Tag | Content |
---|
EnhancerAtlas ID | HS187-10267 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr17:29106920-29108350 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr17:29107599-29107616 | TGCTTTCCAGGAGTTCC | + | 7.33 | IRF1 | MA0050.2 | chr17:29107469-29107490 | TAATTGAAAGTGAAAGTGATC | - | 7.94 | PRDM1 | MA0508.2 | chr17:29107478-29107488 | GTGAAAGTGA | - | 6.02 | SOX10 | MA0442.2 | chr17:29107831-29107842 | TTCTTTGTTTT | - | 6.62 | Zfx | MA0146.2 | chr17:29107052-29107066 | CCGGCCTCGGCCTC | + | 6.28 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr17 | 29107170 | 29107220 | chr17 | 29107427 | 29107570 | chr17 | 29107579 | 29107752 | chr17 | 29108210 | 29108284 |
| Enhancer Sequence | GCCTCAGCCT CCTGAGTAGC TGGGATTACA GGCGCCTGCC ACCACGCCCG GCTAATTTTT 60 TTGTATTTTT AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC CATCTCCTGA 120 CCTCGTAATC TGCCGGCCTC GGCCTCCCAA AGTGCTGGGA TTACATGCGT GAGCCACTGT 180 GCCTGGCCAT TTATTTTTAC AGCGAACTAC ATTTGCCACT GTACTCCAGC TCGCTGTAGC 240 CTCAAGCTCC TGAACTCAAG TGATCCTCCC ACCTTAGCCT CCTGAGTAGC TGGCTAATGC 300 CTGACTATGC CTGGCTAATT AAAAAAAATT TATTTTGGTA GAGATGGGGG TCTCATCATG 360 TTGCCCAGGT TGGTCTTCAA CTCCTGGCTT CAAGCAATCC TCCCACCTTG GCCTCCCAAA 420 GTACTGGGAT TACAGGTGTG AGCCAGCAGT CCCGGCCAAA CTTGCTAATT TTAATTTGTG 480 TCTTTTTGCT TTACTAAATA GTAACCATGA GTGTTCTGAG CTTTTCTGAG TTCTGTGAGT 540 CCTGGCAAAT AATTGAAAGT GAAAGTGATC TTAAGCACCC CTGAACACAT TTACCACGCA 600 TGGCCCACTT GCATTCATCT GGTATTGGAG GGAAACAAAT TTCTAGAGTT TCAGTTGCTA 660 CTTTTCAGTT GTTCCATGGT GCTTTCCAGG AGTTCCAGTC GATGATATGG GGTTTCGCCT 720 GTCATCACAT CTGTCAGGCT TTGCGCCTTC TTCATCCTGC ACAGACACTG AGATCATGCA 780 GGTCTTGTAT CTGTTTGTAG TTCGTCTTCA CTAGCTTGTA TTTTGGGATT TGAGGGGGTA 840 AGTGGTCACC TAGTCTTACT GTAGATATTA TCCAGGGGAT TTTGCTTTTG TTATCTATCT 900 AGTTGCTCTA TTTCTTTGTT TTGTTTGTGT TTATTTATTA AGAGATGGGG TCTACCAATG 960 TTGCCTAGGC TCACTGCAAC CTCGAATTCC CAGGCTCAAG CAATTCTCCC ACCTCAGTCT 1020 CCTGAGTAGC TTTGGAACTA CTGGTGGGCA CCACAACACC TGGCTAAATT TTTTTTTTTT 1080 TTTTTTTTTT TTTTGAGACA GAGTCTTGCT CTGTTGTCCT GGCTGGAGTG CAGTGCCAAG 1140 ATCTTGGCTG ACTGCAGCCT CCACCCCCCG AGTTCAAGCA ATTCTCCTGC CTCAGCCTCC 1200 CATGTGGCTG GGACTACCAG CGTGCGCCAC CACATCCAGC TAATTTTTGT AATTTTAGTA 1260 GAGACAGGGT TTCACCATAT TGGTCAGCCT GGTCTCGAAC TCCCGACTTC AGGTGATCCA 1320 CCAGCCTAGG CCTCCCAAAG TGCTGGGATT ACAGGTGTGA GCCACCACAC CCAGCCAAAT 1380 TTTTTTTTTA AGTGAATAAA AAATGGCTAG GCATAAGCCA CCATGCCCAG 1430
|
| |
|
|
|