| Tag | Content |
|---|
EnhancerAtlas ID | HS176-16558 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr17:46013010-46013840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr17:46013101-46013113 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr17:46013105-46013117 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr17:46013109-46013121 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr17:46013113-46013125 | AAACAAACAAAC | - | 6.32 |
|
| | 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 |
| GH17I047935 | chr17 | 46013021 | 46014114 |
|
Enhancer Sequence | ATCTCTTAAG CCCAGGAGGT CAAGGCTGCA GTGAGCTATG AGTGTGCCAC CGTATTCCAG 60
CCTGGGCAAC AGAGTAAGAC CCTGTCTCAA AAAACAAACA AACAAACAAA CAAACAAAAA 120
AAACGAAAGA AAAGAAAAAA AACCAAAACA ACAAAACACA CACTCAGCCC TGCTCCCACC 180
ATGTGCAAAA ATGTCCTGCA CCCTACTCAC CATACGTAAC ACCCATCATA CTGAAAAGCT 240
TAAAAAAGTG GTTTATGCAT AAACATTACA GATTAGCATT TTTTGAGCAC ACCTTGTGGG 300
CTAGGATTGT GAGAAGAAGC CAGAGAAAGT TAAGAGATGT GGTCCCTCTC GTGAAGGAGG 360
TCCCATTCTA ACAGGGAATA CCAGCCACCC ACAATGTATT TGGGAAGCCA TCTATAAGCA 420
CATGCAAGGA TCGTTTAGAG GGTTAGCCAC AAGCACCAAC AGGCAGGACA CCGATAAGTT 480
TCAGCCTCCT CTGATCTCGT CCCAAGCCTC TGAGGACCCA CCTCCCTTGG GCCTCTGATA 540
AACCCACTCA GGGCTTAGGC ATCTGCTGGC AGAGCACCAA GCACACGCCC TTCTGTAAGT 600
CCTGGTGTTG CTACTCTTGG GGCTCCAAGC TGAGTTCACT TCAAGGCTGG GCCCAAGAAT 660
TCCTGAGCTT CAGGCCCTCC AGCACACCCC TTGCTCTGCT ATCAGCCTTC TTCCTCTCAC 720
CTCTTAGAAA GCTGGACACA GGCCGGGCAT GGTGGCACAC ACCTGTAATC CCAGCACTTT 780
GGGAGGCTGA GGCAGGCGGA TCACCTGAGG TCAGGAGTTT GAGACCAGCC 830
|
