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EnhancerAtlas ID | HS187-07603 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr14:71684830-71685450 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:71684865-71684883 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr14:71684861-71684879 | TTTTCTTTCCTTCCTTCC | - | 7.52 | EWSR1-FLI1 | MA0149.1 | chr14:71684873-71684891 | CCTTCCTTCCTTTCTTTC | - | 8.57 | EWSR1-FLI1 | MA0149.1 | chr14:71684869-71684887 | CCTTCCTTCCTTCCTTTC | - | 9.6 | Nr2f6(var.2) | MA0728.1 | chr14:71685232-71685247 | CAGGTTAAGAGGTCA | + | 6.71 | ZNF263 | MA0528.1 | chr14:71684861-71684882 | TTTTCTTTCCTTCCTTCCTTC | - | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCATTCAAC AAAGGAGTTC CTTTTCTTTT CTTTTCTTTC CTTCCTTCCT TCCTTTCTTT 60 CTTTTGACAG GGTTTCACCA TGTTGGCCAG GCTGAGCTTA ACTCCTGACC CCAAGTGATC 120 CACCTGCCAA GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACTGT GCCTGGCCAA 180 GGAGCTCTTA TTGTCATCTC TGCACTGTGC TTGACCCCAG AGCCAGGACT AGGCTGGGGC 240 CAATGAGGCA TTGAGCAGAC AAAGTTTAAG GAGAAACTCA CTTGCACAAC CCTGAGAGTG 300 AGTGCCACCT GGCATTGTCT GCCCTCCACC CCCTCCTGGC CCTTCCAGGC ACAGAGGAAA 360 CAAAGATTTT TTTTTAAGCC ACTTTCTTCC TCAAGACACC CACAGGTTAA GAGGTCAGAA 420 ACAGGGCATA CCACACTGGC CTTTGGCACC TCAATTGCTC ACTTCACAAG AGCACAAAAT 480 GTCCCCTAAG AAGAGCAGCT GAGTATAATG GAAAAAGTTA AGTGTCCTCT TCTGACCTTT 540 GATGATTCAA AAGTTTAGAG TCATTTTTAA CACTATTCAA AGGAAATGTG ACACTCATAT 600 AAACTTGATG CTACATGTCA 620
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