Tag | Content |
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EnhancerAtlas ID | HS105-45054 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:113715960-113717010 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:113716578-113716597 | TACTGCCATCTAGTGGGGA | - | 6.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AGCTGTTCCT CCCATCTCCA CCACCCTCTC CATCTCTTTC TCACGTTGCT CTATCCTTAA 60 TTATAGCAAA ACCCATAGGA AGTGTTATAG AGACCCCCCT TTCTGTAATT TCTCCTGTTC 120 TATTTTAAAC TTGCCCCCAA AGTACACTTA CCAAAGTGGC TGTAGTCTCC GCCACTGCAC 180 CTAAACTTCC CTTGCTGAGG TCATCACCAG CCTGCACGTG GCCAAACCCA CTGCTGTCTC 240 TGCTCTCCTC TTATTTGACT TTTGAGTCAT GTGAGCACAT AAATGATCCA AACGGCAACA 300 CTCCTAAGAA ATGGTTGTAC CTGGACAAGA GGCATAAATT GGGGCCGTCT TAGGAAAGCA 360 GATATACAGC CATCCTACCT TTAGGCACTC ACTGTTGGAT GCAATTGGTC ACTCTTCCTT 420 GGGACCTTTC CGCCATTGGC TCCACTATAC GCACTCTCCT GGTTTCCTCC CCTCTAGCCG 480 CTGTCTTTGG TCTCCTTTCT GATTTTGCTG CGTCCTCTGT CCCCTGAATG ATTGCTTCTC 540 CACTACGGGG TGATTTTGCT CCCCAGGGGA CATTTGGCAA TATCTGGAGA GGTCTATGGT 600 TGTGTTTGAG GGTGTTGCTA CTGCCATCTA GTGGGGAGAG GCTAGAGATG CTGTTAATGC 660 CCAGGACAGT CCCCATAACA CAGAATTATT CAGCTCAAAA TATCCATGGT GCCAAGATCA 720 AGAAACCCTG CTCAAATATT AGCATGTGCT GAAGGCCCTT CTCTTTCCTT TAGCAATATC 780 TGCCTCCTTA GGGATCTTTT CTAGTCTCAG TGGTTTAACA TTTAAAATCC CAAATTAGGC 840 AATAAATTGG GCCCCAAACT TCGTTAGTAT AAAATGTAGA ACTGTGTTAT TAGAAGGCTA 900 ATAAAATGAC CTGGTGAGCA TCTGCAGCTA GCCTCTGAGC AATTCTGGGG ACCACGTGCA 960 AGATAAATCC ATCTGTTCCC TCTCTGTAAT GTGGCGCTAC CTTGTGGCCG ATTTTTCCTC 1020 GGGTTAAATA TCTCTGGGGA TGCAACTTGT 1050
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