| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06635 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:116678510-116679960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr11:116679116-116679127 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr11:116679116-116679127 | TTCTTATCTGT | + | 6.62 |
|
| | 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 |
| GH11I116807 | chr11 | 116678420 | 116680295 |
|
Enhancer Sequence | CGAGGGGAAG CCAGGGAGCA GGGCAGCCTG AGCCAAGGCC AAGCCCAGTT GAGGACAGGA 60
AGTGGAAGGA GGCACCTAGG AAGGCTGAAG ATGCAGAGGA GTGTGTTCCA GAGGCAGTGG 120
GAAAACTGGG AGGGAATAGT TCTCGGGATG TTGGATAGAG AGAATAAGCA AAGAACAATG 180
CAGGAAGAAG AGTGGGGTGG GAGGCCGTGA CCTTGCTAGA GAGCCTTATG TTTTGGGCTA 240
TGACCAGGGC TGACAGAAGT GTGAGGCATG GCGGGTTCAG AAGAGAGATC AATGATGCAT 300
CGCACATCTC TAAAGCTGAT GAAGGCAGCA ATTGGCACTG AGGCCAACCT GGTTGGGACT 360
CAGAGAGGTG GGACACATAT TGTGTGCCAG GCACCCTGCC ACATCTTGGA GAGAATAAGA 420
CACAAACCCT CATCTAGTGG GTTGGGGAAA TGATGCAGGG CTCAGTGTGG CTAGCGCGTT 480
GGGGTGGGAA GCAGCCTGGG CACGCCCACA AGGCTCTCTG CCTTCCAGAA TCTGGCCCAG 540
TTGGGTTTGA AAAGATTTAA TGACAATGAG CTCTCTATGG ACCTACCTTG TGCCCAGTAT 600
TTACCTTTCT TATCTGTAAC GCTCAAGTCA ATACTCTAAG GTAGGAATTG TTATCCTCAT 660
TTTATTTACA GAGAAACTGG AGTTCAGAGA GATTCTTGCC CAAGGTCTTG CCCTGGGCCA 720
ATTCCAGGTC TATCTAACTC CAAAGTCCAT GCTCAGTACA CTGTCTCCTG CTTGGGAGCA 780
AAGAGAGGAC TTTGCTCCTA AGACCAGACC CATACCACAA AGAGCCTCAA CACTTAACTA 840
CTGGGAGAAA ACACCGTCCT AAGTAAAAAG CCAGGTGCTC TTCCCCTTAC CCCAGGGGGT 900
TTAGGATTTG GGAGAAAGAG GCCTGATGGA ATATAGGGGT ACCAGGTCCA TGTGTTAACT 960
GATCTGGGTA CAAGAACAGT AACTCAAGGC CAGCCAGGGA AAGAACAGCC AAGCCGAGGC 1020
ACAGCTGCCA AGTCATCACC TCTCGTTCCT TGTCCCACCA TGCCTTGTCT CAGCACGAAC 1080
ATAACCCCCT CAGTTTCCCT CTTCTCCTGT CTCCTGCATA GGCAGAACCA GTTCTGAGTG 1140
ATAGCCAGGA CAGCAGGTCC TCGGGTCCTC AGGCTTGCCA CTACAACCTG TTTACCCTGC 1200
GCAGACCATG ATCCATCAGG TCGAGAAATG CCCCACTGCT AGATGTTTGT GTCAAAAATG 1260
CCTGCCGGTG GTGCAACAGC TGGGTGGGAC CAGTGACGTG GACTTGAGTG CCACAAAATG 1320
TACCGAACAC ATTCTGAGTC AACATAGTGA TGGTGTGCCA ACTCCAGATA AAGATTTTCA 1380
TTATTATTTG TTTGGGTTTT GTTTATATGT ACTCCTCTTC ATCACCAAAG ATTTGAGGCT 1440
ACAGAAAATG 1450
|
