Tag | Content |
---|
EnhancerAtlas ID | HS183-04384 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr4:3496200-3498540 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr4:3496827-3496837 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr4:3496824-3496839 | CAAGCCCCGCCCCTC | + | 6.34 | SP2 | MA0516.2 | chr4:3496823-3496840 | ACAAGCCCCGCCCCTCT | + | 6.94 | SP4 | MA0685.1 | chr4:3496824-3496841 | CAAGCCCCGCCCCTCTC | + | 6.6 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_37486 | chr4:3492383-3497475 | HSMMtube | SE_40841 | chr4:3495357-3497003 | Left_Ventricle |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 3497032 | 3497267 | chr4 | 3498161 | 3498265 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH04I003491 | chr4 | 3493028 | 3499818 |
|
Enhancer Sequence | CTTTCCTTAC CACCTTGTCC TAGTCCGTTG CCCAGCCCTC TCCGCCTCCT CGCCCACCCT 60 CCACGTGGGG CCTCTGCCTG GATGCGAAGT CCCCGGGCCC GGCTTCCCTG GCCTTTATCT 120 CAGAGAGTGC GAGAGGCCTC ATCTGTCTTG TGAGCCTTGG GCCTGAATGC TGTGGTGTGC 180 GGAGAGGCAG CTCCGGGCAG CCCCCGGGCT GGGATGTGCA TGTGTGGTGT GTGCACGTGT 240 GGCACATTCC TGGGTGTGTC CTGGAGACCA CAGTGGGGTC TGCAGTAGTC CCTCAGGCAT 300 GGGGCTCCTC AGGTCCCGGT GAGGGCGGAC CTCAGGAGGG GGCTGGCTCT GAGCCCAGGG 360 CCCCTGCCCT GCCTGTCTCC CCTACATGGG GCCGAGTTCC AGGCTTGTCT CAGTCACCCC 420 TGCACATCTG TGTGGGTGCC TGCCTGCCCC CTCACCCGCC ACCCTGTTGT GGGTGCCTGC 480 CTGTCCCTTT GCCTGCCACC CTGTCAGGGA CTGACTCTGA GCGGGGAGTT CTGGAGGGCT 540 TCTGCAGCAG TGCCTGGTGA GCAAGCGTGG GCTTTGGGGA CTGAGTTTGG GCCACATCCA 600 CTACCTGCTG GCTGGGTGAC CCTACAAGCC CCGCCCCTCT CTGAGCCTCA GTTTCCTCTT 660 GCAAACGGGA TGACAGACCC CGCCTCACTG GGCTGCACTG AGGGTCTGAT GAGGTCACTC 720 TTCAGGCGCT CAATAGCTGC CCGTCACCAT TACCCCTGCT GCTGTCACCT CCGGAGGTGG 780 CCGCGCCAGT CTTGTTGCAG GACGAGTGAG GCTGTGGCTC CTTTGCTGGG GAGCCAGGCC 840 CTTCCCGCTA GTCTTCATCA TCCACGCTCA GCCCTCTGTG TTCCCACGGG TCGCCTGCCC 900 AAGGCTAGTG GGGGCAAGGT CCCTCTGATG GGACCAGACT GAAGCACCCC ACAGCGGTGG 960 CCTGGAGTCA TGGGGCCTCT TGCCTGGCGG GGCTGGGCCC CTGGACAGCC TTTCCCTGTG 1020 GGGATGCGGC CGGGACATCT GCCTCTCCTC ACGATGCTCG TGAGTGGGCC TCGCTCCGGG 1080 CGTCTGAAGG TTCCGGCCAC CGCCTGCTAC GGCAGCCCAG GGTCTCCAGC CTCAGTACCC 1140 AGTTCCCAGG TGGGTGGCCA ACAGGCTGGG GGCTCCTCCT CAGGCCAGGG GCAACCAGAT 1200 GGGACAGACA CTGGTTCTGT TTTCTTGACG GCCCTGGAGC ACCTGGGCCT GGCCAGGCAG 1260 GGGACAGGGT GGACCTTCGC TGGTTCGGGC TCTGCACCAT CCACACCTAC CCGCCTGCCC 1320 CCACCGGGAG CAGCTGGGGA GGGGCCCTCT CAGGAGCCTG TGTATGTGAT GAGCTCAGGG 1380 GGTGTCGGCC TGTTGTCAAA GGTTCTCAAA GTCTAGACCA GCTCAGTTTG CTCAGGGGGC 1440 CTCGTGTGAG GGTCCCAGCC CTGTGACTGT CTGCCCTTGA GTCTGGCCTG CACCAGTGCT 1500 AGGTGCTGAG CCCCCATTTC CGGCCTCCCA GCCCCCACCC ACGAGGCCCC TCAGAACAGG 1560 AGGGTGCTGC GCCTTCTTTC TAGCTGCCGG CTGCCGGAAC CCATGTGGGA CATTGTCTTG 1620 GGCTGGCCCC GCTTCTGCTC ATCTGGGCTG GAGGTGGGCA GGAAGCCTCT GCTCAGCCGT 1680 GGGCCGCTGT CCCTCCCGCA AGCGCCCTTC AGACCCCACC ATAGGCTCCT CCAGGGACTT 1740 GGGGCACCCC GTTAGGCACG GCCCACTTCA GAGGCCCAGG AGAAGGTCGC CTGCAGTGTC 1800 AGGGAACTTT GCTCATCTCA TCTGGGGCCT CCCAGTGGGG CATTTTCCAG GGGCACCCCC 1860 CTGCGGAGCC TTCCCCACCA GCTGCAGAGA GCAGGGCCCA CACCCTCAAG GACGGGAAAG 1920 GAAATCACAG GCACCCTCGG AGCAGCCGCT CAGCTCTGAG GTCGGAGCCC AGACACTACC 1980 TTGCATGGGC GTGGTACTCC TCCGATAAAG CTCTAATAGC AAAATAGTGG GGCTGGACTG 2040 GGCCTCAGGG CTGGGAACCG CCCCCTCCCC AGATGCCGAG GCCTCCAGCT CCCCCATGGG 2100 TGGTTATGGG GGCTACCACC AGGCTGGGTG GTCAAGGCAG TGGGTGGCCC GGAGATCTGG 2160 GGGCTGTGGG GCAAAGGGCC CTGGAGAGAA GGCATCAGGT ATGGCGGGCT GGACTCCCTG 2220 CAGGTGACCC AGGTCCCCCA GCCTGTGTCA CTCTTGGGGG GTAGTGTCCT TGTTCTCGGT 2280 GGCCCCCCGG GCACAGGATG AGGGGAAGAC TGAAGGATGC ACTGACCCAG GTTCTCTTTG 2340
|