| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13659 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:44017750-44018910 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr17:44017855-44017868 | CAAATGATGTCAT | + | 6.18 | | JUND(var.2) | MA0492.1 | chr17:44017854-44017869 | TCAAATGATGTCATC | + | 6.16 | | MEF2A | MA0052.3 | chr17:44018544-44018556 | TCTATTTTTAGA | - | 7.22 | | MEF2C | MA0497.1 | chr17:44018543-44018558 | CTCTATTTTTAGATT | - | 6.09 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_03683 | chr17:44016721-44019722 | Brain_Angular_Gyrus | | SE_05693 | chr17:44016402-44028022 | Brain_Cingulate_Gyrus | | SE_07407 | chr17:44016244-44028031 | Brain_Hippocampus_Middle_150 | | SE_68134 | chr17:43999844-44033224 | TC32 | | SE_68411 | chr17:43970687-44036061 | TC71 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTCAGAGTCC TCATCTGTGA GTTGGGGAAT CTGGACAGAA TCTACCCCAT AGGGCGTAGT 60
GAGGATGTGT TGAATTATCC CAAGTGGCTA CACAGAGTAA GCACTCAAAT GATGTCATCG 120
TTGTCATGAT TGCTGTTACC AGAGCCTAGA GTTCATTCTG ATACTCGAGT CTGTGGCCCA 180
TCCAGCCCAG GTAAGGAATA GTTGGAGGAG TTGGGCATGT TCAGCTTGAA GAGGAGACGA 240
CAGGGGATAT GGGATAGTTG AATCTGTGAA GGGCCCCCTG GGATGAAGAA CTGGCATGTT 300
CTGTGTGGCT CCAGGGCACT GAGCAGGACC CATTTGCCAA AGTCTCAGGG ACACAGTTTC 360
TAGCTATAGA CAGAAAAATT TTCTGTCACT CAGAGGATGA AAATAGAATG AGCCCCCTTA 420
AGAGGTAATG AGCTCCCTGT CATTGGAAGG ATTCCAGAAG AGCTAGGTAA CCACTTTAGG 480
TGCTATCAAG GGGCTTTTTT CTTTAAAGTC CTTTCCAAAA GCTTCTGAGA TTGCATAAAC 540
AATAGGAAGC CATCTTGGTG CTTTAACACA AACTCTCCCC AGTGATGAGG GTTGAGCCAA 600
AGCCAGATTG GCAAGCAGAG AGGAGACTTG TGTACAAGGA GTTCCTCGAG TCAATTGCTT 660
TTTCCTTGTT CTAGCCAGCC AGAGGGCTCC TGTTGGAAAA CAGGAGACCG GAGAGGCTGA 720
GGCCTGACCA AACCAGCTTC TGCAGGCCAG CTGGGAGGCC ACAACTCCTA CCTACGGGAA 780
AACTGAAGGG CATCTCTATT TTTAGATTAG CAAAAGAAAA TAAATTTAAG TTTGAGTCTC 840
CTTTGCAACT TTTAAAAGAC ATCTTTATTG AGATGATCAT TCACATTCTA TAAAATTCCC 900
CCACTTTGAG TTACAATTCA GTGGTTTTAG TCTTCCTTGA TGATTTTGAT GGTCTTTTCT 960
TAAGGCTCTT GGAAGACCCA GAAGCCTCTC AGACACAGGT GGGTGTGGAG GGCGTAGCAC 1020
AGAGGCAGAC TTCTCATTTC CTGGGTCTCC CCTTTAATGA CTCTCAGAGA CCCCTCCTTC 1080
CCCCTGCCCC TGGCTTCTAC CCCAGGGGTG TAGAGTTTTG CCATTTTCCA AGCAGAACTT 1140
CATTTCCTCT TCTGTGTCTA 1160
|
