Tag | Content |
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EnhancerAtlas ID | HS080-25709 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr4:4397420-4398880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr4:4398387-4398398 | AATGACCTTGA | - | 6.32 | ESRRB | MA0141.3 | chr4:4398455-4398466 | AATGACCTTGA | - | 6.32 | Esrra | MA0592.2 | chr4:4398388-4398399 | ATGACCTTGAG | - | 6.02 | Esrra | MA0592.2 | chr4:4398456-4398467 | ATGACCTTGAG | - | 6.02 | Esrrg | MA0643.1 | chr4:4398388-4398398 | ATGACCTTGA | - | 6.02 | Esrrg | MA0643.1 | chr4:4398456-4398466 | ATGACCTTGA | - | 6.02 | KLF4 | MA0039.3 | chr4:4398107-4398118 | CCACACCCTGT | + | 6.14 | Nr5a2 | MA0505.1 | chr4:4398387-4398402 | AATGACCTTGAGCTT | - | 6.53 | Nr5a2 | MA0505.1 | chr4:4398455-4398470 | AATGACCTTGAGCTT | - | 6.53 | RREB1 | MA0073.1 | chr4:4398350-4398370 | ACTCTGTGGGTGGTTTGTGT | - | 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 |
chr4 | 4398239 | 4398522 | chr4 | 4398536 | 4398757 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I004396 | chr4 | 4397961 | 4399008 |
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Enhancer Sequence | GTCCCACTAG TGACTGGACA GCTTCTGTGC AGCTCCCTGG CCCAGCCATC ATCTTAGCTC 60 TTTCATCTCC ATGCATGAAT TGCAGGAATG GAATCTCGCC TTTCCGATCT TGAAGTGACA 120 GGTAAATCGT TTGTCCCCTC CTCTCTCCAA TTTGTGTAGC TCAGAAGCAC CTCATCTTTA 180 TAGGCGTTTG GATGGCATCC TTGAAACGGA GTGTCTTTTT GCATGCAGCT TTCTGATTGT 240 CACTTGGGGA TTAATCTCTT GGCTGTGAGG TTACTAGGCT GGTTGCTAGG TAACTGCTGA 300 CTGGGAGAAG GTTCTGAGAG ACTCCGCCAC ACGGGATGGC AGGAGGACTC CCCCAGCGGC 360 GGCCAGCTGC TTGGGCTTCC AAAGAGGTTC TTGTCAAGGA AAGCAGTCGC TTAATTAACT 420 GGAGGCATAT TTACAGTGAG AATAAACACT GGCTGAGATG TTTCTCAACC AAACCTAAAC 480 ATTTTTGAAA TTGCACTTCC CCACTGATGC CTGCAGAGTG GCGGGTCGGG GCTGCTGGGG 540 CCGCTGCTTG CAGTTCTCCT TCCGGTCTGG AGACTGTCAT TAGGGGCCGT CATCAGACAG 600 GTGACAGGAA GGCTCCCTCA GGGCCCGCTC CAGCCCTTCG TGCTTCGTGA TTCCGGTGAT 660 GACCGGTTGC TGACGCTGGA GAGGTCTCCA CACCCTGTTT GCCTGTGATG TGAGGTCAGG 720 TTTGGGTGGT CCAGCCTTGA CCCTCACCGG GTACCATGTC ACCCTGGGGC CTTGAGAGAT 780 CTGAAGGTCG GCTTTGCACG GGAACACCTT TCACCGCCAG CACAGGGCTG GGGAGTGACT 840 TGGCAGGAGA GCCCTCGTTA GTCTGCGTGG TCCCCCTGGT TGGCAGTCCA GACTCTGGTG 900 GGGACGTCCC TCTGCATCCT GTCGCAGAGG ACTCTGTGGG TGGTTTGTGT CTTTTCTTCA 960 CATCCCTAAT GACCTTGAGC TTCCTGCGTG CCCATCTGTT TCCACATTCT CCAGTAAGCC 1020 CCTGGTGTGT TCCCTAATGA CCTTGAGCTT CCTGCGTGCG CATCTGTTTC CACATTCTCC 1080 AGTAAGCCCC TGGTGTGTTT CAAGATGCAT TTCTTAAATA TTTATGAAGA GTGATGCCGT 1140 TTCCTTGGCA TTCAGCAGTG GGGGTGGGGG TTCTTCCCGT GGGGGTGGTA TTGGAGACCC 1200 TGAAGGTGTG TGTGGACGCC CCCTCACCTT TAGCTATGCG AGCATCTTGT AGGATCCTGG 1260 GGCTGTGGTT GCAGAGCCCA CCTTCCCCAG GCTAGCTGTA GTGTGGGGGC TTCGGCTGAA 1320 TCAGATACCA CGTGGGTTCA GTCATCTGTG TGTGTGTGTG TGTGTGTATG TATTCACTTT 1380 TGTGTGGGTT ACCTAAAATA TTTAGTGCTG TAAACGCTTG AAGATGTCGG GATTCATCTT 1440 CTTTTTCCAA GTTTTTTCCT 1460
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