Tag | Content |
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EnhancerAtlas ID | HS095-09053 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:58797500-58798360 |
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) |
RFX1 | MA0509.2 | chr14:58797921-58797937 | AGTTGCCATAGTAACG | + | 6.91 | RFX1 | MA0509.2 | chr14:58797921-58797937 | AGTTGCCATAGTAACG | - | 6.92 | RFX2 | MA0600.2 | chr14:58797921-58797937 | AGTTGCCATAGTAACG | + | 7.19 | RFX2 | MA0600.2 | chr14:58797921-58797937 | AGTTGCCATAGTAACG | - | 7.24 | RFX5 | MA0510.2 | chr14:58797921-58797937 | AGTTGCCATAGTAACG | + | 7.41 | RFX5 | MA0510.2 | chr14:58797921-58797937 | AGTTGCCATAGTAACG | - | 7.45 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I058329 | chr14 | 58796705 | 58798651 |
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Enhancer Sequence | TTTTCTTTAT AATATTGCCA TGTCATTTAT AATATGCATA TAATTGTAGG AAATCATCCA 60 TGGAGTACTT CATGATTGCT TATATGAATA CTGTTGTTTA TTCTGCAGTG TTGTATCAAA 120 TGGGATAAAC TGTCTAGTAC ATTTTTGGTT GTTACGGGGT AAAAGGGTTT AGGGGCAAGA 180 CAAAGACAAT GAATTTACTG AAAAGGGGGA CCTATTTGAG CATGAAAAAT ATTGGCCTGG 240 AAAAATGTGG GATTCTTGTT TCTGTTTTAA ATACACAAAT ATGAATTTAT GAAATGAAAC 300 GAGTATAGTC ATATGTAATG AAGGGCATAC GCTATTTCTT TCCTTTTACT TCCCCTGCAG 360 TATTTGGTTT TTTTACACTC TGAAATCAGA ATGGCGGTTC ATACTTACAG GCTGCCTACA 420 GAGTTGCCAT AGTAACGTGC TGTTGGTTTT AAGTGAGCAT GCTCGGAAAG ACAGGAAGGT 480 TTAGCAGAGG CTTGGCAGTT TGCCAATGGA GGTTTGCCAG ATGCTTTGAA ATGGGCTGTC 540 TTTCTTTTCC TTTCATGTAA TGTCTGATTT TTATGTGGAA GAGAATGTAA GTAGTGCTGT 600 ATAACCCTGC GGATGCTATG CCCTAAGAGG GAAAGCAAAT ATTTGCAAGT CAGACTGAAA 660 AATGTCCAGA CCCTGTACTG ATTAAGTAGA AGGGGAATCT AACCACTTTG CATTTGAAAG 720 AAAATGCAGC ATATAGGTAA GATTTTTTTG TGTGTTTAGT TACCATTTTG ATTGCCAAAA 780 ACGGGATTAA ATAAGAATTT TAGGTATTGA TGATGTAGCT GATAGGGAAG GACTCAGAAC 840 CAAGCGATAT TCTTTCTTGT 860
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