Tag | Content |
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EnhancerAtlas ID | HS092-19877 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:87889310-87890630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr16:87889322-87889343 | GGAGGAGAGGGGTGGGGGAAG | + | 6.71 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_26742 | chr16:87869316-87891392 | Esophagus | SE_31703 | chr16:87879174-87891256 | Gastric | SE_37207 | chr16:87880767-87897470 | HSMMtube | SE_41970 | chr16:87888022-87890510 | LNCaP | SE_46353 | chr16:87883260-87891139 | Osteoblasts | SE_57166 | chr16:87888011-87890219 | VACO_400 | SE_65609 | chr16:87884681-87892290 | Pancreatic_islets |
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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 |
GH16I087841 | chr16 | 87874627 | 87897571 |
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Enhancer Sequence | GGGTCCAGTG TTGGAGGAGA GGGGTGGGGG AAGGGCCAGT AACAGGTGTG TTCAATATGG 60 AGAGCAGGTG GGACCTGTGG GCCCCGGCTG GGTGGGGACC CCGCAGGCCC CATGAACCCA 120 CCCCACACGG ACTAATGCCT GATTCTTTCA GGTAATAAAC ATGTACCAGG TACAGGAGCA 180 TCCGTGGATA GGGTTCAGGG TCAGCCACAA TGAAAATCCT CTCTGTTGGC CACAGAGGCT 240 GCTCCCTGGG CCGCCGGTCC TCACCTGCCC CCGAGCCAGG CACAGCAGTG AGTCCTGCAG 300 GGCTCAGCAC CTTGGCCTGT CTGTAAGTGG GAGTACCCAG TGAACATGAT CCTCCCGGGC 360 CCCTTCGAGC CCAAACACAG CCACTGTGAG TGCCCCAGGC AGGCGTCCAG CCCAGGCAGG 420 CATCCTGCAG TCCCTTCTGT CATTTTCAGA CCCAACAGAA ACAGAAGTGC TCCTGCCAGG 480 CCCCCGAGGA CTGCCTCCAG GAGTCATCTG TAATGACAGG CTGTGTTCCG CGCACGGTTT 540 CAGAGTCTGT CCAGAGGGCC AATGCTGGGG CTGGGGCAGA GATGGTCCAA GGCCTGTGAG 600 CTGTGCAGCT TTATAGGCAA ATGACGATTG TTTACCCAGA ACTGCCTGCT GGAGACAGCA 660 CAGAGGAAGT GGCCGGCAGC TTCATCAGTT CCAGGAAGCC CAGGCAGCCT GGTCCCCCAG 720 GGTGCACCGG GCACAGCAGT TCGCACGGGG CCGGAGAGCG GCAGCTGACC ACAGCAACTA 780 CAGCTGGCCC GACACCGGGC ACAGGTACCA GCCCAGCCCA GTCCCGCCCA GTGCAGCCTG 840 TGGCCCCTAG CGGAGCCAGC ACCTGGCAAA CCTGACACCC AGCCTTGGAG CTTGGGCCCC 900 CCTCTGCAGC TGGCTGGGGC TCCTGAGACA GCTTCTTTGT CGGAATCCAC TCGGTACGCA 960 CAGGGCCCCG AACTTGGTGG CTGCCCAGTG CACATGGGGC TTTAGTAGAA CCAGTACCTT 1020 CCTCCCTGGC CCCTTCAAGT CTAAATATCC CCTGCTCTGA GTACAAGCCT CCACCTTCTC 1080 CACCGACAGA CAGCCCCCAC CATCTCCCGT GTCATCCCCC GGGGGAACTT ATAAAAGCAG 1140 TGGTGGGGGA GGCGGATGGA AACCCAGAGC TTCTGATCAG GCAGGTCCGG GAGATGGAGA 1200 CAACACATCT GCACAGAACA AGGTCCCAGG GAGGCTGGTG CTGCCGGCCT GGGGAGCGCC 1260 CCCAGCACAG GCGCGTGCTT CCCTGATGGA CACGTCACCG CCCCGGGCTC CAGAAAATGA 1320
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