Variant report

Variant	rs56145517
Chromosome Location	chr3:150054246-150054247
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs28573339	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35674456	0.89[ASN][1000 genomes]
rs62269235	0.91[ASN][1000 genomes]
rs73003243	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73869210	0.80[ASN][1000 genomes]
rs9917701	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][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	nsv829755	chr3:149992023-150156001	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150043400-150059600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:150050800-150055200	Enhancers	HMEC	breast
3	chr3:150052400-150054600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:150052600-150054800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:150052800-150054800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr3:150052800-150055000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:150053000-150066600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:150053400-150062000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:150053400-150062000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:150053600-150057800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr3:150053800-150054800	Weak transcription	NHEK	skin
12	chr3:150053800-150061800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:150053800-150062000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr3:150054000-150054400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:150054000-150054600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr3:150054000-150054800	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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