| Tag | Content |
|---|
EnhancerAtlas ID | HS108-24388 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr2:230645470-230646700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:230645662-230645681 | TATCCACTAGATGGTGCTA | + | 6.24 |
| | | 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 |
| GH02I229780 | chr2 | 230645257 | 230646775 |
| Enhancer Sequence | TACTTTTCTT CCACATGGCC TAACATATAT GTGTACATGA ATGTGTGTGT ATGTATTGGC 60
CTCCCCAAAC TAAAAGATAA GCTCCATCAT GGGGGTGGGA GTACTTTGTA TATTCTGTTC 120
TGCACTGAAT CCCAAGCACT AGAGGCCTGA GGAACAAAAG AGAAGCAAAG AAAAACCTGC 180
AGTAACACAT GGTATCCACT AGATGGTGCT AGTCAATTCT CCTTTTGGCA TAACATTATC 240
CCAGGTTCAA CAGAAGTCAC AGATCAAATT AGTCTATTTC CTTCATCCAA TGCTGTTGTT 300
TCTAAAAGGA TTCTTAAAAT ATTAAATCAC TAAAAGCACT TCCTCTGTGA GCCTCTGCAG 360
AAGGTGGAAG GCCCAGGTCA TGTTTGCTTT GCTGATACAA CCTGGGGGTG GCCAGCACCC 420
CCACAGAGTA ACCTGATCTC TTCAGGGATT ATCATTCTAC CCAACTACAC CACTAAAAGT 480
GTAGGTACTT GGTTGAGCTT CATTTTTCTT TTTAAAGGAA AGGAAAGCAT AAAACCCCAG 540
AAACAGAAAA ACAAAAGTTT GACAACTTGA CTTAAAATGG AATCTTTTTC TCTCAAAACT 600
AACACATACT GGCACTTATT ATGTGACAAT GGTCTGAGTG TTTCACACAT TGCAGCTCAT 660
TTTATCATTC TAACAACATG AGGAGGCAGC TGCACTAATT ATGTAAAGGG CTGAGAGGAC 720
ACTGATGAGT TTATGTTAAC TTGCCCAAAA TCACATAGCC AGTAAGTGGG CAGGCCAGGC 780
TCCACATTCC CTGCTCCTGA TCTTCCACAT TCCCAAAAGG ATACTGGGTC ACTGGGTCAT 840
TTGTAACCCT AATCCTGGGG GTTTGGGTGG CTTGTGAGCC CAAAGACTGG TATAATCCTT 900
CCCTGGCTTA CCAATCATCC CAATTCAAAT AGGAGCCCAC ACTGTGACCT GACATTTTCA 960
CTGGGATTCT TCTAGAGCTA GTTAGAAATT CTTCCTAAAG GCCACCAGCT GACATGTACA 1020
GCTGAATTTG AATCATAACC TGAAGCCCTA TGCATCTCAC AAAGTCAGTG CTTGTGAGGT 1080
AGGGGTGGAG GTACTTTCCC CTTCCCCAGT GAAGCAGCTC CTGGAATCTT TTCCGAGGTC 1140
AACAGGTAAG ACCCATGAAG GAAGGGCATA AAATCTTGAC CTTACATTAG CAATCCAATC 1200
CTGCTCCTTA GAACAACCTG TGTGAAGACA 1230
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