Tag | Content |
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EnhancerAtlas ID | HS080-16670 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr19:6765250-6766740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr19:6766358-6766375 | AGGTCAGCCAAAGGCCA | + | 6.68 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_17561 | chr19:6764993-6770046 | CD4p_CD25-_CD45RAp_Naive | SE_18804 | chr19:6765256-6769968 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23570 | chr19:6765105-6765564 | Colon_Crypt_1 |
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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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Enhancer Sequence | TGGGTGAACA TTTTTGATCA TGTGACCAGG AAAGGTCTCA TTGAGTAAAG TCTGGAAGGA 60 ATTCTGGGGA GTGTGCCAGG TGACTCTGGG TGAAAAAACA TCCCAGTCAG GGGGAATTTA 120 ACTTACAAAC ATCCATGGCT TCTCGGCAAC CTATGCGCAC ACTCAGAGGT TCTCAGGATA 180 GGTGCAGATC TAACCCCTAT TCTTTGCTTT AGAATGCAAC GCTGGGGGCC AGGCGCGGTG 240 GCTCACTCTT GTAATCCTAG CACTTTGGGA GGCAGAGGTG GGTGGATCAT CTGAGGTCAG 300 GAGTTTGAGA CCAGCCTGGT CAACACAGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT 360 TAGCCAGGCA TGGTGGCGTG TGCCTGTAGT CCCAGCTACT CAGGAGGCTG AGGAGAGAGA 420 ATCGCTTGAA TCCAGGAGGC AGACCCTGCA GTGAACCGAG ATCACACCAC TGCACTCCAG 480 CCTGGGTGAC AGAGCAAGAC TCCGTCTCAA AAAAAAAAAA AAAAAAAAGA ATGTAACCCC 540 AGGGTTAAGA TTTTTAAAAG GTCACATTTT GTAGCAATGT CAGCAAACAG CAATGTTGCC 600 TTTGCAGATC CTTCTATTTC GGAGCCCATA CATGTGGTTA TCATGATGAT TGAATTTGGA 660 TCTCAGACAT TTTGGTAGTT TCCCGATAAT CTCACAGGCC TCAGGGCCAG TGTGTCTCAG 720 GTGTCTGGTG GGGGAGATTT CTCTGGATGG TCCAGAAGAA GATAATCTGC TTCTTACTCT 780 CCTGCAAGCT CTCCCTGCAG CCCTGCAAAG TCTTCTGGTG GGGTCTGCAG AGAAATTCCT 840 GCCTCCTGAG TCAGCAGGAA GTTCCCAGAC CAGCCCTAGG TGGCTTTAGG GGAGGAGCGC 900 TGGGCAGGGA GCCAGCTGCC AGTGCCGCAT ACCTGAAGCC AGGTGTGTCT TTGCAATGCC 960 TGCGCACTTC CTGTTTGTCA CCTGGACCAG GGCTAGCCTC GGTCGCAGAG TTTCCCAACC 1020 CCAAGTTCCT GTCTTGTGTC TCCCTTAGTG AGAGTGAAGT TGAGTCAATG GCAAGGTTCT 1080 GGTTAGTTTG AGGACACAGG GTGGCCATAG GTCAGCCAAA GGCCAACTAA GCCATCTCCT 1140 GCCTCTGAGT CCTTTGGGAT CATTTATTCG GGCACGGAAG AGAAGAAACG GGCAGAATCA 1200 GGAATCAGAC CAAGCATAGA GAGAGGAGAG AGGGGATTAT TCATGTTCCA GTTGGATCAT 1260 AAACATGTGT CCACGTGTGG GGAGGACGTG GAGGGTGGGA ACCACCAGCA CAGGCAACAC 1320 AAACACAGAT GTAGGCAGGA CTCGCTTTTG ACGTTGGACG ACCATTGCTG GAGCACTTGC 1380 TGTGCACCAG GCTCTGTTCT AGGACCTAGA GATACAGTGA CTAAGGAGAT TAAAGCTCGG 1440 CACCACCCTG CCCTCCAGAG CTTGCAGTCG GCTGCGCAAG ACAGACTGCA 1490
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