| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00752 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:22144700-22145950 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:22145357-22145368 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:22145357-22145367 | GCCCCGCCCC | + | 6.02 | | MEF2C | MA0497.1 | chr1:22145564-22145579 | TATATAAAAATAGCA | + | 6.26 | | Nr5a2 | MA0505.1 | chr1:22145074-22145089 | GCTGACCTTGACCGC | - | 6.38 | | RREB1 | MA0073.1 | chr1:22145039-22145059 | TGGTGTTGGGTGTTTGGTGT | - | 6.98 | | SP1 | MA0079.4 | chr1:22145354-22145369 | CTGGCCCCGCCCCCC | + | 6.51 | | SP3 | MA0746.2 | chr1:22145356-22145369 | GGCCCCGCCCCCC | + | 6.11 | | SP4 | MA0685.1 | chr1:22145354-22145371 | CTGGCCCCGCCCCCCGC | + | 6.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I021818 | chr1 | 22145094 | 22145798 |
|
Enhancer Sequence | CTCCATGTTG GACAGGCTGG TCTCAAACTC CTGACCTCAA GTGATCCACC CGCCTTGGCC 60
TCCCAAAGTG CTGGGATTAC AGGCGTGAGC CTCCGCACCC GGCCTCATGT TACATTCATT 120
AATAGTCATC ATGCCTCTTT AGGCTCCCCT TGGCTGTGGC AGTTTCTCAG GATTTCCTTG 180
TTTTTAATGA TCTTGACAGT TGTGAGTACT GCTCAGGGAT TTTGTAGGAT GCCCCACTAT 240
TGGGATTTAT TTGATACTTT TCTCATGAAA AGACTAGAGT TACAGTTCAC AGAGGTGAAA 300
TGCCATCTTC ATCACATCAC ATCACACCAA ACATGACTTT GGTGTTGGGT GTTTGGTGTT 360
GGACGGTGGT TGACGCTGAC CTTGACCGCC TGGCTGATGT CTGCCTCATT TCTCCACCGT 420
TACTTTTGGT CCCATCTTTC CCCACTGTAT TCTTGGGAAG TCACTATGTA TAGCCCACTT 480
GAGTGGGGAG TTATGCTTCC CCGCCAGAGG TACCTTTTAA AACAGTAAAT CAGGTTATGT 540
CACTATCCTG CTCAAAACCC TCATCACATT CAGCAAAGGC AAAGCCTCGC CCGGGCTCAA 600
AGGCCCTGCA CGATCTGGCC CTGCCCCTTC TTTCCTGGCC TCGCCTCTTC CTTCCTGGCC 660
CCGCCCCCCG CCCCACCCCT CCCTGGCCCC GCCTCCTCCC TGCCCCACCC CCTCCCTGGC 720
CCCGCCTCCC CTCCACACTC CAGCTTTGTT CTGGCCTTTG CAGTAGCTGT GTCCTCTACC 780
AGAAGACTTT TCTTCTGAGA TCTGCATTGC AAGCTCGTTC CTTTGCTTCC TGGTGGGTCT 840
CTTTAAGTTC TTCCCTGACT CCTTTATATA AAAATAGCAA CCCTGGCCAG GTGCGGTGGC 900
TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCGAGGTGGG CGGATCACCT GTAGTCGGGA 960
GTTCGAGACC AACCTGACCA ACATGGAGAA ACCCCATCTG TACTAAAAAT ACAAAATTAG 1020
CTGGGCGTGG TGGCATATGC CTGTAGTCCC AGCTACTTGG GAGGCTAAGG CAGGAGAATC 1080
ACTTGAACCC GGGAGGCATA GGTTGCGGTG AGCCGAGATC GCACGGTTGC ACTCCAGCTT 1140
GAGCAACAAG AGCGAAACTG TCTCAAAAAA AAAGTTATTA TTAGTAACTT ATTATTATAT 1200
TCTAATATGT ATATTAGATA TGCTTCCTGT ACAGCCTGCA GAACTGAGAC 1250
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