| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13222 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:23537180-23538360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr9:23538015-23538029 | GTTCCCTGGGGACT | - | 6.41 | | ZNF263 | MA0528.1 | chr9:23538135-23538156 | TTCTCCGTCCCCCACTCCTTC | - | 6.17 |
|
| | 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 |
| GH09I023537 | chr9 | 23537599 | 23538198 |
|
Enhancer Sequence | AACTGAACAA GACAGGGCAC CAAAGCCACT CAGCTGACTG TCATCTTGAA ATTATGGATT 60
CTGTGTCCTA ATTTATCACC CTCATTCTGT TCTAGCCTTT CTGATGCTTG GCATTAATTT 120
TCCTTTTCTG AGCACTGACC CCACCTCTCC TATTCTATTC CTCCACTGTT GAACCGGAAC 180
AAAGGTCACT TGAAAGCGAA GCAAAACTCA GCTGTTACCA AAGGCGCAAA GATCAAAGTT 240
GGCAGCTACG CTAAAGTTCA GGATTCAGAG ACTTCCTCTT TAAGATCAAA ATTCCAGATG 300
ATCCAAATAT AGGCAAATGA GCCCCAGTAG AACACTCAGC TTTCTGTGCT GAATCCAGGA 360
AAGAAGCAGA AATCACCATA GAAGCAACTC AGTTTCACTC TTTGCAACCC CGTGGGCTCT 420
ATGCTAATTG CCTACCCCAA GAGTGAGATC GCATTTCAAA ATATGGTCAA ACGCAAAACA 480
GCCAAGTCAA TCAAGCATTA AGTATTCAAG CACAATTATC CGAACACATG CCCAAGGACC 540
AGCAGTGAAG CAGCTTAATT TGGGAGCGGC TCCGTAATCA TCTCTCCGGG CAGCTGAGAT 600
TTTAACCTCT CCCCTCGGGC CTCCTGTTCG GGGCACTAGG CTAGCTCTCT CTGTGTGAGA 660
GATCACAACG GGAGCCGCTG CCCCCCAGTT GTGAGGCTTC ATTTAAATTC ATGCTAAGGG 720
TAAGGGAGGG GGAGGGGGCA GAAGGTCTGC AGAAGCCCCC ATTGTTGGGG AGAGACGTGT 780
GGGAGCAGAT GGTCTGGCTG GTCACTCAGT CTGGCTGTCA GATGCTCTCT GTCAAGTTCC 840
CTGGGGACTG CAGGGTTTTC TTTCCACTCT CCGCTCTGGT CATATGTGTT TGCTCAGCGT 900
GAGCGAGGGG TCTTTTTCTT TATCACCCCT CAGACTTCCA GGGGGCTGAG TTGCCTTCTC 960
CGTCCCCCAC TCCTTCCCTC TGCTTTCTCT GCTTTTTCTG GACCAGCTAG TGCCGCGCCT 1020
CCAAGGGCCC GCTCGCTGCA GAGAAAAGCA AGCGATTTCC TTTGTCTCTA ATTGATGCTG 1080
CGCTCTCATC CAGCAGCTTC TGACTGGCAT GCTCACTCGG TTATTTAACA AATTACTCCA 1140
CAGCCCTCAT TAGAACTATT GACATGTACA GCTAACCAAC 1180
|
