Tag | Content |
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EnhancerAtlas ID | HS105-60729 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:77616880-77618030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr4:77617612-77617628 | GGGGTCACAGTCCAGT | + | 6.3 | NKX2-5 | MA0063.2 | chr4:77616998-77617008 | CTCAAGTGGT | - | 6.02 | Nkx2-5(var.2) | MA0503.1 | chr4:77616993-77617004 | AGCCACTCAAG | + | 6.62 | RFX2 | MA0600.2 | chr4:77617488-77617504 | GGTTCCCATGGTTACC | - | 6.05 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_01606 | chr4:77616834-77618109 | Aorta | SE_24309 | chr4:77617569-77617855 | Colon_Crypt_2 | SE_31802 | chr4:77617215-77617911 | Gastric | SE_43754 | chr4:77607361-77625162 | MM1S |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I076695 | chr4 | 77617143 | 77618082 |
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Enhancer Sequence | CCCAAAGTCC TGAGTGTCGT GGAAGATACT CTGGATTATT GGTCCTGACA TCAAAGCCTC 60 TCCATTGCAG TGTGGAGTTA ACTAGGCAGC CAGAATCTCA GGACCATTTC CTCAGCCACT 120 CAAGTGGTGC CACGTTGGTC TATTTCCAGA CCCATCGAAG AAGCCCCTCA GCATGCAGAG 180 ACCTTTGGAG ACACTGGACT GAAACCAGAT GGTGCAGAAA GAAGCCCCTA AGCAAAGTGT 240 TGCTTGCAGC CCTGTATTTG AAAGAGTGCC ACTGTGTACC AATTATGTCC ATCCAAATGA 300 GCCGTATTAT TTTGGGGCAA AATGACTGGG AAATGAAATT ATTAGGACTC TGCTCTCTGA 360 TGGGGAAAAA ATAAATCTGG AAGAAGAACC TACAAGGATC TTAGCTGTCT GCTTGTCTCT 420 GACACTCTCG AGGCCTTGTG CCAGGCTGCT TTGCTGTGCA AAAGCTCCAC TTCAGTCTTT 480 TAGTCTGACT CACAATAGAC GCACATGGTT GAAGTTAGGA GAATTGCAGG ACTGTCACTT 540 GAAGTCCCTC TCAGCCTCTT CACCATCGCC CCCAGCCTCT TTCCCTCTAA CATTAAGCCC 600 TTTGTGTCGG TTCCCATGGT TACCTCCTCA CTACTGGCAG CTGGAATGTG ATAGTGAGAG 660 GAGGCTGCCT CCCCTACTGA GCCAGGTCTG GCTGGGGCGG AGGCCATTGA TCCGCAGCTG 720 GATTTGTGAA ATGGGGTCAC AGTCCAGTAC CTTCTCTTTG TCGTGGGTTC TATACCTTTC 780 CCAGGCTTGA CATATCAGGG TTGCAGTGGG AGGGGACATG GTGGGTGATG GACTGCTCAC 840 AGGACATGTC CTGTCATAGG CTGGCCTGGC CTGGCGTCCC TGACCTGCCA AACTCCTCCC 900 TGAGGTCACC CTTCCATGTG TGAATGCCCA TTGAGGGGGA AGGGGCTGCT CTGCTTGGTC 960 AAATAAAAAT GATGACTCAC TTCTCTACCT GCTTTCTGCT CAGATTCTGT TCCCAATACC 1020 ATCTGTTCTT AAGTTAGTCA ACATTAACAA GGGTGGGCTC CAGTCTGGAA AGAATTTGCA 1080 TCAAAGGCAT GTTTTCACAT CCAGCTTGGA AGACCAGGCA GGCTCTGGGA ACTGGGGGAT 1140 AGCATAGGGA 1150
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