Variant report

Variant	rs2684929
Chromosome Location	chr15:34368766-34368767
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:34362589..34365348-chr15:34368462..34371323,3	K562	blood:
2	chr15:34361453..34364220-chr15:34368679..34370797,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10775220	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11630826	1.00[YRI][hapmap]
rs12917199	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1865924	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2243764	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2257058	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2632074	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2632089	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2684938	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2684942	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2684948	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2684949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2684957	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2702275	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2705351	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2879445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4411478	0.96[AFR][1000 genomes]
rs4780200	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4780201	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4780202	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs486970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs499142	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs527470	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs537920	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs542890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs545484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs547824	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs572179	1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs591999	1.00[AMR][1000 genomes]
rs612992	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs643827	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6495507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6495516	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs681873	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs682484	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs683417	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7162728	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7494971	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8027337	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8030334	1.00[YRI][hapmap]
rs8041507	1.00[AMR][1000 genomes]
rs919470	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv903985	chr15:34279319-34370487	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	nsv1035579	chr15:34363159-34501115	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34354200-34372400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr15:34354200-34375600	Weak transcription	Brain Substantia Nigra	brain
3	chr15:34354200-34376400	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr15:34354400-34379600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:34355000-34369000	Weak transcription	Liver	Liver
6	chr15:34358600-34393000	Weak transcription	Aorta	Aorta
7	chr15:34361800-34375200	Weak transcription	Left Ventricle	heart
8	chr15:34364800-34375400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr15:34365800-34378000	Weak transcription	HSMMtube	muscle
10	chr15:34367800-34369600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr15:34367800-34369600	Enhancers	NHEK	skin
12	chr15:34367800-34375600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr15:34367800-34375600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr15:34368000-34379600	Weak transcription	Fetal Brain Female	brain
15	chr15:34368000-34391600	Weak transcription	Right Ventricle	heart
16	chr15:34368200-34378200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr15:34368400-34369000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr15:34368400-34375600	Weak transcription	Primary B cells from cord blood	blood
19	chr15:34368600-34368800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr15:34368600-34374600	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr15:34368600-34375000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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