Variant report

Variant	rs10929614
Chromosome Location	chr2:9923308-9923309
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:9916325..9919455-chr2:9921227..9924824,4	MCF-7	breast:
2	chr2:9921109..9926354-chr2:9930407..9935197,5	K562	blood:
3	chr2:9920939..9923701-chr2:9941195..9943026,2	MCF-7	breast:
4	chr2:9694755..9696304-chr2:9923143..9926045,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000271855	Chromatin interaction
ENSG00000151694	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10186112	0.89[EUR][1000 genomes]
rs11674480	0.93[GIH][hapmap]
rs11887400	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11896311	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1515326	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2357266	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2357267	0.81[CHB][hapmap]
rs4669455	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4669456	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4669460	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669461	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6432035	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6712066	0.86[EUR][1000 genomes]
rs7599932	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7605035	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469405	chr2:9814374-9964947	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv580930	chr2:9814374-9964947	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv1003026	chr2:9854939-10012516	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv470443	chr2:9857018-9975557	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv873619	chr2:9870631-9956981	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1013969	chr2:9888703-10023951	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv873620	chr2:9906145-9951970	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv524327	chr2:9913515-9954768	Bivalent Enhancer Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv948591	chr2:9922257-10141191	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
10	nsv580931	chr2:9922283-9927532	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
11	esv3486179	chr2:9922334-9929480	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9915000-9924800	Weak transcription	Left Ventricle	heart
2	chr2:9917800-9923600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr2:9918000-9923400	Enhancers	Fetal Intestine Large	intestine
4	chr2:9918000-9923400	Enhancers	Fetal Intestine Small	intestine
5	chr2:9918200-9924000	Enhancers	Primary T cells fromperipheralblood	blood
6	chr2:9918600-9923600	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr2:9919000-9923400	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr2:9919400-9927000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:9919800-9923400	Enhancers	Placenta	Placenta
10	chr2:9920200-9923400	Enhancers	HMEC	breast
11	chr2:9920200-9924000	Enhancers	Primary T cells from cord blood	blood
12	chr2:9920600-9924200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr2:9921000-9923400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:9921600-9923400	Enhancers	Duodenum Mucosa	Duodenum
15	chr2:9922000-9923600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr2:9922000-9923600	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr2:9922200-9923600	Enhancers	Fetal Thymus	thymus
18	chr2:9922600-9923400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr2:9922600-9923400	Enhancers	Esophagus	oesophagus
20	chr2:9922600-9927200	Weak transcription	GM12878-XiMat	blood
21	chr2:9923000-9923400	Enhancers	NHEK	skin
22	chr2:9923000-9923600	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr2:9923000-9923600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr2:9923000-9924200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr2:9923000-9927000	Weak transcription	Fetal Kidney	kidney
26	chr2:9923200-9924000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr2:9923200-9927000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:9923200-9927000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr2:9923200-9927000	Weak transcription	Adipose Nuclei	Adipose

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