Tag | Content |
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EnhancerAtlas ID | HS187-21151 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:36996850-36997870 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:36997206-36997225 | AGACCACCAGGGGGTGGCA | + | 6.51 | FOS | MA0476.1 | chr6:36997332-36997343 | GATGAGTCACA | - | 6.14 | Foxd3 | MA0041.1 | chr6:36997414-36997426 | GTTTGTTTGTTT | + | 6.32 | JUND | MA0491.1 | chr6:36997332-36997343 | GATGAGTCACA | - | 6.14 | ZNF263 | MA0528.1 | chr6:36997051-36997072 | GGAGGAGAGTGAGGAGAAGCA | + | 6.05 | ZNF263 | MA0528.1 | chr6:36997129-36997150 | GGAGGAAGGGTGACGGGAGGA | + | 6.44 | ZNF263 | MA0528.1 | chr6:36997048-36997069 | AGGGGAGGAGAGTGAGGAGAA | + | 6.67 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10059 | chr6:36996866-36998910 | CD14 | SE_40024 | chr6:36997037-36998421 | K562 | SE_61011 | chr6:36971402-37041202 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 36997200 | 36997653 | chr6 | 36997320 | 36997527 |
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| Number: 2 | ID | Chromosome | Start | End |
GH06I037029 | chr6 | 36996777 | 36997780 | GH06I037030 | chr6 | 36997848 | 36998834 |
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Enhancer Sequence | TGCAAGGTGT TTTATGTGGA TTATGTCATT TTACCATCCA GAGTTATCCC CATTTCCAGA 60 TGAAGACACC GACTCAGAGA GGTTTAGTAA TTGGCTCAAT TGGTCATGTA GCTCGTAGAT 120 GCCAGAGCCA GGTTTTAACC CGGTGAACTA AGGTCAAAGC TCTTTCTATC ATGGAGCAGA 180 ACAATAAGAC AAGCAGAGAG GGGAGGAGAG TGAGGAGAAG CAAAAGAGAG GGAAAGAGAG 240 TGAAGAAGCT GGGAAGACAA GAGAGAAAGG TGAATGGTGG GAGGAAGGGT GACGGGAGGA 300 GCATCCCTGT CCCCTCATCC CCACCTCGCT GGTGGGTGAG GATGCTTTTT CATAAGAGAC 360 CACCAGGGGG TGGCAGTGGT CAGCAGGCCA CATGCAGTGG CCCCAGCAGT GGCCAGAACA 420 CCCTCAGCTG CTCTCAGCAG GTCCAGCCAT TGCTGGGCTC TGCCCTGAAA GGAGGAAGCA 480 TGGATGAGTC ACAGGTTTTT GTCCCATCAC AGGCCCAGCA GCTTTGCCTG CCTCCAACCT 540 GAGGCCACTT CCCTCCTGTA GGGTGTTTGT TTGTTTATTT GAGACAGGGT TTTGCTCTGT 600 CATCCAGGCT GGAGTGCAGT GGTGTGATCA GAGCCCACTG GAACCTTGAC CTTCTGGGTT 660 TAAGCTATCC TCCTTCCTCA GCCTCCTGAG TATCTAGAAG CACAGGTGCA CGCCACCACA 720 TCCAGCTAAT TTTTAAAATT TTTGTAGAGA TGGGGTCTCA CTATATTGCC CAGACTGACC 780 TCAAACTCCT GAGCTCAAGC AATCCTCCTG CCTTGGCCTC CTAAAGTGTT GGCATTATAG 840 GCATGAGCCA CCATGCCCGG ACAGCATCAG CATTTTATTT ATTTTTTATT TTTATTTTTA 900 TTTTTGAGAT GGAGTCTGTC ACTCTGTCAC CCAGGCTGGA GTGCAGTGAC GCCATCTTGG 960 CTCACTGCAA CCTCTGCCTC CCAGGTTCAA GTGATTCTCC TACCTCAACC TTCCAAGTAG 1020
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