| Tag | Content |
|---|
EnhancerAtlas ID | HS003-03806 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr1:222628060-222629210 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:222628642-222628661 | TAGCGCCACCTACTGACCA | - | 7.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGACAACACT CCTGTTCCAG CGCCTCAAGG GATCTCCACT CTCCTACCTT CTCACGTAGG 60
TGGGAAAGGT GGCGTCCTCA CCTACATGTA CGGCCAGGAC TCCCATAATT TAAGAAGAGC 120
CAGCTAGATC ACTAAAATGG TCTCCATGCT ACACGTTACA ACTGCACATC TCAGCACCCA 180
AAGCCTTCAC TGGAGAGAGA AAACCGTGCC TGGGTGACTC GTGACTCGAC ATTGGCTCCG 240
GACGTGTCAG TACAGAGGAA CGTCGGTACC GGATCCCAGA CATAGGGCTG AGCCCAGCTG 300
GTTCTCATTC TCTTCTGGGG CCAGGCCTGC TGCTGGTTTC ATTTAATTGA ATATTTTGAT 360
TGTTTGATTT CTGTAGCCAG AAGCCTGTAG GCAGTAAATG CCCTTTTCCA TCAGTTCAAG 420
AAAGAAAATG TACCTGCCGA GGTAGTATCT GCTTCGCTGA GCTGCTGACT TATTTTAAGA 480
ACTAAATCTT TCCTGTTACT ATATTTTTCA CTCTGGGGTG TGCGCGCTCC AAGACTGACA 540
GTAACTCAGG TCTAGGACAG GAGCGTCCTC TCGGCGATGA CTTAGCGCCA CCTACTGACC 600
ACTTGCTCAA CAGCGGCCAC GTTCAGCAAC CACGGTGATC TCGACAGACA CGAAAATGTT 660
CTGTGCTCTC AACGAGAAGT TCTGCATGTA TTCTTCCCTT CTCACATAGC AGAGCTTGCC 720
TAGCAGAATT GTGCTCCTTT TATTTTTTAA TATAAGTAAG TTAAGACACA GGGCTCCAGC 780
AAGAAAGCTG AGCAAGTTCT CCATTTGGCA ACTGTTTCAT ACTTCCCGAC TTTGGCGGCT 840
GTCATTTATA AATGATGAGC TCATGAGTGA GGAGGCTGAT GCAACCCCCA GGGGCCCAAA 900
ACACAAGCAT GGAGAAAGAC AGCCCTCCTG TGGGATCTGA TGCAATCGTC TTGTCTTCTT 960
TAGGCTTTGA TACCAGTGTT TCTAAACTTT AGGTGCAAGA TTATCCTCAC AGCACCTCTA 1020
AGGAGTATAA ACCCCAGGGT TATTACTTAC CGGTTACCAC AGCAACTCAT ATGTAAAGAG 1080
TTGGAAAGTC CTTCCTCTGT GGTGATTGAG AGTAGACATG GAGCTGTTTG CAACCCCCTA 1140
AACACATTGC 1150
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