Variant report

Variant	rs10930443
Chromosome Location	chr2:171719836-171719837
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10208705	0.82[EUR][1000 genomes]
rs10930444	0.82[EUR][1000 genomes]
rs10930445	0.82[EUR][1000 genomes]
rs11895068	0.82[EUR][1000 genomes]
rs12472230	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12614879	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12620730	0.82[EUR][1000 genomes]
rs1894915	0.82[EUR][1000 genomes]
rs1894921	0.82[EUR][1000 genomes]
rs45501695	1.00[EUR][1000 genomes]
rs4667664	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4667665	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4668337	0.82[EUR][1000 genomes]
rs4668338	0.82[EUR][1000 genomes]
rs4668339	0.82[EUR][1000 genomes]
rs6433258	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6433263	0.82[EUR][1000 genomes]
rs6713482	0.82[EUR][1000 genomes]
rs6734495	0.82[EUR][1000 genomes]
rs7564818	0.82[EUR][1000 genomes]
rs7575296	0.82[EUR][1000 genomes]
rs7576508	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7578938	0.82[EUR][1000 genomes]
rs7580088	0.82[EUR][1000 genomes]
rs7602737	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7603048	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7606814	0.82[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	nsv508179	chr2:171708404-171736003	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv523717	chr2:171719565-171722926	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:171699000-171730000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:171705200-171725200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:171710400-171725600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:171713800-171724000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr2:171717000-171729400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:171718200-171729400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:171718400-171729200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr2:171718600-171729400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr2:171718600-171729600	Weak transcription	Right Atrium	heart
10	chr2:171719400-171720400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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