| Tag | Content |
|---|
EnhancerAtlas ID | HS136-19412 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr8:101278600-101280110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:101278981-101279002 | CCTCCCTCCTCACCCTCCCCA | - | 6.83 |
| | | 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 |
| GH08I100266 | chr8 | 101278829 | 101279735 |
| Enhancer Sequence | AAATGATTTA TAGGTACATG TGGTACAACA GTCTCTCTTT CCCTTCTAAG TATCTGAATA 60
GTTTTGTTTT CAGCAAAGCC TTGCTTTGAA TAACTACATG AAAAATTACG ATCAGCTAAT 120
ATATTTTGAA ATTTTTTATT TTTTCTCTCT TTTTTGGAAA TAGGGTCTCT CTGTGTCGCT 180
CAGACTAGAG TGCAGTGGCA CGATCACAGC TCACTGTAGC CTCAACCTCA CGGGCTCAAT 240
CAATCCTCCC ATCCCAGCTT CCTTAATAGC GGGGGCTACA GGCATGCACC ACCACTCCCA 300
GCTGATTATT TAGTTTTTTG TAGAGACAAG GTGTCACACT GTGTTGCCCA GGCTGGTCTC 360
AAACTCCTGG ATTAATGCAA TCCTCCCTCC TCACCCTCCC CAAGTGTTAG GATTACAGGC 420
ATGAGCCACC ACACATGGCC CAACATTTTT TAAAGTCCAG GTTTACTCAC TTAAAACCTT 480
CAGAAATAAA TATGTGACTT ATAAATATGT TTGTCATCAG CCCCAAAACT AATTTTTAAG 540
AAATAGTATA TATTATTTTT CTGATTATAA AATGTATGTT GAATATAAAA AATTCAGCTG 600
TTTTACAGAA GAAGATCAAC CTTATTCCCA GTCGGGTCCC AGAAGTTAGA AACAGAAATA 660
AAGGAAACAA AAGGAAACAG ATCTGACTCA AACGTAACAA TTTTGTAACA ATTAGTAGCC 720
ATTTTACAAC AGAATGGATT GCTTCATGAG TTGGTGGTTT CCCCATGACT GAGTTCCCAA 780
ATAGCTACTG AAACTTAATC ATGGAACTTA TATTAAGAAT TCATGCATCT GAGTTCAAAT 840
CTCAGCTCTG CTTCTTTGTG TGTAACTGAA GATATATTAC ATAAACTTTC CTAAATCTCA 900
ATATTTTAAC ACACAGAGAC CGAAATATCG AGGTTGCTGC AGGGTTAAAA TAAGTAAAAG 960
TACATACAAC ACCTATGACA CAGTATGACA ACCTTTAGAT CCTTTTTTTA TTTTAGAGAT 1020
AGGATCTTGC TCTATCACCC AGGCTGGAGT GAAGTGGCAC AATCACAGCT CACTGCAGCC 1080
TCCACTTGCC CATCTCAAGC AATCCTCCCA CCTCAGCCTC CCAAGTAGCT GGGACTACAG 1140
GTGCATACTA CCATACCCAG ATAATTTTTA AATTTTTTTG AGAGATGGGG TCTCACTATG 1200
TTGTCCAGGC TGGTCTTGAA CTCCCAGCCT CAAGTGATCC TTCTGCCTCA GCCTCCCAAA 1260
GTGCTACGAT GACAGGAGTA AGCCACCATG CCCAGCTTGT TAGTTCTTTT TTTTTTTTTT 1320
TGAGATGGAG TTTTGCTCTT GTTGCCTAGG ATGGAGTGCA ATGGTGCAAT CTCAGCTCAC 1380
CGCAACCTCC ACCTCCCAGG TTCAAGTGAT TCTCCTGCTT CAGCCTCCCG AGTCTGGGAT 1440
TACAGGCACC TGCCACCATG CCTGGCTAAT TTTTTCTGTA TTTTTAGTAG AGATGGGGTT 1500
TCACCATGTT 1510
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