| Tag | Content |
|---|
EnhancerAtlas ID | HS150-06859 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr20:61983390-61984100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr20:61983894-61983905 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr20:61983895-61983905 | GGGGCGGGGC | - | 6.02 | | SP1 | MA0079.4 | chr20:61983893-61983908 | GGGGGGCGGGGCTTT | - | 6.6 | | SP2 | MA0516.2 | chr20:61983892-61983909 | CGGGGGGCGGGGCTTTA | - | 6.28 | | SP4 | MA0685.1 | chr20:61983891-61983908 | GCGGGGGGCGGGGCTTT | - | 6.2 |
|
| | 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 |
| GH20I063352 | chr20 | 61983781 | 61983950 |
|
Enhancer Sequence | GGGCCAGGCT CAGCTCTGTG GAGGGCGCTG GGGCACGACG CGTCGGGGGG AGCGGCTGCC 60
CAGCCACACA CCTCCTGCTC CACCTCTGCC AAGCTGCCTG GACCCCTGCC CATCCCTCCT 120
CTGCCTCATT CCCTGAGAGC CTGCTCAAAG GCCAGGGCCT CTCCAGGTAC TTGGGCAGAG 180
CTGGCGACTG TTCCCTGAGC TTCCTCTGTG CCTGCCCCCG AGTCCCAGGG CTGGACCTGC 240
ACCTCAACCT CCCTCCCAAC CCTCAGGGAC CCTCCCTTTG TGGAGCCGCC ACTGCTGGAG 300
CTCTGCCCTC CAGGTCGTGG AGACCTGGCC CCCCACGGTC TCAGTCGGTG CTGAGCCTCT 360
GCCCCCCTGA ACTGGTCCTG AGCCAACACC GCCGGCTGGG CTGCCGCTCA GCTGCAGAGG 420
GAGGGAGACC CAGCAAGAGC CACCAGCTGC ATCTCAATGC GGCTCCGGCC CAGCACAGCC 480
TGGCTCCCGA GCGTCCCTCC AGCGGGGGGC GGGGCTTTAC CACCAAGTCA GTCTGGGTGG 540
AATCAGGCTC AAGTTTGCTC CCTCTCCCCA GCCCATCTCT CCAAAAACCA ACGCCCTCCA 600
CCTTCTGAGG CACAAATTAA AAGATTCTCA TATGGCAAGC GGGTGACTAC TCTGTTCAGC 660
ACACACTCTA CAGGGAACGC CAGGGCCATG CTCAGGGAAC AGTGCAGGTC 710
|
