| Tag | Content |
|---|
EnhancerAtlas ID | HS091-29429 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:238484120-238485890 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr2:238485307-238485318 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chr2:238485307-238485318 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_32293 | chr2:238483069-238485350 | Gastric | | SE_41966 | chr2:238482997-238485143 | LNCaP |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I237574 | chr2 | 238483317 | 238484786 |
|
Enhancer Sequence | TTCCTGAAGG AAACAGCCAC AAAATCCAGC GCTGTTTATA AGAGAGTTTC CTAAGGACAC 60
CTGGTTCACT TCCAACAGTA AGATCCGAGA AAGCTGCAGC CGTGGAGCCC GCACTCCTCC 120
ACGTTTCGTG TCCAAGTTGT GTTTCTTGGC ACTCCTGAGC AGCCAGGACC AGGGAGGGGC 180
GGGGTGTGCT CCCTGGAAGA GGCTCTTCCT CTAGCTGGCG GGGTGCGGCC TTCCTCCTCC 240
TGCAGGGCCT GGAAAGCCAA GTCCCCACCC CCAGGTTCCC CTCCCATCAT GCCTGTTGGC 300
ACCTGTGGGC TTTGATGCTG GGCAAAGAAC CAACTGAGAA CCCAGGAAAC ATGAGGCAGA 360
GGGAGGCCCC TGGACGGCAC CCACCTGGGC CCTTCTTCTG GGGAACCCTC ATTTTCCAAC 420
ACAGCTCTCC TCTGGGGAGA AATGGATGTC CCAGAGCAAA GGCAAACCAG AAAACAGCAG 480
GCTTGCAACG GGTGACCAGG AGAAAGCATT CATGGGAAGG CCACAGCCTT GCCCAGGAGT 540
CGAGGGTGGC CGAGGAATGG GGGCCTTCCT GTGCAGGCCC CTCCCCTGGC CTCCGGGACT 600
CTCCCAGGAA GAGGAGCCTG TGGTGGATCC CAGAGGGCAC AGCTCAGGCT CCTGACTGTC 660
CAGCCAGACA TGGAGCTGGC AGCAGGTGTG GCCGGCCATG CCCCCAGCTC TCGCACCATC 720
CACCATCGTG AGTGCACTCC TCCTGTCCTG GCCCGGAGAT CCCTCGGCCG GCCCTGCATT 780
TGTCCCCACT GAGCTCCCCA GCCAGCTCCC CAGACAGACG CTCCAAACCC ACCCTGGCCG 840
CCCACTGCCC CTCCAAGCCT TGAGTAACCT CGTGCCCATG TTTTTGTGCC TGCCCAAGCA 900
CACAGCCCAT GTAGTCACTC TCAGAGGGCA CAGCTCTGCT GCCAGGATCC TCTCTCCCCC 960
ACCCCAACTT GCAACGAGGG CTCAGACTGA CGCTGTCTCC CTTTGCTCCC CTTGCTCTCC 1020
CCCGAGATTC TCCAAAATCT TCACCCCACT TCTCCATCTC TCCACAGCCT CCATTGAAGC 1080
TGGGGCCTTT TCTCTTTGGG AGGCGCGCCC GTCGGTCTAA GCCCTGAGTT GGGTCTTCCC 1140
CTGCGCCAGC CTCTAGTGTG TGTGGGGTCT CCCCATCAGC CACTTGTCTG CAGCTGTTTA 1200
CACGGTCTTC GTCCTAAATG TGGTGGGGGA GGTGGGATGC CGTGGAAGAG AAACAACAGC 1260
GACACCTGGG TGACCGCTGC CTCTGCCTGT AAGGAGGACT GACAAAACTC GAGTGAAGGA 1320
GGCTACATTT GCACAGAAGC CCCTTCTGGG AACAGAGTAG GGAAGGGAGC CCTGCTGAGG 1380
AACTAGATCA CTTTTCTCGT TCAAGCCGAG CCCACCCTGC AGCTGCCGCC CTGCCCTTCC 1440
CTCTGCCGGC CACTGGGCTT GAACTGCCAT TGCACTGGGC CTGAGTTTTT CAGGAAAGAC 1500
CGGAAATCTT TGACTAAAAG AGAAACTCAG GTGGAAAGCT GTGTGTGTGT GCGTGTGTGT 1560
GTGTTCACTT GTAAATGTGT GTGGGTGCAA GTGAGAGTGA ATGTGGGGGG TGTGCATGTG 1620
TGTAAATGCA TGTGGGCGTG TAGAGGTGTG TGTGCACATG TGTAAGTGTG TGCGTGTGTG 1680
GGTGTGCGTG TATGAAAGTG TGAGTGCCAA GGTCTTGACA CAGGCGGGCA GGGCTCTCTC 1740
CTGCTGTGGA AGAGCAGAGC AGGGTCTCCT 1770
|
