Tag | Content |
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EnhancerAtlas ID | HS193-17303 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr2:26290950-26292240 |
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) |
ALX3 | MA0634.1 | chr2:26291298-26291308 | TCTAATTAAA | + | 6.02 | JUN(var.2) | MA0489.1 | chr2:26291638-26291652 | CTGAGTCATTTCCT | - | 6.73 | NFE2L1 | MA0089.2 | chr2:26291634-26291649 | CTTGCTGAGTCATTT | - | 6.88 | Nfe2l2 | MA0150.2 | chr2:26291636-26291651 | TGCTGAGTCATTTCC | - | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09566 | chr2:26289818-26294619 | CD14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 26291005 | 26291914 | chr2 | 26291590 | 26291772 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I026066 | chr2 | 26289807 | 26293562 |
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Enhancer Sequence | CTGTCCTGGG GAAATGACAT TTATACTGCT ACATGAGATA TGATTAGAAG TTAGGTAGAA 60 GAACATCATT CCAGGCAGAG GAAGTGGGCA CAAAAAGGTC CTTAGTAAAG GAGCTTTTTG 120 AGTTCAAAGA ACTGAAAGAT GATGTGTGTT GCAAATGTGA CTTGTGAGGC TAGCAGAAGC 180 AATAGATGTT GAAGACGTGG GTTTGAGCCA GATTGTGCAG AGCCTGGTAG TCCATGCTAA 240 GGATTCGAAT TCCATGGAAG GTTTGAGCAG GGATGTGACA TGGTTAGATT CAATTTTTAA 300 AAGATGGTTG GCCCAGAAAA TGTGGAAAAT GGATTGGAGT TGGAATTTTC TAATTAAAGA 360 CTTATCAAAG ATGTGTTTAA ACTCTTACTG TATACTATTT AATCTTTAAG GATTATGAGC 420 GATTATATGT GAAAATACCT GTCAGTGACT GTGACAGTGA GCCTTTAATT TTTTTTTTGA 480 GGTGATCTTT TTAGTGCCAA ATACATCAGA CAATCCTGAG CCAAGAGACA GAGTTCTGAT 540 CATAGTTAAT TTGGTTTGTG AGCTTGAGCA AGTCATTTAA ACTCTGAGCC TCTTTCTTTA 600 TCTGTAAATT GGGCGTGTTT GAGAAATGTG TGCTTAACTT TAATTGTGTT AATCGCTTAA 660 CTCTGGTTAA CATATGGGCT GAGTCTTGCT GAGTCATTTC CTCAGACGTT GTGGGCAAGG 720 CTTAAAACCA GCTAAGCAAA TTTAGTGATG ACACATTTTA CCTCTTCTGT AGAAGTCAGA 780 TGAAAGAGCT GTTTCAAAAA TGTTTCACTT ATTGTTTTCA TGCAGATTAT CTCTTCGTGG 840 GGGAGAGAAT ACAGTACACA TAGCTCAGGA ACTACTGATG CACTGCCTTC CATTTTAGTG 900 GCAGTTTGAA TTTAAGAATT TCTAGTTTGT CTTAAGCTTT TCTGTAATCT CTCACATATA 960 TATTCTTAAT TTCAACTGAT AATTTCTTTC TTAATGTCTA ATATAGCCTA TTTGCCCTCT 1020 GAACAGCATT GAGATGCTTT GAAATTTTAA TGCCCAAAAA GTTGGCTTTG GTAAGGTGGT 1080 TTTCATTTCT GCAGTAGAAC CATGGTTGAG GCTAATGGTC CCATCAGCAT TAGCAGGCCT 1140 TTGGCTAGTT GCACAGTAAA CTGCATGTTT CCCACTAGTA AAAGAGATAA CCCCAACAGT 1200 TTTAGGATTA ATGCTGAGTT GTAGTGTTCT TTGGGATTTA CAGATTTTTT TCTATAATTT 1260 AAACTTTTTG AGACATATCC TGAGGATAAT 1290
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