| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13523 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:97737600-97739070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr9:97737681-97737702 | TATTTGTTTCACTTTTAGTGC | + | 6.08 | | MSC | MA0665.1 | chr9:97738706-97738716 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr9:97738706-97738716 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr9:97738706-97738716 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr9:97738706-97738716 | AACAGCTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 97738128 | 97738262 | | chr9 | 97738417 | 97738842 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I094976 | chr9 | 97738481 | 97738630 |
|
Enhancer Sequence | TGTGTCTGGC ACACAGTAGG TGTTCAATAA GCAGTAGCTT CTAGTTTTAT GCCTTTTCTT 60
GGCAGTGGAT AGAGGACTTT TTATTTGTTT CACTTTTAGT GCCACGGTAG AATAGTGTCT 120
GTGTGTGCAA GTACTAACTA TGTTAAAGCA GAATTTGCCA ATGAACTAAC CCTCTGAGTT 180
GGCCGAAGAC TGTGGCACAG GCAAATTGTA TGCAGCCACA TGCTTCCTAC GGAAAGTCAT 240
CCTGCAGAGA TTCCTGGGGC CCACTATCTG CACAGTGTCT CCCAACCCTG CAGCTGGACT 300
GCTTCAGTGC TGCCCTGCAG ATCCGTCCCC TGCACGCCAC ATCCATGTGG GCCGCTCTCG 360
TTGCCTCCTG CAGAAACATT CTGCAAGTTC TGGTGTGGTC TCCCTGCCTC CAGCCTCTTC 420
TCCGCTTTTT CTTCCTTGAC TCAGTTCTCT GCCGTGTCCC TCTGCAATTT TGCTCCAGAG 480
CCTCCTTGAC AAAGGCAGGG CCCGGTAGCA GGGACTGCAG AGTCCCCGCA GGACCCGCTG 540
TTTTCTTTCT CAGCTCATTC TGGAGGCCAG CCCCACTGAG CTGAACGGAG TCTGCACACT 600
ACTGCACTGG CATTCCTGCT CCTGCTATCT TTGCCCCGAT GTGCTTTTCT TCCATTTCTA 660
TTGGCTTTGC CCCACCAGGA CCCAGTCATG CATGGCCTTC TTAGGAAGCC TCTCCTGATG 720
CACCTCCTCT TGTCCTGTTT TACCTATCCC ACCTGCAGCA GTGGTTCTTC AACACCTAGA 780
GGACCATCAT CTCTACAGGC GCTGGTAGCA TTCTGCCTGG TGTCTATTAC ACATCCCTAA 840
TCCACAGTCA CTCCCTGGGT TTTCCCATCC CAGCCTTCCA CAGAACCTTT GCCCAGCAGC 900
CATCCAGCGA ATGTTTGCCA CATAGAGAAT GTTGCCTGTT TTTCAGTCTT CTCTGGTGAA 960
GACTTTGGAC CTCACTTAAT AACATTCCAG GGCTCAACTC CCCAGCCCCC ACTCCATGCC 1020
ACCCCTAGAG AAGCATCTGT AAGTGAAAAT TCCCCAAAGG AAATTTATGT CCGTGTCTTC 1080
ATATTCACTC CCCCATGCTG ATACACAACA GCTGTTCACT GTCTTTTGTA AAATCACTCA 1140
AAAATAGCAA TTAAGTCGCT CCTCGGACTT CTCTTCTCTG GGATATTTAA CCTCAGTTCC 1200
CTTTACCTCC CTTGTGGGCT CTTCCCCTTT TGATCGTCAC TATTGCTCTC TCTAAGTCCT 1260
TTCCAAATTC TGCATCTTCC TCTTAAATAT CTTATGGGAA AGGTGGAGAC TTGTTTTCAG 1320
TTCAGAAGAC AGCCTCTTTT TTTTTTTTTT TTTCTTTTTG GGGGTTTGAG ACAGGGTCTC 1380
ACTTTGTCCC CAGGCTGGAG TGTAGTGGTG TGATCCAGGC TCACTGCAAC CTCTGCCTCC 1440
CAGGCTCAAG CCATTCTCCC ACCTCAGCCT 1470
|
