| Tag | Content |
|---|
EnhancerAtlas ID | HS118-13220 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr3:125401330-125402780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr3:125402324-125402335 | TCTGCCAAGTA | - | 6.62 |
| | | 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 |
| GH03I125682 | chr3 | 125401391 | 125403445 |
| Enhancer Sequence | ATTCTCTCAC TGAGACCTCA GTAGCCTAGG GGACAAGGAT GCTGTCCTGA TTTCAGATGG 60
AAGGCTCTGG AAGTCTCAGG AAGTGAATGT AACTTGCCTA AGCACATCAC ACTAGTCTGC 120
AAATCTGGAC CCTGGAGCCC ACAGCCTGTG ACTTTCAAGT CTGCACTCAT TCCTATGCCC 180
TGACCTTTTT CAGAGGGCAC GTCCCCTGGC CCAAAGGGGA AGACTGGCCA CTGTGGGCTG 240
GGCAGTGTCA GTCCCTTAGG GATGAAGGAA CTGGCACTGA TGGAGAATGT GGCCGAGCCT 300
GGCTCCGTGA AGCTCTCTGC CAGGAGTGAG CATGCTCTCT GGGTGCTCTA ACTGAAGAGA 360
TGCCTCAGCA TAGAGTCGTT ATTGGGAAAC TGGTCCACCT CTTCCTTCCA GGAAACCTAT 420
CACACTGGGC TCAGAGCCCA ACTCTGGCCT CTGGGAATTT GCAGCCAGAT TCTGGTTTAC 480
AAACTTACTC ATTTATCCTC ATAGTTCTAA CTTCATGACT CCCTGGGAGC CAGGTGGGGA 540
GCTCAGGAAA TTGTGATAAT GAGATTTCAG AGGAAACCTG AACTGCTGAG AACCTTGTCT 600
CTGAGGGTCA GGGAGCAGGA CTCACCTTCC ACCTGGGGGC TCTTCTTGGA GGCCAGCATG 660
GCCAACCCGA GTCGAGTAAG GGGCAGCAAG AGTCAGAATG CTACACGTAG AGCCACATGG 720
CTCAGCCCTC TGTTTTCTGA GACTCTCCCT CCACAGCCAC AGCCAAGGGC TAATCCAATG 780
TCTGTCCTGG CTTGCCTGTG TTTAGATTGG ATTAGAGTGA CCCAGCTGAG CTAAGAGTCC 840
CCTGGAGGTG GGAGTCCCAG GCGAAAGATC AAGAACTCTT TAGGGCCATT CTCCTGACTC 900
CTGGGCCTGT GGGGGCTGGG GCCTGAAGGA TCACCACCCA TCCACAAAAA AAAAAAAAAA 960
AAAAAAAAGG CACAGAGAGG TCCCAGGCAA AAACTCTGCC AAGTAAGTTT GGATTTGTTC 1020
TGAGAAGAGG CCTGCATGAG AGAACCCCCT CCCAGTGTGG GGGATGTACT GGGCTATAAA 1080
GACCAGACAG GCTCAGATAC CATAAATGGT GAACAAGGCT GAGAACGCAG CTGCACTCTC 1140
AGGCCCGGCA GCATTTGGGC TCTCTTGGCA CAGGATTGGA GCAGGGTGAG CCTGGCAGAG 1200
TGACACCCCC TGGCATGGTG CCCTGAGACA CTCGGGAGGC TCGGGGCTGC TCCCTGCACT 1260
GTCCTCCACT GTGGAGTTTT TCTGACTTGA TTGGCAGCCC CGTTGGCTCT GGGTCCTTGG 1320
GGGACAGCCT GGGCTGGGAG AGATGATCAC AGTGGAGGTG TTTGTTCCCT ACTGCACTGA 1380
TGGCTGCTTC ACCCCTCCCT TAGCTGTCCA GGTCCAGCCC TCTCTTGCCC TTAGTGTGGC 1440
ACCAGGCCAT 1450
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