Variant report

Variant	rs3822106
Chromosome Location	chr4:79784527-79784528
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:79696750..79699065-chr4:79783549..79785777,2	MCF-7	breast:
2	chr4:79530033..79532299-chr4:79783489..79785388,2	K562	blood:
3	chr4:79530799..79532363-chr4:79783489..79785979,2	K562	blood:
4	chr4:79700005..79702087-chr4:79782609..79785586,2	MCF-7	breast:
5	chr4:79769174..79772080-chr4:79784280..79787147,3	K562	blood:
6	chr4:79781834..79784550-chr4:79800015..79801943,2	K562	blood:

Variant related genes	Relation type
ENSG00000260278	Chromatin interaction
ENSG00000138756	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10018189	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10023100	0.85[ASN][1000 genomes]
rs10025599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10034295	0.86[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs11724233	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs1275045	0.96[ASN][1000 genomes]
rs1275046	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1275047	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs13108247	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs13138117	0.95[CEU][hapmap]
rs1480718	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1979444	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2288254	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2554395	0.86[ASN][1000 genomes]
rs3937772	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4512020	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs62308043	0.84[ASN][1000 genomes]
rs6533951	0.80[CHB][hapmap];0.84[JPT][hapmap]
rs6534083	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6534085	0.94[ASN][1000 genomes]
rs6534086	0.94[ASN][1000 genomes]
rs6534087	0.94[ASN][1000 genomes]
rs6534090	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs6846743	0.85[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs6854347	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7656083	0.94[ASN][1000 genomes]
rs7688534	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[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	nsv1007685	chr4:79732468-79788768	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv879504	chr4:79759796-79874275	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79738800-79793200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:79744600-79793800	Weak transcription	Psoas Muscle	Psoas
3	chr4:79745800-79786400	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr4:79747200-79815600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr4:79748800-79823600	Weak transcription	Small Intestine	intestine
6	chr4:79749200-79793600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr4:79749400-79792400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr4:79749400-79793800	Weak transcription	Gastric	stomach
9	chr4:79749600-79784600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr4:79749600-79793000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr4:79749600-79793600	Weak transcription	Brain Germinal Matrix	brain
12	chr4:79749600-79793800	Weak transcription	Fetal Brain Female	brain
13	chr4:79749800-79786800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr4:79749800-79788000	Weak transcription	Lung	lung
15	chr4:79749800-79793400	Weak transcription	Thymus	Thymus
16	chr4:79749800-79793600	Weak transcription	Colonic Mucosa	Colon
17	chr4:79750200-79786600	Weak transcription	Left Ventricle	heart
18	chr4:79750200-79787600	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr4:79750400-79786800	Weak transcription	NH-A	brain
20	chr4:79750400-79791400	Weak transcription	Colon Smooth Muscle	Colon
21	chr4:79750400-79792200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr4:79750400-79792600	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr4:79750400-79793600	Weak transcription	Stomach Smooth Muscle	stomach
24	chr4:79750400-79797000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr4:79750600-79792600	Weak transcription	HSMMtube	muscle
26	chr4:79750600-79793600	Weak transcription	Fetal Kidney	kidney
27	chr4:79759600-79786600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr4:79759600-79786800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr4:79759600-79787800	Weak transcription	Fetal Stomach	stomach
30	chr4:79759600-79792400	Weak transcription	Rectal Smooth Muscle	rectum
31	chr4:79760000-79792400	Weak transcription	Fetal Lung	lung
32	chr4:79760600-79787800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr4:79760600-79787800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:79760600-79794800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:79761000-79791800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:79761200-79786800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr4:79764600-79787800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr4:79764600-79792400	Weak transcription	Brain Anterior Caudate	brain
39	chr4:79767400-79789200	Weak transcription	Brain Substantia Nigra	brain
40	chr4:79768400-79811400	Weak transcription	Hela-S3	cervix
41	chr4:79768800-79787200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:79771400-79801000	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr4:79772800-79786800	Weak transcription	Adipose Nuclei	Adipose
44	chr4:79772800-79792000	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr4:79774200-79786800	Weak transcription	Osteobl	bone
46	chr4:79774400-79793600	Weak transcription	Right Ventricle	heart
47	chr4:79774600-79793400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr4:79774800-79793200	Weak transcription	Brain Hippocampus Middle	brain
49	chr4:79775000-79788000	Weak transcription	Fetal Muscle Leg	muscle
50	chr4:79775200-79786600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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