Tag | Content |
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EnhancerAtlas ID | HS182-11619 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:50152940-50154120 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr19:50153934-50153947 | CCTGTGACCTTTG | - | 6.44 | Nr2f6(var.2) | MA0728.1 | chr19:50153185-50153200 | TGCCCTCTTGACCCC | - | 6.36 | ZNF263 | MA0528.1 | chr19:50153187-50153208 | CCCTCTTGACCCCTCTCCTTC | - | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53947 | chr19:50152939-50154526 | Spleen |
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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 |
GH19I049649 | chr19 | 50152940 | 50154526 |
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Enhancer Sequence | GGGCTTTCTC CATGTTGGTC AGGCTGGTCT CGAACTCCCA ACCTCAGGTG ATCCATCCAC 60 CTCGGCCTCC CAAAGTTCTG GGATTACAGG CATGAGCCAC CCCACCCGGC CATAAAGGGT 120 GTTGGATGAA TGAACATACC CCCATTTTAT AGATGAGGAA ACTGAAGTAA GACACATTGA 180 TCCACTTGCC TGTGGTCATG TGGCTGGTGA GGGCCAGCCC CTGGATCAAG GGGTGGCTCT 240 GGTGCTGCCC TCTTGACCCC TCTCCTTCCC TGGCACTGTC CTCACACCAC TCTGCTGGCA 300 TCCTTGCCTG TGGTGTGGCC TCTGTCAGCC ATCTCCATCG TGTGACTGTG GCATCATGAC 360 TGTAGTACTT AGCACAGTGC AGCGGGCTCT TTGGGGGCGA ATGAGGTGAC ATACGAAGCA 420 CCATGCCTGG TTTGGAGGAA GAGGCAAACC TTTGTCATTG CCACTGTCAC TGGTCAGTGG 480 TGTCTTTGAG TCCTGAGCAG ATGTAATTCC TTGGGTGGGG ACTCAGCACA GAGTGAAGAG 540 CTTGGGGTGA AGACCAGCCT TCCTGGGCTC CCCAGCTCTG CCATTTCCTG GCTCTGCACT 600 GGAATCTCAC CCTCTACCAA ACGGGAGAAA CTCCCACGAG AGGCAGCTGG CGCAGCAGGC 660 CAGAGCTTGT TTTTGTCTTG GAGGGGGACT TAGGTTTGAA TCCCAGCTCT CCCCCTGCAG 720 CCTGTTTTCC TGTTTCTTCT CCCCCCAGGA TGGAGTGTGG TGTTGTGGTC ATAGCTCACT 780 GCAGCCTCCA CCTCCTCCTG GGATGGGTCG CCGGCACTGG TCAAGATAGT TCCTAGTTTC 840 AAGGCCAGGG TACATTGCCC AGGGTCAGGC CAGTGCTGTC TCAGGATATG GGAGTGCAGG 900 TTCGGGGCCG CACTGACTGA GTTTACACCC TGACTGCTGC CTTCTCTCTG TGTGCCCTTG 960 GGGAGGATAC TGCAGCCCTC TGCCTCAGTT TCCTCCTGTG ACCTTTGGGT TAAGAACCAT 1020 GGTGTGCAGT TGTTGGGAGC ATCCTACGGC TGGCTCCTGT GAAGCACTTG GGGCTTCCTG 1080 GGCAGGACCT GGTGGCCCAG GGAGTGTCCA CGGCTGGGCC AGCAAGCAGG CACCAGGAGG 1140 GAGGCAAAGG CCCTGACCGC CTCTCTCTCC CTGTTCCTTT 1180
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