Variant report

Variant	rs9985620
Chromosome Location	chr4:152176269-152176270
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10006091	0.82[ASN][1000 genomes]
rs10011948	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10012999	0.82[ASN][1000 genomes]
rs10016704	0.82[AMR][1000 genomes]
rs10019075	0.82[ASN][1000 genomes]
rs10857257	0.82[ASN][1000 genomes]
rs11099797	0.82[ASN][1000 genomes]
rs11099798	0.82[ASN][1000 genomes]
rs11099799	0.82[ASN][1000 genomes]
rs11733473	0.82[AMR][1000 genomes]
rs11734727	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12501397	0.82[ASN][1000 genomes]
rs12505382	0.81[ASN][1000 genomes]
rs12508449	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2291978	0.82[ASN][1000 genomes]
rs2407166	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28650996	0.82[ASN][1000 genomes]
rs28651657	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35245353	0.82[AMR][1000 genomes]
rs4339187	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4473634	0.82[ASN][1000 genomes]
rs55812154	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55855806	0.82[AMR][1000 genomes]
rs62328350	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62328351	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62328353	0.81[ASN][1000 genomes]
rs6535780	0.82[ASN][1000 genomes]
rs6535781	0.82[ASN][1000 genomes]
rs6535782	0.82[ASN][1000 genomes]
rs6823844	0.82[ASN][1000 genomes]
rs6824159	0.82[ASN][1000 genomes]
rs6824195	0.81[ASN][1000 genomes]
rs6849875	0.81[ASN][1000 genomes]
rs6851493	0.82[AMR][1000 genomes]
rs7663659	0.81[ASN][1000 genomes]
rs7665657	0.82[ASN][1000 genomes]
rs9994652	0.82[AMR][1000 genomes]
rs9996742	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034948	chr4:151590115-152202687	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv537302	chr4:151590115-152202687	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv530159	chr4:151624865-152203910	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv880262	chr4:151712054-152519899	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv881526	chr4:151968295-152489087	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	esv3418115	chr4:152174852-152177850	Weak transcription Genic enhancers ZNF genes & repeats Enhancers Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152130200-152187800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr4:152149200-152185200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:152149200-152197600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr4:152156000-152179800	Weak transcription	Fetal Stomach	stomach
5	chr4:152158800-152178800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:152158800-152181800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:152164800-152176800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:152165400-152189000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr4:152169400-152176600	Weak transcription	Fetal Intestine Large	intestine
10	chr4:152169600-152176600	Weak transcription	Fetal Intestine Small	intestine
11	chr4:152172200-152178600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr4:152172200-152183400	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr4:152172200-152184000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:152172200-152184000	Weak transcription	Lung	lung
15	chr4:152172800-152190600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr4:152173000-152184000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:152173400-152176800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:152173400-152180600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:152173400-152189400	Weak transcription	Aorta	Aorta
20	chr4:152173600-152176400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr4:152173800-152198200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:152174000-152177200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:152174000-152177400	Weak transcription	Colon Smooth Muscle	Colon
24	chr4:152174000-152178800	Weak transcription	Brain Substantia Nigra	brain
25	chr4:152174000-152179600	Weak transcription	Ovary	ovary
26	chr4:152174000-152187200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr4:152174000-152192200	Weak transcription	Brain Angular Gyrus	brain
28	chr4:152174200-152183200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr4:152174200-152183400	Weak transcription	Right Atrium	heart
30	chr4:152174200-152183600	Weak transcription	Brain Anterior Caudate	brain
31	chr4:152174400-152177000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr4:152174400-152178800	Weak transcription	Fetal Heart	heart
33	chr4:152174400-152183800	Weak transcription	Brain Hippocampus Middle	brain
34	chr4:152174600-152177200	Weak transcription	Liver	Liver
35	chr4:152174600-152178000	Weak transcription	Pancreas	Pancrea
36	chr4:152174600-152179600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr4:152174600-152181800	Weak transcription	Left Ventricle	heart
38	chr4:152174600-152182400	Weak transcription	Psoas Muscle	Psoas
39	chr4:152174800-152176800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr4:152175200-152178800	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr4:152175200-152183600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:152175400-152177400	Weak transcription	HepG2	liver
43	chr4:152176000-152177400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:152176000-152180000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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