Variant report

Variant	rs4819212
Chromosome Location	chr21:44977455-44977456
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	chr21:44976320..44978488-chr21:45138337..45140856,2	K562	blood:

Variant related genes	Relation type
ENSG00000160209	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1003280	0.87[CHB][hapmap];0.83[JPT][hapmap];0.82[EUR][1000 genomes]
rs1073522	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs11089020	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1122873	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs11701518	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs11701746	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12627667	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs1378079	0.87[CHB][hapmap]
rs1378080	0.87[CHB][hapmap];0.83[JPT][hapmap];0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs141521	0.87[CHB][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs1436291	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1454648	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs1454650	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs1454651	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs1584917	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs1584918	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs1595167	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1598206	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs162344	0.87[CHB][hapmap]
rs162345	0.87[CHB][hapmap]
rs162366	0.87[CHB][hapmap]
rs162371	0.87[CHB][hapmap]
rs162372	0.87[CHB][hapmap]
rs162375	0.87[CHB][hapmap]
rs162376	0.87[CHB][hapmap]
rs162377	0.87[CHB][hapmap]
rs162378	0.87[CHB][hapmap]
rs162388	0.87[CHB][hapmap]
rs162402	0.81[EUR][1000 genomes]
rs1836854	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1836855	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1836856	1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2246602	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs229357	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2329442	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838316	0.87[CHB][hapmap];0.82[JPT][hapmap]
rs2838317	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838319	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838321	0.87[CHB][hapmap];0.83[JPT][hapmap];0.82[EUR][1000 genomes]
rs2838323	0.87[CHB][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs2838324	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838328	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838330	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838331	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838336	0.87[CHB][hapmap]
rs2838337	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838338	0.87[CHB][hapmap]
rs2838339	0.87[CHB][hapmap]
rs2838341	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs2838343	0.87[CHB][hapmap]
rs2876854	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3788062	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs4818843	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4818850	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs4819219	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs4819270	0.93[CHB][hapmap];0.83[JPT][hapmap]
rs4997353	0.81[EUR][1000 genomes]
rs56369437	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6417729	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6518268	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6518301	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs6518302	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs6518309	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs7276215	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs7276633	0.87[CHB][hapmap]
rs7277539	0.82[JPT][hapmap]
rs7278003	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7278282	0.90[ASN][1000 genomes]
rs7279958	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs7279968	0.87[CHB][hapmap]
rs7282704	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7283362	1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8131020	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[ASN][1000 genomes]
rs8133523	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs86139	0.87[CHB][hapmap]
rs9306159	0.87[CHB][hapmap]
rs9976441	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs9977258	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9978811	0.86[CHB][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs9979187	0.86[EUR][1000 genomes]
rs9980185	0.83[JPT][hapmap]
rs9981291	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs9981790	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs9983763	0.87[CHB][hapmap];0.83[JPT][hapmap]
rs9984002	0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv913873	chr21:44879869-45142427	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv587689	chr21:44884252-44986050	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
3	nsv1061539	chr21:44915533-45041824	Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv1067171	chr21:44921187-45039471	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
5	nsv521700	chr21:44925334-45041790	Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
6	nsv470903	chr21:44925334-45061501	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
7	nsv459289	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
8	nsv587690	chr21:44925334-45064600	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
9	esv1837818	chr21:44949285-44987079	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv511632	chr21:44963686-44987079	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv1065359	chr21:44967209-45029878	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
12	nsv3537	chr21:44967340-45013104	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:44970400-44982400	Weak transcription	HSMMtube	muscle
2	chr21:44973800-44982400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr21:44975600-44982400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr21:44976800-44980400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links