| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00117 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:2431160-2433550 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr1:2431551-2431562 | TACTTCCTGGT | - | 6.02 | | Myod1 | MA0499.1 | chr1:2433488-2433501 | GGGAGCAGCTGCA | - | 6 | | Tcf12 | MA0521.1 | chr1:2432775-2432786 | CAGCAGCTGTT | - | 6.32 | | ZNF263 | MA0528.1 | chr1:2432367-2432388 | CCTCCTTCTCTCTCCTGCCCC | - | 6.4 | | ZNF263 | MA0528.1 | chr1:2432354-2432375 | CCCCTCCTATCCCCCTCCTTC | - | 6.96 | | ZNF263 | MA0528.1 | chr1:2432211-2432232 | TCTCCTCCCCTCCCCTCCCTC | - | 7 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I002499 | chr1 | 2430966 | 2432034 |
|
Enhancer Sequence | TGAGTGTCAC CCCCTGCCAC CAGCCATCAT GGGGAGGGGC CACACCAGCC CCTTGTCCCA 60
TGCCCCCCCA TGTGTCCCCA GTGCTGGGTC CTGAACTCAG GCAGTGAGGC CTAGGGTCCC 120
CTCCCCGGGC CTCTGCTCCT CTATCTCAAG AGGGGCTGCT GTGGGGGCCT GGCTCCTGAG 180
CCACCAGTGC CCACCTCTGA TCTCAGGGCT GGCTTTGGGC ATCTCGGGCA GGACAGGTCC 240
TGAGTGCTCC GGGCCTTGCC CCGCCCTGTG TCACCCATGC CTGTCTCAGA CTCTTGGGGG 300
CCTTGCAGCC TCCACCCCTA CAGTGCTGCC ATCTGGCTTC TCAGCAGGGA CCGAGTGATG 360
CCCCTCTCCC CTCTACTACC CCCCACCCCT CTACTTCCTG GTGTCACGTG GAAGGCAGCT 420
GCCCGGGTTT GCCTGTGACT CCACACCCAG CATGTCTGTC CCCTGCCCCA GGTCAGGGTG 480
GGGCCTCGGC TTCCGCAGGA AGTGGTCTTG GTGCCAGCCC TGCTGCCCTG GCTTTGAGCT 540
GGGGCCCAGT GCCCTCTGGG TCCTGCTGGC TGCAGCTGGC CCTCGGGGAA CCCGCACACA 600
CAGCAGGAGG GGCCTGCCCA GGCCCAGTGC TGACTCTCTC CTGCCATGCT CTCGGGCCCA 660
GAGGTGCCAT CCAGCCCCTG CCGTCTATCC ACCCATCTGT TCCTCGTCCC CCAGGCTGCA 720
GGGCTCCCCA CGCCACTGCT GTGGCCGCCT CACCTGCTCC CCCTGTCTCT TTGGTCTTGC 780
AGTCGGCTTC TCTATGGCCA CAGCCTACTT TTAGAAGTGC AGCTCTGTTA GGAGCCTTGA 840
AGGTACCCGG TGCGCGGGAC AGTGCGGCCC GCCGCCCCTG CATGCCCAGG CCGCACCCCA 900
TTAGCATCCA TGATTCCTGG TAGCATTTGG AGACTGTCGC TCATGTGACG TGGATCATGA 960
CATGGCTCCG GGGGCCCTGG CCATCCCCAG CCATAGTGGC ATTTACGAGG CAGATCCAGG 1020
GTTCAGCTGG GTGGCCGCCT TCTCACTGGC CTCTCCTCCC CTCCCCTCCC TCAGTCCTCC 1080
CTCCCCTCCC TCAGTCCTCC CTCCCCTCCC TCAGTCCTCC CTCCCCTCCC TCAGTCCTCC 1140
CTCCCCTCCC TCAGCCCCTT CCCTGGCGGG CAGCCCGCTG GAGCCCCCAC TGTGCCCCTC 1200
CTATCCCCCT CCTTCTCTCT CCTGCCCCCA TCTCGGACCC TCAGGCTGTT GGTTCTGAGT 1260
TCGCCTCCCA CTCCCTCCCT GTCCTTGCCA ACCATGCCAG TGCATGGGAT GAGGGCACCC 1320
CTGAGGCCGG CGCTCCGAGC CAGAATCCCG GATCTGCTTC TAAATGGCTT CCCAGCCACT 1380
GTGACCAAAT GCGTAGATTT GGGATCTTGA ATCAGGAAGC TGATTCAAGT GCTGGCCATC 1440
TGAACGCATC TGCCCAGAGG CGCCCCTGCA GGGGGGTGAC CCACCTGCCG GGCCTGGGCC 1500
GCTCTGTGCA CGAGCACGGC TCGTCATGGG GGCGCGGTGG GTGCTGTCTC GGGGGCATCT 1560
GGCATGTGAG GGCCCCTCTG GCCTCTGCGC CCTGGAGATG CGGCTGCCTC CCTCTCAGCA 1620
GCTGTTCTGC CCAGGCAGGG ACCTCCTGGG CCCAGCTGTC CAGGAAGATT GGCTGTGGCC 1680
AGGTGCTGGT GGGCTGGGAG TCTGAGCCCA TCTTGGCAGG GCTCAGGGGG CAGCAAGCCA 1740
GCTGCGGGCC TTGGGGGCTC ACATGAGTGG AGGGCAGGGC AAGACCAGAA AAGGCTGCCT 1800
GGGGGAATTC AGGAAGGCTT CCTGGAAGAG GTGGTACTTC CTAGGGCACG AGTATCACCA 1860
TGGGAGTGGG CAGGACACGG GCCGGGCAAG TGGGCCTCCC GCTGCACCTG GCTACTCCTG 1920
CTGTGGACCA GCTACTCCTG CCTGAGGGTG GGGCACACAC AACCAGGGAG TGCCACGCCA 1980
GTGTCCCCTG CTAGCGCCGG GGGCTGCGGG CCTCTGAGCA GGTGCAGGCT GTGGTGGGCC 2040
AGGCTGGGGC TCGAGGTCTC TCCTCCGGAG GGAAAGACCT TCTCTCCATG CCCCTCAAGG 2100
GCCCCACATG CCCTGGACAG GTCAGGCGAG GGCAGTTTCT GCCGGAAGGG TGGGGTGGGC 2160
CATGTGTACT TAGATCTGTA GCAGCTACTG TCCCAGGCAG AGCTGCCCTA GGGACCCTGC 2220
TCCTGAAGGC CCTGGTGTGT CCACACACCC CCAGCCTGAG GTGGCCCAGC CCCTCGGACC 2280
GAGACACGCA TGGCACGTCT GTGGCACGGT CTGGAGAGCT GGCCCTGGGG GAGCAGCTGC 2340
AGCTGGGCTG GGACCCCTGG CAACAGCTAC ATGGGCTCCT TCTCTTGCAG 2390
|
