Tag | Content |
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EnhancerAtlas ID | HS105-48496 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:237486400-237487820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr2:237486972-237486987 | CCTGACCTTGACCTG | - | 6.57 | REST | MA0138.2 | chr2:237486535-237486556 | GCTGCTGTCCCTGCTGCTGCC | - | 6.47 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00605 | chr2:237475122-237490782 | Adipose_Nuclei | SE_28108 | chr2:237484181-237488584 | Fetal_Intestine | SE_28893 | chr2:237484168-237488685 | Fetal_Intestine_Large | SE_42057 | chr2:237485490-237488875 | LNCaP | SE_48031 | chr2:237485489-237488874 | Pancreas |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I236578 | chr2 | 237487130 | 237488810 | GH02I236575 | chr2 | 237483928 | 237486754 |
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Enhancer Sequence | TGAGGGTCAT TTCTTTCTAG CCCCTGTGAA TGGCCCAAAC CCCAGGATTT ATGGCAGCTT 60 CTGCTGTGTG GCTGTGCCAG TGGGGACAGA GCAGGGAGCC CAAGCCAGGC GCCAGCCGAG 120 CTCCCTCTGG ACCCAGCTGC TGTCCCTGCT GCTGCCCAGC TGTGGGGCGG TCCTCCATTC 180 AAGCTCCTCT GCTCCCCGGG ACTCTGGGGT CAGATGAGAT CATGGGGGAA AGTGTTTTGG 240 AAACCAAGCC ATGATGCAAA TGTGTTTCGT TTTAAGGAAA TGGGAGAAAG GAACAAGGAT 300 TGTTGCAGTA GAGCCATGTG GGGAGAGCAA AGGTGAAATC CTTGTCTCCT GGCATCACGG 360 GGTGGAGAGT GGAACGTCAG CTCTGGGTCA TTTGGTGGCC AAGGAAAGAT GGCGATAGTA 420 GCTTCAAGGC ACGGCCTGGG GTTGCCCGTC CACCCTGGAG GCAGTCTGGC AGGACAGGGT 480 GTCCTCAGCT CCCTGCTGGG CCTACGTCCT TTTGGAGTTC TAGAGCTGCG TCTTAGGACA 540 AGTGTGCCAA GCCTCCTGCT TTGAGTTTCT GTCCTGACCT TGACCTGGCT CACCTCCATG 600 GGCAGCCTCC CATGCTTGGG CATCAGGGCT TGTCATAAGT CCGTGGTCAC AGGGCTTGAT 660 TCCTCCTAGT GGGTGACTCT GAGGACGGCC AGGCCTCCCG CTGCAGGACC AGCGTGGTTC 720 CCTCCATGGA AGGCTTTCAG AGTGTGGAGG GGATGCGGCT GTCTTGGGAG GCCCAGCCCT 780 TTCTGTCAGC CGTGGAGGAC ACTGAGTCAG GTTAGGTCAC GAGGAGGGGA CCCCACAGTC 840 ATTTACATCC CGCAGAGGGA AGTGCCCAGA AGCCCGCAAC AGTCTCCGCT AAGTGGGGTT 900 CACGCCAGGT CCTCTGCTGT GAATGTGGAG GCTGTGGAGC CGAGGCCGCG AAATTTCTCA 960 CTTTTCAGGG ATTCTGTTCA AGTTGTCCCA AAGGAGAAGC CCATCAAACA ACCCAGTCTC 1020 TGTGCGAGCT CCCCCGGGGG CATTTACTAC TCAGCCAGTG AGAGCCAGGT TTCCAGGGGA 1080 ATAGAATTAA ACAAGGTTCT GCTTTTTGCT GAAGGGAAAA ACCGCTCCCT TAGGTGGGAG 1140 AATCCCCAGG GTTCTTTCTT CCTGGCCAGG GAGGGAGAAG GGGGTGACGT TTTATTGAGC 1200 ATCGGCTAGG GCCAAGCTCT CAATTAGGCC CTTTCTTCTT TCTTCTTAGG GTATCTGTGA 1260 GATAGGTGCT GCTGTCCTGG GGAGGTAGAT GCAGACAGAT TAACTCTCAA GGTAAATGCT 1320 AATGAATAGA GGAGCCAGAA TCCCAACCCA GGAATGTCTG ATCTCGGAGT GGGCGGCTTC 1380 CCAGCTGTGG CTTTGCATAC CGCTAGCGTA GCCACCCGGA 1420
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