| Tag | Content |
|---|
EnhancerAtlas ID | HS145-27143 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr9:139119640-139120970 |
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 | | IRF1 | MA0050.2 | chr9:139120933-139120954 | AAAATAAAAAAGAAAGAAACC | - | 6.14 |
|
| | 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 | TAAAACCCTG TCTCTAAAAA AAAAATACAA AAAATTAGCT GGGCGTTGGT GGCGCACACC 60
TGCGGTCCCA GCTACTGGAG AGGCTGAGGT GGGAGGACCG CTTGAGCCCG GAAGGCACAG 120
GCTGCAGTGA GCCGGCGACA GGGGGAGGCT CCACCTTAAG AAAAAAAAAA AGTCCCTATT 180
TGTTCGTTTA AAGTTTGTTT GAATCAAGAT CCCAGCGAGG CTTGTTGGTT ACTGCTGGTG 240
GGTCCTGGCA CTTTCCTTCT CTGGGTTTGA CTGACAACAT CCCGGACTCC TGGCATTTCT 300
GTAACAGGGC ACTCAGATCT AGATTCTTGT CTGATTTGTT TGGTGACATT ACTTTGTAGG 360
TAGTGGAACA TGCTTCCACC CAGAGGCAAG CGACGCCTCT CTCCTTAGTG ATCACGACCT 420
AAATGCATTA ATGCACCAGG GCTGCAGTGA AATGGTGACG TGTCATCTCT CACCGTTTGC 480
TCATGATGAG CTGGGACAAT TCTGTAAAGA GAGACCTGCC CTCACTGCAA CCCAGCGGAA 540
TGACTCACAT GAGGAAGGGG AGTGCCTGGC TCGTGCTTCA GTCACCAGTA TCAAAGTCAT 600
GGTTTCCGAA GCTGACCAGT GAGGTTTTCT TTTTAAAAGA TTTGTGTTCT TCCTCTGGGA 660
TGTAAAAATT GCACTGCCAA CAATTCACAA ATATTTCCTG GCTCCTCACT CTGTAGGGGT 720
CCTTCCAGGC CCTGAGACTT TGAGGGGACA GCCTAAAGGG GCACCACTGG GTCAAGGGAT 780
GGGTGCTGGC TATCCTGGAG CCTGGAGGCC TCAGCAGAGT CGGCAGTGTG GCAGGGCACG 840
CCGCACCGTG GGAGAGGCAG GTGCAGAGGC GAGACCCAGG CACCCAGCAA ATGGACCTGC 900
CTGGAGGAAT GGAGCCAGCC ACGTGGGGTG CTGCCCTGGC ACAGCCTTGT GACCGGAAGC 960
CCAGTGATTT CTGAACGGGA GGGAACGTTA TGTCTGCCTG TCACTGAGAT ACTGATGAGG 1020
CTCTTTTTTG CCTTGTATTC CGATTCTGCC CACTTGTCTA AATCAATGAT TCCACTATAA 1080
ATCATGTAAA AAGAGTAAGA GTCTTTTCTG AGAGCGAGCT ATGATCTCAA ACTCCAGAGG 1140
TTCTGTTAAA AGCATGCCTG GAAGAGACGG AACATATCAC CAGACTCTGT ACAAATATGA 1200
AGGCTTGTGT GTGTTAGCGG TTCAGATTGC TATTTTTCTA CATAATATAC CACAGCTCTG 1260
TTTCAGATAC TGGCCTTTTC TCCCTGTAAT TTAAAAATAA AAAAGAAAGA AACCTCTTTC 1320
AGAAACAATG 1330
|
