Tag | Content |
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EnhancerAtlas ID | HS109-11767 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr2:9919550-9920800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr2:9920557-9920568 | TGTGCCAAGTA | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27173 | chr2:9919761-9920622 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 9919769 | 9920108 | chr2 | 9920201 | 9920597 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I009779 | chr2 | 9919287 | 9924010 |
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Enhancer Sequence | GAAGGAAGAT GGCCTGCTGG TGCCCCAGTT GTTGCCCGGG GAGACCTGCT GCGGACTTCT 60 GACCTCCAGA ACTATAAGAT AGTAAATGTG TCTTGCAAAA TAACAAATTA GTGGCTTAAA 120 ACCATGAAAT TTGTGGTAAC TGTGACAGCA GCAATAGGAA ATTGATACAA GTATGTATCC 180 GACTATTATT ATATGTGTTA AGTGTTGTTA GAGTAGCGAG AAACAGACAT CAGCTTTAGC 240 AAAAAAAAAA AACCCACAAA AAACCCAGAA AATGTATGAA AAGATACTGT CCCAGCTCAC 300 AGGATCAAAG TGCTGAGCGA CCACTCACAG GAAGCAGGAA ACACGGAGGC TCTGGGTGGA 360 TCAGTGAAGC AAGAAGTTCC TGCCCTTCTC TCAGGGCACC TGCCTGGTGG AGGCTCCATG 420 CAAGTCCCAG GCTCCATGAA CCTGGATCCC AAACTCACTG GAAAGGGAAA TCCAGACCCA 480 GCCTGCCTCT GCCTGTGATG GCTAGGAGAG GGAATTGCTG GGCCAGGAAG CCACCCCTAT 540 GGGTACCTGC TGGAGCCCAA AGCCCCGTTC TAGTAAGCTG CAGCTGGTGC AGAACTTAAA 600 CCTGTGGCCC CAAGGCCACG CCTCCCTCCA GGCCACAGTT GCTCTCAAAG GCAGGCTGGT 660 GAGGAGGCGT GTGTGGCCTG AGCAGGATGC TAGAGAGCCG GGGAAGCTGA GGCAGGAAGA 720 GGCATTGGCT CCAGCTGGCA GAGCCCTGGA GTCAGGAGGA GAAGCCGGAG AAGCTCATGA 780 AGCCCAGAGT CTGCGTGCTA GGGACTCGCG AGCCGCATTT GGCCACAGAC GGTTTTATTC 840 AGCTTGCGTG GTTTTTGTTT GCCTGTCTGT ATAATGGCTA CAATATGCTG AAGACATTAA 900 CAAGATGGAT TTGCAATTTG CTTTCAAATC GTGTTTCTTT GCAGCCTCCC ATCTCCAAAG 960 TGAGGAATGA GTTCATGGCT TCAGAGAAGG AGGTGAGGTT TCTACCCTGT GCCAAGTAAA 1020 AGGTCTTCAC TTTGAGACTG AAAGTTCACT TTTCAGAGCA CAGAGAACTT TTAGGGGTTG 1080 GCACATGTTT CTGCTGAGGG CTGGGTAGGG AATCTTTTAG GTCAGTGGGT TTGTGGTCAG 1140 CAGGCTTGTG GTCTCGATTG CAACTCCTCA ACACTGCTGT TGAAACACAA AAGTGAGCGA 1200 ACATGGCTGT GATTCAATAA AACTTTATCG GTCCTGGAAT TTGCACTTCA 1250
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