Variant report

Variant	rs17198941
Chromosome Location	chr2:190379162-190379163
allele	C/T
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]
rs10206543	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11677198	1.00[CHB][hapmap]
rs11677494	1.00[CHB][hapmap]
rs11682165	1.00[CHB][hapmap]
rs11694976	1.00[CHB][hapmap]
rs12474223	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12616162	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12622578	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12622601	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1371468	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1371469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17198934	1.00[CHB][hapmap]
rs4145236	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4508634	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6732419	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs751663	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs751664	0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7608796	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7609427	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv533029	chr2:189812229-190554339	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv875615	chr2:190215527-190444392	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190375600-190380600	Weak transcription	Stomach Mucosa	stomach
2	chr2:190376000-190386000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:190376400-190382000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr2:190376600-190384800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr2:190377400-190383000	Weak transcription	Fetal Lung	lung
6	chr2:190377800-190379600	Weak transcription	Aorta	Aorta
7	chr2:190378000-190379200	Enhancers	Ovary	ovary
8	chr2:190378200-190385800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr2:190378400-190380200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr2:190378400-190382000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr2:190378600-190379600	Weak transcription	Adipose Nuclei	Adipose
12	chr2:190378600-190379800	Enhancers	Psoas Muscle	Psoas
13	chr2:190378800-190380800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr2:190379000-190380800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	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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