| Tag | Content |
|---|
EnhancerAtlas ID | HS042-31754 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr3:45379410-45380720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr3:45379866-45379876 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr3:45379866-45379876 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr3:45379866-45379876 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr3:45379866-45379876 | AACAGCTGTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTATAAAGT CAAAGATCAA TGTTTAACAA AAATCAAGTC AGCCTGGAAA TCTTTTATTC 60
TCCTGAGCTG TGTAGGCGGC TTTTCTGATA GGGAACGCTC ACTCTGCGTT GGCGTTTTGG 120
AGGTGTTCTG CATTTGAAAA GCACCCTGCA ATCTGCTTTC CCCCCCAACA CCCAGGCAAA 180
GTTGACGGCA TTTTCCCCTC AGTCCTTTCT ATTAGTGCCG CAGGACAAAG GTTGGTCACA 240
AAGCTCCAGA TTCACTATAT CCATCCAGCT CTGCCAAATG CAGATCACAG TTTAACAATC 300
TAACTTCTCG AGAGAGGTCT GCACTCCAGG CCCTGTGCTA AATGGGGAGG AACAGAAATG 360
AATAACGTAT GGTCTTGGCA CCGAGGACTT AGAATTGTGG AGGCAGAAAC AGACACACAA 420
ACAAAAACAT ATGACAGTAT TATGGGAGCC ACCAGGAACA GCTGTTGGAA TCCAGTTGGG 480
CACAAGGAAG GGAATGGTCC CTTCTCCTCA GTGTTATTCA GCTGGCTGTA AGTCGTGGGG 540
CTTTCCAAAG GATGGAAAAG AGGGATCTGG GACCAGCATC TCAACACACG CACTTTGTAC 600
CAAAGCTCCC AGCCCACCCA CCTTTTCCCA GGCATCTCTG CTTCCTGAGG TTTCTCTGGC 660
ACCTCTATTA CTGTGTTATC TCCAGGTTTC GGGGTCTGCT CACCCAAACC CTAGAAAGAA 720
AAGCCCAGTA CTTTCTGTGA AAGCCAGGTA GTGATGTAGA AAGTATCTAC TCTCTCAACA 780
GCAGGTACCC AAAACCCTCG TAGAGAAGCC AGCCTGGGGA AATACAATGA TAAACTTCTT 840
AAAGGCAGAG AGGGGAGGTT ACAGGGTAAG AACCCAAAGG TAATGGTTAA TGAGAGAGTA 900
AAAGGAAGTT GTTGTGCTCC TGAGAGGAAG AAGGAAAGAG AAAGGAGGCA AAGGCACAGA 960
GAAGTGGAGA GAAGCTGGAG GGTTACTGAG AGGGTGGGTC CCTGGGGTGA AGGTCACAGA 1020
AATGACCCAC ACTGGGGGCC AAAAGGAATT TCTAAGAATG AGGACGTCTG GCAGCCAATT 1080
GTAAGTCATA AACCCTTCTT CACATGCCAT CACCATCACT CTCCCAATAT GCATGCTCAT 1140
GTGCACACAC ATTTTAGAGA AGACACTATA CTCAGTAATA CTTGGAGGTC TTTTGGTCAA 1200
AAACAAAGTG CTGAGCCTCG TGCCTGGGTG AATGCCCTTT GGCACAGAGA TGGGGGCTAG 1260
ATGCAGGGGC AGGTCCAAAT TTCGTGGAAT CTGAAGCTCA GTCTGGTGAG 1310
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