| Tag | Content |
|---|
EnhancerAtlas ID | HS045-01321 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:38096350-38097380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr1:38096924-38096934 | CTCAAGTGGT | - | 6.02 | | RREB1 | MA0073.1 | chr1:38096495-38096515 | ACCCCACACTCCCCCACACA | + | 6.09 | | RREB1 | MA0073.1 | chr1:38096505-38096525 | CCCCCACACACACCCACACC | + | 7.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTCCCCTGA TCAGATGTGT CTGGGAAGTT GGACATCTGA GCCCAACCTG GGAGTGAGAA 60
TGAAAACCCT GCTTCCCCGT CACGGGATCA CACACATGCT CTGATGCTCT CAAGGTTCTT 120
CCACAGCAGC GGCCTGCCCA CGCACACCCC ACACTCCCCC ACACACACCC ACACCACAAC 180
AGAGCATGCA GGCCAATAGC ACAGAGTCTC TGTAGATGCC AGGGAGCCAT CACCTTCCCC 240
TCCAGTGGCT AGATGCCTTC GAACAAGTCA TGTAGCCTCA CTGAACCTGT TTCACATCTA 300
TAAAATGGGG ACAAGCATGA CTATGTCACA GGCTAGCTGA GAGTCAGAGA GTTCAGGCTC 360
AGGAATGAGA AATCTGAGGT GCTGGAGTGG AGGTGCCCCT CCCACCCCCT GTCCTAATCC 420
TTTCCCCTCT AGGCTCTTCA GTGCCAGTCC ACCCCCTCGC CTGTCAGGGA GGCCCCAGCA 480
GAGCCCACCT GCACGGGAGA TAAATCATTA TCCCCTAAGG GAGTTCAGTA CCTCCCTCCT 540
TGGCCTCTCC CGCTGGCTTT GAAGGCCAGA CACACTCAAG TGGTTAAGCT GCCTGTGAGA 600
AGTGTTTACA TGAGGCTGAT GGATCCCACC TGGTGCTGTG GCCTGAGCCA GAGGAGATGC 660
CCCCAGCTAC CCCCAAATGC CCGTCAGCTG CCAACCCCTG CACGCCCCTC CAGTACTCCC 720
TGCCTGATTT ACCAAAGCCT TTCTATCCTC CCCAGCCCCC ACTACACAAT TCTCTCACCC 780
ACAGATTATA GATGTCCAGT TGAGTTTATC AAACTGGGGT CTTCTGGCCC AAGTCTGTAG 840
TCTCAGAGGC TGGCTGTACA GCATGATAGT CACGGGCATA AACTTCAGAG TCAGACTGCC 900
TGGATTTGAA TATTGGTTCT GCTACTTATT AGCTATGTTA CCTTGCTTAG CTGGTCTGAG 960
CCTGTTTTCT TATCTGCATG AAGGTTATTG TTGTTTATAA CTTAAATGAG TTAATACACA 1020
AAACTGCTTA 1030
|
