Tag | Content |
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EnhancerAtlas ID | HS182-06583 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr14:75118480-75119580 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:75118986-75119004 | GGAACAAAGGCAGGAACG | + | 6.01 | RARA(var.2) | MA0730.1 | chr14:75118510-75118527 | AGGTCAGGCCAAGGTCA | + | 7.54 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 75118891 | 75119132 | chr14 | 75119239 | 75119563 |
| Enhancer Sequence | ATGGAAGAGC AAAGGAATTT AGCTATACCC AGGTCAGGCC AAGGTCAGTA CCAGTGGACG 60 TGGGAGAGGC AATGTTGGAA TTAAGAGGAT GTTTTGTGAT TTACAAAACA CTATTCACAT 120 CCATTGTCTC ATTTAAGCTT TACGTGCCCT CTGTCGGGTA CACTTGTACG TTGTTAGAAT 180 CACTATTTCC CAGTTAAAGT TAAGAGCGAC TAAGCAATTT ATGCAGAGTA TACACCTAGG 240 CAGTGGCAAG TCAGAAATTT GAACCCAGAT CTTCCAAATT CAAATCCACA ACATAACCAA 300 AGACAACTGT GGATAGTGGT TTACTATTGC TAACTACTAA TTTTTTTTTT TACACTTAGT 360 GTCAGACACA GTACCGGCAC TTTTCATGAG TTCTCTTATT TAATCCTCAT ATCCTCTGGC 420 ACGAGCCAGG TTTGAAGGAT GGGGAGGTAG CAGGGAGGAA GGACGGGATG GGCCTCATTC 480 CTTGCAGAGT GCACAGAACA AGTAAAGGAA CAAAGGCAGG AACGAGCTGA GATGGTTCAG 540 ACCACGTTCA CTGAGAGCTG GTGGTGCTTC ACAGCCACCG TCCTTGGGCC TCTGGCCTGG 600 TCAGGTAAGC CTCCTAGAAC CTTTCATCTT AGTAAAAATG GGCTGTGCCC ATGGAAAGTG 660 GCCTCTGGCT CAGCCCTGGA AGCAACAGCT GGAAGAGGCC TGTGGCCTGT CACTATCCAC 720 ACGGTTGCTT CTCTGCAAGA CAGAGGCCCG CCACGGTGAG CTGGTCTGTC CAACCAGCTC 780 CTGAGTTGCC AGTCAAATGA TGGGCTCGGC CTCAGCGCTC AGCTTTGAAG TTTAATGGGG 840 ATCCTGGTAG CCCACAGGTC TTGGCCAGAT CTTGCCCTTT AGTAAGTGTC TTCTTCCACT 900 TCCCATCAGG GGCCTGGAGC CTGGCCAACT CCCTGAGGCA TCTCTCCCAG CTTATTTGGA 960 TTGAGGGATG GAGGGTGCCT CCTGCCCTGG AGAGGGAGGT GGAGAATGGA ACCCGTACCC 1020 TGATTGGGAA ACAGAAACCT CAGGAGGCAC CAGGCAGCAG GACTGGACAA AGAAGTGCCG 1080 GCCAGACTGG CTCCCTGGGG 1100
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