Variant report

Variant	rs9377212
Chromosome Location	chr6:149704901-149704902
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149681410..149684153-chr6:149703161..149705168,2	MCF-7	breast:
2	chr6:149703892..149707802-chr6:149748749..149751962,4	MCF-7	breast:
3	chr6:149704358..149706531-chr6:149865675..149867741,2	K562	blood:

Variant related genes	Relation type
ENSG00000131013	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs2143076	0.85[ASN][1000 genomes]
rs2262617	0.80[EUR][1000 genomes]
rs2789488	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2789492	0.85[ASN][1000 genomes]
rs489551	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4895788	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4897124	0.80[EUR][1000 genomes]
rs504985	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs506268	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs511100	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs514839	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs521845	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs536203	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs537354	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs540538	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs544947	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs560051	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs562428	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs564961	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs577001	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs579789	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs580011	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs585022	0.81[EUR][1000 genomes]
rs628488	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs638407	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs652807	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6570965	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9285519	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9322178	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9373589	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9373592	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9390677	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][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	nsv1024106	chr6:149622349-149745053	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv522875	chr6:149643709-149762537	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv530444	chr6:149654540-149848997	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149682600-149709200	Weak transcription	Psoas Muscle	Psoas
2	chr6:149686000-149709000	Weak transcription	Stomach Mucosa	stomach
3	chr6:149687800-149726400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:149695400-149709600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr6:149697200-149705400	Strong transcription	Primary T cells fromperipheralblood	blood
6	chr6:149697400-149706400	Strong transcription	Dnd41	blood
7	chr6:149697400-149708200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:149697600-149709000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr6:149697600-149713600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:149698400-149709600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr6:149698800-149705200	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr6:149698800-149705200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:149698800-149705800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
14	chr6:149698800-149707600	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:149699000-149705400	Strong transcription	Primary T cells from cord blood	blood
16	chr6:149699000-149706800	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr6:149699000-149707000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr6:149699000-149707200	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr6:149699000-149707800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:149699200-149705000	Strong transcription	Fetal Muscle Trunk	muscle
21	chr6:149699200-149705200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr6:149699200-149705200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:149699200-149705200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:149699200-149705200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr6:149699200-149705200	Strong transcription	Fetal Intestine Large	intestine
26	chr6:149699200-149705200	Strong transcription	Fetal Muscle Leg	muscle
27	chr6:149699200-149705200	Strong transcription	Fetal Stomach	stomach
28	chr6:149699200-149705200	Strong transcription	Lung	lung
29	chr6:149699200-149705200	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr6:149699200-149705200	Strong transcription	Stomach Smooth Muscle	stomach
31	chr6:149699200-149705400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr6:149699200-149705400	Strong transcription	Duodenum Mucosa	Duodenum
33	chr6:149699200-149705400	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr6:149699200-149705400	Strong transcription	Fetal Lung	lung
35	chr6:149699200-149705400	Strong transcription	Placenta	Placenta
36	chr6:149699200-149705600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:149700400-149709000	Weak transcription	Fetal Heart	heart
38	chr6:149700400-149728400	Weak transcription	Hela-S3	cervix
39	chr6:149700400-149732400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr6:149700600-149705000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr6:149700600-149708000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:149700600-149709200	Weak transcription	Pancreas	Pancrea
43	chr6:149700600-149721200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr6:149700600-149721200	Weak transcription	Colonic Mucosa	Colon
45	chr6:149700600-149721200	Weak transcription	Right Ventricle	heart
46	chr6:149700600-149730800	Weak transcription	Fetal Brain Male	brain
47	chr6:149700800-149706800	Weak transcription	HMEC	breast
48	chr6:149700800-149721000	Weak transcription	K562	blood
49	chr6:149700800-149721200	Weak transcription	Aorta	Aorta
50	chr6:149700800-149732800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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