Tag | Content |
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EnhancerAtlas ID | HS092-22091 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr19:778660-779940 |
Target genes | Number: 32 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:778709-778724 | GAGGTCAAGAGTTCG | + | 6.24 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_35289 | chr19:778437-779863 | HeLa | SE_37813 | chr19:778619-779677 | HSMMtube | SE_42931 | chr19:778786-779860 | Lung | SE_54264 | chr19:778823-779615 | Spleen | SE_65841 | chr19:778619-779829 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 778993 | 779222 | chr19 | 778831 | 779582 | chr19 | 779666 | 779796 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I000778 | chr19 | 778481 | 779755 |
|
Enhancer Sequence | GCTGGGAGTG GTGGCTCACG CCTGTAATCC CAGCACTTTG GGATCACCTG AGGTCAAGAG 60 TTCGAGACCA TCCTGGCCAA CATGGCAAAA CCCTGTCTCT GCTAAAAACA CAAAAATTAG 120 CTGGGCGTGG TGGCTTGTGC CTGTAATCTC AGCTACTTGG GAGGCTGAGG CAGGAGAAGC 180 GCTTGAACCC AGGAGCCGGA GGTTGCAGTG AGTCGAGATT GTGCCACTGT GCTCCAGCCT 240 GGGCAACAGA GCGAGAGTTC GAATCAAAAC AAACAAAAAA AGCCACAGGC GGCCACACAT 300 AGACCGTCAC TGACCTCCTG GAGCTTCTCT TCTCAGGGAA AGGAACTTCC AGACTCAGAA 360 AACTGGGGCA GGAAACATCC AGGCCAGTTT TTCCAGCCCA CCGGATCTCA GGCAGCTTCC 420 AGGAGGATTG CCTGAACTCG CTGAAATTGC CCAATTCCCT CCTGGGCACA TGGTTTTCAG 480 ATGATGAACA CACACCCTGC ACCGGGGCTG AGGCCTCACC CTGGCGTTTG AATCCTGGGC 540 CCCGGGTTTA GTCCACAGGA GGAGAAGCCA CACTGGCTGC TGGGAGGGAA TGGGAAGCGG 600 GCAGCCGCCG TGGAAAACAT GGATCAGTGC TTCAGAAAGC CAGACAGCGG CGCCGTCTAA 660 CCCCACCGTG CGGCTCCGAG GAATCCACCC CAGATAACCG AACACAGCGG CTCTCAATAA 720 ACATGTTCAC AGCAGCATGA GCCACGGGAG CCAGGGGTGG ACGGAAACAG TGGCACGAGC 780 CACAGGAGCC AGGCGTGGAA GGAAACAGTG GCACGAGTTA CGAGAGCCAA GCGTGGAAGG 840 AAACAGCAGC ATGATTCACG GGAGCCAGGC ATGGACGGAG TCCACAGGAG CCAGGCGTGG 900 AAGGAAACAG TGGCACGATT CACGGGAGCC AGGCGTGGAT GGAAACGGAG AGGAGCAGAG 960 AGCAAGGCTC TGACGCCAGC CACAGCGCAG ATGCACCCTG AGGATGTAGG GCTCAGACGG 1020 ATGCCCGACA CGAAAGGCCA CACAGCGTGT GATCCCATTT CCATGAAATG TCCAGGGCCA 1080 GGCGTGGTGG CTCACGCCTG TGATCCCAGC ACTTTGGGAG GCCGAGCCGG CGGATCACGA 1140 GGTCAGGAGA TCGAGACCAT CCTGGCTAAC ATGGCAAAAC CCCGTCCCTA CTAAAAATAC 1200 AAAAATTAGC CGGGTGTGGT GGCGGGCGCC TGTAGTCGCA GCTACTCAGG AGGCTGAGGC 1260 AGGAGAATGG TGTGAACCCA 1280
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