| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22494 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr18:61185180-61186150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr18:61185847-61185866 | CTTCCACTAGATGGCGCTG | + | 7.05 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 61185797 | 61185958 | | chr18 | 61185548 | 61186106 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH18I063518 | chr18 | 61185761 | 61185958 |
| Enhancer Sequence | ATCCCAACTA CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AACCGGGAGG TGGAGGTTGC 60
AGTGAGCTGA GATTGCCCCA CTGTACTCCA GCCTGGGCAA CAGAGCGAGA CTCTGTCTCA 120
AAAAAAAAAA AAGAGAATTT TAGTTTTGAA AACTTTTTTT TTTGTATAGA ACGATTTTAA 180
AGGTCCGCCG GTAAAATAAA AGCAGCTGTC AATTCAGATT TCATCTATCT ATGCAACTTT 240
AGCTCTATAA CTGTAATTAT TTTTGATGCC CTTTTCCCTT TCAGAATTGT CCTGGTGTGG 300
AAGAATAATT ATATGGTCGC GCTCTCTATA TAACAGGGCG GAATAGTAAA AATGCTCTCC 360
AGAAAGGAGC TTTTCAGGTT TTCTTCATCT CCATTGGCCT CAGGAGAGGT GTTATTTTTG 420
CTAGGTATGA AGTTTTTTCT GGTTGTTGTC TCGACCCTGA CACCATAGAG TTTGCTTCTT 480
TGTCTGGGTG GATGTCAGGG CTGAGAAGGA AACAGCTCTG TCACTTGAGA ACTGGCTTAA 540
TCTGTGGGGA AATCAAACTT AGTCTCTATG TTTCCTCTGT AAAATATTAA CTGTTAAGGT 600
GCCTTCCGAC TCAAACGCAA TGTTATCATC AACCTTTAAG AGAATCGGTC ACTTCTGTTC 660
ATTTTCTCTT CCACTAGATG GCGCTGTCCG TCACATTATA ACAGTGCTGC TCAGGGCCTG 720
GAACGGTCAG TTGCTACAGC TTTTCTTTAA GGTCTGTGAA CTCCCGCCCT GCCTTAGACC 780
TTCTGCCCCT GCTGCTATGG GGACGTTGTT GAAGTGCTTT CTTCTCCTTG CCACCAAGAC 840
ACTCTGCAAC ATTCCTTAAC GTTTCATTCT AGGCCACCTC CCCAAGCTTA AAAAATTTGT 900
TTATGGTAAG AACGGTTAAT ATGAGGTGTA ACTTCCTAAC TAATTTTCAG TGTACAACAA 960
TATATTATTA 970
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