Variant report

Variant	rs35314445
Chromosome Location	chr1:194026099-194026100
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs58271974	0.95[AFR][1000 genomes]
rs72644118	0.95[AFR][1000 genomes]
rs72644123	0.95[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv872834	chr1:193889533-194482304	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv872835	chr1:194014041-194051568	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv275445	chr1:194021985-194026943	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv467016	chr1:194022818-194037890	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv548665	chr1:194022818-194037890	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194020400-194030800	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr1:194020800-194030800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr1:194021200-194027600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:194022200-194030600	Enhancers	Primary T cells from cord blood	blood
5	chr1:194022200-194030800	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr1:194022400-194027600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:194022400-194029600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr1:194022400-194030800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:194023400-194027000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:194024600-194026600	Enhancers	Fetal Thymus	thymus
11	chr1:194024600-194027400	Enhancers	Thymus	Thymus
12	chr1:194024600-194030600	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr1:194024800-194026200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:194025000-194027000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr1:194025200-194029200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr1:194025400-194026200	Enhancers	Right Atrium	heart
17	chr1:194025600-194027200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr1:194025800-194029200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:194026000-194026200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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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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