Tag | Content |
---|
EnhancerAtlas ID | HS130-16044 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr20:61691070-61693570 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr20:61692005-61692023 | ATGACACGCCCCCTTCCC | + | 6.41 | KLF14 | MA0740.1 | chr20:61692006-61692020 | TGACACGCCCCCTT | + | 6.99 | KLF16 | MA0741.1 | chr20:61692007-61692018 | GACACGCCCCC | + | 6.32 | SP4 | MA0685.1 | chr20:61692004-61692021 | CATGACACGCCCCCTTC | + | 6.04 | SP8 | MA0747.1 | chr20:61692007-61692019 | GACACGCCCCCT | + | 6.27 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ACAACGGCCA CAGCATAGCC TGCAGCCAAG GGGCGAGGGC TGATCGCGAG GGCCTGTGGT 60 CATTCCTCCA CCTTCGGTGC CCTGCCTGGG CACCCCCGTG CAGCTACCAC GTGGGGAAGG 120 CACTTGGCCT CTTCCCTCAT CTGCAGACTC AGCCAACTTC TGGGGCTCCC TCGGCAGTTG 180 GGGCTAACTC AGTGGGTCAG GTGGACCCCG GCTGTGCGTG CAGCCCCCGA GAGGGTCAGC 240 AGGGGCGCGG AGGCCCCCTT GGCTCTGCTT TGTTCTGCCT GCGGCTCCGG TTGGTTTGTG 300 ATATCTTTGA TTCCATCTCT TGCCCCCATG TGACCCCATC GTCTGCCTGG CCGGGGGCTC 360 CCTTGTTGGA GTGTGGGGCG AGCCCCCACC CGTGTGGGAA GAGGAGAAGG CCAGGCTCTA 420 AGCCCCACTC AGCTCCTCGT CCTCGGAGGG GTCCTGGCCC TAAGAGGGCT TGTTGGGGTC 480 ACGCAAGCTC ACAATGGCTG TGGTCCTCAG CAGGTGGGAC AATCGGGCTG TTTTCCGATG 540 GTGTTTGGCA GAAAGTGGGA GTCAAAGCTT AGAAAAGCCC TGACAGAAAT GGTTCCCTGA 600 GGCTGGCGGG AGAGTGGCAC TCGGGATATT AAAACAGCGA AGTCGGTCCT GGCCAATTAT 660 CAGCCAGCTG GCCTTGCTCC GGCGCCCAGA GCTCACAGGG TGAGTCACCA TCTGCGGCTG 720 AGCATCCCTG TTCAGTGAGG GAGACAGATC CTGTCCTGGT CCCTCCTCCC AGCTGTTTGT 780 GGCCTCCCTC CTCAGGCTGC CTGGGAAGCT GTTTCAGAAC CTTCCAGTCC CCTCCTGGCT 840 GGCCCTGGGG CTCTGTGGAA GTCCTGCTTC CCCCAGCAGT GCCTGGCCCT TTGTCCCCGA 900 CCCAGGAAAA GGTGAAGTGG GGGTACTTCC TGTGCATGAC ACGCCCCCTT CCCTTCTCCC 960 AGCCTCCTGC CTCGGGGCTC TGGCAAGAAA GAGGGCCTGA GCTGCAGGAG AAGGGCTTCC 1020 TTGAGCAGGA AGAAGCCCTG GCCCAGGGCA GGGTGCCCGG AAGGCGGAAG GATCCCAGCC 1080 CAAGCCACAG CCCCACCAGA TGGGTGGGGG CCTTCATCAC AAGAAAGATC AGAGAGTTGC 1140 CCTCTGAAGC CTTCGCAGTG GCCCTGACAC AGGCTGCCAG GGATCCGTCA CTCAAGGGAA 1200 GGCCCTGGGG GTGGGGGGCT CTGGCAGGGG TGACCACAGT GGTTAGGGGC CTGGGTGAGA 1260 AAAGGGACCC CTGATGTCCC ATCAGGGCCG GGAGGGGAAC TGGAGGACCT CCTGGCACTC 1320 CCTGGCCCCT CCTCTGGTGC CTAGCACCTT CCAGTGCTTT TCCCAAGAGG AAGGGAGAGC 1380 CTGGTTTCAT TACTAAGCCC TCCATGTCCT GTCCGTGTCC GTGTCCTGTT TGTGTCTGCG 1440 TCCTGTCTGT GTCCATGTCC TGTCTGTGTC CGTGTCCTGT CCGTGTCCTG TCTGTGTCCT 1500 GTCCGTGTCC TGTCCATGTC CACGTCCTGT CTGTGTCCTC TCCGTGTCCG TGTCCTGTCC 1560 GTGTCTGTGT CCATGTCCTA TTCATGTCCG TGTCCTGTCC GTGTCCTGCC TGTGTCCGTG 1620 TCTGTGTCCT GTCCGTGTCC TGTCTGTGTC CGTGTCCTGT CCATATCTGT GTCCGTGTCC 1680 TGTCCATATC TGTGTCCGTG TCCGAGTCCG TGTCTGTGTC TGTGTCCATG TCCATGTCCT 1740 GTGTCCGCGT CTGTGTCTGT GTCCATGTCC ATGTCCTGTC TGTGTCCATG TCTATGTCCT 1800 GTCCGTGTCC TGTCAGTGTC CTGTCTATGT CTTGTCCATA ACCTGTCTGT GTCCGTGTCC 1860 TGTCCATGTC TGTGTCCTGT CTGTGTCCTG TCTGTGTCCG TGTCCTGTCC ATGTCCATGT 1920 CCTGTCCGTG TCTATGTCTT GTCTGTGTCC ATGTCCTGTC CATGTCTGTG TCCGAGTCCT 1980 GTCCATGTCC ATGTCCATGT CCTGTCCGTG TCTGTGTCCA TGTCCGTGTC CTGTCCGTGT 2040 CTGTGTCTGT GTCTTGTCCA TGTCCGTGTC CTGTCCATGT CCTGTCTGTG TCCGTGTCCT 2100 GTCCATGTCC GTGTCCTGTC CGTGTCCGTG TCCATGTCCA TGTCCTGTCC ATGTCCGTGT 2160 CCTGTCCGTG TCTGTGTCCA TGTCCGTGTC CTGTCCATGT CCGTGTCCTG TTTGTGTCCT 2220 GTCTGTGTCC GTGTCCTGTT TGTGTCCTGT CTGTGTTCGT GTCCTGTCCA TGTCCATGTC 2280 CTGTCCGTGT CTGTGTCCAT GTCCTTGTCC TGTCCATGTC TGTGTCCTGT CCATGTCTGT 2340 GTCCTGTCTG TGTTCGTGTC CTGTCCATGT CCGTGTCCTG TGTTCGTGTC CTGTCCATGT 2400 CCGTGTCCTG TCTGTGTTCG TGTCCTGTCC ATGTCCGTGT CCTGTCTGTG TCCATGTCCT 2460 GTCTATGTCC GTGTCCTGTC CGTGTTCTTC TTCACCCTGA 2500
|