Tag | Content |
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EnhancerAtlas ID | HS091-07053 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:10624800-10625950 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS3 | MA0737.1 | chr11:10625194-10625208 | TGCCCCCCACAAAG | + | 6.1 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_01546 | chr11:10624293-10626559 | Aorta | SE_09736 | chr11:10617530-10636071 | CD14 | SE_10512 | chr11:10625398-10636066 | CD19_Primary | SE_11292 | chr11:10622400-10636276 | CD20 | SE_25798 | chr11:10617606-10629692 | Duodenum_Smooth_Muscle | SE_27162 | chr11:10624462-10626575 | Esophagus | SE_39068 | chr11:10624738-10629673 | IMR90 | SE_53459 | chr11:10624554-10631450 | Spleen | SE_54561 | chr11:10624920-10626610 | Stomach_Smooth_Muscle | SE_59736 | chr11:10619159-10666414 | Ly4 | SE_63010 | chr11:10625185-10682031 | Tonsil | SE_64956 | chr11:10625412-10626339 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I010598 | chr11 | 10620462 | 10632701 |
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Enhancer Sequence | GAACAGGAGT AGGAGCATCA CCTGGGGTCC TCAAATAATG TTATGGACTA AATCAGCAGT 60 CCCCAACCTT TTCGGCCTCA GGGACTGGTT TGGAAGACAA TTTTTCCACA AACCTGGTGG 120 GGGCGATGGT TTGGGGATGA AACTCTTCCA CCTCTGATCA TTAGATTCTT ATAAGGAGGG 180 TACAACCTAG ATCCTTCGCA TGCACAGTTT ACAATAGGGT TCGTGACCCT ATGGGAATCG 240 AATGCTGCTG CTGATCTGAC AGGCGGCGGA GCTCAGGAGG TCATGCTCTC AGGCAGCTCA 300 CCTCCTACTG TGCAGCCTGG TTCCTAACAG GCCATGGTTT GGTACCGGTT TGCGGCCTGG 360 CCCAGGGGAT GCGGACCACT GGGCTAAATG TCTGTGCCCC CCACAAAGTC ATCTGCTGAC 420 TTTTGGGGGG ACATATCCTA ACTCCTCAAT GTGATAGTGA AGTGGGGCCT GGGCGAGGTG 480 ATTAGGTGAG GAGAGTGGAG CCCCACGAAT GGAATTAGTG CTCTTATAAA AGGGACCCCA 540 GAGAGTTCTG TTCTCTTTCC ACCATGTAAG ATATAATGGA AAGGTGGTAG TCTGCAAGCC 600 AGAGATGGCC CTCACCAGAA CCCGACCATG CTGGTGCCCT GATCTTGGCC TTCCAGCCTC 660 CAGAACTATG AGAAATAAAT GTTTGCCATT TAAGCCACCC AGTCTAAGGC CCTTTGTTAC 720 AGCAATTCAA ACTGACTAAG ACACACACCA AGCCTAGACT CAGCTCTCAT GAAAGCAGCT 780 CTGGGCCCCA TCCAGGCTGA GAGAAGTGGC CTCTGCAGGG CCTGGGCCAC AGTTTCTTCT 840 GGTGCTTGGA GAAGCCCAAT GTGAACACGC TATCCCTGGC GCCTGAAAGT AGGAGTCACA 900 CCCAGGCCAC CCTGCCCCCT TCTGAGAAGC TCCCAAGGCT TTGGAGGACC TGTCCACAGC 960 CCTGAGGGAA CCAGGCCTTT GGGATCTCTG CCTCAGTTCC CCCCAACTCT CTGAGGAACA 1020 CTGTCAGAGT CTTGGCTCAA TTTTTCACTT CAGGAGACTA TACTTGGTAC CTGAGAGAAG 1080 CATGACACCC TGTATGGCCC TTGGGGACAG TCTCTGCTCC AGGGATTCCT CACATCAGGC 1140 TCCACAATTA 1150
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