Tag | Content |
---|
EnhancerAtlas ID | HS091-15976 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:1882200-1883980 |
Target genes | Number: 38 | Name | Ensembl ID |
|
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr16:1883704-1883714 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr16:1883704-1883714 | GGCACGTGCC | - | 6.02 | ZNF263 | MA0528.1 | chr16:1882762-1882783 | CTCTCCTCTCCTTCCTTCCCT | - | 6.23 | ZNF263 | MA0528.1 | chr16:1882759-1882780 | CTTCTCTCCTCTCCTTCCTTC | - | 6.61 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_12522 | chr16:1883218-1883464 | CD34_adult |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr16 | 1883240 | 1883546 | chr16 | 1882837 | 1883199 | chr16 | 1882695 | 1882750 | chr16 | 1882570 | 1882641 | chr16 | 1882551 | 1883874 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I001832 | chr16 | 1882613 | 1884275 |
|
Enhancer Sequence | AAGTCTTGCT CTGTTGCCCA CGCTGCAGTG GCATGATCTC GGCTCACTGC AAGCTCCGCC 60 TCCCGGGTTC ACGCCATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGCGCCC 120 TCCACCACAC CCGGCTAATT TTTTTGTATT TTTAGTAGAG ACAGGGCTTC ACCGTGTTAG 180 CCAGGATGGT CTACATCTCC GGACCTCGTG ATCCACCCAC CTCAGCCTCC CAAAGTGCTG 240 GGATTACAGG CGTGAGCCAC CGCGCCTGGC CTATTTTCCT CTTTTTCTTA AAAATATAAG 300 TGTCAGCTGG GCACGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCGAGGTGGG 360 TGGATCACTT GAGCCCAGGA ATTCAAGACC AGCCTGGGCA AAATGCCAAG ATCACTGTCT 420 CTACAAAATG TTTTAAAATT AACCGAGTAA GGTGGCTTCT CCTGAGCTCC TGGACACGGG 480 GCTCAGTGGA GGGGGCACCA TACCCACTCT TGCTGAACCA ACAGTGGGAG CCAAGCCAGC 540 ACCAACCACG ACACCCTCAC TTCTCTCCTC TCCTTCCTTC CCTGTCCACC CTCCCCATTC 600 ACCTGGCTTC ACAAACCCCC CAGTTCTCCC CAAGGGAGGA TGGAAGGCCT GTTCTGCACA 660 ACTAGGTCAA GTCGTTCATT ACCTTATCAC CACAATTTGG ACACTTAGGG GTGAACCTGC 720 ATCCCTCCTC TGTGGCTGCA CATGGTAAAA GCCAGATAAA ACATGACTGA CGATGGTTTA 780 TCTCCCAACA CCAGCCTTAG GAAACAGTTT CATATACTCA CTTTTTCCTT TTTTTTCAAT 840 CCTGTGGTGG AGGGCATGTA GCCTTCTAAA GTACCAGGTC AAACCTCCCA GGCCGTGGGT 900 CAACACTGAC CTTAGCGGTG GGTCTTCACA GCTGGAGTCT GCGCCCTGAA GCAAGTGACT 960 CTCAATGGTG TGCAGTTGAG CCGTTTACTT TGTGGCTGCT GCAAAGCAAA CAGATAAAGT 1020 GGCAGCTGTC GTCCTCATGT CCTGAGTAGG TCCCCCTCAG AGTTCTGAGA CCCAGGCATG 1080 CTCATGAACC TTTTGAAGTT GGTCTCCTCC CAGTTGATTC AGACTCAGTC ATGTCAGCCC 1140 TGAGCCAGCA AGCCTCCACA AGCACTGGGC ACTCCAGTGT GTCACCAGAG AAGACCAGGG 1200 ACTAGAAGAG CCCCAGGTGC TCAAAGCAGT CGCACAGGAT TGCCCACGAC TTTGGCTATT 1260 CCCACCCAGC ACCAAGAGCC CCTTGCCCTC ATCCTGTCAG ATCTGTCAGA TGACGAGTCA 1320 CCACCCAGCT CTCAGAAAGT AGTCTTTAGA GGTACTTTTT TTTTTTTTTT TTTTTTTTTT 1380 AAGACAGAGT CTCGCTCTGT CGCCCAGGCT GGAGTGCAGT GGCTGGATCT CAGCTCACTA 1440 CAACCTCCTC ATCCCAGGTT CAAGAGATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC 1500 AACAGGCACG TGCCACCACA CCCAGCTAAT TTTTTGTATT TTTAGTAGAG ATGGGGTTTC 1560 ACTGTGTTAG CCAGGATGGT CTCGATCTCC TGACTGCCTT GGCATCCCAA AGTGCTGGGA 1620 TTACAGGCAT GAGCCACCGT GCCCAGCCCT TGAGGTCCTA CTCTTTTTCC AGGGAACCAA 1680 GACAAATAAT AAACTGGCTT AAGAAAATAA ATCATTCACT CAGGATTAAG AAACTCACTC 1740 AAAGCCGTTC AACTACATGG AAAAGAAAAT AAATCATTCA 1780
|