Variant report

Variant	rs534731386
Chromosome Location	chr11:18165223-18165224
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	esv11709	chr11:18138662-18200717	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3509521	chr11:18159957-18188401	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv3509522	chr11:18159957-18188401	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv3367251	chr11:18159957-18196082	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv518373	chr11:18164687-18195348	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv975090	chr11:18164912-18189697	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv1949763	chr11:18165006-18165493	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
9	esv3520283	chr11:18165133-18165363	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
10	esv3520281	chr11:18165145-18165340	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
11	esv3324860	chr11:18165165-18165310	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
12	esv3475497	chr11:18165185-18165290	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
13	esv3520282	chr11:18165195-18165312	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
14	nsv39555	chr11:18165199-18165285	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
15	esv3475509	chr11:18165199-18165310	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
16	esv3520284	chr11:18165199-18165310	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
17	esv1004442	chr11:18165203-18165289	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18157200-18165600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:18164000-18166000	Enhancers	HMEC	breast
3	chr11:18164800-18166600	Enhancers	NHEK	skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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