Tag | Content |
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EnhancerAtlas ID | HS195-01713 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr12:120754800-120755990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr12:120755593-120755603 | ATCACGTGAC | + | 6.02 | KLF5 | MA0599.1 | chr12:120755419-120755429 | GGGGCGGGGC | - | 6.02 | MYC | MA0147.3 | chr12:120755499-120755511 | AGCCACGTGCTC | + | 6.04 | MYCN | MA0104.4 | chr12:120755619-120755631 | GGCCACGTGGCT | + | 6.37 | MYCN | MA0104.4 | chr12:120755619-120755631 | GGCCACGTGGCT | - | 6.37 | NRF1 | MA0506.1 | chr12:120755382-120755393 | GCGCCTGCGCA | + | 6.62 | SP1 | MA0079.4 | chr12:120755417-120755432 | GAGGGGCGGGGCCTG | - | 6.22 | SP4 | MA0685.1 | chr12:120755415-120755432 | CAGAGGGGCGGGGCCTG | - | 6.17 | TFEB | MA0692.1 | chr12:120755593-120755603 | ATCACGTGAC | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_48023 | chr12:120754608-120755524 | Pancreas | SE_65438 | chr12:120753829-120756250 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I120316 | chr12 | 120754472 | 120756202 |
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Enhancer Sequence | GTGGGGTAAC AGCAGCTGTA CCTGCGGAAG AAGGACAAAG CTCAAGAAAC TTCCAGAAGT 60 GACCCAGGCT GGGTTCTGAA AGATGAACAT GCCTTCACGA GGTAGGAAAA GGGAGGAAAC 120 CACTCATGCA AAAAGCATGG CTGTTACACC ACCAAATCTC TTCGGTTTTT TTTTTCCCTT 180 CAATGTGGGG GTGGAAATTT AAGTGTAGAT TTGGGGCGCC TCAGAGGCCT GTGGCTCGCC 240 CAACATCCCC TTGCCTCTCT GCTTGGCCAC CTCTCCTCTC AGCTCCCCTT TGTTCCCTGC 300 ACCCCACTTT CCCTACCCCC TAATCCGTCC CCGGGATAAA AGCAATGCAG GCGATGCCCA 360 CAGGAAACCG GCAGGAGGAG CTGGGTGACA GGGAAGAGCG ACCCGGAGAG TCACATCCAC 420 GTGAGTTCGC CCTCTTTTCA CACTCTAGCG CCCATTCTGT CCTTCCTGCT GGATTCTGGC 480 TCAGGAGAAG AGCGCCGCCA GGACCCCAGG AAGCTGCAGA CAGGAGCCGC TGACACCTCC 540 ACCTCACGCG GACGCCACCT AGTGTGACCA TTACCAGCCA CTGCGCCTGC GCAGACTCGG 600 GTTTTCTGTG CGCGCCAGAG GGGCGGGGCC TGGGCCGGGA AGGGGCAGAA GTAGACCGAC 660 GGCTGGGCCG CCATTCACCA ATAGAAAAGA GAGATCGAGA GCCACGTGCT CATAAGATAT 720 CCAATCACAA TCACATCCTG TGGCGGCGGA TTGGGGGGCG TGGACTAGAG GTTGATCGGG 780 TTGGGCACAC AGCATCACGT GACACGAAAA GGTAAATAAG GCCACGTGGC TTTTTCTCCT 840 TGGCTTCGGC GAAACATTAC GTCACACTAC CGTCTCTGAA CAATTATTTA ATGAACTTAT 900 GTGATGCGCT AGACAATGTG AAGACAATGC GGTTGCTAGA AATTGTAATC TCTCCATCAA 960 ATTACTCTGT CCAGCTTATT TCCTTGTTTC TTCATTCAAA TCATCCTAGA CATTCAACTA 1020 GTTTTCCGTA TCCTACTTTC ATACAAATGC TCATTTAAAG ATAATTAAGG GAATTTATTC 1080 TCTCTTTCCC AAGCCTTGAT AATGAAAAAG AGGTAGGTTA TTTTGTTGTT GGTTTTTTGT 1140 TTTCTTTTTT CTTTTTTTTT TTTTTTTGAG ACAGGGTCTC ATTCTATCAC 1190
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