Tag | Content |
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EnhancerAtlas ID | HS176-19864 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:26290850-26292180 |
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 | POU6F1 | MA0628.1 | chr2:26290905-26290915 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr2:26290905-26290915 | ATTAATTAAT | - | 6.02 |
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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 | CAGAAACATC AAACCAGAGT AGTTCTCTAG TTAGTAAAAT GAGAATAAAC AGGTTATTAA 60 TTAATCTATT TCAGAGGATG GTCAGGTGGC CTAGAGAATG CTGTCCTGGG GAAATGACAT 120 TTATACTGCT ACATGAGATA TGATTAGAAG TTAGGTAGAA GAACATCATT CCAGGCAGAG 180 GAAGTGGGCA CAAAAAGGTC CTTAGTAAAG GAGCTTTTTG AGTTCAAAGA ACTGAAAGAT 240 GATGTGTGTT GCAAATGTGA CTTGTGAGGC TAGCAGAAGC AATAGATGTT GAAGACGTGG 300 GTTTGAGCCA GATTGTGCAG AGCCTGGTAG TCCATGCTAA GGATTCGAAT TCCATGGAAG 360 GTTTGAGCAG GGATGTGACA TGGTTAGATT CAATTTTTAA AAGATGGTTG GCCCAGAAAA 420 TGTGGAAAAT GGATTGGAGT TGGAATTTTC TAATTAAAGA CTTATCAAAG ATGTGTTTAA 480 ACTCTTACTG TATACTATTT AATCTTTAAG GATTATGAGC GATTATATGT GAAAATACCT 540 GTCAGTGACT GTGACAGTGA GCCTTTAATT TTTTTTTTGA GGTGATCTTT TTAGTGCCAA 600 ATACATCAGA CAATCCTGAG CCAAGAGACA GAGTTCTGAT CATAGTTAAT TTGGTTTGTG 660 AGCTTGAGCA AGTCATTTAA ACTCTGAGCC TCTTTCTTTA TCTGTAAATT GGGCGTGTTT 720 GAGAAATGTG TGCTTAACTT TAATTGTGTT AATCGCTTAA CTCTGGTTAA CATATGGGCT 780 GAGTCTTGCT GAGTCATTTC CTCAGACGTT GTGGGCAAGG CTTAAAACCA GCTAAGCAAA 840 TTTAGTGATG ACACATTTTA CCTCTTCTGT AGAAGTCAGA TGAAAGAGCT GTTTCAAAAA 900 TGTTTCACTT ATTGTTTTCA TGCAGATTAT CTCTTCGTGG GGGAGAGAAT ACAGTACACA 960 TAGCTCAGGA ACTACTGATG CACTGCCTTC CATTTTAGTG GCAGTTTGAA TTTAAGAATT 1020 TCTAGTTTGT CTTAAGCTTT TCTGTAATCT CTCACATATA TATTCTTAAT TTCAACTGAT 1080 AATTTCTTTC TTAATGTCTA ATATAGCCTA TTTGCCCTCT GAACAGCATT GAGATGCTTT 1140 GAAATTTTAA TGCCCAAAAA GTTGGCTTTG GTAAGGTGGT TTTCATTTCT GCAGTAGAAC 1200 CATGGTTGAG GCTAATGGTC CCATCAGCAT TAGCAGGCCT TTGGCTAGTT GCACAGTAAA 1260 CTGCATGTTT CCCACTAGTA AAAGAGATAA CCCCAACAGT TTTAGGATTA ATGCTGAGTT 1320 GTAGTGTTCT 1330
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