| Tag | Content |
|---|
EnhancerAtlas ID | HS042-49425 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chrX:18893040-18894090 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chrX:18893442-18893453 | CCACACCCTGC | + | 6.62 | | USF2 | MA0526.2 | chrX:18893849-18893865 | GGAGGTCACGTGGGCC | + | 6.5 | | ZNF263 | MA0528.1 | chrX:18894028-18894049 | GGAGGAGTGGTGGAAAGGAGG | + | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGGAGCCTCC ATTTATCGTA ACCACAACCA CATCCCGGGA CCATAGCAAA GATGAGAGCG 60
AATGTACGTG AAGCACGTAG CACAGGAAGC GGTATCTCGT TGTAGTGGAA GCTGTTGGCC 120
CCGCTGCATC CCCTTTATTG GCCGGTGCAC TCATCCTCCA GCTTCTAGGA ATGTTGGGTG 180
CCAGCAACGC ACAGCGACCC CCTTTCCTGG TGCATTGCCC TGGACTGATG GGAGGTGCTT 240
GCCTAAGAGC TTGTGTCCCA TCCGCGTCCC CCCCAACTGC CCCCATTGCC ACCCGCGGGC 300
AGCCAGCAGT CACTGGCTAA CTGATGGCAG AGGCTGCTTT TATCTTGCAG TGCTCACTCC 360
AGAGCCCCCT GTGGCGTCGG GCTGGCTGGG TTCCACCTGA TGCCACACCC TGCTCAGCTC 420
CTTCCCCTGT CACTCTTGCT TCCTTCCAGG CTGCTCCCTG GAGCACACTC TTGGCATTTC 480
ACTTGTACAA CATGCCTGGC CCTGGCACGC TGCTGGTGCT GGTGTGCACA CTGATCACAT 540
AAGCTTGTGA GCATTCAGCG CTGAAGGCCA AGGATGCCTT GTGCTCTGAG AATGGGATCT 600
GCTTGGGGGC AGGAGAGACT TGGGGTCGGG GTGCGTTGCT GGGGAACAGA CAAGGGATCT 660
GTCGCCTCCT GGGAAGCTGG GAAATGGTGT GGGGTGGGGC GACTGGGAGA GGACGGCCAG 720
GGACAGCTTC AGGCCTGGTG TCCTGCAAAA CCTGACACCT AGCAGATGGG AAGATGCGGC 780
TCAGCTACCT CCTCCCGGAG CCAGGCTGAG GAGGTCACGT GGGCCCAGGA GGTTCAGCCT 840
CAGTTGGGCT GTGCTTGGGG AAATAAATCA TCAGGACTCA ATGCAGAAAA ATGACATGAA 900
TTAGGGGGCT CGTCTGGGTG CCACGCGAAC CTCTCCCTGT CTCTCCACCT TGCAGGCATG 960
CTTTTGGGTA CCGACACATG TTCCTCCAGG AGGAGTGGTG GAAAGGAGGA ATCCTTTGGC 1020
CTCCAACCCT GGAAGAAGGT GTATAGTTTT 1050
|
| |
|
|
|
