| Tag | Content |
|---|
EnhancerAtlas ID | HS145-27068 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr9:133227370-133228300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr9:133227548-133227559 | AATGAGTCACA | - | 6.62 | | KLF16 | MA0741.1 | chr9:133228089-133228100 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr9:133228089-133228099 | GCCCCGCCCC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr9:133227417-133227432 | TGAACTCCTGACCTC | - | 6.22 | | Nr5a2 | MA0505.1 | chr9:133227409-133227424 | GCTGGCCTTGAACTC | - | 8.25 | | RARA | MA0729.1 | chr9:133227414-133227432 | CCTTGAACTCCTGACCTC | - | 6.73 | | SP1 | MA0079.4 | chr9:133228086-133228101 | GTGGCCCCGCCCCCA | + | 6.33 | | SP4 | MA0685.1 | chr9:133228086-133228103 | GTGGCCCCGCCCCCACC | + | 6.57 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 133227579 | 133227879 | | chr9 | 133228000 | 133228065 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I130351 | chr9 | 133227155 | 133228200 |
|
Enhancer Sequence | GTATTTTTAG TAGAGGTGGG GTTTCACCAT GTTGGCCAGG CTGGCCTTGA ACTCCTGACC 60
TCAAGTGATC CTCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGTCACTGT 120
ACCTGGCCCA AATTTACTAC TTCTGATACC ACTTGGAATT ATGATTTACT TTTCTTTAAA 180
TGAGTCACAC TTCCTTACAC TGAAACACAT TTATTTAAAT ATCCCTTATT CTTATAAAGG 240
ATATTTAATA TCGAAACTGT AAGCAGAAAA CCAGTTTCGC TTGGCTAAGG AAGCTGAAAA 300
AACAAACACA CCCCATAGAG CAATGTTGTA AATTCTCGAG GCGTGGACTC CGCAGAGGGC 360
ACCCAGCCTG CATCTGCACT CTCTGTGCTA AAAAGCGGAG AGTAGAAAGT GCTAGAAAGG 420
TTAGGGACAT GCATAGTAGC ACCAAACGGA GCCTTTCCTT GCTGTAACCC GGATAGAAGG 480
AGATTTGGGA GGGGCGTAAC CATTCCATTC TGAGATGCAG TTATTTCATG CTGTGCCCAT 540
GTGCCCCTAG CATTGTCCTG GGTAGCATCG GTGGTGAGTG ACCAGCCCTG TGTGAAGTCC 600
TCATCTAGTC CAGCCTCTCA TTTCACAGAT GGGGAGACTG AGGCCCAGAG AGGGGAAGTG 660
GCTCACCCCT GGTCTTCCAG TATGTTAGAG CAGAGCAGGG CCCAGAATCC AAGCCTGTGG 720
CCCCGCCCCC ACCTCCTGCA CCTTCCACAC CAGCATGTCC CCATGCTGGC CTCTCCCATC 780
TGTCCCCAGA CCCCTCCCCT CCTTGTCCAC CATGCCTTCC CTGCCCCCGC AATGGAAGCC 840
TGTGGTGTGT CTTGTGGCCC AAAGGCATGA GTCTGCTGCC CTGGGGAAGA TGCCAGAGGC 900
CTCAGCGGCT GCCTGTGACC AGCCCCACCT 930
|
