| Tag | Content |
|---|
EnhancerAtlas ID | HS161-08929 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr2:70608330-70609540 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr2:70608930-70608941 | TCCTTATCTGT | + | 6.14 | | IRF1 | MA0050.2 | chr2:70608875-70608896 | AATCTCTTTCTCTTTTCCTTT | + | 6.37 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_36401 | chr2:70607326-70610314 | HMEC | | SE_56436 | chr2:70607793-70609878 | u87 | | SE_64949 | chr2:70607746-70610100 | NHEK |
|
| | 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 |
| GH02I070380 | chr2 | 70607669 | 70610677 |
|
Enhancer Sequence | GTATAATGAA TTCTGGCTTG ATGCCTCATT CTTGAATTCT CCAGAGGTGA TGAGGATCTC 60
CCCTTCTGAG CTGCACCCTT TACAGTAAGT CTTAGTGGCC TTCAGGAGAG GGCTGCTGAG 120
CAGGCTCATG AAACCTACTG GAAGTCCCTG GTCAACTGTC CTGGAGAAGG CAGGGGCCAC 180
TTCCTGCCCT GCTAGGGAGA CTGATTTCTG GGGTGAGGAA GAATGAATCA CGACCCTCTT 240
GGACCCAATC TACCTGCCTA TGAGAGGTTG TAGTGAGTCA CCCTTACTTG CTAATGACAA 300
TGTTTAAATG ACTCTGAATG ACCTCAGAGG TTTGCCTCTA CTCTCCTGAA AGTTCTAATT 360
TATAGAATGA TGCCCTCTGG TTTCATAACT GGACAAAATG CATATCAACA GTTGAGAAAG 420
AGTGAGAAAG AGAGAGTGAG AAAGTTGGGG GAGAGAATAT ACTAAGCCCT CATGAAGTTT 480
CTATAATAAC CTATGACATA GAAAACTCCC ACCAACTCTT TAGATGTGAC TCCATTTTAT 540
AAAGAAATCT CTTTCTCTTT TCCTTTTTTC TTTTGCCATT CTCTTCTCTG CTGCAGGAAG 600
TCCTTATCTG TCCCTTGAAC GCCCAGTTTC AGTTTTTCCC TCTTGGTGAG GCTCCTCTGG 660
GCAATCCCGT CCACTCATCA CTGTCTTTTC TGCATTTCTG GTGTGTGTGG TCAGAGTTTC 720
TACCCAACAC TTGCTCACAC GCAGTCTGGA TTGCTTTCTG ATAGTCCCCG GCATTAATCT 780
CCTCTTCCCT GTGCTGTCAT CTCCACAAGG GCAGGGCAGG GCTGTGCTGC CGACCTCATC 840
TGCATGCCCT GGGGGATCGA GCTGACACTG GGTGCAGCAG GAAGTGTGGC CCTGGTAGAA 900
TGTTCTCACC CATTCCAGTA TAGGATTGGG ACTTCCTGTC CTCATCCAGG CTGTGGCGGT 960
TACATTTAAA CCTTTCCCAC ACCTGGGTCT CTACCTCAGT TGTTGTCCTA GCAGGTTGGG 1020
TTGGTTCATC CTGCCCTGGG CATTCCTAAG GCTATTATAA GTGTGTCAGG TCTGGGTCTT 1080
TATCTTGATT AGAATAATAA CTTCCTGAAT TTGTCCAGTG GGCAGCCTTT CCTTAATGAA 1140
TGAAAAAAGA ACTGGAATGT TACTGCAAAT GAGTATCTAC CCTGTTCTCT TTCCACAGAA 1200
CTCTTAGCAT 1210
|
