Variant report

Variant	rs17061347
Chromosome Location	chr3:59873472-59873473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs17061336	1.00[AFR][1000 genomes]
rs17061337	1.00[AFR][1000 genomes]
rs17061338	1.00[AFR][1000 genomes]
rs17299290	0.89[AFR][1000 genomes]
rs17365142	0.89[AFR][1000 genomes]
rs17365190	0.89[AFR][1000 genomes]
rs4368451	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv460564	chr3:59821071-59927727	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv590384	chr3:59821071-59927727	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv460565	chr3:59842644-59877988	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv470616	chr3:59842644-59877988	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv590385	chr3:59842644-59877988	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv590386	chr3:59846067-59912377	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	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	chr3:59868800-59882600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:59869400-59873600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr3:59869400-59873800	Enhancers	Primary hematopoietic stem cells	blood
4	chr3:59870200-59874000	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr3:59870400-59873600	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr3:59870400-59874000	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr3:59871400-59879200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr3:59871800-59873800	Enhancers	Primary T cells from cord blood	blood
9	chr3:59872400-59873800	Enhancers	Fetal Intestine Small	intestine
10	chr3:59872600-59874000	Enhancers	Fetal Intestine Large	intestine
11	chr3:59872600-59880600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr3:59872600-59880600	Weak transcription	Fetal Thymus	thymus
13	chr3:59872600-59884200	Weak transcription	Dnd41	blood
14	chr3:59873200-59904200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr3:59873400-59873600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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