| Tag | Content |
|---|
EnhancerAtlas ID | HS091-43804 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr7:50535010-50536680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr7:50536168-50536178 | GGGGATTTCC | + | 6.02 |
| | | 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 |
| GH07I050467 | chr7 | 50535499 | 50536470 |
| Enhancer Sequence | ATGCTTCAAA GAGGAAAGGG AAAATCTGTT TTTCTCATGG CCATTTAATT CAGAACTTAA 60
CTACCTAGAA AACCTTATTA GACTGCCCAT GTATAATTCA TTTAGACGCT CTTGGCAATT 120
TTCCTCAAGT GCTTTTACCG TTCACTGACC AGCTGTTTCC AGGCAGGCTA AGAAACTCAT 180
TCCCTACATT AGCACAGGTC TAGTGTCCTC AGAACACCAA TTGTCATTTT CTTCTGTTCA 240
TGGGACTATT CTTATCCCAC CCAAACTGTC TTTTATAATG TTAGAATAAA CACCGTGAGG 300
AGGTATTTGA TCATTCTGGA AGAGACAATG GCTAATGCCC ATCGAGTTGC TCCTCTGTGC 360
TTGAGGTGCC AGCGCTCACC ACTGCGGCAT CCTCAGGACA GCCCACAACA CAGAAGATAT 420
CATGATTATC CCCATTTTGG AGATAAGAAA ACAGGCTGGG AGAGGGTGAG CGACATGCCC 480
AAGGTGCACC CGGAGGCCTT GGCTGAGCTA GGATTCTAAG GCAGCCTGAT GGAGCTGCAG 540
CTCTGTGGCT GCCACAGCTG TTGCTCCTCC TCCGCGTTTG CCACCTAGAG CTGGGCATCC 600
TGTCCGCTCT GTCACATTCA GAAACGGCCT TCCTCTCATT GAATATCACA CTGACCTTAT 660
TTCACTTCCA AATAGTTATA GAACTCAGAA GCTATTCAGA CAGCATGTGA TCCTAGGAGA 720
AGGAGCCCTC CGTGGCGTAG GCCCGTGCCT TGCTCATTCT AAGCCCGCGG ATACAGCAGG 780
GCCCCCATGT TGCAGGTGCT GGGGAGGACC TGCGGAAACG CGGCGCCTCG CGGGCAGGGG 840
GTGGCTGGGA CAAAAACACG TGTCATACGA GTGGTTCCTC GTCATGCCAC CAGAGAGCGC 900
CAAAGACCTC GGCCTCATGG GCGATCCCGA AAGCCGGTTC CCGCCCAAGG AGACAGGCTT 960
TGAGCATCGC TGGACTCTGC TCCTAAGGCA GGATTGGGTC CCCTTTAAGA AAGAAGTGGA 1020
GTGTGTTTTA AACAGGAGCC AGCATGATCA TAACTAGTTG TCCTTGAGCT TAAAGACGTC 1080
ATCATTGTGG GGAGATAAAT CCCTTATTTT TTGGCTTTCT TTCCCCAAAA AAGCTGAATT 1140
CGTCTCAAAT GGGTAGAGGG GGATTTCCTA CCCAGGAATT CATATACATA CTCCTTTCCC 1200
AGTTCTCGCC CCCAAACAGG TCCTCATAGT GCTCGGCAGC TCCTGGAACT GTCCTCACCG 1260
AAGCTTTGGG AGTAGGCAGT TCATGGCACA TCCTAGGCAT TCTATGAAGC TTGCAGATGG 1320
ATGTGTTTAT ATATGCTGTG CCACAGAGGA GGTGGCTGGG GACACCTGCC CCTGCACACC 1380
TGGTTGTGAA GTGGCAACAG GACTTAAAAT GGAGGGCTGT TACCATCACT AAGGCTGAAT 1440
ATCATAAGTG TGCTTGTTCC CATGAAGCCT GGGGACCTCT GTCCATCAAG ATGAGGCCAC 1500
AGCTTAGGAA GGACACCAGG ATCAGAGAGA GCCAGCAGAA CAGCAGCAGG CCTTCTGCAG 1560
CTGGCTAAAC GGGTGGCTCT AGGCAGATCC AGGCTCATAT TCAGGACTCA GTTTCCTCAT 1620
TTTTTTTTTT TTTTTTTTTT TTGGTGAGAC GGAGTCTTGC TTTGTCACTC 1670
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