Tag | Content |
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EnhancerAtlas ID | HS098-23452 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:17922000-17923190 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr17:17922494-17922514 | ACACACCCCACCACCCCACC | + | 6.54 | RREB1 | MA0073.1 | chr17:17922497-17922517 | CACCCCACCACCCCACCCCC | + | 6.69 | ZNF263 | MA0528.1 | chr17:17922677-17922698 | CCCTTCTCCTACACTTCCTCC | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I018018 | chr17 | 17920827 | 17922030 |
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Enhancer Sequence | CTGAGGGAAG GACAAGACAA GTTGCTGGGT GAGTGGCCAG TGCCTGGCTG CCTCCTGACC 60 AAAGCCACGT TCCATTCCAA TAGGTTGGCT GAGGGCAACA GGTTTGTATC TTGCCAAAAC 120 ACATGAGACA TGCCTAGGGG GAGGTGGCAG GTAAGAACAC CCAGGTACGC CAGACACGGT 180 GGCTCACGCC TGTAATCCCA GCACTCTGGG AGACCGAGGC AGGAAGACTG CTTGAATCCA 240 GGAGTTCAAG ACCAGCCTGG GCAAATATGG TGCAACCTCG CCTCTACAAA AAGGTTTAAA 300 AATTAGCTGG GTGTGGTGGG GGTGCACCTG TAGTCCCAGC TATTTGAGAG ACTGAGGTAG 360 GAGGACTGCT TTGAGCCCAG GAGGCTGAAG CTGCAGTAAG CCAAGATCAC ACCGCTGCAC 420 TCCCACTTGG GCAACAGAGC AAGACCCTGT CTCAAAAACA CCACACACAC ACACACACAC 480 ACACACACAC ACACACACAC CCCACCACCC CACCCCCAGG GAGCCGGAGC AGGCACCTGT 540 GCTCTCTGTG GCATGGATGG TCTGGAAGAA GTGCAGTCCA GGCCCAGGCC CAGGGCCAGT 600 GGCTGCCCAC CCACCACTGG GCAGGCTGGG TACCAGAACC ACCCATGTGA CTTCTTTGAG 660 GAGGCCTTAT GTGCCATCCC TTCTCCTACA CTTCCTCCCA GAAAGCCTGT GAATGGACAG 720 CCTCTCCAAG TTGCCTTGCC ATGCTGGGCT ACAAGTGCCC CCCAGCGCCA TGTGGGTGGA 780 ATAACTAAAT CAAGTAAGGC CACGCAGTGG CTTCAACTCT GACTCTTGTG GTAGTCACAG 840 AACTACAGAT GCCTCTGCTC TGCACACTGG GGACAAGTTG CAGATTCTCT GTCTGGAGCT 900 CTAAAAACAA GAGGGAGGAA CGCTCAGACA CACGATGTGG CTGTCCAGAC AGTGTAAGTC 960 CAACCAAACC TTGCTGGCTC CTCCCTGGCT AGTTGCCCAA GAGGCCTGGC CTGGCCGCCC 1020 CAGCTCATCC AGGAACTCAG AATCCACCAT GCTACACAAG CTATTTGAAC TTCTGGGCTG 1080 CCTGGTCCCA AACTGTACAA TTGTAATATG TCATCTGAAG AGTATTCCAT ACTTTCATTG 1140 TATACCATCA CATACATAAT TCAGGTTATT CCTCTGTTTG TAGAGGATCG 1190
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