Tag | Content |
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EnhancerAtlas ID | HS176-05933 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr10:99400940-99402250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:99402138-99402159 | TCGAAGTTTCTTTTTCTTTTT | + | 6.09 | IRF1 | MA0050.2 | chr10:99401586-99401607 | AGCTACTTTTTCTTTCATTTC | + | 6.31 | STAT3 | MA0144.2 | chr10:99401506-99401517 | CTTCTGGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr10:99401506-99401520 | CTTCTGGGAAAGGG | + | 6.38 | ZNF263 | MA0528.1 | chr10:99401129-99401150 | GGGGGAGGAGTGAGCGGAAAA | + | 6.28 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28882 | chr10:99399491-99402317 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 99401200 | 99401600 | chr10 | 99401742 | 99402052 |
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Enhancer Sequence | GCGGGGGTGG GGACCGCCGC CGCGGGCTGA GGGCCGGCGG CGCTCCTGGG GAGTTGGGGG 60 CTTCGCACAG CCAGAGGGAA AAGGGAGAAA CTTCACAGTA CCAGCCCCTG GCAGGATTTA 120 GGGATGCCAC TGAGGACTGG AGCTGGGGAC GCTCTGCGGA ATGGAGAAAT AAATCAGAAC 180 CTACTTGGTG GGGGAGGAGT GAGCGGAAAA TGAAAAGAGG AAATTGACCA GATACGGGCC 240 GGGGGCTCAG CGGTGTGGTG GGGCAATCCG CCGCTGGACA GAGACTGCTT TCTAGTAGGG 300 TACTTAGCTT CACACTACTG GGACAGCTAT TCGGCCGCCG ACTTGCAGAT TTGGGGCTTT 360 AGGCCTGTTC TCTCTTTTTG GACCGACCGA ACCAGTGTGT CGCTGTTCAC GGAGGAGGAT 420 GGGTGACCTA TCAGGGGATC TGAGAATTCA GTTCCAGCCT TCTATGTTGT GGGGGATGTC 480 CCCTGCCACC GTCCCAGCTC TTATTAACAG ACGTTGAAGA AAGAATGGGC GGACTCACCA 540 GTTTCATCTG CCCTGGGTAT TGCTCACTTC TGGGAAAGGG TTCAAATACT TTTTGACGAC 600 TCCAAAGTTT AGATAGAACT TGGAGTTTTA GAAACATGGG GCCATCAGCT ACTTTTTCTT 660 TCATTTCTCT CCCAGGGCTA TCAACAGCCT GCTTTTCAAC TAAGGCAGAG CGTTTGCCGA 720 CCTTTATTTT GTCCCCTGCC TGTATATAAA GGGGGATGGT TATAGGATGG GGCATGGAGT 780 GACCAGGGTA TCTGAGAAGT GACCTTTATC CTTTTGAGAA CTGCAGAATT TAAGAAATAC 840 CAAGTCTTCC CTGTTTTCAG GGAAGTTTCA GGGAAATTTT CAGGTGTGCT GCAATGGGTC 900 ATTGGAAAGA TGTATTGTTA TTTAAATTAT GGGTGTCAAA GTTTCCTCAG ATTTTCCCTG 960 ACATCTCTCC TGTGTGAACT CTTTAGATGG CCAGGGTGCT GTTTTAATAG GAGTCCTGAG 1020 TGGCCAGGAC GGGCTGTTAC TTGTAGCTCT TGGTTCGGCT CATTGAATGA TCTAGTTATT 1080 CACTCAGAGT TTGAGTCGTC CCTGAATTAA TCAAGAATTA GAGAACAATT CTGCCATGAA 1140 CTCAGTTTCT CAGTTTACAT AAACTGAGTT GGGGAAAGCT TTGCGAGTAA TAAGTCTTTC 1200 GAAGTTTCTT TTTCTTTTTT TTTTTCTTTT TTTTTTGAGA CAGAGTCTTG CTCTGTCGCC 1260 AGGCTGGAGT GCAGTGGCGC GATCTCAGCT CACTGCAGCC TCCGCCTCCC 1310
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