Variant report

Variant	rs4614410
Chromosome Location	chr11:102625598-102625599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10895358	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11225388	0.81[CEU][hapmap]
rs11225389	0.81[CEU][hapmap]
rs11225394	0.83[EUR][1000 genomes]
rs11225399	0.83[EUR][1000 genomes]
rs11225400	0.90[CEU][hapmap];0.83[EUR][1000 genomes]
rs11225415	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1892886	0.90[CEU][hapmap];0.83[EUR][1000 genomes]
rs1938897	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1940465	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34546185	0.83[EUR][1000 genomes]
rs4121365	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61893957	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61893958	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61893959	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61895560	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102620600-102628600	Weak transcription	HMEC	breast
2	chr11:102620600-102628800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:102622800-102632400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr11:102623000-102632600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr11:102624200-102632400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:102624400-102628800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:102624600-102628600	Weak transcription	NHEK	skin
8	chr11:102624600-102632400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr11:102624800-102628800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr11:102624800-102633600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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