Tag | Content |
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EnhancerAtlas ID | HS136-15032 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr4:120021550-120022540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr4:120022354-120022369 | GAGGTCAGGAGTTCA | + | 6.22 | SOX10 | MA0442.2 | chr4:120021759-120021770 | AAAACAAAGCA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATGGAAGAA ACAAATCCGA GGAGAGAGTT TATGGAAAAT GGAGAAAGGA CAATGAGAAC 60 CGACAAAGAT TGAATAAGAG AGAGTAAAGA ACAAGATGGT GACGTAGACT ACTTATTCAT 120 TCTTTCTTTT TTCCTTTCTG CCGCAAGTAT TTGTTAAGCT TTGCTAAGTG CCAGGTATTC 180 TTCTAGGCAC TGGAGATATA GCAGGGAACA AAACAAAGCA CTTTCCTTTG TAAGATTTAT 240 ATTTTAGTGT AGGGGCTGGC CAACTTTTTC TATAACAAGC CAAATAGTAA GTATTTTAGG 300 CTTTGAGGGC CATGCAGTCC CCATTAGGAC GTCTGAACTC TGCCATTGTA ATGCAAAAGT 360 TGTCACAGAA AGACAAACAT GTGGCCATGA CTGTGTTCCA ATAAAACTTT ATTTACTGAA 420 ACACATGACA GGCCAATTTG TCCTGTAAGC CATAGTTTGT GGAGTGCAAA GGAAAGAAGG 480 AAGTCCAGGA TGACTTCAAA GATTCTTGCT TAAGCAACTT AGTGACCATG ACAATAAACA 540 GTTTCCATGG AGCAGTACAG AGAAACTGAA GAAAGCAAGT GTAGACAAAT TTTTATGTTA 600 AAAGGGAGCA AAGAAAAGGA CCACAGAAGG TGTTTTATTG TGCTTGTCTC TATTTGCAAG 660 GTATTTTGCT TTTGTTTGAT GTGAGAAAAA AAGCATAGCA TGTTTCTATG ATGATGGAAA 720 AACTCCAGTA GAAAACAGGG CTGGGTGCAG TGGTTCATGC CTGTAATCCT AACACTTTGG 780 GAGGACGAGG CAGGCGGATC ACCTGAGGTC AGGAGTTCAA GACCAGCCTG GCTAACATGG 840 TGAAATCCCT GTCTCTACTA CTAAAAATAC ACAAATTAGC CCGGCATGGT GGTGGGCGCC 900 TGTAGTCTCA GCTACTCGGG GGTTTGAGAC AGGAGAATCA CTTACCCAGT AGGCGGAGGT 960 TGCAGCCAGG GCTACACAGC GAGACTCCAT 990
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