| Tag | Content |
|---|
EnhancerAtlas ID | HS044-03636 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:132662730-132663930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr12:132663148-132663162 | TGTCCCTTGGGATT | - | 6.24 | | KLF16 | MA0741.1 | chr12:132663670-132663681 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr12:132663670-132663680 | GCCCCGCCCC | + | 6.02 | | Myod1 | MA0499.1 | chr12:132663005-132663018 | TCCAGCTGTCCCT | + | 6.16 | | SP4 | MA0685.1 | chr12:132663667-132663684 | CGAGCCCCGCCCCCTCC | + | 6.16 | | ZNF740 | MA0753.2 | chr12:132662876-132662889 | CCGCCCCCCCCAC | + | 7.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr12 | 132662941 | 132663228 | | chr12 | 132663524 | 132663727 | | chr12 | 132662936 | 132663290 | | chr12 | 132663332 | 132663875 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132178 | chr12 | 132662746 | 132663750 |
|
Enhancer Sequence | TCGAGACCAG GCTGGGCAAC ATGGCAACAA AAAAAATTAA AAACTTAGCT GGGTATGGCG 60
GTGTGCACCT GTAGTCCCAG TGACCGGGGA GGGTGTGACG GGAGGGTGGG GAGCCCGGGA 120
GTTTGAGGCT GTACTGAGCT CAGAACCCGC CCCCCCCACC CCCTGCACTC CAGCCTGGGC 180
GACAGAATGA GACCCCTGAA AAGTGTTGGT TTCTGACTTT TTTCGTTTTT GAAATCGTTT 240
CCGGCTGGCC CAAGTCGAAA AATAATGCAG ATGTCTCCAG CTGTCCCTGA GAACACTTCC 300
TGTTCCTTGA TCTGTGGCTT GTGATTCTCC CCCCGCCCCC ACTCCCCTTA CATGGGGCTG 360
TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC CTCAGGATTG TATGACTGCA GGTTGGGCTG 420
TCCCTTGGGA TTCAGGGCCT CAAATGTACC TGCTGACCAG TTGAAGAGTG CTGACCAGCT 480
GTCCTGCTGA ACACCTCTCA ATCTGGATTT TTGACATTTC CCTGTGATTA AATTCAGGGA 540
ATCCAGCTTT GGTGACAGAG CCACTGAAGC AAGGCTGTTC CCTGCTTGGA GACGCACCCA 600
CTTTACACGT GTAGGGTGGC GAGTCTGACA AACGCAGCCA CAGGCAGCCC CCACCGGGGG 660
AGCCGGACGT TTCCATCCAC CCAGACAGCA GCGTTCACGC CCAGGACCAT GTGGGCCTGC 720
GCCCCGGGCC GCACCTGCCT CTCCTGCATT CCGTGTCTGG CATCTTGTGT CGTTGCCACC 780
CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA GCGAGTGTCC TCCGTGTCTC CGAGTCGCGC 840
CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA GAGCTGTTGT TTGTTTAGGG ATGTATCATG 900
TTTTCAGCTT AACATTTGTG CCATTCGTGT GCCCTGGCGA GCCCCGCCCC CTCCAAGTTA 960
CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT ACTCTTCCTG CTGTCGCCAG CGCAGCCGAA 1020
GCACCAAGCA GGAAGCTCTG CCGAGTTCTT GGCTTCAGGT AACGTGTCAG ACCCAGGGCA 1080
TGAGCTCCAG TCCCTCTTGC CTCCACAAAG GACAGCACAT TTCCAGTTCA GGGTGCTGTG 1140
GCCGACACCG TGCGTGTGGC TGGGGCCAGT GTCACCGCGA ATCTCGGCTG CTCCACGCCC 1200
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