| Tag | Content |
|---|
EnhancerAtlas ID | HS091-44149 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:75682320-75684140 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr7:75683063-75683081 | CCTGCCTGCCTGCCTGCC | - | 6.1 | | GLI2 | MA0734.2 | chr7:75682995-75683010 | TGACCACACACGGTG | + | 6.19 | | PRDM1 | MA0508.2 | chr7:75683227-75683237 | TCACTTTCAC | + | 6.02 | | TFAP2A | MA0003.3 | chr7:75683585-75683596 | TGCCTGAGGCT | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 75683400 | 75683991 | | chr7 | 75682868 | 75682922 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I076053 | chr7 | 75682437 | 75684775 |
|
Enhancer Sequence | GCCTGAGCAC GAGAGTGAAA TGATTAAGAC TTTGATTTTG GGAAAGCATG CTTTGGAGGT 60
GTTGCTGAGT ACCTAAGTTA GATAACGGAA TAGAATGAAG AGGAGGAGCG GGTTGGGAGG 120
GTGGTTGAGC TGCCAAGTTC TTCATGTCCT GACTTGATGT CTCTGATAAG AAGGAGGTGG 180
CAGAAGATGG TTCTAGAAGT TTACATTTAG TGAACACAAG TGCCATTTGG GACCAGGGAT 240
GGAGGGAGGG GGGCAGGATA AATGGACAGT TGAGTTTGTG GAACCCATGG AACGCCTAAC 300
AGAACTGGGA ATGCAGAGCT GGGATTTGGG AGTCCCTGAG ACTCACACAA GATGTGGGAG 360
TGAGAGCTGA AGATCCAGAA GTGGGTGAGG CTGAGCCTGC CCGACCTCAG GTTCTGAGCG 420
GGTCTGACAG GTTCAAGTTT CCAGGCAGCC AGGGGTTCAC CTTTAAAGCA CCAACTTGAA 480
ACTCAAAAAC CTGTTTGAAT TCAAATGTTG GTTGTATATG CTTCCACAGT TTAATTTCCT 540
GAGCAGAAAC CCACTGGGTA AGCGTCTTGA TTCGGATTTT GGTTTGTTGG GTTTTGGTTT 600
CTGATAACCA AAGCCTGTTA TTAGCTGGCC TCAGCTACTG TAGAAGACTG TGCAGTGATG 660
CTGTCAGGCC CCAGATGACC ACACACGGTG CCGAGAGTTC CCGTGTCTGC CACTTTGTTT 720
GCCTCTTCCC TCACTGGTAG CTGCCTGCCT GCCTGCCTGC CAGGGATCGG CTGTGCTTCT 780
CATTTGTGAG TTTAGATCAG AAACAAGCTC CCTGGGTATG GCTGTAATTT TGGTCAGACC 840
TTGAGTGAGA CCTAGAGGGG AAGAGTGCCT TCGAATAACG GGAGTGATTG CTGGATGCGG 900
GGCCGGGTCA CTTTCACCCC ATCACTTTCC TAACTGTTCC AAGCTGAAAT GCCCAGGGCC 960
AGCTGCTACT TTGCTGCCTG TTCTTCTGAT TAGCCTGGTA TGAAACAGTG ATTCTCAAAC 1020
TGTTTGGTAT CAAAATCATC TGGGGAAAAT GGCAAAAATG CCAAGGCCTA AGCCCCATCC 1080
CGCTTCCAGG AGCCTAGTCC TGAGTGGGCT TCATTAGCTC AGCAGGTGGC TCTGATGCAC 1140
ACCTAGGCTG GAGAACCAGT GTGAGATACT GGAGCCCGAG ATGACAGATC TGACTCACCA 1200
GGAGGGTTGG AGTCTTTCGC AACGTACGTA ACCCCTTCCA CCTCTTGTTA GGCAGCTCCT 1260
TGTCCTGCCT GAGGCTCCAG CCACAAGTTT GCTGCCTGGA TGAATCTTCT CTGATTCCCC 1320
ACCCCTGCAG GGAGTTGATT GCCGCAACCC CATCTGCCCT CTTGCACAAG GGGCTTCTGT 1380
GACAGTGTTC TCCCTGCTCC TAATGCATCT CATTACCTGT CTCCTACAGA GCCAGCAGGG 1440
ATCTTCCTGC AACCTCAGTT ACCGGGAGGG CCTGTTGCTA GGCACTCAGT GTGTGTTTAT 1500
AGTTTATAAA GCTGCAGGTT GAAGGGAAGG CTGCTGTTAC CAGTCCAGCT GCCTGATGGA 1560
GTCCAGCTTG TTCTTCATCT TTCAGGAGGG TTTTGAAGTA CCCTGAGTAT CACAGACTCT 1620
ACAGACATAA ATTCTCCCCA TTTGAAAGTG GACCTTTGGA ATGAAGGTCC TGAATTCTTC 1680
CAGAATGAGA CTGTTACAAA TACAATGATT GTATCTTGCT TTGGCAACTG CAGTAAAAAG 1740
AGGCCCAGTG CAACATTATA GGATACCATG TGAATCCTTT TCATGCTCAT TTCCTCCTAA 1800
GAGTCCTTTC TCTGTGCCTC 1820
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