| Tag | Content |
|---|
EnhancerAtlas ID | HS091-35117 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:129247940-129249710 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr3:129248421-129248431 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr3:129248421-129248431 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr3:129248421-129248431 | ATTTTCCATT | + | 6.02 | | RREB1 | MA0073.1 | chr3:129249371-129249391 | ACACAACACACACACACACA | + | 6.19 | | ZNF263 | MA0528.1 | chr3:129249548-129249569 | TCTGCCCCTTCCCCCTCCTCC | - | 6.07 | | ZNF263 | MA0528.1 | chr3:129248685-129248706 | GAGGCAGGGAGAGGGGAAGAG | + | 6.12 |
|
| | 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 |
| GH03I129530 | chr3 | 129248844 | 129249644 |
|
Enhancer Sequence | TGAGCCGGGT GTGGGTGGGG TGTGCAGGAG CCCGGGAGCA TGGAGGGGTC TGGGAGAGTC 60
CCGGGCTTGG CGGTGGTGGC TGAGAGGCCT TCTCCCTTCT CCTGTCCTGT CAATGTTATC 120
CAAAGCCCTC ATATATTCAG TCAACAAACA CCATTCATGG TGATAGCCGG GCTGCTGTTT 180
GTGCAGGGCT GGCACTGAAC ACTGCCTTGA TCTTATTTGG AGCAATATGC GCTTGTCTAA 240
TTTCACAGCA AGAAAACTGA GCTGAGGCTC AAAGAAGTCA AGCGCCCTGC TGGGGCGTCA 300
CACAGGGACG GGTGCAGAGT TGAGTTGGAA GCCCGCATCT ATCTCGGGCC ATGTTTGCAG 360
CACCAAGCCT CTGTTTCCCT TGGAGCAGCT GTGCTGAGTC AGACCCAGGC TGGGCACTGA 420
GGGAGAGCTG GGCAAGCCAG ACCCCTCCTC TCTGGGGGCC CAAGCTCAGG GTGGGAAGTG 480
GATTTTCCAT TCTCCAGTCA TTGGGTCTTC CCTGTGCTGG GCAATGGGCT CGGTCCCCTC 540
TGGCATCCTC TGCCTCCCCT CTCAGCCCCT GTCCTCAGGT GCCCCTCCAG CCTCCCTGCC 600
GCGTTCCAAG TCTCCTGGTG TTGAGAACCG CAAGCAGCCG CTCTGAAGCA GTTCCTTTTT 660
GCTTTAGAAT AATGTCTTGC ATTTAACAGG AAAACAGATG GGGTGCTGCA GGGATAACAG 720
ATCCCACTTA ACAGAGAGGA AAACTGAGGC AGGGAGAGGG GAAGAGACTC ATTTAGGGAT 780
GTGGCCAGGC AGCAACAAGA GCCTAGGTCT CCTGGCTGTG ATCCAGGAAT ATCTCTGCTG 840
AGATGCAGGA GGAGACGCTA GAAGCAGCCA TTGCAAAGCT GGGTGACGGG GAGAGCTTAC 900
CGCCAGCCAC AAGCGTCTCT CTGCCAGCCT TGCCCTGTCT CCCCCATGTC CAGGCTGCTG 960
CCTCGGTCCC ATTCTCAGGG AATCTCTGGC CATTGTTGGG TGTTTGTTGC ATTCAATAAT 1020
CACAGATCAC TCAGTTCTGG CCAGAAGGTG GGTGTGCCAC TTACGGGTGG TTGTTCTCTG 1080
CAGGGTCAGT CCCAGTTTAC AAATATTGTC CCTTTCACTG TTAGGAATGT CCCAGTTTGG 1140
TTGATTAACT ATATGGCCAC TCTCCCTATG GAACTTCATG GGGTGGTGAG CAGGACAGAT 1200
GTCTGAATTC CATCATTTCC TTCTTCTTCC TCTGGGCAAA ACATTGCACA TTGCTTCATG 1260
GCTCCTAGGA GAGGCCCCCA CATGTCCGGG TTATTTCATT TCCCGAGAAG GGAGAGGGAG 1320
GAAGGACTGC CAATTCTGGG TTTCCACCAC CTCTGCATTC CTTCCCAACA AGGAACTCTG 1380
CCCCACATTA GGATGCATTC TTCTGCTAAA CACACACACA CACACACACA CACACAACAC 1440
ACACACACAC ACACACACAC ACACACACAC AAAACTCCCT ACCGGGTTCC CAGTTCAATC 1500
CTGACCCCCT GATCTGATTC GTGTCCCTTA TGGGCCCAGA GCGCTAAGCA AATAACTTCC 1560
CCCATTCCCT GGAATTTCTT TGCCCAGCTC TCCTCAGCGT GTGGTCCCTC TGCCCCTTCC 1620
CCCTCCTCCC AGCACCAAGC TCTCTCCTTC CCCAAGGCCT CCTCAAATCC CTCTCCCACT 1680
CCTGGTTGCC TTCCTAGCTA CCCTCTCCCT GTCTAGGGGG GAGTGCACCC TCCTTAGGCA 1740
GTGGGGTCTG TGCTGACCGC CTGCTGACTG 1770
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