| Tag | Content |
|---|
EnhancerAtlas ID | HS046-03092 | Organism | Homo sapiens | Tissue/cell | Fetal_muscle_leg | Coordinate | chr1:222627660-222629400 | 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 | GGCTGTCTGG CCACTTTAGT TGTAAGCTTT CTCTGCTTCC AAGAGATGTG AACTCATTTC 60
AAGCAGCTCA TTGGCAGCCC TCCTGCCCAT TCTATGCATA TTTTACAGAG GAGAGCTTTG 120
AAGCTTAAGC AAAATGGCAT TTGCAAGGTC ACAGAGCTCA CTGGTGGCAG AGCTGGGATA 180
CAGGACTATT GGATTCAAAG CCCCCCACCC ACTCTTTACC TCCCTCCCCT TTCTAAAGCA 240
TGACCCACTG GAGCTTTCAC GGTGGGGGCT ATAGATTGTG GAAAAAAGTG GCAACATGAC 300
TGTGAACTTG CATCTGATCC AGTGATTCCA AATTCCCTTA CAATTGAGGC AGAGACTCCG 360
CCAAAGGGAC TGGTGAGCCC TGTGACTGGC CCCATCACCA TGACAACACT CCTGTTCCAG 420
CGCCTCAAGG GATCTCCACT CTCCTACCTT CTCACGTAGG TGGGAAAGGT GGCGTCCTCA 480
CCTACATGTA CGGCCAGGAC TCCCATAATT TAAGAAGAGC CAGCTAGATC ACTAAAATGG 540
TCTCCATGCT ACACGTTACA ACTGCACATC TCAGCACCCA AAGCCTTCAC TGGAGAGAGA 600
AAACCGTGCC TGGGTGACTC GTGACTCGAC ATTGGCTCCG GACGTGTCAG TACAGAGGAA 660
CGTCGGTACC GGATCCCAGA CATAGGGCTG AGCCCAGCTG GTTCTCATTC TCTTCTGGGG 720
CCAGGCCTGC TGCTGGTTTC ATTTAATTGA ATATTTTGAT TGTTTGATTT CTGTAGCCAG 780
AAGCCTGTAG GCAGTAAATG CCCTTTTCCA TCAGTTCAAG AAAGAAAATG TACCTGCCGA 840
GGTAGTATCT GCTTCGCTGA GCTGCTGACT TATTTTAAGA ACTAAATCTT TCCTGTTACT 900
ATATTTTTCA CTCTGGGGTG TGCGCGCTCC AAGACTGACA GTAACTCAGG TCTAGGACAG 960
GAGCGTCCTC TCGGCGATGA CTTAGCGCCA CCTACTGACC ACTTGCTCAA CAGCGGCCAC 1020
GTTCAGCAAC CACGGTGATC TCGACAGACA CGAAAATGTT CTGTGCTCTC AACGAGAAGT 1080
TCTGCATGTA TTCTTCCCTT CTCACATAGC AGAGCTTGCC TAGCAGAATT GTGCTCCTTT 1140
TATTTTTTAA TATAAGTAAG TTAAGACACA GGGCTCCAGC AAGAAAGCTG AGCAAGTTCT 1200
CCATTTGGCA ACTGTTTCAT ACTTCCCGAC TTTGGCGGCT GTCATTTATA AATGATGAGC 1260
TCATGAGTGA GGAGGCTGAT GCAACCCCCA GGGGCCCAAA ACACAAGCAT GGAGAAAGAC 1320
AGCCCTCCTG TGGGATCTGA TGCAATCGTC TTGTCTTCTT TAGGCTTTGA TACCAGTGTT 1380
TCTAAACTTT AGGTGCAAGA TTATCCTCAC AGCACCTCTA AGGAGTATAA ACCCCAGGGT 1440
TATTACTTAC CGGTTACCAC AGCAACTCAT ATGTAAAGAG TTGGAAAGTC CTTCCTCTGT 1500
GGTGATTGAG AGTAGACATG GAGCTGTTTG CAACCCCCTA AACACATTGC CCCCTTGCCA 1560
CACAATAGCA AAAATTGAGA ATTATCATCC TGTCACCACC CAGTGGCTCT GGGCCCTCAA 1620
GCTCCCAATT ACTTACAGAT ATCTACAGCA GAGTCTCTTG ACCTTCGCAC CATCGGGTCA 1680
GATAGGTCTT TGTTGTTGGG AGGCTGCCTG CGCATTATGA GCATTTAGTA GTATCCTTGG 1740
|
| |
|
|
|
