Variant report

Variant	rs2605442
Chromosome Location	chr3:59775628-59775629
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs1352020	0.82[EUR][1000 genomes]
rs780359	0.82[EUR][1000 genomes]
rs780360	0.82[EUR][1000 genomes]
rs780361	0.82[EUR][1000 genomes]
rs780362	0.82[EUR][1000 genomes]
rs780371	0.87[AFR][1000 genomes];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014601	chr3:59666609-59888166	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv1003387	chr3:59756364-59831340	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv460562	chr3:59760118-59826778	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv590381	chr3:59760118-59826778	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv590382	chr3:59763809-59793062	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
6	nsv460563	chr3:59772342-59827390	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv590383	chr3:59772342-59827390	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59760400-59776000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr3:59769800-59791400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr3:59770000-59779000	Weak transcription	Thymus	Thymus
4	chr3:59770200-59775800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr3:59770400-59775800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:59770400-59776600	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr3:59770400-59825200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr3:59770600-59776200	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr3:59773000-59776000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr3:59773400-59775800	Weak transcription	Fetal Heart	heart
11	chr3:59774600-59775800	Weak transcription	Primary T cells from cord blood	blood
12	chr3:59775400-59777200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr3:59775600-59776200	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr3:59775600-59777400	Enhancers	Fetal Thymus	thymus
15	chr3:59775600-59777400	Enhancers	Dnd41	blood

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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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