Tag | Content |
---|
EnhancerAtlas ID | HS176-11904 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:101148980-101150230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:101149512-101149533 | CACTTCTTTTTCTTTCACTTT | + | 6.07 | MEF2A | MA0052.3 | chr13:101149370-101149382 | GCTAAAAATAGC | + | 6.44 | MEF2B | MA0660.1 | chr13:101149370-101149382 | GCTAAAAATAGC | + | 6.92 | MEF2C | MA0497.1 | chr13:101149368-101149383 | GAGCTAAAAATAGCA | + | 7.91 |
|
| 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 |
GH13I100497 | chr13 | 101149482 | 101150468 |
|
Enhancer Sequence | GGTGCCTTGG GAGCCAGTAA GTAGATGTCA CCCAACCTGG TAGCTCAGGG AAGGCTTCTG 60 GAGTTGATGA CACCTCAACT GTGACTTAAG GTAATGATTA TGAGTCAGCC AAGCCAAGGA 120 AAATGGGGAG GATACTGTAG AAGGACATGA TACCATGAAC ACAGCCATGG AGCCACGAAA 180 CTTCATGGTG TGTTCAGGTC GCTACAGTGG CTGGCAGCTT GAGTTCTAGG ATGGAGTTCG 240 GAAGATGTCA CGGAATCCCA GTATGGCAGT ACAAGTGCAC TTGTTCTCAC GGGAGGCTGG 300 AAGCAAAGGC TGTGCTCCTT GTTCCTCAAA AGCTCTAGGG TCTCTTTTGT CTCTTAATTC 360 CATAGTTCTC TCTCCCCTAA TTAACACAGA GCTAAAAATA GCAGAGAAAT GGGGAATTGG 420 GGGGAAGATT ATAGTCAAAG AAGTTTCATC ACAGGATGCA CAGTTAATTT GGTTGCACTG 480 GAAATTGGTT TCCTTCTCTT AGAAAATAAA AATCATCTTT GCAAAAAATT GTCACTTCTT 540 TTTCTTTCAC TTTTTTGAGG GTGAAAATTA GTGAAAAATG AAAATATGAA CAAGTTGTGC 600 AAATAAAACT AAAAAGTCAC CGAATTTGGC TTTGAAGTAT GCATCTGAGA AGCCTACTAT 660 TCTTTGGCTT GAATGAGAAG TGTAAGTTGT GGAATGGTAA AGCAGTGTAG CCTCTTTGAC 720 ACCCAGCCAA TTTAATTTTT TTTTTTTTTT TTAATTTTAG TGGCAGTAAG TACTGACTTA 780 CCAAGGCTTG GGGTAGCAGA TACTATCACA GCTGCCAGGA CTTTTCCAGG CTCCTGTCAA 840 GAAACTGCTG CAATTCTGCA AGAGTCTTCA GATTAAATTC ATGCCAAGTC ATTTCCTCTG 900 TTCTTCTACC AGTGAGGTCA CCTTTGCAGC TGACCATTAG TGATGCTGTC AGCAAGAAAA 960 GGATTATGAA CTGAGGTCTA AATTTCAGTG ATGTCTAGGC AAAAATAAAT GTTCAAAAGA 1020 ATTTAGCGAG GTTTCCAAGA CCTGGTAAAT TTCTCCCTAA GAGAAATTGC CAGATTTGTG 1080 GGCTCTTGAT TTTAGCCTGA AGAATCACAT TCTTCAGCAC TGGAAGTTTT TCCTTCTTTT 1140 TTTACTTTTC TTTTTTTTTA GACACAGGGT CTCACTCTGT CACCCAGGCT GGAGTGCAGT 1200 GGCAGGATCA TAACTTACTG TAAACTTCGA ACTACCGGGC TCAGTTGATC 1250
|