| Tag | Content |
|---|
EnhancerAtlas ID | HS034-22075 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr3:186131220-186132420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr3:186131764-186131776 | GCTATTTTTAGT | - | 6.18 | | MEF2B | MA0660.1 | chr3:186131764-186131776 | GCTATTTTTAGT | - | 6.62 | | MEF2C | MA0497.1 | chr3:186131763-186131778 | GGCTATTTTTAGTTC | - | 6.41 |
|
| | 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 |
| GH03I186413 | chr3 | 186131314 | 186133044 |
|
Enhancer Sequence | TGTCTCTCAG GACAAATGAG GAATTACAAA TAAACCGTAT TAATTCATCT GTGAACTCCA 60
AGCCTCTGGC ACAGTACCCG GCAATATTTT ACATGGTATA TAGCACCTAA CAGGCTATAT 120
TCAAAAAATA TCAGAAGATA GACGGGAGGA GACGGTCACC ATGCCAGGCA GGGAATGTTT 180
CCAGGGAGAA CTGTAGCTGC AGGGAGTGGG ACTTATCCTG ACTGCCCTGG GAGATCGCTA 240
ATTTAGAGCA CACCAGTGTG ACAGTACATT TCTTTTGAAA TGCAACTCAA AATCCGCTTC 300
CTCCAGGAGG AATGCCAAGT GGCGTCCCGG AACAGGACAA GTTGTACTTC ACAGGAGATG 360
GGAAGCTAGA GGGGGGAAAT GCCATCATTA ATCCACCAAG CAGCAGGGGG TGGGGGCGCT 420
TGCCTCCAAC AGGCATGGCT GGAAAAATAA GCAGCTCTGG CTTGTGCTCC TCCCTGTGTC 480
CCTGCCACGA CTGTGAAGGG CTAAGAACAC AGCAGAAAAG GTTCCAGTTC ATTTACAAGC 540
CTCGGCTATT TTTAGTTCAT CGATCCCTGG GCGCGGTGTG TGTGTGTTGA GGGGGGCCGG 600
GGGACGGGGC TTGCAGAGCT CACGGTTTGA GGTGGAAGCT GGGGAAAGCT TTAGAATTCT 660
TTTCATAGAA CAGGTACTCT GTTCACTACG CACCATCCAG CCTCTGGAGA CCTAACCGCT 720
TTTCTTGGGG CAGGAAGAAG GAGCAGTGTC AGGGGAGGGA GGAGACTGAA ATGAGAAAGG 780
GAACGAGGCA AGAGGCGGTG ACGCCCTTGT GCCAATGACC AAATTGGGTC AGAAAGAACA 840
ACCTTTTGAA TGCAAGTCAG GAAATGTGAA TCGCTGCCTC AGCAGGGCCA GGTGCATGCC 900
TAGTGGGTGC CGGCCCAGCC TGACCAGGGA ACTGTGACTG TACCTCCTGC CGCTCTAGAG 960
AACCAGACCG ATGACCATCT AGAAGTGCAC TGATCTTTAT TCCTTGCCTG GTGCCCTGTG 1020
GCCAGTTCAA TTCCTATTAT CAACCCCTCC TTAAAGCTGT CAGGGAAAAG GAAGGAGAAG 1080
TTCACATTTA AAGATGGATC TAAATGGTGA AAGAGGTGAA AATCATTGCC TTAAAAGAGA 1140
TCACCTGTGG ATTTTGTGAG TTATTAATTC TATGATCCCT ACCGTGTCTG ATTCTGATTG 1200
|
