Tag | Content |
---|
EnhancerAtlas ID | HS118-18888 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:142244270-142245650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr8:142245470-142245480 | CACTTCCGGT | - | 6.02 | ELK4 | MA0076.2 | chr8:142245469-142245480 | GCACTTCCGGT | + | 6.02 | ERG | MA0474.2 | chr8:142245470-142245480 | CACTTCCGGT | - | 6.02 | ETS1 | MA0098.3 | chr8:142245470-142245480 | CACTTCCGGT | - | 6.02 | FEV | MA0156.2 | chr8:142245470-142245480 | CACTTCCGGT | - | 6.02 | FLI1 | MA0475.2 | chr8:142245470-142245480 | CACTTCCGGT | - | 6.02 |
|
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_24873 | chr8:142243734-142245171 | Colon_Crypt_3 | SE_41505 | chr8:142243777-142245539 | Left_Ventricle | SE_42811 | chr8:142243762-142245872 | Lung | SE_65316 | chr8:142243357-142246494 | Pancreatic_islets | SE_68924 | chr8:142244392-142245633 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I141233 | chr8 | 142243828 | 142246657 |
|
Enhancer Sequence | CTCGTCCCTC GGAAACCTCA GCCCTAGCCT GCTGGTGCTG GTGGAAGGCA GCCTGGTTTG 60 AAGGAAAAGT GCTGGCCTCC AATTCACATT CTTCATTCAC CGTCAGGACC TCAAGGAGGT 120 CACCTTTCCC TTTGGAGCCC TGGTTTCTAG AGACAGAGGC CACCTCCTCG TGGGCCTAGC 180 TTGGGCTCTT CCCAGGACTG AAGGGTGCGG GGTGGGCTTC CTGGCCAGTG TGGAAGAAGG 240 GCGTCCGTTG TTTGTTCCCT GCTCATGGCT GGCAATTTGA ACCCTATTTG CTACCCCATT 300 TTGACATTTC CCTTTCCTGT TACTACATTT AGCATCTTTC TACCCAAACA GGGTCGCAGG 360 TGGCCTGGCT TCCCCAACAG GACTCCGTGT GCACCAGCAA AGGGTCCAGA GGTGGGCAGG 420 GAGTGTTACT TGCCAGCTTG AACCTACCCC AGGTCCTGAT GCAGTCTGCC TGCCGTGGGA 480 TATTCTCCTG CGCGCTGCCA GGAGAGGGCC CTTAGACCCT GTCAGGGCTG TGGCGGTGGC 540 CTGAGGTGAC CTCCCTGATA ACTACACTGA TGACAACAGG CTTTGGAGAG GTCTCGACTG 600 GCACAGGAAA GCTGGACACA GCTCACCTCC ACGTTCCGCT CTGGCCCCTC CCCCCAGCAC 660 AGCCAGGCTC CAGCAGGACT CGACCTCCTG GGATTGCGTC ACTGTGAGCT TTTGCTCCCC 720 AGCCTGGAAC GGCTGTCCCC CTTGGTGACC ATGATACTGG CTGTTTAAAT GTGTGTCCCC 780 GCGCTGGTCT GCCTTCCCCG AGGACAGGAA TGCGCCCGCT ACCTAGCAGG TGCTCGGAAG 840 GCACTCTGCA AACCGAAACT GACTCTCCAG CACTGGGTTT GTTGCTTCAT CTCCGAGTGA 900 AGGTGCAGGT GACCACGCTC AGCTCTCCAC CCACAGGAGC CATGGCTTGG CTTGTTAAGG 960 CTTGTCCAAG GTTGTCACAC TCCGAAGCCC CCGACCCACA GCAGCAGCAG TACTGAAAAC 1020 CAGGTGATAT GAAACCAGCA GGGAACGGCA CTGACTGCTC AAATGCCACC CCCCTTCTTC 1080 ATGCAGGTGA AGCAATTTAA ATGCATGAGA CACACAGGCG GCCCCATTTA TAAATCATGA 1140 GCGTCAGGTT ACCGTGAGGG GCATTTCAAC CCAGGGCACA GCGGGTGTGT CTGTAGAGTG 1200 CACTTCCGGT GTGGCTGCAG TTAAATCATG CTCGGCTGTC ATGGTCTAGC AAGGGTCACG 1260 GTGACGAGGA GGACGTATTC GTATTCTGGA GAATATGAAG GACCAAAGAC CCTCTGTGAA 1320 CCCCACAACG ATTCTAACGT AAAGCTTATA AGAACTGGTG AATTATCCGA AGAAAGCACA 1380
|