| Tag | Content |
|---|
EnhancerAtlas ID | HS030-11952 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr3:186130980-186132350 |
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: 2 | Chromosome | Start | End |
| chr3 | 186131140 | 186131200 | | chr3 | 186131407 | 186132227 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I186413 | chr3 | 186131314 | 186133044 |
|
Enhancer Sequence | CACGTGCTCT TAACCACTGT ACTCCATTAC CATGTGTGGA GTGCCTACTG GGTGCCAAAA 60
TATAGCATAA GACAGAAGCA GCCAAGGCCA TTCCCGGGGA CCCCAGACCC CAAGGGAAAT 120
GCCTTCCTTC CCCCCAGCCC CTGGAGATGT CCTTGGCTGC CTCCTTCTCA CTGTGCTCTT 180
GACCTTGGCT ACTCTTGGGC AGTACCCAAA AGACCCAGGG AACACACTTC CCCTATTCCA 240
TGTCTCTCAG GACAAATGAG GAATTACAAA TAAACCGTAT TAATTCATCT GTGAACTCCA 300
AGCCTCTGGC ACAGTACCCG GCAATATTTT ACATGGTATA TAGCACCTAA CAGGCTATAT 360
TCAAAAAATA TCAGAAGATA GACGGGAGGA GACGGTCACC ATGCCAGGCA GGGAATGTTT 420
CCAGGGAGAA CTGTAGCTGC AGGGAGTGGG ACTTATCCTG ACTGCCCTGG GAGATCGCTA 480
ATTTAGAGCA CACCAGTGTG ACAGTACATT TCTTTTGAAA TGCAACTCAA AATCCGCTTC 540
CTCCAGGAGG AATGCCAAGT GGCGTCCCGG AACAGGACAA GTTGTACTTC ACAGGAGATG 600
GGAAGCTAGA GGGGGGAAAT GCCATCATTA ATCCACCAAG CAGCAGGGGG TGGGGGCGCT 660
TGCCTCCAAC AGGCATGGCT GGAAAAATAA GCAGCTCTGG CTTGTGCTCC TCCCTGTGTC 720
CCTGCCACGA CTGTGAAGGG CTAAGAACAC AGCAGAAAAG GTTCCAGTTC ATTTACAAGC 780
CTCGGCTATT TTTAGTTCAT CGATCCCTGG GCGCGGTGTG TGTGTGTTGA GGGGGGCCGG 840
GGGACGGGGC TTGCAGAGCT CACGGTTTGA GGTGGAAGCT GGGGAAAGCT TTAGAATTCT 900
TTTCATAGAA CAGGTACTCT GTTCACTACG CACCATCCAG CCTCTGGAGA CCTAACCGCT 960
TTTCTTGGGG CAGGAAGAAG GAGCAGTGTC AGGGGAGGGA GGAGACTGAA ATGAGAAAGG 1020
GAACGAGGCA AGAGGCGGTG ACGCCCTTGT GCCAATGACC AAATTGGGTC AGAAAGAACA 1080
ACCTTTTGAA TGCAAGTCAG GAAATGTGAA TCGCTGCCTC AGCAGGGCCA GGTGCATGCC 1140
TAGTGGGTGC CGGCCCAGCC TGACCAGGGA ACTGTGACTG TACCTCCTGC CGCTCTAGAG 1200
AACCAGACCG ATGACCATCT AGAAGTGCAC TGATCTTTAT TCCTTGCCTG GTGCCCTGTG 1260
GCCAGTTCAA TTCCTATTAT CAACCCCTCC TTAAAGCTGT CAGGGAAAAG GAAGGAGAAG 1320
TTCACATTTA AAGATGGATC TAAATGGTGA AAGAGGTGAA AATCATTGCC 1370
|
