| Tag | Content |
|---|
EnhancerAtlas ID | HS105-57052 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr3:121714000-121714860 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:121714563-121714582 | TAGCTCCCTCTTCTGGCCA | - | 6.92 |
|
| | 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 |
| GH03I121994 | chr3 | 121712875 | 121715130 |
|
Enhancer Sequence | CATTTCGTTG TTTTTGTTTG TGCTTTTCTA TTTTGGGGTA GTTGTGGCTG AGTGCCTCAT 60
GTTTCCTAAG GGCTCTGCCT ATCCACGCGT GTTGGACGTG TGCCTGTACG TTAAGTGCAG 120
GAAGTGCCAG CCTCAGTGTG AACGAGGTTA GGCCCCAGCC TGGCATTCTC AGTTCCTCCT 180
TGCTTCCCTG GGCCCTGTGG CCACCCCTAA AACAGCAGGG CCACGTACAG TAGAAGGGGG 240
CAGAAAGCTG GCATCCTGAA CACAGCCACA TAGGGTGTAG GGTTTGCCAA GGCCAGCAGC 300
AAAGGGGTCA TCCAGTGGGC TGCTCAGTGA TTCCAGTATG AAACTTCCAG CACAACAGGA 360
AGTGGTTGTA ACAGAGTCCC CAGAAATGTC CGGAGCTCCA ACCCTCAGTG TGAGTCACAG 420
CCTAGCCTGG AAGAAATCAG AGGCAAACTT GCAGCAGCTC CCCCAGCAGC TACACCTTCA 480
TGCCAGCTGA TCACCTGGAG CCTCCCTGAA GACAGGTCCA CAGGCTCAGC ACTGCCCTCT 540
CCCTCTGCAG AGATGCCTCT CCCTAGCTCC CTCTTCTGGC CACCACCAAC ACACATACTG 600
GAATGCCCAG CCTTATACAT GTAATTTACT TTACATAAGC TAACTAGTTC TCTGAAAAAT 660
CTCTTCACGT GGGAATCCAA TGAGGAAGCT GGGCTCAGAG AGATTACCTT CCCAGCCTAA 720
GGTCCTACAG CTAGCGACTG GCAGAGCCAG GGTGTGAACC TGTGTGACGC TCAAGCCTAC 780
ACTCTTTGTG TGCCGCACCG CCAAGTCCCC AGACTCCTTT ATTTTCTGTG ATGAAGCAAA 840
AAACCTTCCC TGCAGGCACC 860
|
