| Tag | Content |
|---|
EnhancerAtlas ID | HS105-57587 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr3:135969400-135970360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr3:135969976-135969986 | GGCACGTGTC | - | 6.02 | | Npas2 | MA0626.1 | chr3:135969976-135969986 | GGCACGTGTC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGAGTCCTG AGGGGCCTAA GTGAGTCCCG CCCCTGGCGT CCGCGACCTA TCACTGCGTG 60
CCCGGCTTGC GGCGTCCGAG GCCTCCCTGC CAATCCGCAC GGTGCCTGGA GGGGCCGGAG 120
CAAGGGTGTT CACCTTGAAA ACCTGTAGCG TTTCTCGTGG AGGCGGGTAT AACCAGCAGA 180
AGCACCTGTG TGCTTTTTCA TACTGTTTAA CCCTTGGGAT TTAGACGGAT CTGGCTCGTC 240
TCTAGCCAGC TCAACACTTA ACATAAGCTT TTGGGCAACT TATTAAATCT CTGTGGGTCA 300
TTTTAATAAT AATTCTTCCT TCACAAGTGT ATCGTTAGAC CATAGATAGC AAAATGATAG 360
GCGCTCAGTA AAAACCATGT GCTTATTCTC GTGCCCCATG AAAGAGTGAT GGTAGGTTCT 420
TTCTCCTTTG TGGAAGCAGG AAAACTGAAC TTGGGCATAC TCCACTAACA TGAAATGGGG 480
GATGTGCGCG TGCAGGAACT TGTGGAACTT CTGCCCGCAG AATGCCTGGT CGAGCTCTTT 540
AGGGCCTTAG CATGCCTCGC CTTGATGGGT AGCAAAGGCA CGTGTCGGAA GCAGGTGGCC 600
TTTCTGGGAG TGCGCAGGCT ACTCTCGATG TTTGGCTGGA CTGAGCAGTT GAAACACTGC 660
CACCCACCGC CTGGGTTTTG AGGCGAGAAT CCAGCTGGCC TTCAGAGATA AGCTGGGCGG 720
CCCATTTTGG AGAGGTGATC CCTGACTTGA AACCAGGCTT GCCCAGTGTG TCCGTGACTG 780
GTGGGTGAGT CTGGACCGTT GTGCTGAACG AATTAACCAA CGGGAAGGTG CAGAAGTGAA 840
ACTCTTACAG ATGAAGAGTA TTCAGGCACA ACTCACAACC ATGAGGGAGG CACTGGGGGA 900
GGGATGGGGT CTTAAAGTGA GGAGATTTGA ACAGCTCTAT ATTTGTCTAA TATTGATTCA 960
|
