Tag | Content |
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EnhancerAtlas ID | HS161-06504 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr17:28690160-28691280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:28690342-28690357 | AAGGTCAAGAGATCA | + | 6.93 | RARA | MA0729.1 | chr17:28690342-28690360 | AAGGTCAAGAGATCAAGT | + | 6.45 |
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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 |
GH17I030363 | chr17 | 28690419 | 28691490 |
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Enhancer Sequence | GATTCCTTTC AACTATCTTG CTTTTCTAAT ACATAAATAA TTTTGCATGT GTCATTAAGA 60 AACTTTCTCA TGCTGATTTA TTAAAGCATT TTAATGCTAC TTAAAGAATA TGAAGTGTGG 120 CCGGGCGTGG TGGTTCACGC CTGTAATCCC AGCACTTTGG CAGGCCAAGG CAGGTGGATC 180 ACAAGGTCAA GAGATCAAGT CCATCCTGAC CAACATGGTG AAACCCCGTC TATGCTAAAA 240 ATACAAAAAT TAGCTGGGCG TGGTGGTGCA TGCCTGTAGC CCAGCTACTT GGGAGGCTGA 300 GGCAGGAGAA TCACTTGAAC CCGGGAGGTT GAGGTTGCAG TGAGCTGAGA TCGTGCCACT 360 GCACTCCAGC CTGGAGACAG AGCGAGACTC CATCTAAAAA AAAAAAAAGA ATATGAAAGT 420 GTGATGCTGA GTGCGGTGGT TCACACCTGT AATCCCAGCA CTTTGAGAGG TGAAGGTAAG 480 AGGATCACTT GAGCCAAGGA GTTTGAGGCT GCAGTGAGCT ATAATCACAG CACTACACTC 540 CAGCCTGGAT GACAGAGCAA TACCTTGTCT CTTTCTCTTA ATTTAGAAAA AAAAAAAAAA 600 AAAGGAAGTG GGCAGACTGC AAGTAAACCC TGAGAACTCC TAGATCACCT CAGTTTGCAG 660 CACCCATTCA CCTCTTTCCT CACCACTGCC TAAGAAGGCA CATGAAGCTT AGTCACTGTG 720 CAGACTCTCA AAACTTTCTG GAACTTCATG CAAAGGTTAA GCCTTGGAAC CAACTCTGAA 780 TTTCCTTGTG GTTTCAAACT TGTCACATTT TCTTCTCACC TTGTCACCAC CCACACAGAC 840 TCAGCCTCCT GGATGCATCA CGCTTGGGTT GCTTCACTTC CTGGCTCCTG GTAAGCCACA 900 ATTGCAAGAG CTATTGCTGG TAAAACTGGT GACCCATTAC AGGCACACAA ATAAGAACAT 960 AGGTGCAGGG GAGCCACAAG TGCACTATCT GAATGTGTCA GGGTGAGAAC ATTATGTTTC 1020 CTCAGCTCTC ACTCATCCTC TGGTGGAGAG GACTCTTTGG TCTTCAGTCT TCCAATAACT 1080 GTCTATAGAA TATTTTTGCA TGCTATTCAT CTATACCTGA 1120
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