| Tag | Content |
|---|
EnhancerAtlas ID | HS105-53356 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:38568540-38569640 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr22:38569560-38569571 | TCCTTATCTCT | + | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27733 | chr22:38568471-38569298 | Fetal_Intestine | | SE_38157 | chr22:38567450-38578612 | HUVEC | | SE_41851 | chr22:38568570-38569776 | LNCaP | | SE_43287 | chr22:38567875-38569862 | Lung | | SE_53822 | chr22:38568366-38569195 | Spleen | | SE_64973 | chr22:38568015-38569139 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 38569323 | 38569554 | | chr22 | 38568686 | 38569301 | | chr22 | 38568765 | 38569142 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I038171 | chr22 | 38567581 | 38570134 |
|
Enhancer Sequence | CCTATTTTCC AGATGCTATG TAAAGCGATT ATAGTTTTCA AAGGAAGTAG CAGTATAGGC 60
TGAGCCTCTG GGGGCTGCAG CCGGGAAGAT GGGGACCTGT GGGACTCAGG CCTGGCCTGG 120
AAGAGCGCAG AGAGGCTACC CCGAGGACGG GCCCACAGGG ACGCGGAGGG GTGCGCCCAG 180
GAAGGGCAGA GAGTCAAGAG CATCCAGCAC CCATGAGCCT CAGATTGAGG GAGAAAGTCA 240
CCAGGGGTGC AGTGAAATCA AAGAAAGATT CCACACACCC CTTCGTCAAT GGCCCAGCCT 300
GTGTACCCCC CACCAGAGCC TGGGGCTAGG GGATGCCCCC CACACACCCA CGACAGCATG 360
GCCACAGAAA CGACAGGCTT GGCTGGCATC CAGCCTTCAG GGTAGGCAGG AGGACGAGAT 420
GACGCAATGG AGGGAAGGTG TCTGGGACAC AGGCCGACTG TGGGCACACA AACAGTGGCC 480
ATTGTTATCA CTAGGTGGAA GAAAGGAAAT GACAGCCACG GGGCCACATC CTGGAACACT 540
CACGGCATTG CCAACCAGGA AGGCGGGCCA GCAGGGAGAA AGTGCTCACA CGTGCTTCCT 600
TCTGTCCCTG CCACCTTGGA CCCTGGAGCC TAGGCTCTTC CCAGCACAGC TGCAAGAGGG 660
GGATGGTGGA TGAGGGCCCC CCGCATCATG CCTCACTTCA TCTCTCCCCC TGGCTTCTCA 720
CAGCGTCCTA CCCTTGACCT TCCCGTGGGG TAGACAATCA CTTTTCCCCA CTGATGACCG 780
GCCCCTCCTC CTCCTTACCT GGGCTTCTCC CTGCACCCCC AGGATGCCCA GGTCACCTGA 840
CACAGACCGC ACCTCGGCTG TGTCAAGCAG CTCTCTCAAA CACCACAAGC AGAAAGACAA 900
AGACCCAAGA CCTTTGGTGG TGGGGGTTGA CAGTGACAAT TCTGCCTGTC CAAGCCAGGC 960
AATTTCCAGG TACCAATTTT GGTGCCCCTG CTGAGGGAAG CCAGATATTT CTGGCCGTTT 1020
TCCTTATCTC TGCTCACCCA TCCTCTGTCA AAACCAAGCT TGCCTGCTGG GTTCATTGAG 1080
GGAAGACTGA CAGAGAGTGT 1100
|
