| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09175 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:2964670-2966840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:2964890-2964911 | TTACCTTCACCTCCCTCCTCC | - | 6.53 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 2964703 | 2964765 | | chr12 | 2965809 | 2965859 | | chr12 | 2966033 | 2966484 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I002854 | chr12 | 2963743 | 2964912 | | GH12I002856 | chr12 | 2965890 | 2966588 |
|
Enhancer Sequence | GGGTGAGGCA CTCCGCTCTC CTTCCCAGGC ACGACCTCTG CCAGCCCAGG ATTCTCATGA 60
GGACGCAGAA GTCCTGGCAG GGCCGCATCT CCATCCCTCT CCTTCCCGGC GGAAGTTATG 120
GCTGCTGCGT ATCATCTTCA CAGTCACTCA TCTTTTGATC TCTTGCCATT GACCATATTT 180
TGGCTTTGAC TTCCCACCCT CTGTACTCAG CTTTCACTCT TTACCTTCAC CTCCCTCCTC 240
CGTTCTGGCA TCCCCACATT CCCACCCAGG AACTGGTGCT CCTTAGAGGG CACATCAGGC 300
CTCAGGAAAT CATGAAGGGA AATGCTCCCT ACCATGCCAA GGGGGGCAGC CCACCTTCAC 360
TTGCTCCTGG TCTTGGCGGT ATACCAGGAA AGTCCTCCAG AAAATAGGGC CAGGGGTTTT 420
CCCATCCCAG ACTCCTCTCA ATACTCATTT GTCCGTCACT GACGCTTTCC TCCCACTCCT 480
CATTAAAACG CTAGTATAGA AAGCATCTAG AATGGCAGCT CCTTCCCCTT TCTGCACCCT 540
GCCCCCCATT AAATAAACAG CAGCAAGTAC ATATTGATGC TGTGCTAAAT ACTTACATGG 600
ATCTTATTGA ACCCCCACAA CTCTATGAGC AAGTATTGCT ATCGTCCCCA TCTCAAAGAT 660
GCAGAAAGCA ACACACAGTA AGGGTAGGTG ACTCACACAG GGTGCTGGTG CCTGAGTGAC 720
AGCTGGGACT TAAGCCCTCT GTCTGTGCTC TTGCTTGGCA TACCATGCTG GGTGAAATGA 780
AATGGCCTTA CTTAGCACAG TGCCTGACTG CAACAAAAAT GTGCCTCTTT TAAAATGCTT 840
CGCCCTCCTA TCCATCCCCA GGGATGTTTT CTTTTTTTAG ATGGAGTTTC ACTCTTGTTA 900
CCCAGGCTGG AGGTGCAATG GTGCAATCTC GGCTCACTGC AACCTCCACC TCCCGGGTTC 960
AAGTGATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGGATT ACAGGCGCGT GCCACCATGC 1020
CTGGCTAATT TGGTATTTTT AGTAGAGACG GTTTCATCAT GTTGGCCAAG CTGGTCTCAA 1080
ACTCCTAACC TCAGGTGAAC CGTTCCCCTC GACCTCCCGA AGTGCTGGGA TTGCAGGCGT 1140
GAGCCACTGT GCCTGGCCCC CAGGACTTTT CTGATTGCAA AAACCCACCT GTTTCTTGAG 1200
CTTGGGCCCC TAAGTCATTT CTACAGGATC ACCCCAGTGG GTGGGGCTGG GAGATGTGGC 1260
ACTAGCCAGG CATCTCCTCT CTGTTCTGAG CTCTGGGTTC CTAGTGTCAT AGGATGAAAA 1320
GGGGAAGACA GCAGAAAATG TATGGGCCAG GCAGTCTGCT GCCCAGAAGA AAGCCTGGCC 1380
CACTATAAGG GACAGCCTGT AGCCCAGTGG GGTACAAAAA GGTAGGCGGC AGAGATGGGC 1440
CACCCCCTAC CTGCAGGAAA GGTTCTTCCA TATGAGATGG GTGACTGGGC CCTCTGAGTG 1500
ATCTTTGCCG GTTACTGGCC ATTCTTCTGG GCCTCAGAGC CAGGAGGGGC GGCTTTGTGG 1560
GGAAGCCCTT TCTGGCACCA TTGTTTACTC CTGGGGTTGC TATGGTGATG CTGCTTGAGT 1620
GGTGATGCAG AGAAGAGGCC CTCACCTGTC CCTGGAGCCT CTTGTGACCC TTGGGCCCCT 1680
GGCTACTTTT CAGGTTAGAC AGGCAGGGGA TAGCACTTTC TTCAAGTTCT GACTGCAAAA 1740
AACTGTAACA GGAGCTGCTG CCGGGCAGAA GAAAAGCAGG GCAGGCTGGC TCCCAGGCCT 1800
CAGGGTGGGG ATGGCAGTGG GAATGAAGCA CCTGTAACTG GGCCCTTCCT GCCCTAATGT 1860
TCAGGGGGCC CTACCCCTCG TGAGCTTGTC TTATTAAGAA CCCTCAAAAG GCCTAAGTTA 1920
ACCAGCAGGT CCAAAGGTCC CAAGGAACAA GGTCAGAGAC GCCAGGGAAA AGAGGTGAGC 1980
TGTGCAGGAC TAGCACTGGG AAAACTGGCA ATTTGTGTTG TCAAGTGTGT GCCTGTGCAA 2040
GTGCTCCAAC TGCTGCTTTG GGTGAACTTC AGGCCTTGCC TCTTCCCTAT CACCATCGTC 2100
TCCATCAACA CCCTCTTTCT TTTCCAGCCT CTCCTGGTGC CTTAGGAATC AGACGCCAAT 2160
AAACCACAGA 2170
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