| Tag | Content |
|---|
EnhancerAtlas ID | HS145-09740 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr17:12880080-12881080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr17:12880292-12880302 | GCCATATGGT | + | 6.02 | | Sox6 | MA0515.1 | chr17:12880601-12880611 | CCATTGTTTT | + | 6.02 |
|
| | 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 |
| GH17I012976 | chr17 | 12880118 | 12881125 |
|
Enhancer Sequence | CTGGCTGTGT AATTGCTAGG CCACAGATGG ACCTGAGAGA TGCAGATGCG GGCACAGTGA 60
GTTCATTGGA GAAGCAGAGT CTGAGAGTGG TGGGCCAGGT GAGGCCGACC AGGAGGAAAC 120
GGACCCACAG GCGGGAGATG GGCTGGGACT GCTTCCTTTT TGGACACTCC TCAGCTTCAT 180
CCTAGTTTCC CATCTTAGAA AGGGGACTCA GTGCCATATG GTATTTGGCA TATAAATGAT 240
ATTTCTAAAA AGTGCTCCTT GAAGATGGAT TCCCCCAGGC TCTGAAGGCA TTCCAGGAAC 300
ATTCTCGGTG GGTGACCTTG CAGAGTTACT TGTGGGCAGG CAATGGCACC CTCTGGTTTC 360
GATTATTTTA AAGCCAACTC ACATTGCTCT ATAGCCAAAT GTCTTTCCCC TTTGCCCGGG 420
CTGACCGGTT TAGTAACTTT TCTTTGGATG TTAGTGTTTT GTGTTTTACA CCACTTTTTG 480
TTCTCTCCCC GCATGGGTTT CTCCCAGTAC AAACAGGTGT TCCATTGTTT TTGTTTGTGT 540
TGTTTGTTTC TGTTTCCTGG ATGTTTGCAG CCCAGATGAT GTTCCCTCGA GTGGCCGGAT 600
TCTCGTTCTG GCTCCCCCTC CCCTGATGGC AGGCCCTTCC TTGCCTCTGA CTGGTTCCCA 660
CCTTCCCACT CCCTACCCCA GGCCCCACCT TCAGTTCTTT CCCTGGCTCT GTCCAGCCAG 720
GCTCTGCCTC CACATCCCGC CCAACTGCTT AGCATGAATG CTAACCCCAA AATTCTCCTT 780
CCTGCTTCTT GGCACCAAGG TCATGGGCTG AGTCATGCAT CTTCAGAGCT AACTTGTCCT 840
CAAACGTGCC TTAAACATGC CTTGTTCAGG TAGCGCCCCT AGTAGCCGCC CTACGCCCCA 900
CCTCTCCCCA CTGGGTCAGC TGCACCTATG CTGGAGAAAG AGGACAAGGC TAAGTGGGTA 960
AATACTTGTT TCTGTGCTGG AGGAAGTGTG TCCGGGCCGG 1000
|
