Variant report

Variant	rs6797160
Chromosome Location	chr3:194850659-194850660
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:194849005..194851034-chr3:194888966..194890875,2	K562	blood:
2	chr3:194846812..194848589-chr3:194850352..194852170,2	K562	blood:
3	chr3:194850288..194852181-chr3:194862414..194864990,2	MCF-7	breast:
4	chr3:194839189..194844993-chr3:194846673..194851288,6	K562	blood:

Variant related genes	Relation type
ENSG00000173950	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11721261	0.81[CHB][hapmap]
rs11917068	0.82[ASN][1000 genomes]
rs1552893	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[ASN][1000 genomes]
rs2131879	0.81[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap]
rs2172695	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.82[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs28573813	0.84[ASN][1000 genomes]
rs4266129	0.91[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs4300953	0.91[CHB][hapmap];0.92[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs4645095	0.84[ASN][1000 genomes]
rs4677663	0.90[CHB][hapmap];0.83[CHD][hapmap];0.86[JPT][hapmap];0.82[YRI][hapmap];0.82[ASN][1000 genomes]
rs4677812	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs58370605	0.81[ASN][1000 genomes]
rs60329099	0.83[ASN][1000 genomes]
rs6794540	0.90[ASN][1000 genomes]
rs7639698	0.90[ASN][1000 genomes]
rs903310	0.81[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs950257	0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9848862	0.83[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007697	chr3:194554814-195009930	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv536873	chr3:194554814-195009930	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
3	nsv997779	chr3:194687093-194885936	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv536874	chr3:194687093-194885936	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
6	esv1813153	chr3:194754532-194851746	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1012592	chr3:194814446-194931562	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv536875	chr3:194814446-194931562	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
9	nsv1001492	chr3:194814990-194935397	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
10	nsv461126	chr3:194817484-194961888	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
11	nsv592981	chr3:194817484-194961888	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
12	nsv878137	chr3:194822098-194900432	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
13	nsv461127	chr3:194833940-194934634	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
14	nsv592982	chr3:194833940-194934634	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
15	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
16	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
17	esv996963	chr3:194845436-194854988	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194827400-194853600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:194827400-194861200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:194831600-194857400	Weak transcription	Pancreas	Pancrea
4	chr3:194832400-194853600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:194832800-194856200	Weak transcription	Primary T cells from cord blood	blood
6	chr3:194839200-194861200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:194839200-194861400	Weak transcription	Aorta	Aorta
8	chr3:194841000-194853400	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr3:194841000-194872800	Weak transcription	HSMMtube	muscle
10	chr3:194841400-194868800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:194841800-194851200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr3:194843800-194856600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr3:194844600-194860000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:194844800-194859800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:194845400-194852000	Weak transcription	Fetal Stomach	stomach
16	chr3:194845600-194858000	Weak transcription	Fetal Intestine Small	intestine
17	chr3:194845600-194861200	Weak transcription	Ovary	ovary
18	chr3:194846200-194851400	Weak transcription	Fetal Heart	heart
19	chr3:194846200-194851400	Weak transcription	Placenta	Placenta
20	chr3:194846200-194862400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr3:194846400-194851400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:194846400-194853800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:194846600-194851600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr3:194846600-194868400	Weak transcription	HepG2	liver
25	chr3:194846800-194854600	Weak transcription	Left Ventricle	heart
26	chr3:194847200-194868200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr3:194847600-194851000	Weak transcription	Fetal Muscle Leg	muscle
28	chr3:194847600-194851400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:194847600-194857800	Weak transcription	Spleen	Spleen
30	chr3:194847600-194858200	Weak transcription	Adipose Nuclei	Adipose
31	chr3:194847800-194856200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr3:194848600-194850800	Enhancers	Primary B cells from cord blood	blood
33	chr3:194848600-194850800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr3:194848800-194850800	Enhancers	Primary T helper cells PMA-I stimulated	--
35	chr3:194848800-194850800	Enhancers	HUVEC	blood vessel
36	chr3:194848800-194851200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr3:194849000-194851000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr3:194849000-194851400	Enhancers	Osteobl	bone
39	chr3:194849200-194850800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:194849200-194851200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:194849200-194851200	Enhancers	NH-A	brain
42	chr3:194849200-194861200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr3:194849400-194850800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr3:194849400-194850800	Weak transcription	Fetal Thymus	thymus
45	chr3:194849400-194851200	Enhancers	K562	blood
46	chr3:194849400-194856000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:194849400-194857000	Weak transcription	Primary hematopoietic stem cells	blood
48	chr3:194849400-194858200	Weak transcription	Lung	lung
49	chr3:194849600-194851200	Weak transcription	Fetal Kidney	kidney
50	chr3:194849600-194853400	Weak transcription	Stomach Mucosa	stomach

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