Tag | Content |
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EnhancerAtlas ID | HS193-10692 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr14:100806880-100808300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr14:100806959-100806969 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr14:100806959-100806969 | GGCACGTGCC | - | 6.02 | IRF1 | MA0050.2 | chr14:100807660-100807681 | GAAGTGAAAGGGAAAGAAAAG | - | 6.93 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09626 | chr14:100805730-100810069 | CD14 |
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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: 1 | ID | Chromosome | Start | End |
GH14I100339 | chr14 | 100805947 | 100809857 |
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Enhancer Sequence | TATTCACAGG CACAATAGTA GCTCACTGCA GCCTTGAATC CCTGGGCTCA AGCCATCCTC 60 CTGAGTAGCT GGGACTACAG GCACGTGCCA CTGCCCTGCC TGAACCTGTT ATTTTTAGGA 120 GGCTGGAGCA GATGTGCCCT CTCTTTTCTA GTGTGGAGAT TCTGATTTTG GAGCTGAAGT 180 CGGGCACGGG GATTTAGAGT GAGGGCCTGG GCGGGCCCTG TTCTGCCCCA CAAGAAGCCT 240 GCAGGCCCAG TGACCGTCTG TAGGCCTCTG TTTTTCCTGA CCTCATGCTA ACTGCTCACC 300 TCGAGGGCTC TACTGGTCCC TAAGTGAATG ATAAATGTCC CAGATCCATA AACAAGTTTT 360 TCTTTTTTCT TTTCTTTTTT TTTTTTTTTG AGCTGGAGTC TCACTCTGTT GCCCAGGCTG 420 GAGAACAGTG GTGCGATCTC GGCTCACTGC AACCCCTGTC TTCCAGGGTC AAACAATTCT 480 CCTGCCTCAG CCTCCCGAGT AGCTGGGATT ATAGGTGCCT GCCACCAAGC CTGGTTAATT 540 TTTGTATTTT TAGTAGAGAC AGGAGTTTCA CCATGTTGGC CACGCTGGTC TCGAACTCCT 600 GACCTCAGGT GATCCACCTG CCTCGGCCTC TCAAAGTGCT GGAATTATAG GTGTGAGCTA 660 TCGCACCTGG CCATAAACAA CTTTTTCCAA ACAACTTCTC AGAAGCAAAA TAAAACAGTG 720 GACTTTTCCA ATGGCGCTTC CCTCCCCACT CTGCACCCTG TGCTCCGGAA GTTTTGGCCA 780 GAAGTGAAAG GGAAAGAAAA GTCTTCAATT ATACCAGCTT CCAACTGAGT GGGGAGAGTT 840 GGTGGAGGGC ATGTCTTAGG AAGTTTTGAT ATGAAAGGCT TCCCCATTGT CAACCAGAAC 900 CTGCTTGGGA CTTTCCAGAA CGGTCAGGGG CAGTGACTCA GAGGGCATGT GACATGCCTC 960 AAATACAGTT CCCAGCATTC CCACTGCAAT CTTCTAGCCT GCAAACACAC ACTTGATTCC 1020 AAAGAAAATG TCAACTGCTT TGTGTAACAG TGAGGCAATT ATATATACAC TGGCTGTTGA 1080 GGAACCAGGC AACAGAACTG GGGCCATGCA AAATAAGGAA GCTCAAACTA ACTTCTCCTT 1140 TTAGTTTCTC TAGTGATTTG TCAAATGTTT GCTGAATGCC TGCTGCATGC ATCCCTCCTG 1200 GGGCCAGCAG GACTGTCCCG TGGATGGACG TTTCTCCGTT CTATGTCTCT CAGTGAGAAC 1260 GCTCTCTGGG AGAAGACCAG CTCATAACCC CTGCTTGGTA ATGGCTGCTC AGGGCCAGGA 1320 GAGCAGTGCT GCTGATTCCT GGTGGTGGAA ACTTGGTCAA GTGGCTGGGC TTCTCTAAGC 1380 CTCATCATCT CATCTTTAAA GGGAATAGCA CCACCACCTC 1420
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