Tag | Content |
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EnhancerAtlas ID | HS093-24441 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr5:360100-361270 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr5:361147-361162 | AAGGTCAGGAGTTCA | + | 6.04 |
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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: 2 | ID | Chromosome | Start | End |
GH05I000361 | chr5 | 360516 | 360715 | GH05I000360 | chr5 | 360822 | 360962 |
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Enhancer Sequence | TTTCCTTGAT GATCTTTTTA TGGACTGGAT GTTTGTCTCA TCCCTTCACC TATTCATATA 60 GTGAAACCCT AATTCCCAGT GTGGCCGTAT TTGTAGGTGG GTCCGCTTAG GAAGAAATTA 120 AGGTTAAACA ACTTCATAAG TGGGGGTGGG GGGTGGCCTG AACTGATAGG ACCAGTGTCC 180 TTAAAAAGGA GACCCAAAAG AACCCTCTGT CCCTCTCTGT GCTGAACACC CCCCAAAGAA 240 AGGCTGTGAG AGAACACAGG GGGAAGGCAG CTGTCTGCAG GCTGGAAAGA GAGCCCTCAC 300 CAGAGCCAAA TCAGCTGCAC CCTGATGACG GGCTTTTAGC TCCAGAAATG TGGGAAAGCC 360 CATTCCTGTT GTTTAAGCCC CCGGACGGGG GTGTTTATTA TAAGCAGCCC AGGCAGAGAA 420 GTGGGGTGCC CTGCACTACA TGCCACATAC CTAAGAATGT GGAAGTGACT TGCAGCTGGC 480 TGGTGGGTGG AGGCTGGACG AGTTTTGAGG TGTGTGCTAG AAAGAGCCCT GATGGCTGTG 540 AAGCAGTTGT TGGTAGAACT ATGGGTGTTA AAGGTGTTGT TGGTGAGGGC TCAGAGAGGA 600 GAGCATTGTA GGGAGAGCTG TGGTCGTAGA GAACACACGT ACCCCATGAA CAGAACACTG 660 ATAGAAATGT GAGCATTAAG GCAGATTCTG GTGAGGAATG TGCCCGTGGA ACGCGAGGAA 720 AGTGATTCTT GTTATAAAGT GGCAAGGACT TGGCTGGACT GAATTCTAGC ATTTTGTGGA 780 AAGTGGAACT TGCAAGTGAT GAAATGGGGT GTTTTGCTGG TGAGATTTCT AAGCAAAGTG 840 TTGAAACCCT TGCTTCTCCT TACTGCTTAT AGTGAAACGT CAGAGGAGAG AGATACATGG 900 AAGGAATTGC CAAAAGAAAA GGAACCAGAA CTTGAAGGTT TGGAAAATTC TCAGCCTATC 960 CACATTGCAA AAAATGAGAA GGTGGGCCGG GTACGGTGGC GCACACCTGT AATACCAGCA 1020 CTTTGGGAGG CTGAGGCGGG TGATCACAAG GTCAGGAGTT CAAGACCAGC CTGGCCAAGA 1080 TGGTGAAACC CCATCTCTAC TAAAAATATA AAAATTAGCC AGGCATGGTG GTGGGCGTCT 1140 GTAATCACAG CTACTTGGGA GGCTGAGGCA 1170
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