Variant report

Variant	rs67469837
Chromosome Location	chr7:21211008-21211009
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12673430	0.92[EUR][1000 genomes]
rs17143980	0.92[ASN][1000 genomes]
rs2390478	0.91[EUR][1000 genomes]
rs2390480	0.90[ASN][1000 genomes]
rs4236302	0.92[EUR][1000 genomes]
rs4273757	0.89[ASN][1000 genomes]
rs58465671	0.80[ASN][1000 genomes]
rs6966877	0.92[ASN][1000 genomes]
rs73279582	0.87[EUR][1000 genomes]
rs7803836	0.85[ASN][1000 genomes]
rs9639369	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3478244	chr7:21044211-21417347	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv3478245	chr7:21044211-21417347	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1020852	chr7:21060791-21375050	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv538799	chr7:21060791-21375050	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:21208000-21211400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:21208600-21212400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:21210000-21212200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:21210200-21211200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr7:21210400-21212400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:21210600-21212800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr7:21210800-21212600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr7:21210800-21212600	Bivalent Enhancer	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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