| Tag | Content |
|---|
EnhancerAtlas ID | HS073-10668 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr3:150888210-150889420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr3:150888233-150888245 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr3:150888233-150888245 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr3:150888232-150888247 | TTCTATTTTTAGTAG | - | 6.57 | | Nr2f6(var.2) | MA0728.1 | chr3:150888281-150888296 | TGAACTCTTGACCTC | - | 7.64 | | RARA | MA0729.1 | chr3:150888278-150888296 | TCTTGAACTCTTGACCTC | - | 6.45 |
|
| | 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 |
| GH03I151168 | chr3 | 150886389 | 150890033 |
|
Enhancer Sequence | TGCCACCATG CCCGGCTAAT TTTTCTATTT TTAGTAGAGA TGGGGTTTCA CCATGTTGGC 60
CAGGCTGTTC TTGAACTCTT GACCTCGTGA TCCACCCACC TCAGCCTCCC AAAGTGCTAG 120
AATTACAGGC GTGAGCCACT GCACCTGGCC TGGAATGTGC TAATTCTTTA CTCTCCCTCC 180
CTGTTGCCCT TTACCGCCCC ATTTCCTTGG CCACTGTTTC TGTGTCTGGG CTTTTGGGTA 240
TAATGGCAAG GGAGGTGAAA ATAAAAATCT CAAAAACCTG AGTGTTTCCT TATTCTAGAT 300
CTGTGCTGCT TAGTTTTCCA TTCAGAGTAG TGTGAGATAT AAAGATGGTA ATACTGAGGT 360
CAGGGCTCAT GTCCCACAGT GGCCAGGCAG GTAGTGGGAA TGAGTCGGGG GATGCTATGT 420
ATAAGGCAGC CTGGAGGTGG TGGGGGTTGA GGTGTCTGGG AAGTGGGCAG ACCCTGTCTG 480
AAGAGGGAAG CCTCTCAAAT TCTTAGATTC TGCTTGGGAT CCACTGTTCC CTGATCATCC 540
AACATTTCAA GAGAAGCTGG ATGTCAAGAT CTGCATGTAA ACTTTCCTGA TTTTAAAATA 600
CTGTGCAGCC AGGCAGTGTG TCTGCTGGCC ATATTCACTC AGATGCTTGT CACTTTTCAA 660
TTCCTGGTAC ATGTCTTCTA CAACATGTAC TCACTTATTT GCTTGTTTAG TGTTTCAGAG 720
CCATTTCTAG TCTGGGTGAT GGAGGTGGCA AATCCTGACA TCCACACAAA GGAGTCGTTA 780
TGTGGACAGT GGGACCCCTG GTTTCCACAT GCTCACTGAG CCTGTCACTT GTGACCTCAC 840
CTCTGAGCAG CTGGAGGAGG AGTTGCTCTC TTTGCTTTTC AGAGGCCTCA GACCACTTCC 900
TTCCTCTTGG CATCTCTCTG TTTGGGATGA GTGTGAGCAC GGAGGCAGCT GCATCTTTAG 960
GGTGCCTCAA GGACATGGAT AGAAGGGACA GGCTAAAGGT GGCAGGAAGA GCTGCCTTTT 1020
CACTTCTCTC TTTGGGGGTC CCAGGAAGCC AGCTTTATCC TGAGTAATGA AAAGATGGAA 1080
CCGGCTGCAC TGGACAGAGT GTTCCTGCAG CAGCATGTGT GTTTCCTCCT TCCCTGCTGC 1140
TAAAACCACA CACCCCAGAC GGGGAAACTT ACATATTTAT TGTTTGGATT TGTTTTATGC 1200
TTAGACTATT 1210
|
