| Tag | Content |
|---|
EnhancerAtlas ID | HS105-83990 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:139119570-139120890 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr9:139120092-139120106 | TGGTGACGTGTCAT | - | 6.78 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_58526 | chr9:139098731-139137766 | Ly1 | | SE_60916 | chr9:139111911-139138466 | DHL6 | | SE_65679 | chr9:139119306-139125149 | Pancreatic_islets |
|
| | 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 |
| GH09I136227 | chr9 | 139119619 | 139120821 |
|
Enhancer Sequence | AGCACTTTGG GAGGCCGAGG TGGGCAGATC GTTTAAGCCC AGGAGTTTGA GACCAGCCTG 60
GGCAACATGG TAAAACCCTG TCTCTAAAAA AAAAATACAA AAAATTAGCT GGGCGTTGGT 120
GGCGCACACC TGCGGTCCCA GCTACTGGAG AGGCTGAGGT GGGAGGACCG CTTGAGCCCG 180
GAAGGCACAG GCTGCAGTGA GCCGGCGACA GGGGGAGGCT CCACCTTAAG AAAAAAAAAA 240
AGTCCCTATT TGTTCGTTTA AAGTTTGTTT GAATCAAGAT CCCAGCGAGG CTTGTTGGTT 300
ACTGCTGGTG GGTCCTGGCA CTTTCCTTCT CTGGGTTTGA CTGACAACAT CCCGGACTCC 360
TGGCATTTCT GTAACAGGGC ACTCAGATCT AGATTCTTGT CTGATTTGTT TGGTGACATT 420
ACTTTGTAGG TAGTGGAACA TGCTTCCACC CAGAGGCAAG CGACGCCTCT CTCCTTAGTG 480
ATCACGACCT AAATGCATTA ATGCACCAGG GCTGCAGTGA AATGGTGACG TGTCATCTCT 540
CACCGTTTGC TCATGATGAG CTGGGACAAT TCTGTAAAGA GAGACCTGCC CTCACTGCAA 600
CCCAGCGGAA TGACTCACAT GAGGAAGGGG AGTGCCTGGC TCGTGCTTCA GTCACCAGTA 660
TCAAAGTCAT GGTTTCCGAA GCTGACCAGT GAGGTTTTCT TTTTAAAAGA TTTGTGTTCT 720
TCCTCTGGGA TGTAAAAATT GCACTGCCAA CAATTCACAA ATATTTCCTG GCTCCTCACT 780
CTGTAGGGGT CCTTCCAGGC CCTGAGACTT TGAGGGGACA GCCTAAAGGG GCACCACTGG 840
GTCAAGGGAT GGGTGCTGGC TATCCTGGAG CCTGGAGGCC TCAGCAGAGT CGGCAGTGTG 900
GCAGGGCACG CCGCACCGTG GGAGAGGCAG GTGCAGAGGC GAGACCCAGG CACCCAGCAA 960
ATGGACCTGC CTGGAGGAAT GGAGCCAGCC ACGTGGGGTG CTGCCCTGGC ACAGCCTTGT 1020
GACCGGAAGC CCAGTGATTT CTGAACGGGA GGGAACGTTA TGTCTGCCTG TCACTGAGAT 1080
ACTGATGAGG CTCTTTTTTG CCTTGTATTC CGATTCTGCC CACTTGTCTA AATCAATGAT 1140
TCCACTATAA ATCATGTAAA AAGAGTAAGA GTCTTTTCTG AGAGCGAGCT ATGATCTCAA 1200
ACTCCAGAGG TTCTGTTAAA AGCATGCCTG GAAGAGACGG AACATATCAC CAGACTCTGT 1260
ACAAATATGA AGGCTTGTGT GTGTTAGCGG TTCAGATTGC TATTTTTCTA CATAATATAC 1320
|
