Tag | Content |
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EnhancerAtlas ID | HS092-24447 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:102062630-102064010 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:102062779-102062789 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:102062779-102062789 | GGCACGTGCC | - | 6.02 | SCRT1 | MA0743.1 | chr2:102062980-102062995 | AAGCACCTGTTGCTG | - | 6.35 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_39690 | chr2:102062883-102066026 | Jurkat | SE_66502 | chr2:102062883-102066026 | 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: 2 | ID | Chromosome | Start | End |
GH02I101444 | chr2 | 102060897 | 102062669 | GH02I101446 | chr2 | 102062862 | 102063991 |
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Enhancer Sequence | GTTTTTGTTT TTTGTTATTC TTTTTGAGAT GGTGTCTCAC TCTGTCACCC AGGCTGGAGT 60 GCAGTGGCGT GATCTCAGCT CATTGCAGCC TCCACCTCCC AGGTTCAAGC GATTCTGCTG 120 CCTCAGCCTC CCAAGTAGCT GGGACTACAG GCACGTGCCA CCACACCTGG CTAATTTTTG 180 TATTTGTGGT AGAGATGGGG CTTCAGTATG TTGGCCAGGC TGGTCTCGAT CTCCTGACCT 240 CGTGATCCAC TCGCCTTGGT CTCCCAAAGT GCTGGGATTA CAGGCCTGAG CCACCGCTCC 300 CAGCCAAGTT GATCAATTAT TAAGTATATG CTGAGCATAG AGTACATGAA AAGCACCTGT 360 TGCTGGCCTT ATCTCATGAC CAGCCGATGT CACTCTTGCC TTTATCTTTG TCCTCTAGCA 420 GTCCTCCTCT TCCTCACCGA TGATAAAGCC TATCTTCCTT CCCCCACAAA GGACACTCCT 480 AGCCCCTCTC TCTGTGACAT CGGAAACAAA CAGAGTCCCC GGGACGCTAA TGGTCTCTCC 540 CCTCTGAGTG CCGAGTGCCT GCCTAGTTAC TTGTTTTCCT GGAGCATGCA GGGCTCTCCA 600 AATTGTCTGT TAGTTAACTG ACTGCTAGGT GCCAGGGGGT GGGGGTGGGG GGGCACACAA 660 TGGAATGCAG GATCTACACC CAGCCTTTCA GGAGCCTACA GATCAGCAAG TGAGAGAACA 720 AATTCGCACC AGGGACATTC TAACAGTCAC TAAAATAAAT CTCTCATTAT AGCTATTCCT 780 TTTCCTAGCT TCTCTATTTT TGCCAATGTA ACTTTTCCAT CCCCGTGACT AAGAGATGAA 840 TAAGAGATGT AAGAGGAAGA GCTGGTTTGG CGCAGAGCAC AGTGACTTTA TTTGAGGTTG 900 AGTTTGAGGT TTAGGTGGGA CAGGCTTGAC TGAATCATCT CTGCTCCCTT CTACTACACT 960 GACTCAACCA ACTGCCAGAT CCTGAAGACC CTGCCTCTAA GAGGTCTCTC AGACCTGCCT 1020 CCTGTCTGAT TCCAGTGCAA ATCTGAACAA CGGCAGCAGC CCTGGGGCCA TCTCCAGGCT 1080 CATCACCCTC TCCTTTCCCA ACTATTCTTA AACCGCAAGG CTGAATTTTC AGTTCTCCAA 1140 TAGCTATTTC AGTGCCCACT CTGGGAATAT GTCCTTGTTC CTGCAGCTGT AACAAAATAC 1200 CTTAGACTGG GTACTTTATA AACAAAAGAA GTTTATTTCT CACAGTTCTG GAGAATGAGA 1260 AGTCCAAGAT CATGGTGCGG GCAGATTTGG TGTCTGGTAA AAGTTTGCTC TTTGCTGCTT 1320 CTTCTTCTTT TTTAACATAC TAATTGTATA CATTTATGGG GTACATGTGA TATTGTGATA 1380
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