| Tag | Content |
|---|
EnhancerAtlas ID | HS091-04175 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr1:227280350-227283080 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:227282478-227282493 | TGGACTTTGGACCCA | - | 7.05 |
| | | 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 |
| GH01I227092 | chr1 | 227280665 | 227282784 |
| Enhancer Sequence | CCAAACATTT TGTTCATAAT TAGAATTTAT GAGTTCAGAA ATTTTAAAAA ATTTACTTCG 60
AAATAATTTC ATTATTATTA GCAAAGTTAC AAGAATAGTA CAAAGAATTT TTGTATACTC 120
TTAACCCAGA TTCCCCAATT GTAAATATTT TACTGCATTT TCTCTATTAT TGTGTATATA 180
CCGATTTTAT TAGTGTTCTT CAGAACCACT GAGAGGCAGC TAGCTGCAGA TATTATGCCC 240
TATTACCCCT AAATACTCCA GTGTGTATCT TTCAAAGTCA AGGACACTCT ACCATAATCA 300
CGAAGCAATC CTCTCAATTT AAAAAAATCA ACATTACTAG AACACTTACC ATCTGAATTC 360
ACAGACACAA TTCAAGTTAT CCCTACCATG TCTCCTTTTC TTATGAAGCC CAGGATCCAA 420
CTGAGAAACA TGTGTTGCAT TTAGTAGTCA TGTCTCTTCA ATTTTCCTTG GTCTAGAACA 480
GTTCCTCAGT CTTCCCTATC TCTCACAACA GTTTTATAAT GTATAGGTCT CTAATTATGT 540
ACAGTGACAC TCAACCTGGG GCCATCTGAT GTTTATGACT AGTCTCAAAG AATTCATTTT 600
TGGCTGGAAT ACCACAAGAA CAATGTTTCT CAGTGCATCC CATCAGAAGG TGCAAAATGT 660
TGATCTGCAC AACACTGACC AAACCTCTTA GGCTAAGGGT GTGGATTCAG AATGAGTGCA 720
GTCCCCAAGA CATGAGATGT GAGAAAGAAA AGAAACTTTT TATGAGAAAT GCGAGCCCCT 780
TTAAATTAGC AGGGCCAGAC AGGCACTGAA ATGTGACTGC AGTCACATCT TATTCTCCCA 840
GTTGAGCTAA GTAATCTACC AGCTATGTGG ACTCCAGACT GAGTGTCACC AATAGCTATA 900
AATTAACCCA ACAATGCCAT ATTCTGGACA CCATAACTCA TACCCTATAG TTCAACAATG 960
TACAGCCAAT CATTAATCAA TGTTATTTCT GCAAACCAGT GAGAACTCCT GACCAAAGAC 1020
TTTTGTATGT TCCCTCTCCT GATTTTTCTT TAAAAACCTG AGCCTCTTTT TTGTTCTCTG 1080
GAGCACTTCT CTGTGTTTCC TGGGCTGCAG TCCTCAACCT TGGCCCAAAT AAACTCTATA 1140
TTAATTTTGT CTCAGTTTCT GTCTTTTGGA CAACATATTG GAACCTTCAG GCAGCAAAAG 1200
ACAGTGCTGA GAACTCTGAA CTCTCGTATT GCTTCAAACC TCTGCAGGTA GAAGCAATCT 1260
CATCCCCTTC CTCAAAGCAG CTATAACCTG AGGCAACCAA CCTGTTTTTG CATAAATCAT 1320
TTATTAACTT CACCTGAAAT AGTTACATCA AAAAGGGAGG CCAACTATCT TTAACACCTA 1380
CCCAATCACT TGTCATTGTC TTCAGGCCTA TGATGACAGT TAAGATCACA GCAGAGACTA 1440
GATATAAAAG CAATGAAGGT GTTAAAGCAT TTTGGCAATT TATATTGGAA GGAGTATGGG 1500
CAGCATACAG AAATGAATTC TAAGAGCTGA GAAAGAAAAT AAACTTTTTT TATCTGAGGA 1560
ATGTGAGACC ATTTAAATTA TCAGGCCCAG AGAGGTATTT AAAATGTGAG AGCAGTCACA 1620
TCTCACTCCC ACCTTGAGCT AAATAATCAC CTCTTGAGGC CACTTGCTAT GTGGGCTCTA 1680
AACTGATGCC AAGTAGCCAT AAAATGCCAT ACACTGGAGA CCATGACTCA CACGCTATAG 1740
TTCAACAATG AATAGCCAGT CACTAATCAA TGTTATTTTG TAAACCAGTG AAAATGCCTG 1800
TCAAACAACT TTGTATCAGC CCAGCCCTTG CCTCCTTTTG CTTTTAAAAC CCTACTTGTA 1860
ACAAAGACCT AATGGAGCAC TCCTCAAGGT AACCTGGAAG TGTGTTCCTG GCAGCTGTCC 1920
TCACTTTGGC TCAAACAAAC TCTTTAAACA TATCCTGTGC CTCAGCTTCT TCCTTCAGGT 1980
CAGAAGGGTG TTACCCCAAG GTGGGTAAAT AAAAAATTAA ATACAGCCAA ATTTATCAAA 2040
TGCACATACT CATCTAGGAT TTGTGGTTTA ATGTGTTGAC TCAATATTCA GGTGTAGTTT 2100
TTCACTGCTA GGCTGAGTAA TTGAAGCCTG GACTTTGGAC CCAATAGTGG CCTACAGTCA 2160
ATTAGCTCGA GATATTTGAC TTACTGAGCA TAAAGGGTCT ACTGGCTCAA AGAGATGAGA 2220
ATGTCAGAGT GGACCTATTA TGTGCAACCT GGTCAGCCAC CCACAAAGCA CTCCTTTCAC 2280
CAAGGCATTA ATAAATACAC CAGTGAGAGG GCACATTAGC ATCCTGGAGA AACACTATGG 2340
TAGGTGTCTT CAGATGACAG TCTGCAAATG ACAGCAGAAA ATGCCAGAAT GGAACTGCAT 2400
TGCCTGATTT TATTGAAAAT AACAGTATTC CAGATTGGCT ATTGCACCAT CTGCTTTACT 2460
TATAGCCTGA TGCTTCCAAA TCCTCATCCT TTCCCTTAAA ATTAAAAGTC ACACTCATTT 2520
ACTTTTAATG AGTTCAATGA ACGTATACTT AATAACATCT ATTTGTGTTT CATTTGGAAA 2580
TCTGAGGAAA ACATCTGTGA TGTGTAGACT TCCTATGCTC ACCTTATTTG ATTATGTATA 2640
TACTAGAAAG CATGGTGAAA GGAGAGGTTA GGGAAAGAGG ATATATGAAC CACAAAATGA 2700
TTCCTTGTTC TCAACCCTAG ATTGTATTAA 2730
|
| |
|
|
|
