Tag | Content |
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EnhancerAtlas ID | HS091-13979 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:94524240-94526440 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RORA | MA0071.1 | chr14:94525132-94525142 | ATCAAGGTCA | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 94524415 | 94524509 | chr14 | 94524800 | 94525527 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I094056 | chr14 | 94522767 | 94527176 |
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Enhancer Sequence | CAGCTGGGGT AGAGAGAGAA AGCTTATTAA TAATAACTAA CAGCTATCTT TAATCAAATT 60 CTTACCAACT GCTGAGCATC CTAAACATTA CAGTCCTTAC CAATACTCTG TAAGATATCA 120 CTTGTATACC CTTTTACAGA AAAACTGAGG CTCGGAGAGA TTAACTTCCC AAGCTATCTA 180 CATGGCTATT CAGCTGTGGA GTCTGGATCC AAATTTGGGA CTCATTGACC CCAACCAACA 240 TGCCATACTC TGCAATGATA AAGACTCCCT TCAGTGAGTT AAATGAGGCC ATACATATTC 300 TGGGTCAGTG ACTCCTCTCC TAGCACCCTC TCATTTACTT CCTCCCAGTG GCACACAGAC 360 TTCCTTGCTC TTCCCCAAAC AAACCAAGCA TGCTCTCACC TCCAAGCCTT TGCACTTGCT 420 ACTCCTTAAG GCCTTAAAGG GTCTTGCCTC AGATGTCCAT ATGACTCACT TCATTACTTT 480 CTTCAGCTCT CTGCTCAATT CTCACTTCAT CAGAGACTGA CCACACATAC CCAATCTCTT 540 TTCTCCAACC CCTGCTCGAC TTACTTCTTA GGATCACTTG GCAGACTGTG GGCTTACTTT 600 GCAATTTATT ATCTCCCTCT ACTAGAATGT AAGCTTCATG AGAGCAAGGA CTTTGCATTA 660 CTCACTGCTG TTATTACCAC CACAGAGAAC AACATCTGGT TCATGGTAAG CACTTGATAA 720 ATGTGTTGGA TGATGTTTCT CAATGTGTGG TTCATGGAAA GTCAAAAGTA CTTGAGGTGC 780 TTCAAAACAT AAGACTCTGG CCCTTCAGGG TCCTCACTCC CTGCATGTCT GAGCTGAGGC 840 CGGGAAATGC AATGCAAATC CTAGTTTGTA AAACATTAAA CTACTGCTCT GGATCAAGGT 900 CAGCAAACTT TTTCTGTAAA GAGCCAGAGA GCATTTCCAG CTTTGTGAAC CACACAGTCT 960 CTATGGCAAC TATTCAACTC TGCCGCAAAA GAGGATATTG ACAATACATA AATGGGTCTT 1020 GCTGTGTTCC AGTAAAACGT CTACTAAAAA AACAGGCAGC AGCCAGGTGT GATGGCATGC 1080 ACTGGTAGTC CTAGCTACTT AGGAGGCTAA GGTGGGATTG CTTGAGCCCG TGAGTTCAAG 1140 TCTAACCTGG GCAACATAGC AAGACCCCAT CTTAGAAAAA AAAAGGGCAG CAAGCAAGAT 1200 TTGGCACGAG GCCTATAGTT TGCCAAGCCT TGTTCTAAGC TAATCTCAGT AAACCACTGA 1260 TACTACTTAC CAATTTTTAA AAACCAGTAA ATCAAACACT TGTTCTAGAA ACTAATTACC 1320 CCATGACCTG ACAAAACACT GGCAAAAGAC ACTTTGTAGT CTGCCTCAAC TTTCCAGGCC 1380 CTCATCTTGA CAATCTGCAC CCCATTCCCT GAGCATCAGT CTGGTCCAAA GGCAGATGGA 1440 CAAAGACATC AGGAATAAGA AATAGCATGG GCTCTGAGGT CCGACAGGCT TGTCTGAGGC 1500 CCAGCTCTAC CACTTCCAGG CAGAGAAACC TTGGGCACAC TGATCAGCTT TTCTAGACCT 1560 CATTTTTCCA TCTATAAATG AGAATAGTGA TAATGGTAAT AAGTAGTAAA GGGACTAGAA 1620 ATTATTAAAG CTAACATTTA GCAATATATA CATACTATGT GCTAGAGACT GTTCTAAACA 1680 CTTTACACGC ATGAATTTAC AATCAATCTT CATAACAACC CTAGAATGGG TTCTATTATT 1740 ATCCAAATAA TGAGAAAATT AAAGTACAGA GAAATTAAAT AACTTGACCA CCTAAGGAGT 1800 GACAGAACTA GGATTTGATT TCAGGCATTC TGGTTCCAGG ATCTGTGCTC TTAACCATGA 1860 ATCTATTCTG CTTCCTCTTA AGGATGTTAG GAGAGTAACT GAATGTGATT CTGAATCTAA 1920 AGTGCCAGCA CAGGACCTAA TCTATTGTCT ATACATTCAA TATTATGTAT TGTCACCTAT 1980 ATTCATTAGT ATTGAAGTTT CTGTATGGCA TTTAACTGCA ACCAAATTCA CTAAATGACA 2040 GTAACCTTGC CAAATGCTGT GCAAAAAAAA AAAAAGGCTA CCTACTACTG AGACAAGGCC 2100 CCTATGACAG AAGGTGGCTT TTCTACCATT TCCCCACCAT CCTGACCCCT TTTACCCCAG 2160 TAACTAACTA GAGGTTAAGC CTCTGGGGAC AGTCCTAACT 2200
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