Variant report

Variant	rs4512243
Chromosome Location	chr6:142971007-142971008
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1848750	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2175165	0.81[EUR][1000 genomes]
rs6902754	0.80[ASN][1000 genomes]
rs6906818	0.84[ASN][1000 genomes]
rs6908599	0.80[ASN][1000 genomes]
rs6924380	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7740440	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7740684	0.84[ASN][1000 genomes]
rs7753052	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9390016	0.82[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	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2762618	chr6:142969785-142972917	Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
4	nsv830828	chr6:142970134-143116517	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142967200-142973600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr6:142967200-142973600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr6:142967200-142975800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:142967400-142971800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr6:142967600-142971200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr6:142968000-142972800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:142968400-142973200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr6:142969400-142973400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:142969600-142972400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr6:142969600-142972600	Weak transcription	Fetal Brain Male	brain
11	chr6:142970400-142971200	Enhancers	H9 Cell Line	embryonic stem cell
12	chr6:142971000-142971400	Enhancers	iPS DF 6.9 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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