| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13492 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:94609510-94610600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr9:94609726-94609739 | TTCATTTGCATAC | + | 6.21 | | Pou2f3 | MA0627.1 | chr9:94609725-94609741 | CTTCATTTGCATACCA | - | 6.6 |
|
| | 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 |
| GH09I091847 | chr9 | 94609813 | 94610748 |
|
Enhancer Sequence | ACTTAGAACC AGAAAGACGG GAGAAGTGCC TGTCCCACTG GACAGAAAGC CTGACCCCTC 60
TGGGAGGCCA CTTTCCCTCC CTCCTGGACC CCTCATTAGG CCTCGCTACC ATCTCCCCAA 120
ATTCCAGAGG TAGTCCTTTG CAGACAAGAT CTACTGCCAG GTCCCTCGAC GCCCCCTTGC 180
TCCTCTGTAC AAGGCACCAA AACATGGGAA GCAGGCTTCA TTTGCATACC ACACATATAC 240
TCCCCCAGAA AGGGCTCCCT AATGCAGTCC CCCCACTTCC CACATAAAGA GACTTGAGGG 300
CGCCAGAGGA GGCCCTGCAG GAGCCAGCTC ATACAGCAAC AGTTCCAGTC TTTCAAAGTA 360
AGCCCAGGCA GGCGGGACCC AACTGCACCC CAGCTCTCCT CCAGAGCCGC TTTTCTCATT 420
TCCGTGTGCA GCCTGCCAGG GCTGAGGGTC GAGAGCAGGC CTGAGAATGA ACCCCACTCC 480
CAGCACATGA TGGATCCTGC CCTTGCCGGC CAGGAGATGC TGGTCGCAGG AAGACATCCT 540
TCACGTCTTC GCTGCCACCA AGAATCACAC TCCCCAGAAC TCAAGTTCCG CTCGACCAAG 600
CTCAAGTCAG GCTTTGATCT TGCAGGAAAC ACCCACGCAG ACTCACTCTC CAGGACGGGA 660
AGGATGCAGG AGCCAGCTTC AGCAGAACTC CTGGCTAGCA GCTCTGCCTG GCAGTACAGA 720
AACTGTCTCA AAATGTGAAA CAGATGAGCC TTTTAAAGAA AGTTATTTAT ATTGTGGAAT 780
CTTTCAGAGC AAGCAGAAAC TTGAAGAGCC TTATCACCTG GGGCACAAAA CCAAGGATAC 840
TCGAGTCTTC TCTCACCATG GAAATGGATG TGATTTTACC AAAACATAAC AAGGAAATAT 900
GTTGGTTTGA TGCTATTTCT TGATTTCTAC TTCTGATAAC GTATGCATGC CAGTCCTAAT 960
CAAGACAGAA TGCCATTCAA TAAGCTGACA AAGAACTCTT TTCCTGCGAA TCCCCTACCT 1020
TGAAGGTCAG TATTAACAGT GAAGCATGGA AATTAAATTA AATTAAACCA GGGGAGCGGA 1080
GCTGTATGTA 1090
|
