Variant report

Variant	rs9366928
Chromosome Location	chr6:37060280-37060281
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:37060206..37065655-chr6:37067548..37072519,8	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs59613460	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6912088	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6918055	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6918118	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6934536	1.00[CEU][hapmap];0.81[JPT][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6941432	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9357237	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9357238	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9357239	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[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	nsv1030015	chr6:36818510-37104446	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv969392	chr6:37052594-37060796	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37045800-37060800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:37051400-37060400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr6:37051600-37060600	Weak transcription	A549	lung
4	chr6:37051600-37063400	Weak transcription	Small Intestine	intestine
5	chr6:37051800-37060600	Weak transcription	Pancreas	Pancrea
6	chr6:37052200-37060600	Weak transcription	Adipose Nuclei	Adipose
7	chr6:37052200-37070000	Weak transcription	Right Atrium	heart
8	chr6:37052800-37069800	Weak transcription	Ovary	ovary
9	chr6:37053200-37060400	Weak transcription	Fetal Intestine Small	intestine
10	chr6:37057000-37060400	Weak transcription	Fetal Intestine Large	intestine
11	chr6:37057600-37060400	Weak transcription	Fetal Stomach	stomach
12	chr6:37057800-37060600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr6:37057800-37061400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr6:37058000-37069000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:37058600-37060600	Enhancers	HepG2	liver
16	chr6:37059200-37062200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr6:37059200-37062400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr6:37059600-37060800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:37059600-37060800	Weak transcription	Placenta	Placenta
20	chr6:37059800-37060800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:37059800-37060800	Weak transcription	Osteobl	bone
22	chr6:37059800-37061200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:37059800-37061200	Weak transcription	K562	blood
24	chr6:37060000-37061000	Weak transcription	Hela-S3	cervix

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