Tag | Content |
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EnhancerAtlas ID | HS136-08643 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:76150470-76151970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:76151926-76151941 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr17:76151500-76151521 | CCTTCTTTCTACCCCTCCCCC | - | 7.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 76150608 | 76150740 | chr17 | 76151038 | 76151473 | chr17 | 76151621 | 76151807 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I078152 | chr17 | 76148740 | 76152220 |
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Enhancer Sequence | AATACAAAAT TAGACAGGCG TGGTGGCATG TGTCTGTAAT CCCAGCTACT CGGGCAGCTG 60 AGGCAGGAGA ATCGCTTGAA CCCGGGAGGC AGAGGTTGCA GTGAGCCAAG ATTACACCAC 120 TGCCCTGAGG CCTGGGTGAC AGGGTAAGAC TTCGTCTCAA AAAAATAAAT AGGTGGGGCG 180 CAGTGGCTCA CACCTGTAAT CCCAGCACTT TGGGGGGCTG AGGCAGGTGG ATCACCTGAG 240 GTTGGGCGTT TGAGACCAGC CTAACCAACA TGGAGAAACC CTGTCTCTAC TAAAAATACA 300 AAATTAGCCA GGCATGGTGA CGCATGCCTG TAATCCCAGC TACTCAGGAG GCTAAGGCAG 360 AAGAATTGCT TGAACCTGGG AAGCGGAGGT TGTGGTGAGA CGAGATCACG ACATTGCACT 420 CCAGCCTGGG TAACAGAGTG AGACTCCATC TCAAAAATAA ATAAATAAAT AAATAAATAT 480 AAAAAGGAGA GTTATCATGA AATTTTCAAA GGGGCACAGA TGAGAAAATA ATTGTTGGTG 540 TCTGTGCAGC CCTGGGCAGG GGAAGACATC CTGATTCTAG AAGGCTGCTG CCGGTTGTCT 600 AGACCAGAGT TGTCAACCTC AGCACTCCTG ACATTTGAGG CCAGACCATT CTTCGCGGTG 660 GGGGCTGACT GTGCACTGTA GGATGCTTTG CGACATCCTT GGCCTCTACC CACTAAATGT 720 CAGCAGCAAC CCCTATTTTT TTTTTTTTTT TTTTGTGGAG ATGGGGTCTT GCTGTGTTGC 780 CCAAGCTAGT CCATCTCCCA ATATTGACAA CCAAAAATGT CCCCAGACCC AAAGTTCCCC 840 TGGAGGCAAA ATTGCTCCTG GTTGAGAGTT ACTGGTCTAG AATGAAACAT GCTTAGTGGT 900 CACACACTCT AGTCTATTCC AGTTCTCTGC TCAATCAGCA GTTTCCTCAT TGCAGGGTGG 960 TTTCCAGAGC AGACATGCCC AGCCGAGCAA AGGCAATTCA TGACGTCGAT GATATTCAGA 1020 TTTCACAGAC CCTTCTTTCT ACCCCTCCCC CAAGCACTGC CCCACCACAC AGTATTCTTT 1080 TTTTCTTTTT AATTTTTCTT TCGATTAAAT AGAGGTGGGG TCTCACTATG TTGCCTAGGC 1140 TGGTCTGGAA CCCCTGGGCT TAAGCAATCC TCCCGCCTTG GCCTCCCAAA GTGCTGGTAT 1200 TACGGGCCTG AGCTACTGTG CCCACCTGAT ACACACTATT CTTTTTCTTT TTTTTGAGAC 1260 GGAGTCTTGC TCTGTCACCC ATGCTAGAGT ACAATGGCAG GATATTGGCT CACTGTAACC 1320 TCTGTCTCCT GGGTTCAAGT GATTCTCTGG CCTCAGTCTT CTGAGTAGCT GGGATTACAG 1380 GCATGTACCA CCATGCCCAG ATAATTTTTG TATTTTTAGT AGAGACGGGG TTTCTTCATG 1440 TTGGCCAGGC TGGTCTTGAA CTCCTGACCT CAGGTGATCC ACCTGCCTCG GCCTCACAGT 1500
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