Variant report

Variant	rs2906694
Chromosome Location	chr7:21790905-21790906
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10156026	0.85[CEU][hapmap]
rs10227372	0.87[CEU][hapmap]
rs10268039	0.82[CEU][hapmap]
rs10268330	0.82[CEU][hapmap]
rs11983051	0.87[CEU][hapmap]
rs17145316	0.82[CEU][hapmap]
rs2072219	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs2214934	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2906680	1.00[CEU][hapmap]
rs2906682	1.00[CEU][hapmap]
rs2906692	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2965355	1.00[CEU][hapmap];0.91[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2965356	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722054	0.82[CEU][hapmap]
rs6461598	0.85[CEU][hapmap];0.91[EUR][1000 genomes]
rs6979777	0.87[CEU][hapmap];0.93[EUR][1000 genomes]
rs7791639	0.82[CEU][hapmap]
rs886788	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs886789	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[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	nsv1018133	chr7:21740118-22055283	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1016063	chr7:21740433-21808410	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:21782600-21798000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:21789400-21794200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr7:21789400-21794200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:21789400-21794400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr7:21789400-21794400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr7:21789400-21794600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr7:21789400-21804800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr7:21789600-21794200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr7:21789600-21794400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:21789600-21794400	Weak transcription	iPS-18 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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