Variant report

Variant	rs41320050
Chromosome Location	chr5:124600904-124600905
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1371372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2408378	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61258184	1.00[AMR][1000 genomes]
rs73784272	1.00[AMR][1000 genomes]
rs73784274	1.00[AMR][1000 genomes]
rs73784284	1.00[AMR][1000 genomes]
rs73784286	1.00[AMR][1000 genomes]
rs73784293	1.00[AMR][1000 genomes]
rs73784297	1.00[AMR][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	nsv882823	chr5:124569471-124639468	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv964934	chr5:124600863-124602044	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124593200-124609200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:124599600-124601800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:124599600-124608600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:124599600-124608600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:124599800-124613400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:124600200-124603400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:124600400-124601000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr5:124600800-124601000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr5:124600800-124602000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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