| Tag | Content |
|---|
EnhancerAtlas ID | HS105-52358 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:19984130-19985300 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_02031 | chr22:19982266-19984583 | Aorta | | SE_29732 | chr22:19982478-19985264 | Fetal_Muscle |
|
| | 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 |
| GH22I019994 | chr22 | 19982424 | 19989050 |
|
Enhancer Sequence | TCAGCCCATT AGGTGCTCTC ATAGGCTGCT CCAGAGCCCC ACAGTCCTGC CCCTGCCAGT 60
CTACCACTCC TCGAAGCACG CGCCGCTGGC ATAATCAGAA CCTCAGTAGG AAATAGACAA 120
ACCAGATACC CTCCCCACCA GGCAGGCGAG TGAAAGCAGA GGCCAGGGAC CAATCTCCCC 180
AGGGGCCAGG GCGGTGCCCA CTGTCAGAGA GCCATAATCA GATTCAGCCT GGAAATTTGA 240
TTTCCCCAGC AGAGGCAATG AGCCAGGCTG GATGAGACGC CATCGGGGGT TGGGTAGAGG 300
GACAGAGATA GCTCCCCAGG CTGTCCACAT GCTCACTCAG TGGCACCCGC TGATCATGTG 360
AGGGACCACT CCCATGTCCA GGGAGAATAC TCAGAAAGGG CCTCTTCCCA CGCTGCTCCT 420
GCCCTGCACT AATGCAGTGC CCAAGGCCAA AGGTGGCCAA GACCAAAGCT ACACTGGCCA 480
GCCCCAGGGG GCATGCTGGA TGGGAGGTCC AGGGGGACTA GGGGCTGTGT GGGGCTGATA 540
CGGAAGCTGG GGTCCGGTCA AGGCAGGGTC ACTGCTGGGG GCCAGGGAGC TGGGAAGCCT 600
AAGGTTAGGG CAAGGGCTGG CTCTAGTGGC CGAACGAGCC CAGTGACTGC AGGCAGGACG 660
TGACAGGTGA GCAGGCAGGG CAGGCGAGTG TCCCAGCAAC TGTCCCTCCT CTGTGGGAGG 720
CATGAGCCAC AGGGAGCCAC TGCTGGAGGT CCCTAAAGGG TCTGGGCTTA AGATTCTCAA 780
TCCAGCAGGT CACAGACACC TGCTCCCTGT GCCAACAGCA GCATCCTTTA AGTCTCCTTG 840
GTCTCCTGAG ACCTGCCTCT CCATGAGGAG ACATGAGATG GGGTGGAAAG GAGTCCTCCA 900
GGTCCCGATT CAAAACAGCC CCCAATGCCC TTCCTGTGCC TGACCCAGAC TCTAGCTACA 960
GCTGCAGCAG TGGGTGGTCC TGCAGACTCC AAGCCGTGGA GTAGTGGCAG TGAGGGGCCA 1020
CATTCTCTGG GCTCCCTGCT GCATCCTGCC CAGGGCACCA CCAAGGGCTC AAAGGCTGGG 1080
GAGCTCCAGG GAGAGGGCTG CAGAGGCTGC CAGTGCAGTG TCTTCTCCCC TGCACACTCA 1140
GCCCACCCAC TCCGCCCCCA ATGATGAGCA 1170
|
