| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13614 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:87668960-87670310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:87669270-87669289 | GAGTGACACCTGCTGGCGG | - | 6.17 | | FOXA1 | MA0148.4 | chr16:87669959-87669975 | TTTTGTTTACTTAATC | - | 7.54 | | FOXP2 | MA0593.1 | chr16:87669960-87669971 | TTTGTTTACTT | - | 6.62 | | KLF4 | MA0039.3 | chr16:87669490-87669501 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr16:87669488-87669499 | AGCCACACCCT | + | 6.02 | | SREBF1 | MA0595.1 | chr16:87670189-87670199 | GTGGGGTGAT | - | 6.02 |
|
| | 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 |
| GH16I087635 | chr16 | 87668633 | 87670751 |
|
Enhancer Sequence | CGGGTGGGGC TTCAGAGGAG GAAAAGAAAC AAGGGTGTGA GATGTGCAGG CCCTGGTGAG 60
AGACAGGCAG CAGCAAGAGC CTGCCAGCCA TACTTACCCA CAAGGCCGGC TGAGGGGCTG 120
TGCTGGCCCA GGGCTCTGGC TTTCGGACCC AGACAATGCT GCTGACCAAG CAGGCCAGGC 180
GCTGAGTGAC TGTCCCAGCG GATCTCCGAG CAGGGTCCCT TGAGCATTAG GAATGCAGCT 240
TCTCAGGCCA TGCCAGCCTG GCAGAACAGG AAGGGAGGGG TACAGCCCTG TGGGGACGCA 300
GCTGTGGCTC GAGTGACACC TGCTGGCGGC CTCATCTCAT CCGCTCTCTG CGAGTCTGTG 360
GTGGTTCTAG TCGGCGTTTC ACGGGCAAGG TTTAGGGGGT TTGTTCCTCA GCTGGGGTCC 420
ACCCACGTCT TCCGACTTCC TCTCTCAGTG TTTGGGCCAT CGGTGGGTGA GGTGGCTGCA 480
GCAGAGCCGG GGGCTCCTGT GTGCGGAGGC AGCACCGACA TCCACTGCAG CCACACCCTC 540
CTGAGAGGGT CTGGAAGGAA GCAGGGCACC CTGCGAACCC ACCTTCCTCT GGGGTGTCTT 600
CCGGGGCCCC AGGGCCAGGG CAACTGGAGC AGACAGGACA TTATCTAGCT CTGGGGGCCG 660
TGCTGACCGA GCCAGACCCT CGCGGCGGCC CACAGAGATG GGCAGCTTGC GGGGCAGCTT 720
TGTCCCCCCG ACACTGGGTC CTGTCTTCAT GCACACAAGC CGCCTGTTCT GCAGGTGACC 780
AGTTAGGTTC GATGGGACAG GCTTTGGGAA TCAGCGGCTT GGGTTTGCCC CCCACAGCCT 840
TGGATCTTGA CCTTGGGAGA GGCCTCCACC ACGTGCCCTG GGGTGGGGTG GGGGCGGGGG 900
CGTCCTGCAT CTGCGCCGTT CAGCTCAGTT GCCCTCAGCC GCGGTTGGCC GCCAAGCACT 960
AGGGTGTTGC TGGCACAGCC AAGGAACTGA GCCCAGACTT TTTGTTTACT TAATCAAGCA 1020
TAAATGCAAA GGGCTGGGGG TGGCCGAGCT GATGGTGCAG GCGTGTGCGC TCAATAGCTC 1080
CGTCACAGTG GCTGTCGCTT TATTGAGCAA CCGAGGGAGC GAGGGAGAGG AGCAACTGCG 1140
GCGAGCGTGG AGGCCCAGCC CGCAGAGCTC CCGTCTGGGG GAAGCCCTGT CCCTCACTGC 1200
CTGTTCCCGG CGCTTTGGTG CCCTCTGCTG TGGGGTGATG AGGTCAGGCT ACGCAGGCAG 1260
TCACGGCAGA ACTGAAGGCC GTGTGCTTTC GTGTAGCCAA ACCCCTTTTC TTACTGATAT 1320
CAGTTATAAA ATCAGAGCTA TGTTCCCACC 1350
|
