| Tag | Content |
|---|
EnhancerAtlas ID | HS108-27961 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:46427420-46428250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr3:46427752-46427773 | CTCTACTTTCACTTTTCTCTG | + | 6.56 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_25650 | chr3:46421412-46429186 | DND41 | | SE_29537 | chr3:46427543-46428506 | Fetal_Intestine_Large | | SE_43552 | chr3:46423866-46429119 | MM1S | | SE_62170 | chr3:46419501-46460269 | Toledo | | SE_67367 | chr3:46423866-46429119 | MM1S |
|
| | 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 |
| GH03I046385 | chr3 | 46427407 | 46428701 |
|
Enhancer Sequence | TGGGGTTTCA CCATATTTTA TTTTATTTTT GAGACAGGGT CTCACTTTGT TGGCTCGCTG 60
CAACCTCTGC CTCCCAGGCT CAAGCAATCC TCCAACCTCA GCCCCCCAAG TAGCTGGGAG 120
GACAGACGTG CACCACCACA CCTGGCTAAT ATTTTGTATT TTTTTTTGTA GAGACAGGGT 180
CTTGCCATGT TCCCCAGGCT GGTCTTGAAC TCCTGGACTC AGGTGATCAG CCTGCCTCCA 240
CCTTCCAAAG TGCTAGGATT ACAGGAATGA GCCACCCCAC CCGACCACAC TCCCATTTCT 300
TGAGTGTGTG CATTTTGCTC TGCAATAAAT CTCTCTACTT TCACTTTTCT CTGACTCGTC 360
CTTGAATTCC TTCTTGTGAC AGCGTCAACA GCCTGGACAC CAGGTGCAGT CAACGTCTCA 420
CCAGTGTTTA GGGACCTCCC CTAATCCACT GGTATCAGCA TGATCAGACT TGCTTTTTCA 480
GAAAAAGCCT TCTGTCCATA GACCAAAGGG AAGTGACTCA GAGAAGGGGC AGGAGGAATC 540
ACAAGCTCCC TGCCTGACCA GGCCTGGACT ATGGCAGAGA CAGTGAGATG GTGAGAAAGC 600
AAGGGTAGAC AGCCAGCCAA ATCCAGAATA TAGAAAGTTC TACAGGAAAA GGTGGGGCCA 660
AGGTGGGACA GGGGGAAAGG AATTGTTGCA CATTAACAGT GCAATGCAGA GCACTGGTCT 720
TGTTTATGTC CAGGTTAGAA CAAACCAATG AGAAAGCACA TCTTTGAGAA AACTGGAGAA 780
ATTTGAACAC TGACTAGATA TAATATTATG TTAATTATGC TTTAATTTGG 830
|
