| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02378 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:222627940-222629420 | 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 | GAAAAAAGTG GCAACATGAC TGTGAACTTG CATCTGATCC AGTGATTCCA AATTCCCTTA 60
CAATTGAGGC AGAGACTCCG CCAAAGGGAC TGGTGAGCCC TGTGACTGGC CCCATCACCA 120
TGACAACACT CCTGTTCCAG CGCCTCAAGG GATCTCCACT CTCCTACCTT CTCACGTAGG 180
TGGGAAAGGT GGCGTCCTCA CCTACATGTA CGGCCAGGAC TCCCATAATT TAAGAAGAGC 240
CAGCTAGATC ACTAAAATGG TCTCCATGCT ACACGTTACA ACTGCACATC TCAGCACCCA 300
AAGCCTTCAC TGGAGAGAGA AAACCGTGCC TGGGTGACTC GTGACTCGAC ATTGGCTCCG 360
GACGTGTCAG TACAGAGGAA CGTCGGTACC GGATCCCAGA CATAGGGCTG AGCCCAGCTG 420
GTTCTCATTC TCTTCTGGGG CCAGGCCTGC TGCTGGTTTC ATTTAATTGA ATATTTTGAT 480
TGTTTGATTT CTGTAGCCAG AAGCCTGTAG GCAGTAAATG CCCTTTTCCA TCAGTTCAAG 540
AAAGAAAATG TACCTGCCGA GGTAGTATCT GCTTCGCTGA GCTGCTGACT TATTTTAAGA 600
ACTAAATCTT TCCTGTTACT ATATTTTTCA CTCTGGGGTG TGCGCGCTCC AAGACTGACA 660
GTAACTCAGG TCTAGGACAG GAGCGTCCTC TCGGCGATGA CTTAGCGCCA CCTACTGACC 720
ACTTGCTCAA CAGCGGCCAC GTTCAGCAAC CACGGTGATC TCGACAGACA CGAAAATGTT 780
CTGTGCTCTC AACGAGAAGT TCTGCATGTA TTCTTCCCTT CTCACATAGC AGAGCTTGCC 840
TAGCAGAATT GTGCTCCTTT TATTTTTTAA TATAAGTAAG TTAAGACACA GGGCTCCAGC 900
AAGAAAGCTG AGCAAGTTCT CCATTTGGCA ACTGTTTCAT ACTTCCCGAC TTTGGCGGCT 960
GTCATTTATA AATGATGAGC TCATGAGTGA GGAGGCTGAT GCAACCCCCA GGGGCCCAAA 1020
ACACAAGCAT GGAGAAAGAC AGCCCTCCTG TGGGATCTGA TGCAATCGTC TTGTCTTCTT 1080
TAGGCTTTGA TACCAGTGTT TCTAAACTTT AGGTGCAAGA TTATCCTCAC AGCACCTCTA 1140
AGGAGTATAA ACCCCAGGGT TATTACTTAC CGGTTACCAC AGCAACTCAT ATGTAAAGAG 1200
TTGGAAAGTC CTTCCTCTGT GGTGATTGAG AGTAGACATG GAGCTGTTTG CAACCCCCTA 1260
AACACATTGC CCCCTTGCCA CACAATAGCA AAAATTGAGA ATTATCATCC TGTCACCACC 1320
CAGTGGCTCT GGGCCCTCAA GCTCCCAATT ACTTACAGAT ATCTACAGCA GAGTCTCTTG 1380
ACCTTCGCAC CATCGGGTCA GATAGGTCTT TGTTGTTGGG AGGCTGCCTG CGCATTATGA 1440
GCATTTAGTA GTATCCTTGG CCTCTACCCA CTGGTGTCAC 1480
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