Tag | Content |
---|
EnhancerAtlas ID | HS091-31017 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:40725450-40727060 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr20:40726564-40726577 | CAAAGGTCAACCG | + | 6.42 | RARA | MA0729.1 | chr20:40725455-40725473 | GCTTGAACTCTTGGCCTC | - | 6.17 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_43799 | chr20:40725223-40727369 | MM1S |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I042096 | chr20 | 40725532 | 40729891 |
|
Enhancer Sequence | GCTGGGCTTG AACTCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACCATGCC 60 CAGCCTCTAG ACCCATCTTT CTAACAGGAA CCCTGGCTGT GTTATACCAC TGTCAACCCT 120 CCAGTGTTTC ACCTTCCTGC ACAGAAAGTA TTTCTAACTG TGCTCCTCCA AACTCCAGTG 180 GTCCCACAAA GGACTGACCC CTCTAAGGGC ACCAGGAGAA AATGAGACAG CAGTGTGGGT 240 GGAAGCCCAA CCCCTGCCTA CTGCTTCATC ATGAGCAGCT TTTGGTCATC CCTATTTCAT 300 ACATTGGGCT TGCATGAAAG CTTTTATTCA TAGAAAGGAT TCTGTCGCTT ACAAAGTAGA 360 AGTCTGAAGC TTGCTATGCT GCCAACCAAG ACCCAAGCTC CTTAGCCTGG CACAGGGACC 420 TCTCTGCAAG CTGGGCTCTG CTGCATTTTT CAGCCTCACT ACATTCTTCT CCTCCTGATA 480 TTCCTCTAGG TCCCAGCCAC ACTGGAACAT AAACTGTTCC GCAAATAAGT CTGTGTATAT 540 TCATCCCCTG CCTCGCCTTT GCCTCTGCTG TTCCCTCTGC CTGAAATGCC TTTTCCCAGT 600 GAGTTCAGCC TCCATATGCC TAAAGCTCCT CTGCCTTCTT CAAGGCCAAA GTCACCTTCT 660 TTTTGAAGTC TTCCCTCACC CTCTGGGCAG AATTCATTGC TCCCTGCTCC TGGCCAACAC 720 AGCACTTCAC TGCTGACCTC TATTATAACA CAGCCACATG AGGTTGGGAC AATGTGCTCA 780 TCTGTCTCTG GAGCAAGACC ATGCGCTTTT GGAGGGCTGA AACTATAGCT CAGGTCTGTT 840 TAAAAAATTT TTAAATTCCC ATCCAAGGCC TGCACAAGGC CAGCTCTCAT ATGGGAATTC 900 AATGTTACTT TAAGTTTTAT TTAAGGCAGT GAAAGGATAG GTTTTTAAAA ATCTGAAGGA 960 CCATTCTCAG CTCTTCCACC CCAGAATGGC TGCCCTGGCA TAGAAACTGT TCCAAGATAC 1020 ACGTCCTGTG TCCTGAGTAT GGGGATATGC TGTAGGCACG TGATGCTTGG AGCTATCAGA 1080 ACAGAGGGGC TAAGGCAGGA AGCCTGCCGG GGAACAAAGG TCAACCGTGA GGAACTGGGG 1140 CTTGGTGGGG TGGTCAGTGG GTAATGTGTC CAAGGTTCAA GTCCCAGGCT CTGTCTGTAC 1200 AGGCTGCATT GCAGAGGGGG AAGGGAGGTG AGTGTGGCCG GGCATCTGGG TATTTTTCAG 1260 GGCTGCAGGT GCTCAGTGCT GGGGGAGGAA GCCTCCTGGC TCTGCAAGAT CTGTGTGATT 1320 TGGAGCAAGA CAATAATCAA TGCTTGTGAG ATGGAGCAAC AGAGTCTGGT CCCGGGCGGG 1380 GAGTTGGACA AAGCCCATAG GCAGGGGGAG TCTTTGCTGG AGGTCTGGGG GGTGACAGGA 1440 CCCTCTGTAG GTAGCAGAAT GGCTTGTCTG ATGCTCGTGG CCAGACACTG CTTATTACAA 1500 GACAGCTGGC TGGGGCAGAT GTGGCAGGCA CCGGCTGTCA AGGGATCTCC CTCCAGGTTT 1560 AGAGCATGGC CCCCCTGACC CACCTAGGGC TTGGCTTGGC CTCCTCCTAC 1610
|