| Tag | Content |
|---|
EnhancerAtlas ID | HS184-16627 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:102857170-102857750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:102857456-102857475 | TTGCGCCCTCTAGTGGCTG | - | 7.46 | | RUNX1 | MA0002.2 | chr2:102857249-102857260 | GTTTGTGGTTT | + | 6.02 |
|
| | 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 |
| GH02I102238 | chr2 | 102854507 | 102858977 |
|
Enhancer Sequence | TTTGCTTTCT TCAATCAACA AGGCTTTATC AAGAACTTAT GGCTCTTTTA ATTATCTGAC 60
TTCCTGGTCA ATCAGCTTTG TTTGTGGTTT TAAATGACCA CAGGATAGTA GAAGTGAACA 120
TAATTTCCTG CCTGTGTAAA AGGATGACAT CAAGAGGAAA AGAAAGCAGC TCACTGGGTG 180
AAGGACCTTG AGAAAGAGAT GAACATTTCC TCTCTTGAGA CACAGGACAA ACAAGGTCAC 240
GCCTGAGCTC GGCAAACAAG GACTTCGGTG CCTGCCTACG GCGCCATTGC GCCCTCTAGT 300
GGCTGCTGAG GAACCGCTGT CCAGCCCGAA GCTCACAGAG CCCCGTTCAG GCTGCCGCAA 360
CCTACCTAGG CGGCCAGAAT GGAGACTTAC AGGTGGGCGG GCATCCCGGG GTGCACACAT 420
TACCTTCTCG GGGCTCTCCA ACTTAAGGCC AAGGATATCT TTCTTCTTTT TCGGCTGCTG 480
AGAAGGTGGA GATAGTGCCA TTTTCGAATG TGTTCCTAAC TCTTGGGCTT CTGAGACTGT 540
CGCAGTCTGT CCAAGGGTGG TGAGTGGGGA TCAGCAGGCC 580
|
