGCCCAGGC TGGAGTGCAG TGGCGTGATC 960 TCGGCTCACT GCAACCTCCG CCTCCCGGGT TCAAGCAATT CTCCTGCCTC AGCCTCCCTT 1020 GTAGCTGGGA CTACCGGTGT GCGCCATCAT GCCTGGCTAA TTTTTTTTTT GTATTTTAGT 1080 AGAGATGGAG TTTCACCGTG TTAGCCAAGA TGGTCTTGAT CTCCTGTCCT CATGATCCTG 1140 ATCCGCCTGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC CACACCCGGC 1200 TAGTGTCAAG TCTATTTCTA GGCTATCTGT GCTGTTCACA GATCCAGAGC ATTGCACCTT 1260 TAATAGGCTT TTCTCTCTCT CTTTTTCCTG AGCCCTGGAG GCTTCCTGGA TTGAGACCTA 1320 GCCTAGGTCT GCATAAGCAC CTTTCCATCT TGTTAATGTT TAACACTGCC TCTGCTGGAA 1380 AACAGCTCTC ACCTCCTCTC TTTCTGTCTC TTATTTTTTG 1420
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