| Tag | Content |
|---|
EnhancerAtlas ID | HS105-52832 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:30182860-30184350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr22:30184275-30184286 | TCCTTATCTGT | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27345 | chr22:30182911-30184477 | Esophagus | | SE_31847 | chr22:30182746-30184651 | Gastric | | SE_34183 | chr22:30182849-30184241 | HCC1954 |
|
| | 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 |
| GH22I029786 | chr22 | 30182837 | 30184246 |
|
Enhancer Sequence | CCTCCAACTC CTGGGTGCAC CCTCCAACTC CCGGGCTCAA GTGATCCTCC AGCCTCAGCC 60
TCCTGCGTAG CTGGGACTAC AGGTGTGCAC CACCATACCC ACCTTATTTA TTATTTTCTG 120
GAGGGATCGG GTCTTGCTAT GTTGCACAGG CTGGAGCAGC TGCCAATGTT AATTAAACCT 180
TGGGATCTCC TCAGAGGATT TAACTGGCAC CAGGTGGAAA GATTTCATCT GGTCCAACAG 240
GATCACTGTA CAGATGGGAA AACTGAGGCC CTGAGAGATG AGGCAGTAGG CGTAGGAACA 300
CCATTCTGGA TGGCCCCTGA GCTGTTTTCA AAGCACCTCT GAAAGAGTGC TTTCAAGATC 360
TGAAATGAGA AAGTAGTAGA TCCTCAAGGG AGATGAAGTT TGACCTGGCA CTACATTCTG 420
AAAAATTTGA AAAACTGACT CCTTCTCAAA TACTTTAAAC CAGGATTTTC ACATGAGGCC 480
TGAACACCAG TCCAGGTGGG TGGGAGGTAT AGATGACTAA GAGAATGTGA GAGGGGCCGT 540
GTGAACAGGA ACAGGTAAGA CCAGTAAATC CTGGGAACTC CCAACTCACC TTGCCTTGCT 600
CCAGGGACAA GCACTGGACC TGAGGAGTTT AGGGAGGTCC CTGGCAAATG CCTCCAGGAG 660
GAAACAGAGT CTTCCTGCTG CCTGTCAGGA CGGCTGACCC TGGGCCTGAT CTCAGCTAAT 720
TCAGCAGCTC AGGGGGAGGA CACCACCCCC GTATCTGCTC TGCATCTCAA ATACACCAAG 780
AGGGCTGGCC AGGCAGAGGG ATTGCTATTG ATTTTCACTT GTGCGGGCTG ACCTAACAAA 840
ACCAATCCAT CAAGTGCCTG TCTGCCTCTG CTTCAGACTC TCATCCTAAG CACGTGCAAA 900
TAAATTGCAC CAGCATCCAG GGTGATTTGT CAAGGTCCAG CCAGGCATGG GCCCTGGCTT 960
CCACTGATAG GATGGGGCTC CAGGCTAGGC TGGGCTAGGG TCAGCCCAGT CAATGCCCCG 1020
CTGTTGACTC GCCATTGAGT GACAACACGC AGTGTGGCCT GGCATCTGCT GCCACGCTAG 1080
GAACTGGTTG GCCATGCCTG GGAAGGGGCT TTGAGGAAAC AGGCCCAAGT CCCACTCACT 1140
TTGACAGGGC TTGGCAGCGA CATTCTCACT TGTTTCTTAA GGTTTCTGTC CGAACTCTAG 1200
ATTTGGGGGG ATTTATTACA ATGTAGATAC AACCATGAGG TGCTGAGTTT GGGTACTGCC 1260
TCTGCCACTG GCTGAATGTC CTTGGGCCAG TTGTGAGATG GAGATGACAC CACCTACAGG 1320
GGTCTAGAAC CCTGTAAAGG CCAGGGTCCA ATCCCTGTTC TGCCACTTCC TAGCTGTGGC 1380
CGGGGCAGGT GCCTTCAGCC CTCGGTGCCT CATTTTCCTT ATCTGTACTA CCGGGCTGAA 1440
AATGGTACCT ACCTCTTACA GTGGAGCTGT CATAACTGAA TGAGAAAATG 1490
|
