Variant report

Variant	rs535513285
Chromosome Location	chr11:106215212-106215213
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048381	chr11:105945117-106561574	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2754854	chr11:106092790-106245790	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1054471	chr11:106168484-106427713	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1041862	chr11:106210820-106238696	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2760288	chr11:106214708-106238708	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106214200-106215600	Enhancers	Fetal Brain Female	brain
2	chr11:106214400-106215400	Enhancers	Fetal Brain Male	brain
3	chr11:106214600-106215400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
4	chr11:106214800-106215600	Enhancers	Fetal Intestine Large	intestine
5	chr11:106214800-106215600	Enhancers	Fetal Intestine Small	intestine
6	chr11:106215000-106215400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:106215000-106215600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:106215000-106215600	Enhancers	Muscle Satellite Cultured Cells	--
9	chr11:106215200-106215600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:106215200-106215600	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr11:106215200-106215600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:106215200-106215600	Enhancers	NHLF	lung

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Input of quick search could be:

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

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