| Tag | Content |
|---|
EnhancerAtlas ID | HS098-05206 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr1:222627930-222629390 | 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 | ATAGATTGTG GAAAAAAGTG GCAACATGAC TGTGAACTTG CATCTGATCC AGTGATTCCA 60
AATTCCCTTA CAATTGAGGC AGAGACTCCG CCAAAGGGAC TGGTGAGCCC TGTGACTGGC 120
CCCATCACCA TGACAACACT CCTGTTCCAG CGCCTCAAGG GATCTCCACT CTCCTACCTT 180
CTCACGTAGG TGGGAAAGGT GGCGTCCTCA CCTACATGTA CGGCCAGGAC TCCCATAATT 240
TAAGAAGAGC CAGCTAGATC ACTAAAATGG TCTCCATGCT ACACGTTACA ACTGCACATC 300
TCAGCACCCA AAGCCTTCAC TGGAGAGAGA AAACCGTGCC TGGGTGACTC GTGACTCGAC 360
ATTGGCTCCG GACGTGTCAG TACAGAGGAA CGTCGGTACC GGATCCCAGA CATAGGGCTG 420
AGCCCAGCTG GTTCTCATTC TCTTCTGGGG CCAGGCCTGC TGCTGGTTTC ATTTAATTGA 480
ATATTTTGAT TGTTTGATTT CTGTAGCCAG AAGCCTGTAG GCAGTAAATG CCCTTTTCCA 540
TCAGTTCAAG AAAGAAAATG TACCTGCCGA GGTAGTATCT GCTTCGCTGA GCTGCTGACT 600
TATTTTAAGA ACTAAATCTT TCCTGTTACT ATATTTTTCA CTCTGGGGTG TGCGCGCTCC 660
AAGACTGACA GTAACTCAGG TCTAGGACAG GAGCGTCCTC TCGGCGATGA CTTAGCGCCA 720
CCTACTGACC ACTTGCTCAA CAGCGGCCAC GTTCAGCAAC CACGGTGATC TCGACAGACA 780
CGAAAATGTT CTGTGCTCTC AACGAGAAGT TCTGCATGTA TTCTTCCCTT CTCACATAGC 840
AGAGCTTGCC TAGCAGAATT GTGCTCCTTT TATTTTTTAA TATAAGTAAG TTAAGACACA 900
GGGCTCCAGC AAGAAAGCTG AGCAAGTTCT CCATTTGGCA ACTGTTTCAT ACTTCCCGAC 960
TTTGGCGGCT GTCATTTATA AATGATGAGC TCATGAGTGA GGAGGCTGAT GCAACCCCCA 1020
GGGGCCCAAA ACACAAGCAT GGAGAAAGAC AGCCCTCCTG TGGGATCTGA TGCAATCGTC 1080
TTGTCTTCTT TAGGCTTTGA TACCAGTGTT TCTAAACTTT AGGTGCAAGA TTATCCTCAC 1140
AGCACCTCTA AGGAGTATAA ACCCCAGGGT TATTACTTAC CGGTTACCAC AGCAACTCAT 1200
ATGTAAAGAG TTGGAAAGTC CTTCCTCTGT GGTGATTGAG AGTAGACATG GAGCTGTTTG 1260
CAACCCCCTA AACACATTGC CCCCTTGCCA CACAATAGCA AAAATTGAGA ATTATCATCC 1320
TGTCACCACC CAGTGGCTCT GGGCCCTCAA GCTCCCAATT ACTTACAGAT ATCTACAGCA 1380
GAGTCTCTTG ACCTTCGCAC CATCGGGTCA GATAGGTCTT TGTTGTTGGG AGGCTGCCTG 1440
CGCATTATGA GCATTTAGTA 1460
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