Tag | Content |
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EnhancerAtlas ID | HS073-09487 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr21:34785160-34786190 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr21:34785339-34785354 | GGTTAATTATTAGCT | - | 6.19 | HNF1B | MA0153.2 | chr21:34785340-34785353 | GTTAATTATTAGC | - | 6.12 | Mecom | MA0029.1 | chr21:34785170-34785184 | TTCTATCTTGTCTC | - | 6 | RARA(var.2) | MA0730.1 | chr21:34785649-34785666 | AGGTCACCCAGAGCTCA | + | 6.66 | TCF7L2 | MA0523.1 | chr21:34785307-34785321 | TGGCTTTGATGTCT | - | 6.05 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00219 | chr21:34785232-34786512 | Adipose_Nuclei | SE_10924 | chr21:34771599-34789021 | CD20 | SE_53174 | chr21:34783007-34786227 | Small_Intestine | SE_53413 | chr21:34785125-34786015 | Spleen | SE_58466 | chr21:34731200-34786233 | Ly1 |
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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 |
GH21I033410 | chr21 | 34782696 | 34787496 |
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Enhancer Sequence | AGGAGTTTAT TTCTATCTTG TCTCATTTAC AGTTTGGTCC GGAGAGCTGC CTTAGACTCT 60 CCAATAAATC TATTCAAACA GCTGCCTCTG TTATCTTGAC TTGCTCCAGG TTTGGAAGAA 120 GCCTGTGTAG GATCTGTGTT TCATTTCTGG CTTTGATGTC TGGGCGTCAG TTTCCCTGGG 180 GTTAATTATT AGCTTAATGT GAAGGCAGCA TTGTGGAAAT TTCTCTGCAT AGTTCGGATG 240 CTATTCAGAT CTGTCTGTGT GACTGTCATG CAGGCCTCTC TGTGTGACTG TGAGGGAGCA 300 TTGACCTGCC ACCACCCCCC TCTGGAAGCA TCCAGTCCCC AACTGGCTTT GGGCATTGCT 360 AGGTCATAGC AGCCACAGCA CACCTGGTGG GCCTGCCTCT TGCCACGCAG CTTTACCTGT 420 CTGCCTTCGG CCCAGGATGT CATGAGGCCT GCTGTGTGTC AGGAGAAGTG TTGTTAGCTG 480 GTTGGGTGAA GGTCACCCAG AGCTCATAGG TGTGGAGGGG AGGGGCATCC TATAACTAAA 540 CAAATGGCCG CAGACTTGGC AATTCATCTT TCAGAAGAAG AGCCAGTGGT CAGGCTGTCA 600 GCTGATCTCT TTGAGGTTGA GCGCATTTAC CGAAAATGTG TGGCTTGAAT TTCCTGCTTT 660 GAATTTTGGA ACAGCATGTT TTTCAAACCT TTCTTCCACC TTCTGGGCAT TTCTTATTAA 720 TCTTTTTGGT CAAAAGCCTT ATCTTGATTA TGTTTTCTTT CTAAGACAAA GGGCTCCCTG 780 TGAAGTACCT GCTTGGGAAA GGGAGGAGTT GTGGCAGTTT CTTCTAGGTC CCCGAAGGCT 840 CCCTGTGAAG TACCTGCTTG GGGAAGGGAG AGGTTGTGGT TGTTTCTTCC AGGTCACCCC 900 AAAGAGAGGG ATTCTGATAT TGGTGGTGTT TCCGGGGGAG TATATTCTTT CTCTGTTTAT 960 TGCCCCCTAA CCTTTTTTTT TTTTTTTTTT TTTTTGGAGA CAGAGTCTCT CTCTGTCGCC 1020 CAGACTGGAG 1030
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