| Tag | Content |
|---|
EnhancerAtlas ID | HS045-27710 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr17:41773530-41774490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr17:41774026-41774038 | GCTATTTATAGC | - | 6.32 | | MEF2B | MA0660.1 | chr17:41774026-41774038 | GCTATTTATAGC | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACTTGGTGCC CGGCCTTTGT CAAGTCACTT CCTCATTTGC AAACTGGGAG AGTTTGGATG 60
AAACTATTGA ATGAAATTAT TTTGGGGGTT TCTTTCTGGC TCTCACAGTC CTCGCATGCT 120
CACCATGTTC CCTTCAATTT CATTAGCACA GCCCAACAAA GGGTTAAGCA GTGGCAGTTC 180
CTCTCGTTCT TTGGTTAGGA CAGGAAGGTC AGGGGTGAGG CCAATACAAG AGGTAGCCGC 240
CACAGCTGAT GCTGGAAATG ACAATAGTTC TTTCCTAGAC TCATATTTGT CCCCTCTCCC 300
TGAAGCTTTG CCTGCAGTGC CCTTGTAAAG AAGTTGGCAA GAAGCAGGAG TGAGGCTCAG 360
CCCCTCTCTG AAATGGATAC GCCGGTTGCT CCCCCTCATG GCTGGTCTCA TTTGCCTTCT 420
TCATTTTTAG ACACATTCCA AACTTTTCAG CAAATTATAG TGTTTGCCAA CTGGCCGTCT 480
GGGGCCCAGG AGAGATGCTA TTTATAGCGA TGCTGGGATG CTGCCATCCC AGAGCAGCCT 540
GGTAAGAAAC GGAGCCAGAG TGCCTGGGAG TGGCGTCCTG CACCCTGGGG AGAGGCCAGG 600
GCCCTGGAGC AGGGTGGCAA AGCTGGTGGC CCGTGGCAAG GACCACTGGC ACATCCCCTG 660
CCTGCCTGGG CCCTGGGGTC TGTGCCCATA CCCCACACGG GGGGCTGCTT CCGTGCTCCT 720
TGGAGAGACG ATGGTGCTGT GGGGCCACTG AGCACAGTAA AGGCTAAGAC CCACCATAGG 780
TCAGCCCTTG CTCATGCTGA CTGTTGCCCC ATTTCCCTTC ATTCTCTCAC TCGTTCATTC 840
CTCAGAATCT GCATCCTGGT TTTGTCACTA CCTGGAGTTG TAAAGATACC ACCAAGCTCA 900
CCTTGTGGTG TGAGCCTTGA TTTTCCCCAT CTGTGTAAAG GGTGGATCTG AGCTCCAAAG 960
|
