| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01749 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:223350620-223352620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:223350907-223350922 | AGGGTCCAAAGGCCA | + | 7.24 | | ZNF263 | MA0528.1 | chr1:223351779-223351800 | AGGGGAGGCTGGGGAGGAGGG | + | 6.64 | | ZNF263 | MA0528.1 | chr1:223352063-223352084 | AGGGGAGGGGGAGAGAGAGAG | + | 6.69 | | ZNF263 | MA0528.1 | chr1:223351782-223351803 | GGAGGCTGGGGAGGAGGGAGA | + | 6.77 | | ZNF263 | MA0528.1 | chr1:223352058-223352079 | GGGGGAGGGGAGGGGGAGAGA | + | 7.27 |
|
| | 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 |
| GH01I223176 | chr1 | 223349824 | 223351742 |
|
Enhancer Sequence | TGATGCTTAT CACAAAGTAG GCAAGTTGAT GTCACCATAT AAATAATTTT AAAAGTTCTG 60
AGCATGCATT CTGGTGGTGT TATATGTTTA GGTGCATGGT CTTTAAACCT CACTAAAATA 120
TTCTTAGCTG GAAATTATTA TCTTTATTGT ATGGGTGAGG AAACAGAAGC TCAGAGAGGG 180
GGGCTACTTG CCTGTGGTCA CAAGAGTGAG ACAGATTTCA GAGCCCAATC TGTCTGCTTT 240
TTATCCCAGC TCCCCTGCCC ACACCTGCCT CCACTGTGTA GCCCCTCAGG GTCCAAAGGC 300
CAGGCTCAGG ATATTTAGGG GTGAGTTTTA GTACAGGTGT CCTTGTGGTG CTCTCACTCT 360
GGGTCCTGGT GGCCCCACAA CATTCTAAAT CTTTTATATG TGAAGGTCTT ACTCTGGCAT 420
TGGAAGCTTG CTTTCCAAAA TTATAATAAT GACAATCACT AACATTTAGG GAGCACCCCA 480
GATCCCCACT GAGGCTTTAT ACATGCATTG CCTCAACCCC TTGAGGCAGG TACTGTCATC 540
ATGCCCGCAG TGCAAGAGGT GAGAGAACTC ACCCAAGGTC ACAGTGAACA AACAGCCCAG 600
CTGGAACTTG AGCTTGGCTT GTCCCTAAAC CCGCCAGTGC TGTCAACCAC TGTATTCTGG 660
GAATTTGAGG AACAAGGAAT GAGGAAGTGG CAGACAGAAA ACGGTGCTCG AGTCTGGGGA 720
CATTCTGAAC ACTTTCAGGG AGGCCCAATA AGAAAAGAGA AATGCAGACA AATGAAATAA 780
AGCAGAGGCT GGGAAGCCAA CGCCCACAAC ACGACCAAGA CCCCAAGTTC CCAAAGAAAG 840
TGCTTTATTA TTTTCAAAAT AGCAATGTGT AAAAACGGCT TTTGCAGAAA AGAAGACAAA 900
AAGGCTAACC TTTACTGCAC CCCCAATAAT GCCAATTCCC CAGCCCTAGC CCAGCAGAAC 960
CGTGGGAAAG CAGCCTTTGC TGTATGTATG TAGGCTTTCA CTCAGGACAG GTAGATTTTT 1020
CATAATGACT TTGCTTTTAA TCTAGGGAAG AGTGTAAAAT TGCACAGCAA GTCTTGGGGA 1080
CTCTGACAGC CCAGTGGACC AGGAAGGAAT CTCCATCCAT CTCTGGGAGT CTCTGGGGTC 1140
ACAGGGAGCC TGTAAGCCAA GGGGAGGCTG GGGAGGAGGG AGAGCGGCTG GAGAGATTTA 1200
TACATAGTGC TGTCCTCCCC CTGCCTTGGA ATTACAGCAC CATGAGAAGC TGTGAGATTA 1260
AATGAAGAGC AGGGCCCTGG AGAAGCTAAA GCATCAGTGG GAACAGGGGG TGCAGCAGGT 1320
GATAAGCGGG AGATGCAGGT TAATTATGAT GCTGGCACAC AGGTAGCCCC GGGAGGAAAG 1380
CAGAAGCCCT GGGGCGGGTG CATGTGTGTG TGAGTGTGTG TGTGAGTGTG TGCATGGTGG 1440
GGGAGGGGAG GGGGAGAGAG AGAGATCCAT GATATCCATT TGTGTTTTGG CCCCATTCTT 1500
TTTTTTTAAA AAACCTAATC AAATCGATTC TCCTCTCCTA CATAGAGGTT TGCATGCCCC 1560
ACCCCCCACT CTCCTTGCCA ATTCATCAAT ATCCTCATCC TCAGAATTTA TCTAAACTAC 1620
TTTATAGGAA AGATTCTTTT ACCTTTAACC CCCTGCACCC CACTGGCCAG GTATGGAAGG 1680
ATGATTAGAC AGCCTGATCC GAAAGAAGGG GCACCAGCAA TGACTAGACT AACTCTTCTG 1740
GGGAGAGGAA AGTCTCTGAG CTCTGCAGAG CGGAGGAGCC CCTCTCTGAT CTGCCTCAGT 1800
AAGTCAAGCA GATACGATGC AAATCCACGC CTTCTGAGTT CTGGCTGTGA GAGAGGAGAC 1860
AACTCCAGGC ATTGTCTGGG GTAAGGAGCC CTCTTTGAGG GAGGGGTGCT TTTCTTTCAA 1920
TGAGTTTAAG CATTTCCTTC ACTAGCTTGA CTCTGTAGCT GGTTCTTCGA TCCAGTCTCC 1980
TCAGAGGTCC CCTTCTCTGC 2000
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