Tag | Content |
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EnhancerAtlas ID | HS176-39755 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr8:50912370-50913860 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr8:50913545-50913559 | TAAAGATAAACAAA | + | 6.02 | NFAT5 | MA0606.1 | chr8:50913735-50913745 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr8:50913735-50913745 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr8:50913735-50913745 | AATGGAAAAT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGGCTGGTA TAATAATTAC ACTGAATATT TCACCTAACT TCATTTGCCT CTGTCCACTA 60 GAATGGAACC TCTTTTTAGG AACTTGAATG ATTTTTTGTC CCCTCTATTT TGTTTCCTGT 120 TGTATTCCCA GGGCCTCGAT CAGTTCCTGG CTTAATACAT ATTGTTGAAT TGAATAATTG 180 TATCTGGTAT TGACTTGCAA TCCTTCTTCA CTACAAGAGA AATAAATCAT TAGTTTGGTA 240 AGGCCAAGAG AAAGTCTGTT CATTCATTTA ACTTTTGTTT TTCATTTAGT GCTGACCATG 300 ATGACTGGCA CCGTGCCACA CTGGTCCAGA TGTCATCTTT TCATACTGCA AGTTCCTGCC 360 ATATGATCTG CTTCTGTTTT TCCTGCTTGT CATTGTGTTG AAATGATTGA TTGCTTACTT 420 CCGGGCTTTT AATATCCATA GCAAAGACAT TTCCATCTCT TTCTGACTGA CATTATTCCA 480 GTTCAGATTT TAAGCAGAAG TATCATCTAG TATATTTCTA AAAATCTATC AAGCTCTATT 540 CCTCCGAGTT TTAAAATCAC AGAATGCTAG AAGTGCCTGT GTGTATTTTG CAAACTGCTG 600 CTCCTCCGAG TTGTTCTGGA ATGGGTCTTA TTTTTTTATG TTGTGCTTTA GTTATGTTTT 660 TCTCCTTCTC TACTCCCCTT TCAGATTCTT TGTACAATGT AAAGGGTGTT TAAAGACTTA 720 CATTTTTGTG AAAAGAATTA AACTTCAGTG CATAACCTGA CTTAAGAAAA GCTTGCCTGT 780 AGTGCAAATA TCACAGACTC TGTGCTACTT CTCATAAGCA ATATAAAATA GTCTCCTTGG 840 CTGCAATAAT TGAAGCTTTT ACGCTCTCGT GCCCCTAAAT GTCACATAAA TGTATAAGAA 900 ATGTATCTGT GCTTTACAAA TGTAGTCAAA AATAACTGCT CCCTGCTAGT TACTTAATGT 960 ACTTCCTTTT ATTCTTGCTA GAGTCCTATA GATCTGGACA AGAGGTTATC CTTCCTGTCA 1020 GTAGCAGACA AATTTGTTTA TTTTAGGAGA ACAAGTGAAA CTGTTTCACC ATATCTGAAC 1080 TCTTGGCCCT CTGAAAACAT CAGAGCACAT TTGCCAAGAG ATAGAGTTGT CAAAGCCTTT 1140 CTTTTGCCTT CAATTTTCTT TCCAGAAACT TATGTTAAAG ATAAACAAAG CAGGACAATA 1200 GTTGACATGG TAAGGACAGA TTTTAATCAG TCATACGCCA CTGCATTAGG GAAAAGAGTC 1260 CAGGGTGAGC TGAGCTCAAC TGTGACTTGT GCAGAAATGA CTGTGTGTTA CACAAGAAGA 1320 ACAAGTGAGT GGGGAGTGGG TGTGCAGGGG CTTAGTATTC AGAGAAATGG AAAATTACAG 1380 AAAGTAGAAA TGAGGGTTCG GTCTGTGTGA AACCTATCTG GGTTTTTTAA TTGGTGCTTA 1440 TTGAAGTTGG ATTCCCACCC TCCCACAGAG ACTGAGAGAT GAGGATCCTG 1490
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