| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17189 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:19207690-19208640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr19:19208171-19208181 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr19:19208171-19208181 | GGCACGTGCC | - | 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 |
| GH19I019094 | chr19 | 19204944 | 19208680 |
|
Enhancer Sequence | AGCCAAGATT GTGCCACTGC ACCCCAGCCT GAGCGACAGG GTGAAACCCT GTCTCAAAAA 60
CAAAAAAAAA GAGCCAAATG CAGAGAGCCA AAGGGGGTGG GCATGCTTGG TCTTTACTCT 120
GCATTTCCAA GTTCACCTCT TAAGTCCACA ATTCCACTGA AGAAAAGATA TTCTCTCAAA 180
GCAATTGGGT CAGCCCTGTT GTTCACCATA GAAACCAGAA CCCCCACTGG CCCCTAAGTC 240
CTCTCAGCTG AACCTGAAAC ACAGACCGAC CCAGCCCCAC GCAGAAATCA TCGCACTCCC 300
AGGGCCTGAC TCAGGCCGAC CGCACAGGCA GTTTTCAAAG TCCATGGGGT CAAAGGCTGA 360
GGTGGCGTCA TCTTCCAGGC CTCCCGACCT TTCCCCGGAT TCCAGGTGAC ATCTCAGAGC 420
AGCAGGCGGG CGGGAGGACT CATTCACCGG GGTCACCACC AGGTGACTGA GGCACAGGGC 480
AGGCACGTGC CTTGAAGTTT AGTGAAGGTC CCAACAGAGC TGGAAGAACA CCTGGATATG 540
GCTGTTGCTC TGCATGCCGG AGAGGAGGGG GTCTGCAACG TGGATCCCAC CACGTGGACA 600
AGCTTGAGGC AGCGGTGGCT GCTGAACCAC ACGCAGAAAT GCGCCAGTGC TGGTCACTTG 660
CCGGGCATCA CACACACATG CCCATTCTCC TCTGTACTGG CAGGCCCCAA CAACATTGCT 720
CTTGGTCCGC CTGGCCAGCC CCAAGGTGGG AGGGACTCAC TCTGCAATGT CTCTTTTCTT 780
TGGTTAAGAA GCTGAGCCTT GGCTGGGATG GTGGCTCACA CCTGTAATCC CTGCACTCTG 840
GGAGGCCCAG GTGGGAGGAT TGCTTGAGGT CAGGAGTTCG AGACCAGCCT GGCCAACATG 900
GTGAAACCCC ATCTCTACTA AAAATACAAA AATCGGCCAG GCGTGGTGGC 950
|
