Tag | Content |
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EnhancerAtlas ID | HS187-21204 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:41286400-41287880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:41286748-41286767 | CCCTGCCCCCTGCTGGCCA | - | 7.51 | FOXP1 | MA0481.2 | chr6:41287297-41287309 | TTCTGTTTACTC | - | 6.27 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_39685 | chr6:41286828-41287727 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I041318 | chr6 | 41286339 | 41288955 |
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Enhancer Sequence | ATTAGGCGCA CTGGGGTGGA ATCCGGCATC TGCATTTCTG AAGCTCCCTA GATGATCCCA 60 GCATGCAGAG GAGTCTGAGA ATGACTAGTC TAATTTCATT TCCACAATAT GCTTGTGAAG 120 CGGTCGCCAC TATCCCCTGT GATTCCCTTA AGGTTCCCCC CAGTGAATTT GTGGCATCAG 180 GAGCCCAGCC CAGCACTCCT TCCACTGCAC GTGCCGCTGT CCTGGAGGAC AGGAAGCAGA 240 GCCAGGGTGC TGCGTACGTG GCTCTTCAGA GGGCTCTTCA GTGTGCCTCC AAGGGCGCAC 300 AGCCGAGTTG AGCCGTCTGA TTACGCTCCG GGGTGATGGA CAGGCTGCCC CTGCCCCCTG 360 CTGGCCAGAG GCTGCTATTG CAGCCAGCGT GCACACGCGT GCGCGCATCT TCAGCCACCT 420 GCAGTTTCTC TGATTCTTCC CTGGTCTCCT CTCTGCAGTG TCGCCAGAAC ACCTTCGCAC 480 ACTCTATTCT TTGTGGCCCT TCTGACTTTC TCTTTGCCGT GTGACAGGGG AGTCCTCCCT 540 AACCAGCAGA CAGTGAAGGT GGAGTCCACG TTTCTCGGCC TCCACGCATA GCGAGTCTCA 600 GACCCCGCAA GGCTGCAGAC AGTGCTGTGT AAGTGGGCCT TCAGTCCTGT GGGGAGCCCA 660 GGTTGAATCC CCAGGAATAG AAGCTCCAGA GGAAGGTCCC CAATCAGTCC GTGGTCCCCA 720 ATCCTGAGAA GGGTTGCCTT TTCTGGGAGG AGCCTGGGTC TCATCGCTAT GCGGGAACAG 780 GGCTCTGGGA GGTGTCCAGG AAATGTGAGA CCGGAAGTCG CCGTCAGGGA ACGGAGTAGT 840 CTGTGGCCCT GTTAGAGGAA ACAGCCCTGG GGGGTCCCCA ATTGCTTCTA GAATCTATTC 900 TGTTTACTCT TCTAGGGAAT ACCTGTAACT TCTTTCCTTG GAACCAAGAT TTAGCACATG 960 AGAAGAATCT GGAAGAAGCT GAGCCCACAA GGGTCCCAGG AGGGCATTCT ACCTGCCCAC 1020 TGACCGTCTC AGCATGCTAC ACCCTCGAGG GAACTCAGGT TCCCTGTCTG TAAAATGCAG 1080 ATTCTCTCCT ATGAAATCTC TGAGGTGAAT AGCTCTGGAT AAACTTCAGT GGCCTTCTTT 1140 TAGATGTTTT TTGTTTTTGT TTTTTGTGGG TTTTTTTTCC CCTTGGGTCT TCCTGCCTGG 1200 GGCCCTCTGC CCTGGGTCTC CTGCAGAGGT TCCCACCAGC TCAGGAAAAC ACTCAAGGGT 1260 GAGTGTCTCA GAGCTCAATA GGCCTGAGTT CCTTTCCCAA TACCTCCTAC CACTCCCTGG 1320 ACATACACAC TAGCACATAC ATGCACACAT GTGTGTGCAA TCAAGCTAAT CAGAGTGGGG 1380 CCTTGATTGA GTCAGAGCTC TTTGCACTCC TCCACATGTC CTCTACAGTG TAGCACTAAT 1440 TCTGTGTCCT CCGGGGTCAG GGCCAGGTGC AGCAGGTGCA 1480
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