Variant report

Variant	rs2067877
Chromosome Location	chr3:155630845-155630846
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:155624319..155626446-chr3:155627585..155631330,3	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10936021	0.90[AFR][1000 genomes]
rs11712694	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12634282	0.86[AFR][1000 genomes]
rs12636569	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12638792	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12638836	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1356252	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1711084	1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs1878211	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2320318	0.97[EUR][1000 genomes]
rs28438758	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2874232	0.88[AFR][1000 genomes]
rs3772112	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs401514	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs406701	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs445758	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4679757	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4679758	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4680222	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs519400	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs60788059	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6441022	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6441023	1.00[CEU][hapmap];0.94[CHB][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6441024	0.85[AFR][1000 genomes]
rs6766927	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6775044	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6777776	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6797289	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6806109	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs819844	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs819858	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs843931	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs847800	0.81[ASN][1000 genomes]
rs9820534	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9825321	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9846097	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9866164	0.82[ASN][1000 genomes]
rs9875112	0.84[EUR][1000 genomes]
rs9883153	0.86[AFR][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	nsv877680	chr3:155438022-155723064	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2753744	chr3:155487298-155707298	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv877681	chr3:155535670-155654017	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155590200-155643000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:155590200-155667400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:155599800-155633400	Weak transcription	Right Ventricle	heart
4	chr3:155603800-155657800	Weak transcription	Esophagus	oesophagus
5	chr3:155604400-155658600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr3:155605000-155632600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:155607000-155633400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr3:155607200-155656800	Weak transcription	Small Intestine	intestine
9	chr3:155607400-155632600	Weak transcription	Gastric	stomach
10	chr3:155607400-155669000	Weak transcription	Pancreas	Pancrea
11	chr3:155608600-155646400	Strong transcription	Dnd41	blood
12	chr3:155608800-155632600	Weak transcription	Spleen	Spleen
13	chr3:155608800-155633400	Weak transcription	Psoas Muscle	Psoas
14	chr3:155608800-155633800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr3:155608800-155654800	Weak transcription	Aorta	Aorta
16	chr3:155609000-155633800	Weak transcription	Stomach Mucosa	stomach
17	chr3:155609200-155657200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr3:155609600-155652000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:155610400-155631200	Strong transcription	K562	blood
20	chr3:155610800-155632600	Weak transcription	Colonic Mucosa	Colon
21	chr3:155610800-155638200	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr3:155610800-155646200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:155610800-155646200	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr3:155611000-155646200	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr3:155611000-155646200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr3:155611200-155631000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr3:155611200-155646200	Strong transcription	Fetal Thymus	thymus
28	chr3:155612400-155648600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:155612800-155646000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:155614400-155635800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:155615000-155631200	Strong transcription	Liver	Liver
32	chr3:155615800-155632400	Weak transcription	Brain Angular Gyrus	brain
33	chr3:155616600-155632400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr3:155616800-155632400	Weak transcription	Brain Substantia Nigra	brain
35	chr3:155617200-155632600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr3:155617600-155632400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr3:155618000-155633400	Weak transcription	Brain Hippocampus Middle	brain
38	chr3:155619800-155635800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:155620600-155636200	Strong transcription	Fetal Intestine Large	intestine
40	chr3:155621800-155635800	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr3:155621800-155641800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:155622400-155632600	Weak transcription	Left Ventricle	heart
43	chr3:155622800-155632800	Weak transcription	NHEK	skin
44	chr3:155622800-155633000	Weak transcription	Fetal Kidney	kidney
45	chr3:155623000-155646200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr3:155623200-155632600	Weak transcription	Thymus	Thymus
47	chr3:155623800-155636200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr3:155623800-155637800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr3:155624200-155635400	Strong transcription	H1 Cell Line	embryonic stem cell
50	chr3:155624400-155635600	Strong transcription	Fetal Muscle Leg	muscle

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