Tag | Content |
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EnhancerAtlas ID | HS093-14042 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr18:12049890-12050990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SCRT1 | MA0743.1 | chr18:12049921-12049936 | ATTCAACAGGTGTGA | + | 6.18 | SCRT2 | MA0744.1 | chr18:12049921-12049934 | ATTCAACAGGTGT | + | 6.27 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 12050102 | 12050320 | chr18 | 12050338 | 12050731 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I012049 | chr18 | 12049800 | 12051173 |
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Enhancer Sequence | ATGGTCAGTT GACCAACCCC CTTTGGAAGC TATTCAACAG GTGTGACCAT GGCACAATGA 60 CCTGGAAACA GGCATCTCTC ACCCTTCCTC TGTTAAAAAA CCTGAAATCC TGAAAAGGCA 120 GAGCAGATAC AATATTTTTA CCTTTTCATT TCCATCCTAA ACTTTCACCA CTCCAAAAAA 180 TCTAAAATGA TCTTTCATAG AATAACTCCA CTTAAATGCC CTCAGAACTT TAGCTGCTAT 240 ATGCGTTGGT TTGGAATGCA GTTTGAAGTA TTTGAGGTTG TTCTAATTCT GCAAAATGAA 300 AAGGGAAGCT AGGCAAATAC TGAAACTTGC AACCACAATA TCTCATTACT TTGCTGAATA 360 AATTGTATAA ATTTAAAATA GAAAAGTCAC AGCACTCCCT GCCTAGGCCA AGTAACTATT 420 GGTAGTGCTC ACAAGCCTGC AGGGCTTGGA GGATCTCCTG ATCCCAGGCA GTACCTTCAA 480 GTCCCAAATG TTGTGGAAGT GCAAAGGATC TCCCAGGCAC GCTATTAGCC TTTGCCTTTG 540 GAGCTCCACA GCCACTATCT TATTGGAGTA GCTGTAGTTG CAGATCTCAG TTCCCTTTTT 600 CAAGTGGCAA ACCTTTAGCT TCCTCTGAGC TTTGAGGTTC AAAATGGCCA CTAAGGTGCT 660 TGACAACAAT TTTCTATAAT GCACGCATCT TCGGTATCAG TGCAATTCAG GGATCTGTTC 720 CAGCTTATCC ACAGAAGAAG GGAGAAAAAT TTATAACTGG ACTTACTACC CACAGCTAGG 780 GATGTGTCCT TGTTGGAGTT GGCCCAGCTG GCACCGGCCT CTGATCTGGC TCCCCCGGTT 840 CACAGCTGGG TGCACAGGGG TTGCGATGTG CTCAGGGTGT GCGCCAGTCC CACTTTCTGC 900 CTCGGTGGCT GCCACTACCT CTCTGGGATC AGCCACAACC TTGTCCCGTC CCTCCTTGTT 960 TTTCTAGTTT CTTGAAGTAG AAAGTTAATT ATCGTTTTGA GGCCTTTCCT CTTTTCTGAG 1020 GTTAACATTT AGTGCTGTTA ATTTCCCTAT CAGCAGGGCT TTATTCAATT CCATGAATTT 1080 CTAAAATTTA TTTTGAGGCT 1100
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