Variant report

Variant	rs9320821
Chromosome Location	chr6:121847718-121847719
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs17083712	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17083744	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17654108	1.00[CEU][hapmap]
rs28455731	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28581202	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34995334	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7757975	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9482172	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9490308	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9490310	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9490312	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9490314	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9490315	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886594	chr6:121837314-122043117	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv1847344	chr6:121845356-121875648	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1844166	chr6:121845356-121880939	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121845400-121850800	Weak transcription	Osteobl	bone
2	chr6:121845400-121854200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:121847000-121848000	Enhancers	Rectal Smooth Muscle	rectum
4	chr6:121847000-121851000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:121847200-121847800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:121847200-121847800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr6:121847200-121847800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:121847200-121847800	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr6:121847400-121847800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr6:121847400-121847800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr6:121847400-121847800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr6:121847400-121847800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:121847400-121847800	Enhancers	Ovary	ovary
14	chr6:121847400-121848200	Enhancers	Colon Smooth Muscle	Colon
15	chr6:121847600-121847800	Enhancers	H1 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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