Tag | Content |
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EnhancerAtlas ID | HS108-22917 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr2:100403690-100404700 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:100404188-100404200 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr2:100404204-100404216 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr2:100404208-100404220 | AAACAAACAAAC | - | 6.32 | Foxq1 | MA0040.1 | chr2:100404619-100404630 | AATAAACAATG | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGTCATAAT TAGCAAACCA CCCGCAAACT CGACTCTTTA AATCAGAGGC CAGTGACTGC 60 CAGGCTGGGG CATAGACGGG AGAAAACAAG CAGAAATGGT CAAGGTGCTC TCTGGAGCCT 120 GCCTTCGGAT AGCTGTGACC CCCACGTTAG GCATCAAGAC AGGGTTCCAC ACCTGCGCCG 180 CCACCCCTGC AGTGTGAGCG CTGTATTTTG CTTTCTGAGA AAGCCTCACG GTTTGGCTCT 240 TTGGTGCATG AGGCTTTAAG GCGATGTGCC CCCTGCCCAG CTGTTGCCCA GCTCCCAGCC 300 CTTGCCACAG ACAGCATACA TCTCTGTTTT AGAAACAAAT CATTTAGTCA CTTAATCATG 360 AATTCCCGAT GATGTACGTC CTGCAGAGGT CTGAGCTGGG GCTGCTGGTC TGAAAGTCTA 420 CGTACTTCTG ACTGGAGACT TAGGCTAGGC TGGGTTTCAA ATTTGGATGA AGACGGTTTT 480 GGCTGAGCAG GGAGAAGAAA ACAAACAAAC GAACAAACAA ACAAACAAAC AACAATCCGG 540 GAGCCTGGAG TTTGCTGAGA GGCTCAGCTT TGGGGAGATC TGGGGCTGGC CATCCTTGGA 600 GTCTGCTTCC TTATCAGCAA ACGCCTCCTA AAGTTGTTAT GATACTTCTC AGAACTAGAC 660 AGCATATATG AAATCAGATA ATGCACAGTT GTGCACTACT TGGTGACATT TTGGTTAATG 720 ACAGACTGCA TATATGAGGG CAGTCCTGTA AGATTATAAT GGAGCTGACG TCCTATCACC 780 TAGTGATGCA ATAGCCATTG TAATGTCACA GTGTAACACA TTACTCACCA TTGTGGTGAT 840 GCTGGCGTAA ATAAACCTAA TGCGATGCCA GTCATATAAA AGTATGGCAC ATACAAAATT 900 ATGTACAGTA CATACTATTT CATAATGATA ATAAACAATG ATGTCACAGG TTTATGTATT 960 TACTACATTA CACTATACTT TTATTATTTT AGAGTGCACT CCTTCTACTC 1010
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