| Tag | Content |
|---|
EnhancerAtlas ID | HS007-16294 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr8:11309010-11310200 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAX | MA0058.3 | chr8:11309115-11309125 | ACCACGTGCT | + | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_55688 | chr8:11309247-11310384 | u87 | | SE_58515 | chr8:11271776-11367112 | Ly1 | | SE_60559 | chr8:11246636-11318640 | DHL6 | | SE_61363 | chr8:11297105-11326062 | HBL1 | | SE_62362 | chr8:11308990-11367697 | Tonsil | | SE_65314 | chr8:11300056-11310270 | Pancreatic_islets | | SE_67671 | chr8:11309247-11310384 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr8 | 11309200 | 11310200 | | chr8 | 11309050 | 11309513 | | chr8 | 11309830 | 11310187 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I011452 | chr8 | 11310026 | 11310392 |
|
Enhancer Sequence | TGTCTGTTTG CCATATCCAA CACCCTCTCC TTTCCTGTGT GGAGGGAGCT CCCCATTTTG 60
TGCAGAACAG CAGGCAGGCC GTGCAGCCTT CTCTGCAACC AGAGGACCAC GTGCTCCTCT 120
TCCCAGCTCA TGCCCTGGTG ACCAGGTGTG AGCATGTGAC CTGAGCTTGG CCAGTCAGCT 180
GTTCAGGCCC CGACTCTGAA TTGGGTGCGT GTGAGTCTCA GAGGAAGGGA TGGTTAGGGC 240
GCATCTGTGA ACCAACCCTG GAGGCAAATG TGAAGTGCAG GGGCGGTGGC ATCCTCTTAG 300
CCAAATTGTC TCTGCTGAAG GACTGGCCCG GGATCTCCTG CCTCTGCCTT CTGGATCTGC 360
CCTGGTTCTG CCTGTTTTCT GGTCTTTACC TCCTGCCAAT TCTGTGGGCA CCTGACAGCC 420
TTACAATAAT GTCATTTTCT CTTGCTCACA ACCAAGAGCT GTAACTGAAA TGAGACAGGA 480
AGCACAACTC ATTTGGTGAG GAAAATATAC AACTGAGAGC AAACCAGTGT CATAAAATGT 540
CATGACAATC CAAAAGGCTC CCTCTGCCAC CATTCCACGT GTCCCTTGGT GGTGGGGGGC 600
AGGGAGGGGG TGCTGTGCGA CCTCCCATTG AGAACCACAG GGTGGATGGT CACTGTCCTC 660
CTAATGAAAT CTTACTGAGT CTGTCCACAT GCAGAGTTGA CTTGTCTCCT AACTCACAAT 720
CCATGACAGG CTATGCTTGA TGAGGACAGA ATGACAATTT CGCATATGAG TGAATTTATC 780
CTTGCTCTGC TCCTCTGGCA GAAACGCCGC CCATGGTTCC CTGTGCAAAA TGGATACATG 840
CTGGGTCATG AGACCAGCCC AGCTGGGCTA CAGCCGGACA TCAGGGCAAA CAACTGAAGG 900
GCCGAGAAGT CTGGTGAGCT GTGCTCTTTT GGGAGTGGTG CCTCTGGGCT GTTTCAGGAC 960
TGTGACAGTC CCCAGAGGGA GAGGGGGTGA GCAGAGGCAG AAAGAGCATG AAGGAGTGAG 1020
CCTGTGGCTG CATCTGTCTC CCACAGGCTG CTGCTTCCTC CACCTGCAGC TCCCTCCCTT 1080
CTCATCATCA GCCTCCACCC CACGAGGTTG CCTCGGGTCT GTTTCTGCAG CCTGAAAGAG 1140
GTGCACTAAC CCTATTCAAA TCCCCATTTT ACAGGTGAGG AAACAGATAA 1190
|
