| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09407 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:12479900-12481780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:12480921-12480940 | TACTGCCCTCTAGTGCTCA | - | 6.32 | | ZNF263 | MA0528.1 | chr12:12480829-12480850 | TGAGGAGGAAGGAAGAGGTGA | + | 6.02 | | ZNF263 | MA0528.1 | chr12:12480824-12480845 | GGAGGTGAGGAGGAAGGAAGA | + | 6.11 | | ZNF263 | MA0528.1 | chr12:12480817-12480838 | AGGGGAAGGAGGTGAGGAGGA | + | 6.32 | | ZNF263 | MA0528.1 | chr12:12480821-12480842 | GAAGGAGGTGAGGAGGAAGGA | + | 6.46 | | ZNF263 | MA0528.1 | chr12:12480832-12480853 | GGAGGAAGGAAGAGGTGAGGA | + | 6.61 | | ZNF263 | MA0528.1 | chr12:12480847-12480868 | TGAGGAGGAAGGAGAAGAAAA | + | 7.35 | | Zfx | MA0146.2 | chr12:12481682-12481696 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 12480299 | 12480985 | | chr12 | 12480187 | 12480422 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I012327 | chr12 | 12480327 | 12481490 |
|
Enhancer Sequence | TGCCTGGCTA ATTTTTGTAT TTCTGTAGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT 60
CTAGAACTCC TGACCTCAGG TGATCCACCC ACCTTGGACT CCCAAAGTGC TGGGATTACA 120
GGCGTGAGCC ACCACGCCTG GCCAAGAGTA GCTTTTTAAC CTAGGTCAGT ATCGTGTTGG 180
TAAAATACGG AGAGAGGATG TTTGAGCAGA AGGACCTACC TCATCTTCTC ACCTGTTCTA 240
GGCTGCTACC TTCTCTTTCT ACAAACCAAA GGAGGGGGCT CATAACTCAA TGGGCCTTGT 300
GGGAAAGGCT AACCAGACTA GTCACTGCTG AATTCCTCTA AGGGATTCCC CTACCCTGAC 360
TGCCCTTGCC ACAGTTGCAC CCACCATCCT AGGGGCAGTA AGTAGAGAGA GCTGTGTGAG 420
AAGAGCACTC TTTCCACTCC AGATGTCCCC TACAACCTAT ATCCTCACGG CCACTAACAG 480
TTTGGGCCCG TAGCATCACT CATCTGGACC GCTCCCATGT GGTCTCCCCA TCACAACAAA 540
GACTGCAGCA AGGTGGACAG AGAACTCCAA GAGAGCCAGG AAAATACCTT TATAAACCAT 600
CACAGAAAGC CTGATTTCCA CTCGCTAAAT CCATTAATAA AGAGAGGAGA AATTTTAAAA 660
TTCCAAGGCA CCTGGTTACT AATCTGATTC TGGCCTACAT GTGGATATTC AATAAATACT 720
TGTTAAGTTA AATTGACTCA AGGTTTTATT TATTCAGCCT ACTTAAAGCT TATGTAAACC 780
CCTTGGAGAT TTGTGTCAAG CTGTTAAGTT GGAAAATATA AGAAAAGTAG TATTTTCAAT 840
AGACCAGCTT TCCTCTTAAT GTACTTTATG AACTTAGTGT AAACCAGGGA AATGGGGGAG 900
GGGTACCAGA AGAGCAGAGG GGAAGGAGGT GAGGAGGAAG GAAGAGGTGA GGAGGAAGGA 960
GAAGAAAAGC CTTTTCTGTC ATTTCCTGCA TTTGTCTTAA TTGCTGTACT TATTAACCAG 1020
CTACTGCCCT CTAGTGCTCA CTGTATTAAG TTCGCATCTG AATTCCATTT TTATCTTTAA 1080
AAACTCTGGT GACACTTGGA AGGGATCAAA TTTCCTGTTT TGCAGATAAG CAAATTGAAG 1140
TCCAGAGGAA AGAGGTATCA AACTGACCCA GGGGACTTCT GGACTCTTTG TTACCTCACC 1200
TATAACTTGT CTGGAAAACT TTATTAAAAG CCTTTCTCAG AAATTTTAAT TGGTAACCAG 1260
TAAAAATTGT AGCATCATGT TAGTGCTAGT TATTATTATT ATTATTTTTG AGACGGAGTC 1320
TGGCTCTGTT GCCCAGGCTG GAGCGCAATG GTGCAATCTG GCTCACCGCA ACCTCCGCCT 1380
CCTGGATTCA AACTACTCTC CTGCCTCAGC CTCCCAAGTA GCTGGAACTA CAGGCGCCCG 1440
CCACCACGCC CGGCTAATTT TTTGTATTTT TAGTAGAGGC GGGGTTTCAC CGTGTTAGCC 1500
AGGATGGTCT CGATCTCCTG ACCTCGTGAT TTGCCCATCT CGGCCTCCCA AAGTGCTGGG 1560
ATTACAGGCG TGAGCCACCG CGCCTGGCCT GTGCTAGTTA TTATTTCCAA TGTTGTTCTA 1620
AATTAAGCTT AGACTGATTG CTGGTCAATT TAAGTAAGGA TATAAAATAA TAGTGGTACA 1680
TTTTTAACTT AGTACAAGTT TAGAAAATGT CTATAATACT TCTTTAAAAA GTTAACTAGA 1740
GGCCGGGCAC GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCGGGCGGA 1800
TCACAAGGTC AGGAGATCGA GACCATCCTG ACTAACACAG TGAAACCCCG TCTTTACTAA 1860
AAATATAAAA AATTAGCTGG 1880
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