Tag | Content |
---|
EnhancerAtlas ID | HS007-17745 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr9:136370390-136371630 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr9:136371610-136371630 | AGTGGGGGGGTGGGTGGGGC | - | 6.51 | ZBTB18 | MA0698.1 | chr9:136371149-136371162 | CTTCCAGATGTGG | + | 6.11 |
|
| 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 |
GH09I133505 | chr9 | 136370572 | 136372600 |
|
Enhancer Sequence | TTTTCTGATT CATGTACTTG TTACTTGCTG GGTGCTGTCT GTGGGATCAG TCAGGCACTT 60 GGCTGCCTAG AATTCTGTCC CACTGCACTG TGATGAGCCC AACAGCCAAG ATCCCTGCGA 120 GCTCACAGCT CAGGAGGCGG TGCCTAGGGG CTTCGCTGGT CCACAGTGAA GACCTCTGTT 180 GGGCCATCCA GTGGCAGAAC AGGGCAGGAC AAAGGAGGCC GTGAGTGCAG TGTACAGCAC 240 ACAGGACTCA GAGACCCCAA ACTTGGGGCC GTGTCCTGGC TCTGTCAGTG TGAGGTCTCA 300 CCCATGCAGA CACTCCGTGG ATCCTTGGTT TTCCAGCTGG TGAGATGGGG AAGCCAAGAT 360 GACTAAGATG CATGGTGATG AGGAAGTGGT CCCAGGTGCG AGAGCCTGGT CCAGGCCTAA 420 AGACCGTCAC GGGAGTGATC TCGACAACTG GTAGGGCGAA GGCACCATGG GACCCAGCAT 480 AGAAGAGCAG GTGTCTGCAG GAGGGACAAG TGGAGCTCTG GGGCCTCTTA GGCTGCCTTC 540 TGTGCTGACA TCTTTGGTTC TGCCATTGTG GTTTCTGGAA TGGGCTGGCA GGCCAGGGGC 600 CAGAGAACGC CCCAGTTTCC TCTGCCCCTC CTCTCCTACC TCTGGAAGGC TCAGGCAGCC 660 AGGGCCGGTG GTCTGAGGCT GCAGCTTCCC GGAGCTCCAA GCCAGCAGCA GACGCTTATC 720 AGCCTGCTGT GGTGCGGGGG CCGAACTCTG CCCAAACGTC TTCCAGATGT GGCCGCAGCT 780 ACTCGATAGC CTGGCTCCAG CCGGGGCTCT AGGCCAGCAG GCTCCCGTTA GCCTAGCTGT 840 TAGGAAAACA AAACCCAATG AAGGCCCAAG GGACCCAGCT TCTCGGAAGG GAAGGGAGTG 900 ATTGGGCAGA AGCCCTGGCC AGGCCCGGCC ACTGGCCCTA AGCTTGGGGT GGTCATGGCC 960 GTCTGCTGGC TCCTCTGGGC TCCTCCTGGG GTGAGCCTGG GCCCCCTGGC TAAAGGGGTT 1020 CCCCTGTGTG CAGGATGCAG CTTTTGTCTC TTTTGCTTCT CCACAGTGTG TGCGGGTGGG 1080 GGGCGTGGGG TCATGTCCCT ATCACCGTAG ACAGGATGGC AGCTTGACAA CATGGTGCAG 1140 TTTGCCGATG AGCCTGAGGG GCCGGTGCAC CTCTGCTGCC TTCCTGGCCC AGGGCGGGAC 1200 TGAACCCAGG CCAGGTTCTC AGTGGGGGGG TGGGTGGGGC 1240
|