Tag | Content |
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EnhancerAtlas ID | HS127-04593 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr10:104486920-104488180 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:104487383-104487401 | TCTTCCTTCCTCCCCTGC | - | 6.06 | Nr2f6(var.2) | MA0728.1 | chr10:104487839-104487854 | GAGGTCAAGAGTTCA | + | 7.64 | RARA | MA0729.1 | chr10:104487839-104487857 | GAGGTCAAGAGTTCAAGA | + | 6.45 | ZNF263 | MA0528.1 | chr10:104487387-104487408 | CCTTCCTCCCCTGCGTCCCCC | - | 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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Enhancer Sequence | CCTGGGGGCA GGGCCGTGGG AGGTACAGCT GCCTGGATCT GCTGGTCAGG GAGCCATACT 60 ATGATAATAA TAATAGTTCT CTTGATTGGT CACTTACCAG ATACCAGGCA CTATGCTACA 120 TTCTTTGCTC GTATTGCTTC ATTTAACCCT CGCAACAACC CTACACTATA GGTACTATTA 180 TTTCCATTTT ATAGATGAAG AACTAGAGTT CTAGAGAAGC TGAAGAACTT GTCCAGGTTT 240 AAACAGGCAG GAAATATGGG TGCCTGGATT TTAACTGAGG CAGTCCTGTG TAGAACCCTC 300 AACAAATAAG CTACCCCAAT TCCCTCTTTA AAAAGTACTT ATTCCACAAT GATTTTAATT 360 ATGTAACACC CAAACAAAAC AATAGGAAGT CCCTTTCTTG GCTTGGTTGG GGAGAGAATA 420 GACTGCCTCT GTAGCTGCTG GACATGTGAC TCTTCTTCCT ACCTCTTCCT TCCTCCCCTG 480 CGTCCCCCAC CCCACGCATT GATTGGTTCA GCTATTGAGC TGGGCTTTGG GCCGGGTGTT 540 GGGAATGTGA AGGCTTCAGT AACCTCCCGT CAAGGAGCTC CCAGTTTTGT TGAGGAGACC 600 AAGAAGTAAA CAGTTACAGT ACAGCTTGGT AAGTGGTAGG TTGGAGGAAG AACATGGGGT 660 TGTGGGAGCA GGAGCATGGA GTGACTTACT CTGTCTCAGG AGGGGCAGGG AAAGGGTCGG 720 GAAGGTTCCA TGGAGGAAGT GATCCCTCTC AACAGGGCAG GGTTGGCCAT GTATGGAAGG 780 AGGAGGGGGA GATATTTGAG GCAGAGGGGC CAGCCTGCGC AGAAGCCCAG GTGCATAAAA 840 CAGTATGGGA ACAAGCTGGG CACGGTGGCT CATGTCTGTA ATCCCAGCAC TTTGGGAAGC 900 CAAGGCGGGT GGATTACTTG AGGTCAAGAG TTCAAGACCA GCCTGACCAA TATGGTGAAA 960 CCCCGTCTCT ACTAAAAATA CAAAAATTAG CCAGGCGTGG TGGTGTGTGC CTGTAGTCCC 1020 AGCCACTTGG GAGGCTGAGA CAGGAGAATT GCTTGAACCT GGGAGGCGGA GGTTGCAGTG 1080 AGCTGAGATC GTACCACTGC ACTCCAGCCT GGGTGACAGA GTGAGACTCC GTCTCAAAAA 1140 AATAAAAATA AAAAACTAGT ATGGGAACAG TGTGGGGACC TGCAGATCAT GTGCTTTGAC 1200 TGGCATACCC TCAGGACTCC CTGCCATCTG ACTTCTCTCT GCCTCTCCTG GCCTTCCTCA 1260
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