| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08715 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:122070360-122071570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr12:122070680-122070692 | TCTATTTATAGA | - | 6.74 | | Pou2f3 | MA0627.1 | chr12:122070439-122070455 | CTGTATGCAAATTCAG | + | 6.46 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_19932 | chr12:122069661-122071593 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22457 | chr12:122069659-122071671 | CD8_primiary | | SE_49991 | chr12:122069663-122070954 | RPMI-8402 | | SE_53935 | chr12:122069702-122071588 | Spleen |
|
| | 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 |
| GH12I121631 | chr12 | 122069807 | 122071506 |
|
Enhancer Sequence | CAGCTAGTAG AATTCCAGCT CTGGTCTTTC TGGCTGGGAG CCAGTTGAAG AGAAAGTCTG 60
GGTCTGTGTC CCGCTGACCC TGTATGCAAA TTCAGCCTAT TCATGGCTTG TAACAAATTT 120
ACTAAGTTGC AACCAACACA TTTTGTTGTT TCTTTCTTTT GATAACTTTG GTACCAAGCT 180
CCTGGTCCTT TTTAGAATGA GATAAGGGTG AAATGAAACA AAGTCGCAGC ACGCATTGCA 240
TCTTGCAAGA CCTTACTGAT GTGCTGTAAG GCTAAATGTT GATTGGTTAA ACTTTTGTTT 300
CTGTTATAAA CGCGTGTGTG TCTATTTATA GAAACATTTG GAGTCCTGGA CTGTCATGGT 360
CAAGACTTTG TAAACCACTG CACACTAGGC CTCAATACCC TCTTAAGAGA TGGTTTGCAT 420
TTGAGGTGGG GCCGGCAGGC TCAGACAGCT CCGGGTGACC CTGCATGGTT GCGGCCTAGA 480
GGGCCTCATG TTCCAGGCTG CAGCCACCCA CCCTCCTAAA AGGGTGGACA AGAAAAGAAC 540
TAGGCCAGGG GAAGGAAGGC TGTGGGACCT GAGGTCAGGC CCAGCATGGG AGGGCTGCCT 600
CAGAGGGCCT GGACTTGCAG GCGCCAGGTG CCCAGGGTCT CCATGGAGCC CAGCAGGAGC 660
CAGGAGAGAT AGCTGGCAAT CAGGCGAGGT GGGCTGACGG CTGGTATGGT CCGTCAGGGC 720
CAGCCAGGCC TTGCCCTTCG CAGAATTATG TAACCCTCTT CTTGGCCCTT GCTAAGGTTT 780
GGCATCTCTA GCCAAAACCC TATTGGGGGG ATCCATGGAC CAGTGTGAGG TGGAGCTGGT 840
GGTCTTTTGC CTTTCCTATC CCTTATAGGG CTTGCCTCGC CAGGTTCAGG CGGCCAGTGG 900
CTGGCGGGGG GCTGTTTATT TTGGGCTGAC GGGCTATATT TACCTTGTGA AGCTGCGTGC 960
GATCTGATCT GATCCAATCT TGCTGGGGCT CAGCTGGGGC TCTGGCAGTC AGCTGCCAGA 1020
TCTGTAGGGC CCCTGGCCCT CCCCCTGCCA CCCAAGGGGA GATTTCCAGA GCAGGAAGTA 1080
TCCTGGAAAA AGTGGTGGCA TTTATTCCTG TGACTTTTTC ATCAAGCTCC ATGACACATG 1140
CCAACCGTTC CTTTCTTCTC ACTTTTTTTT TTCCCAGTTG CAAGATTTTA TTAAAATTTT 1200
TTTTGTTTGT 1210
|
