| Tag | Content |
|---|
EnhancerAtlas ID | HS145-14313 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr20:5046140-5047060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr20:5046738-5046753 | TGCTAAGTCATGGTC | - | 6.25 | | Nr5a2 | MA0505.1 | chr20:5046853-5046868 | CCTGGCCTTGGGCTT | - | 6.16 |
|
| | 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 |
| GH20I005064 | chr20 | 5045439 | 5047732 |
|
Enhancer Sequence | TCCCTCTAAT GATCTCTTTG AGGCTAGCCA GCAGGGGAGA AGTGGCTGTG AGTGGGGCCT 60
ATTTTCCTGG CTTGCAGGAA GCCAGGGGGC CAGAGCAGAG GCCCCCTACT GCCCTTCACT 120
CCTCACTACC ACCAGCTTCC CAGGTGTCCT GGACGCATGT GGGATGCCTC TGAGATAACC 180
GGGTTAAGGC CAGGGCCTGT CTAACGCCTG GGCTCTGGAG CAGGACCCGG GTTCTGTGGG 240
AGCTCATATG AAGGACAGGA AGTGACCAGT CCACAGACTG GACCAAAGGT CTGTGACTCA 300
CTGGTTGTAT GTAGTAGGGA TCACGCCCCT GCCATGCCAA ACACCAAAAC TGTAGGTCAG 360
ATTGGAGTTG TACTGGAGTA ATACCATGAC GAGGAGTGGG CTGCACTGGA GACCCCCGTC 420
CCTGGAATGA CCGGGGAAGC AGGGGCTGAT GTGAGGAAGG GTGGAGAGGG GCTGCGGTGA 480
TGGCGAAGGA GGCCACAAGT TCCCGGTTTT GGCATGCTGC TCAGGCCTTC GCCTCCCCAT 540
GCTGGCTGTA TTCTACCCGC ACACCCATAT TGGCCCAGAC TGGGAAACCT CACAGCTTTG 600
CTAAGTCATG GTCAGGTTAG TCAAGGCCAG TAAACCACGT GGGTGATGCA TCATTGCCAC 660
CCTGGCACGC CTCCTTCCAG ACCAGGCTGG GACTGGCTCT CCACATCCCA GGGCCTGGCC 720
TTGGGCTTCT CTGCCAGCTG GTCAGGGTGA GTCACTCTTC TTTGGAGGAT GCTGCCTTCC 780
TCTAATGTTG GACATGAAGG GCTTTTTTGT CCTCCTAGAG TTCTGGAGCA TCCCAGAAAA 840
GGCAAAACTA GGGAGCAGAG GAAAGAGAAC ATTTTTTAAA AAACAAAAAT GTTGCCTGGG 900
CGCGGTGGCT CACGCCTGTA 920
|
