Variant report

Variant	rs976417
Chromosome Location	chr6:167517835-167517836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:167516694..167518621-chr6:167521648..167524357,2	K562	blood:
2	chr6:167511835..167514028-chr6:167517104..167518840,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs149887	0.90[AFR][1000 genomes]
rs150109	1.00[EUR][1000 genomes]
rs150111	0.92[AFR][1000 genomes]
rs17550857	0.98[ASN][1000 genomes]
rs2039320	1.00[EUR][1000 genomes]
rs2236311	0.86[CHB][hapmap]
rs3093020	0.92[ASN][1000 genomes]
rs3093021	0.90[ASN][1000 genomes]
rs33985243	0.92[ASN][1000 genomes]
rs34393102	0.92[ASN][1000 genomes]
rs36226075	0.92[ASN][1000 genomes]
rs36226079	0.92[ASN][1000 genomes]
rs3756845	0.92[ASN][1000 genomes]
rs3756847	0.92[ASN][1000 genomes]
rs41427544	0.84[ASN][1000 genomes]
rs41451345	0.92[ASN][1000 genomes]
rs41479146	0.84[ASN][1000 genomes]
rs41518347	0.92[ASN][1000 genomes]
rs4710184	0.96[ASN][1000 genomes]
rs57161866	0.87[ASN][1000 genomes]
rs60646330	0.92[ASN][1000 genomes]
rs61357184	0.94[ASN][1000 genomes]
rs61582484	0.92[ASN][1000 genomes]
rs6938521	0.88[CHB][hapmap]
rs9356556	1.00[EUR][1000 genomes]
rs975821	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948634	chr6:167200671-167838993	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
4	nsv532074	chr6:167320656-167781977	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1031039	chr6:167324021-167741439	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
6	nsv538543	chr6:167324021-167741439	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
7	nsv1026972	chr6:167335031-167671042	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
8	esv2752099	chr6:167448181-167579102	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1018193	chr6:167491589-167797294	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv538544	chr6:167491589-167797294	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv469673	chr6:167500376-167658532	Flanking Active TSS Genic enhancers Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv482439	chr6:167500376-167658532	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
13	esv2758094	chr6:167501204-167845935	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	esv2759492	chr6:167501204-168176733	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167503600-167527200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:167509000-167525200	Enhancers	Primary B cells from peripheral blood	blood
3	chr6:167512600-167518800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:167512800-167518000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr6:167512800-167518400	Weak transcription	Thymus	Thymus
6	chr6:167515600-167518000	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr6:167515800-167518200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:167516400-167518000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:167516400-167518000	Enhancers	Fetal Intestine Small	intestine
10	chr6:167516400-167518200	Enhancers	Fetal Intestine Large	intestine
11	chr6:167516600-167518200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr6:167517000-167519800	Enhancers	Primary B cells from cord blood	blood
13	chr6:167517200-167518200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:167517200-167518400	Enhancers	GM12878-XiMat	blood
15	chr6:167517400-167518200	Enhancers	Primary hematopoietic stem cells	blood
16	chr6:167517400-167523800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr6:167517600-167518000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:167517600-167518200	Enhancers	HepG2	liver
19	chr6:167517600-167523800	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr6:167517600-167529800	Weak transcription	Spleen	Spleen

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