| Tag | Content |
|---|
EnhancerAtlas ID | HS150-09238 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr6:41546030-41546670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr6:41546476-41546488 | TTCTGTTTACCT | - | 6.14 | | ZNF263 | MA0528.1 | chr6:41546273-41546294 | CTCCCCCCTTATCCCTCATCC | - | 6.09 | | ZNF263 | MA0528.1 | chr6:41546256-41546277 | TCCCCCCTTCTCTTATCCTCC | - | 6.25 | | ZNF263 | MA0528.1 | chr6:41546590-41546611 | TGCTCCCCCCACCCCTCCCCC | - | 6.63 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27953 | chr6:41545075-41547681 | Fetal_Intestine | | SE_28956 | chr6:41545059-41547604 | Fetal_Intestine_Large | | SE_31492 | chr6:41544285-41547331 | Gastric | | SE_65317 | chr6:41542070-41547775 | Pancreatic_islets | | SE_69040 | chr6:41544748-41547426 | H9 |
|
| | 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 |
| GH06I041576 | chr6 | 41544339 | 41547426 |
|
Enhancer Sequence | GCTTAGCCTC TTTGTCCCTG TCACTCAAAG TTTGTCTGCA GCTCTCCCTG TCTCTTTGTA 60
CCTCTCTCAC TGTTTGTTCT CCCCTGCCTC TTCCCTTCAG GGTCTCTCTT GGTCACTTCT 120
CATGTTTCTG CGTCCCTGTC GGTCACTCCC TCTGTCCCTC TGTGTTCCTG TGTCTGGGGC 180
TCAGCCCCTC CCAGGCCATC TCTGTTGCTG CAGTCACGTC ACCAAGTCCC CCCTTCTCTT 240
ATCCTCCCCC CTTATCCCTC ATCCACCAGC TCTCTCGCAG TCTCTCCATG CTTCCTGTCT 300
CTTGATGTCT CTCTGTCTCT TTTGTTTTCC TTTGCACAAT CTGCCCTTTT TTCCCCTTCT 360
CCCTTCCCTC CAGCTTGCCA GCCCATCTGG CTGGCTGGGG GAGGGGAGAT CTGTGGGGGG 420
TGGGCGGGGG GTGGGGGAGC CAGGCCTTCT GTTTACCTTT TGTGTCACAA AGAACTTGGG 480
AGAATTGCAG TCTGAGTCCG GGTTGGGTCA CTACTCGGGC AGCCACTCCC CTCCCCCTCT 540
GCCCAGCAGC CCGGGATCCA TGCTCCCCCC ACCCCTCCCC CAGCAGAGGG AGGCTCAGAA 600
TTGGGGAAGG GATTAAGCCA GGCTTTGAAA GGAAGTTTAT 640
|
