Variant report

Variant	rs4936514
Chromosome Location	chr11:120168201-120168202
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:120101055..120116563-chr11:120160593..120179156,52	K562	blood:
2	chr11:120104352..120110604-chr11:120164438..120175098,43	MCF-7	breast:
3	chr11:120166386..120168824-chr11:120169274..120170936,2	K562	blood:
4	chr11:120163792..120168404-chr11:120169163..120175266,6	MCF-7	breast:
5	chr11:120104320..120113596-chr11:120167938..120177639,38	MCF-7	breast:
6	chr11:120105986..120110139-chr11:120162692..120168380,9	K562	blood:
7	chr11:120151169..120153171-chr11:120166306..120168232,2	K562	blood:

No data

No data

No data

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

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11217802	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11217803	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11217804	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11603274	0.85[EUR][1000 genomes]
rs11603307	0.85[EUR][1000 genomes]
rs11603757	0.85[EUR][1000 genomes]
rs11607289	0.85[EUR][1000 genomes]
rs12225696	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17123780	0.98[EUR][1000 genomes]
rs4142654	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4938794	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6589804	0.85[EUR][1000 genomes]
rs744984	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120166600-120170200	Weak transcription	Hela-S3	cervix
2	chr11:120166800-120170400	Weak transcription	Fetal Intestine Small	intestine
3	chr11:120167000-120170400	Weak transcription	Fetal Intestine Large	intestine
4	chr11:120167800-120168400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:120167800-120168400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:120167800-120168400	Enhancers	HMEC	breast
7	chr11:120167800-120169400	Enhancers	NHEK	skin
8	chr11:120167800-120170800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr11:120168000-120169600	Enhancers	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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