| Tag | Content |
|---|
EnhancerAtlas ID | HS042-07729 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr11:47175810-47176720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:47176615-47176636 | CTCTCTCTCTCCCTCTCCCCC | - | 6.46 | | ZNF263 | MA0528.1 | chr11:47176659-47176680 | CCTCTCTCCCTCCCCTCCTTA | - | 6.65 | | ZNF263 | MA0528.1 | chr11:47176642-47176663 | TTCCCTTCCTCCCTCTCCCTC | - | 6.6 | | ZNF263 | MA0528.1 | chr11:47176654-47176675 | CTCTCCCTCTCTCCCTCCCCT | - | 7.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_08437 | chr11:47173499-47177374 | Brain_Inferior_Temporal_Lobe |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I047152 | chr11 | 47174281 | 47176259 | | GH11I047154 | chr11 | 47176404 | 47177530 |
|
Enhancer Sequence | AAGAAAGATA AAGCCAGAAG GACCTGATCA GAAACAGATT GGGGGCCCGC CCCACCCCAT 60
CTGATAGCTT GGCGCCTGCC TGGCATGTGA TGGAGCCCAG CAAACGCTCG TTTCCTTCTC 120
TTCTTGTCCT GGCTCAGATG AGGTGCTGAG CAGAGGATGA ACATAGCCTT GGTCGGATCC 180
CTTTATGAGT CAGACGGTTT TCTTCCTGTG AGGTGGGTCC TCAGTGGGAG GGACTAGAGA 240
CAGGAAAACC GTTGGGTGGG CAACCTGTGA ACATGGATGC AAGGAGGAGC AGGGCGGCAG 300
CACAAGATGA GTGTGGGTTT TGACCCTCAC AAGTGCAGAT TCCCCAATAG CTCTTTGCCC 360
TCTCCCCTTG TCTGCCATCT GTGCCCCAGG GTGGCGGTGT CTGTCGCTGT TCTGGCCCTT 420
TGGTAGCTTA TTAAATCTCA GTACCACTTG CCAAGACCCT TTAAACCCCT TAGCTGTTCT 480
TTTTGCCTTT TCTGATCAGC TGTATTTATT CTGAACTAAA TGGTCCTCAC GGCAGAATGA 540
AAGGATTTAC TGCTTAAGTA TATGAAAAGA AACCTTGGCT GCATTACAGT TGCACCCTCT 600
CCTCGCCACC CCCTGCCCAT GCTCCATCCG CTAGCTGGTG CCACTGAGAC TGAACCGGGA 660
GCCCGCTCTG GGTACAGTGT GGTCAGTTCA GTTTGGTGGC AGAGTCCAAT TGATGGAGCA 720
GTGAGGTGAC TGGGAGGAGC TTGCTTTTGG GAGCCCTCTC CTAAATGTCC TGCTGCCCCA 780
GGGGAGACTG GCGGCCCAGG AACAGCTCTC TCTCTCCCTC TCCCCCGCAC TTTTCCCTTC 840
CTCCCTCTCC CTCTCTCCCT CCCCTCCTTA AACCTCTCCC CCATTCTCTC TCTCAGATTC 900
TCTCTTTCCC 910
|
