| Tag | Content |
|---|
EnhancerAtlas ID | HS044-02164 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr11:995550-996700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:995740-995761 | TTCCTCCCTCTCCCCTCCCTC | - | 6.24 | | ZNF263 | MA0528.1 | chr11:995735-995756 | CCCTCTTCCTCCCTCTCCCCT | - | 6.79 | | ZNF263 | MA0528.1 | chr11:995744-995765 | TCCCTCTCCCCTCCCTCCACC | - | 7.93 | | ZNF263 | MA0528.1 | chr11:995726-995747 | CTTCCCTCCCCCTCTTCCTCC | - | 8.31 | | ZNF263 | MA0528.1 | chr11:995729-995750 | CCCTCCCCCTCTTCCTCCCTC | - | 8.79 |
|
| | 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 |
| GH11I000995 | chr11 | 995741 | 995890 |
|
Enhancer Sequence | GTGCCTGCCC TGGCAGTGTG CTGGTTGGGA GGGTGCTCAT GTCGGAGTCC TGGCACTCCT 60
TGGCGGGGAC CTGCTTATGT GCCCCGGCTG ACCATGTGTC CTGCCCCTCT GGCCGACAGT 120
GCAGGGCCTG CCATGGGGCT GGTATCCAGG CTGAGCCTGA CATCTCAATG AGCAGTCTTC 180
CCTCCCCCTC TTCCTCCCTC TCCCCTCCCT CCACCTAGTG TCCTCTGTGC AGCCCCTGTC 240
CCCCCGTGCC CTCTCTCTGT GTTGTTTGTG GCACGCTGCT GTGCCCGCCA TCTGGAGGCT 300
TGAATTGCCT GTGAGCTCAT CCTGGAGTGA ATGAAATGAA TGAAAGATGT GACTCTTTCT 360
CCCAAGGTGG GCGTCTTCCC TTCACGCCTG AGCACCTTCA TGCTTATGTT TCTCATGTGC 420
TCTGTAGAGC TGGTGACCTG CTTTTGACCC TGTCTCCTCC CGTGGGACGT CACTAGCCAG 480
GCGCCTAGTG CAGCAGGCCT CTGTCACTCC TCTAATCCAT CTCTCCCTCT CCTTTGGACA 540
TCTTGACATA GGTTTCTGGA GGCAGAAACT TGCTTGTGGA GATTTGTCTG TGAGCTGCCG 600
GAGCAGGGGC CTTCCCGTGG GTGCTGGGCC GGCAGCGGCT CCGCCCTGCA GAGAGGAGGA 660
CGCGGCCCCA GTTGGGTGAG GAGGCGAGGG CAGGATGACG TGATCCAGGG GAGGCTGGTG 720
TGCAGGGATT CCTGGAGGCC GGCTTTCAGC AAGGGCACTG TGAAGTCTTC CACGGAAACC 780
TGGGATTGCC TGTTGGAAGC TGGGAAGGCA CCAGGTGCTC TCGCTCCCCT CCAGCTGCTT 840
TGACGTTAAG AGGAACTCGC TGAGGGAGCA TGGAAAGGGG CTGTAGGATT GTCTTCAGTC 900
TCTCTTTGGT TCTTATTTGA TGTTTCTTTT TAATGTGGGT CCTGAGAAGT GAGGTGTGCC 960
CATACCCCAG GCCTTTGATC ACACCCAGGT TTGTCCGGCT AGGCTCAGGG TGGACTTTGG 1020
AGGGCCTGGC CTTGACTGTG TGGCTTAGGG ATCAGATGGA AGCTTCTGGA CCCTGGGAGT 1080
GAGAGCAGTG TGCTGCCCTC TGAAAAGGAG GATGAGGGTC CAGTGAGGTT CAGCATTTCT 1140
GTAAGGTGCC 1150
|
