| Tag | Content |
|---|
EnhancerAtlas ID | HS098-54242 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr8:22986360-22987780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:22986855-22986876 | AGAGGAGGGTGGCAGGGAAGA | + | 6.03 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH08I023128 | chr8 | 22986417 | 22987510 |
| Enhancer Sequence | AAAACCAAAC TTTGAAGCTA ATATATTATA TTAGATGTTT TGGTCAATAC ATTCATTTGT 60
CTCATTCTTT TTAACAAAAG CATAGTAGCT TCTTTCATAG TGGAACTATG GTCCATTCTA 120
CTGTTGCCTT CTGTGGGTAG TTGCATTTGT TTTTGAAAAT TCTAACAGCA ATCATCTTGT 180
AGGTATCACA TATCCAGATA GTCATGTGCA CTACTTAAAA GCAGAATTGC GGAGTCGATG 240
AGTTAATGAT TTAAAAATTT TGTTTAGATT TTGACAAATT GTCCTCCAAA AGAAAATTAC 300
AACAAGTTTA CTCTCACACC AAGAGTCCTA CACCCTTGCT ACTCTGAACT TTCATTCTTT 360
GCTAGTCTAA CAAGTAAACA ATGGTGCATC TCACTGTTGT GGTTTTGATT TCTCAGCATT 420
ATTTGAGGAT TTTCCAGGGT CCGGGAGTTT TCTGAGACTG AGTGTAAATG ATCCGCAGAC 480
CTCAGATGAG ATGGCAGAGG AGGGTGGCAG GGAAGACTGA ATTCCCAGCT GTGCACTTGG 540
AAAACCGTGG TCAGCTGGGG CCAGTCCCCA CCACCTGCCA TGGCTGTGAA TGGAGATAAG 600
GTCTCTGTCC TCAAGCTGTC AGGATGACCT CAAATGAGTC TGGAGCTGAA CTCAGTTCCT 660
GACCCCAGGT CCTCGCTCTG TCAGTGCTGG GCTGGTCCAA TCTCTGTACC AGGTCCTTCC 720
ACCCCGCCCC TCTGTCTATC AAAGTGAGAA CTGAGAAATT CTGAAGGCTC AGAAGCTTAG 780
ACACTCAGGC TGTCAAAGAG CCCAGAGATT GGAGGCTAAA GACGGCCAGG GTTGGCGGTG 840
CTCCTCTTCA ACTCTGTGAC TCTGGTGTGG CCCAGCTCCT TCTTGTAAAA TAAGACAGAG 900
AGGCCTTATT TATGCAGAGG GCCTGTATAA ACCGCAGTGG ACTGTGTTGG CAGTGTGAGG 960
TTGTGTGGGA GGACAAACCA CATCCTCAGG GCTTGTGTCA GTCACTCTGG ACTGGATTCC 1020
CAGGGCACAT GTCCTCCACC CAGCAGAAGC TGCACCTGCT CCTACCTGCG CCTCAGTACC 1080
GGCTCCCTCA GCTTGGGGCA GAAGCTTCTA AAGACTAGGT TGGAGTGCCA TGGGGAGGGG 1140
CCATGGAGGA ACAGAGGTGC CAGACTGCAA GTGAGGACAG CGATGGCACT ACAGGGCCAC 1200
AGCCTGGTTT ACCTGCCATA TTTCCAGTTG TCCTTCTGGT GGGTGCCCTG CCCAGGTTGC 1260
AGTTTGAAGA GTGAGCAGGA AAGGTGTCTG TCGCTCCCAC ATCTAGGTAA TGTAAAAGCT 1320
AAACCCTCCA GGGGAACTGT AAAAGTTGGG GTACTATATG GGTGGCCTAA GCACTTGACT 1380
CCTCGGGGGA GAAGCTGGGG GTTGGGAGTT TTCTCCTGAT 1420
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