| Tag | Content |
|---|
EnhancerAtlas ID | HS045-71514 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr9:138188770-138189880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr9:138189791-138189812 | AGTGCTGGCCTGGGTCCTGCA | - | 6.56 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGTTCAGCT GCACCTGTGT CCCTGGCTGT GTCTGTCTGG AATAGCAGAA AAGCAGGGTC 60
AACCTGAAGG TCAGACGATA GGAATTGATT AAATAAACCG GGGGGGGGGG CATGCAAGTG 120
GGGAGCCACT CTGCCGCCTG ATAAATGTGG CTGCCTAGAC TCAATGGCAA GAAGCCAAGG 180
TTACAGCCTG AAAAGTGAAA CGGCAGCCCC TGGTCCCCCG CCACCCCGTC CCCCACCACT 240
CCTGGGCTGC CTGAGACAGC CAGCACGGGA GGCTGCCAGG CGGCTGCCTG TGCTGTGGGC 300
CCCGAGAGGC TGGAGGCTTG GAGCTGCCTC CCTAGTGCTT ATTGGAAGCA CCTGCCATTA 360
ACTTGCTAGT TTCTTTTTTT TCAGGGCACT ATTGGCGCCC CCAGGATGCT GACAGGCAGG 420
CAGGGGTCCT GTGGCATTCA CTGTCTCTTG AGAACCTTGC AAAACATTGC AAACCCCATC 480
ATTGAGAGCA AGTTCCCACT CCAAAAGCAG TGAACTGAAA TCTCAAGTTT AAGCCCCACC 540
TCCAGGCCTC CTCGAGGTTA CCCAGGCACC AGGCCAGAAC CCGCAGGACC CGTGAGATGC 600
TGGGTCGAGA CCCCCTGGGC TCCGACAGAG GAACTGCCTC AGGTCAAGGG TGTTCCTTTC 660
ACACAAGAGA AGTCAAAACT CCGGGTGTGA AATCTGCAAA TACCTCTGTG TTTTCCTCTT 720
TTCCAGGGCA TGGCCTCAGG TGAAACTCAC ACAGTCTTCT GGAAGCATGC CTGGGTTTTA 780
GAGTACCCTG TTCCCTCCCA ATACAGGCGT GAGGAGAGCA ACACTCTCCG TCTCTAGCCC 840
CTGGACTAGA ACCTGGATCT GCTGACACCA TTGGGGCCTG TCAGACACCT GCCAATCCTG 900
ACGTTGGATG AGAAAAGGCT GCTAAGACCA CGGGGTCCCA CCGGTGGAGA CAGCCATGCC 960
CACAGGTGGG AAGGGGCTTG CCAAGGCTAC CAAGCAGATA GCAACGGCCG GGAGCCAGCG 1020
CAGTGCTGGC CTGGGTCCTG CACCTGCACA TATAGTCACT CAGTAAACGT TGGCTGCATG 1080
AGTGAGTGAG TGAGTGAGTC TGGCTTTTCC 1110
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