| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08457 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:109987450-109988350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr12:109988280-109988295 | AGGTCACCTTGCCCC | + | 7.16 | | NEUROG2 | MA0669.1 | chr12:109988119-109988129 | AACATATGTC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 109987636 | 109988075 | | chr12 | 109987550 | 109987600 |
|
Enhancer Sequence | GCACTGAAAA AACAAAAACA AAAAAGCCAA AAAAAAAAAA AAAAAACTCT TGCAGCTCCA 60
CCAATGTGTC TATTTCCTTC ACAAAAATTC TCAGACACAG AGTTGCAGGA CTGTAAGGTA 120
CACACCTCTC TAGGACTTTC ATGCACATTG CCAAATTGCC CTCCTGAAAG TTCATACCGA 180
TCTCCACTCC CTGCAACCGT GAGAGTCAAC ATTTCTCTCT CCCCGCTGAA GTCAGCAGGT 240
GGAAAGCCAT AGGCTCAGGA CTCTTTCCAG CTGCTGGGAT CCTGCAGCTG GACCCCCGAG 300
GGCCATAGAA ATACAGTTCT CTCTCTTCCA CTCCCCAGTC AAAGCACCTT GAGAGAGTCC 360
CTGGCCGGGC CGGGGCAGGG TCCTGAGACC ACCTGGCATG CCCACTCGCA GCCCTTACCT 420
CCTCCCTCTC CCTGTGCACG CCTGGATGTC TTTTCTCAAG GCCCGATGCT CACACCGTGT 480
GGCAGGGTAG CAAGCTTTTG AGTTATAGTG AACCTTATTT CCCTCTACAG CTCCCACGGA 540
GTTAACAGAT GTACGCACGT CTGAGGCAGT CATGCGGCAA GAGACTTTGG GCCCAATCCT 600
TTCTGTTTTG ACAGTGTGTA ATCGAGGTGA AGCCATAAAT TTTATAAACA AGAATAAACG 660
ACCCTTAGCA ACATATGTCT GCTTGACCCT TCCAAGGTGA TTGTAAATAA AGGCACCTGC 720
TGACCAGTGA GGGCCATCGG CACTGCAGAT GGACAGTGAT GAGAGCCGAA GGACCGGTGC 780
CTTGGGAGCT TGCACTGGGA GGCATTTCGG CAGTGAGGGG CGGGGGGAAG AGGTCACCTT 840
GCCCCCCGCT CGGGTCCTGA GTCAGTTAGA CACCTTCATG CTACTTATGT ACTCCGTTCT 900
|
