Tag | Content |
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EnhancerAtlas ID | HS091-27394 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:120197830-120199130 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr2:120198692-120198703 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr2:120198692-120198703 | CTGAGTCACCC | - | 6.02 | KLF4 | MA0039.3 | chr2:120198245-120198256 | GGAGGGTGTGG | - | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00730 | chr2:120197517-120199731 | Adipose_Nuclei | SE_27766 | chr2:120196802-120199730 | Fetal_Intestine | SE_28652 | chr2:120196991-120198896 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I119439 | chr2 | 120196803 | 120199731 |
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Enhancer Sequence | CACCTGCCCG GGAGACCAGC CATCAGCCCA GGAGGAGAGG ACAGTTCTGT GCCTGGAGCC 60 CTGCTCACTC CCCCAGTGAC TCCACGCAGG CCCTGCCACT CCTGCCCAGC TGCCCTGTCC 120 CCTAGCCTGC AGGCCACGCA GATTGACTGT TTCCAGCCCC AATGTCCAGT AGCTACTGAG 180 GGTCCCCTCT CTCCTGGGCA CATGCACCTG CAATCTCATT ACATCGTGTC TTAAAGAAAG 240 GACTTGTGCA CCTTGGGACA AGTGTGTGCC CTTGACATTA CAAGAGCAGT GGTGGGGAAA 300 GCTAGCTCCC TGGCCCCCAG GCTGAGAGGA AAAGAATCCC GGATTAAGCC AGAGGCTGAG 360 TTCTCTGAAG GTCTGGGGCA CTGACAGGGG CTACTGGGCA GAGGGCCAGC TTAGAGGAGG 420 GTGTGGTCTG AAGGTGTGGG TAGGGCAAGG CCTGACTCCA CTCAGTGATG GGTCCCCAGT 480 GATTTTAAGT GATTTAAGAT GGGTCCCCAC TTATTCCCAG GAAGCCACCC AAGCTCAGAA 540 CTGATCTGGG AACTAGGGAG TTTCTCTTTG TAAATTTCCT TCACAATTCC CAGCTGCAGC 600 AGCTGAACCT TTGAAGCTAG GCTTGATATT TGATTTTTGG GAAACATCAA AGATCACTCC 660 CATTCAAGTG CAACAAACCA GATAGATGGT CAGTAGTCAC AGAAAGCCTT AGCTCATGTT 720 AACCACATAG CTCTGTATGC CCAGAGCCTG GGGTCCTGAC CCAGATGCTC CATGTGAGGC 780 TCGAGTCCTC AAAGTGAGTG TGCAGTCTCC CAAGGAGTCA GTGCTCATCT GGAGGTCCCT 840 AAGGATTGAG CTGCAGACAG TTCTGAGTCA CCCGTTTCAC ATATGGGCAG ACTGAGGCCC 900 AGAACAGGGC AGTGACTGAG ATCGCCCATT AAGCAAGCAG CAGGGCAGTC AGGAACCTGG 960 GTTCTGCCCA ACTTTCCTCC TGCATTTGCT GAACAGATCA ACATCGGCAC CAGGAATGCT 1020 TGTTAAAAAA CACTTTCTCA GACCCCAGTC CAGACCTACA GAATTTATTT CTGTGGAATG 1080 AGAAACTAGG AACAGGGTCC AGCCATGGTT TGAACAAGCC TTGCTCCCAT TAAGCAAATT 1140 CAGACTCCTA AAAGAACTGG CCAAGCCACC TGCCACCAGA CCCAGGACTC CCTCTGACCC 1200 TTTCCATCCC CCTTCCTACC ACCCCTCCCA GGTAGCTCCT TCTGACCCGG AAACCAATGG 1260 CTAGGAGCTC TCCTGGGTAC CTGGGTGACC CAAGACTACT 1300
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