Variant report

Variant	rs6741630
Chromosome Location	chr2:55549480-55549481
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs10153861	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10181997	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10184362	1.00[EUR][1000 genomes]
rs10186158	1.00[EUR][1000 genomes]
rs10196295	0.81[AFR][1000 genomes]
rs10199332	1.00[EUR][1000 genomes]
rs10201075	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10202943	1.00[EUR][1000 genomes]
rs10209908	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10518764	0.89[AMR][1000 genomes]
rs13383527	1.00[EUR][1000 genomes]
rs13384739	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13389151	1.00[EUR][1000 genomes]
rs13389799	1.00[EUR][1000 genomes]
rs13390100	1.00[EUR][1000 genomes]
rs13398447	1.00[EUR][1000 genomes]
rs13402277	1.00[EUR][1000 genomes]
rs13404740	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13405460	1.00[EUR][1000 genomes]
rs13406929	1.00[EUR][1000 genomes]
rs13408706	1.00[EUR][1000 genomes]
rs13411077	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13411257	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13412682	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13416519	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13417988	1.00[EUR][1000 genomes]
rs13419337	1.00[EUR][1000 genomes]
rs13424499	1.00[EUR][1000 genomes]
rs13426160	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13426766	1.00[EUR][1000 genomes]
rs13429863	1.00[EUR][1000 genomes]
rs17046801	1.00[EUR][1000 genomes]
rs17046820	1.00[EUR][1000 genomes]
rs17046828	1.00[EUR][1000 genomes]
rs17046829	1.00[EUR][1000 genomes]
rs17046835	1.00[EUR][1000 genomes]
rs17046837	1.00[EUR][1000 genomes]
rs17046881	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17046896	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17046898	1.00[EUR][1000 genomes]
rs17046954	1.00[EUR][1000 genomes]
rs17046959	1.00[EUR][1000 genomes]
rs17046963	1.00[EUR][1000 genomes]
rs17046964	1.00[EUR][1000 genomes]
rs17264948	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2043716	1.00[EUR][1000 genomes]
rs28434193	1.00[EUR][1000 genomes]
rs28498550	1.00[EUR][1000 genomes]
rs3861571	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3975804	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56201519	1.00[EUR][1000 genomes]
rs57623398	1.00[EUR][1000 genomes]
rs59695161	1.00[EUR][1000 genomes]
rs60920006	1.00[EUR][1000 genomes]
rs6545485	1.00[EUR][1000 genomes]
rs6545486	1.00[EUR][1000 genomes]
rs6704701	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6707774	1.00[EUR][1000 genomes]
rs6710128	1.00[EUR][1000 genomes]
rs6714932	1.00[EUR][1000 genomes]
rs6715991	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6719677	1.00[EUR][1000 genomes]
rs6726757	1.00[EUR][1000 genomes]
rs6729144	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6734415	1.00[EUR][1000 genomes]
rs6735009	1.00[EUR][1000 genomes]
rs6738517	1.00[EUR][1000 genomes]
rs6748541	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6754036	1.00[EUR][1000 genomes]
rs6758229	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6759625	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6759763	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6761771	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72918961	1.00[EUR][1000 genomes]
rs72918964	1.00[EUR][1000 genomes]
rs72918965	1.00[EUR][1000 genomes]
rs72918972	1.00[EUR][1000 genomes]
rs72918975	1.00[EUR][1000 genomes]
rs72923130	1.00[EUR][1000 genomes]
rs72923156	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72923157	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72923183	1.00[EUR][1000 genomes]
rs72923187	1.00[EUR][1000 genomes]
rs72923194	1.00[EUR][1000 genomes]
rs72923197	1.00[EUR][1000 genomes]
rs72924917	1.00[EUR][1000 genomes]
rs72924922	1.00[EUR][1000 genomes]
rs72927340	1.00[EUR][1000 genomes]
rs72927384	1.00[EUR][1000 genomes]
rs72927388	1.00[EUR][1000 genomes]
rs72929306	1.00[EUR][1000 genomes]
rs7561604	1.00[EUR][1000 genomes]
rs7562535	1.00[EUR][1000 genomes]
rs7577510	1.00[EUR][1000 genomes]
rs7589558	1.00[EUR][1000 genomes]
rs7594907	1.00[EUR][1000 genomes]
rs9309264	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522016	chr2:55404794-55560298	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv874156	chr2:55474026-55636351	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv874157	chr2:55483020-55571085	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv874158	chr2:55513738-55619923	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv874159	chr2:55513738-55636351	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv457941	chr2:55517491-55585915	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv582030	chr2:55517491-55585915	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1006170	chr2:55530179-55809251	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55510000-55553600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:55510000-55578800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:55510200-55559000	Weak transcription	Psoas Muscle	Psoas
4	chr2:55510200-55616800	Weak transcription	Fetal Intestine Small	intestine
5	chr2:55512000-55549800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:55512400-55577400	Weak transcription	Right Ventricle	heart
7	chr2:55514800-55549600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
8	chr2:55515800-55550400	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:55518600-55591400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr2:55519800-55579000	Weak transcription	Primary B cells from cord blood	blood
11	chr2:55520200-55554400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr2:55520400-55591200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr2:55521400-55591000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr2:55523000-55584400	Weak transcription	Aorta	Aorta
15	chr2:55523200-55584800	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr2:55523600-55600600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:55526400-55549600	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr2:55534200-55589400	Weak transcription	Pancreas	Pancrea
19	chr2:55535200-55549600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr2:55535200-55549600	Strong transcription	Dnd41	blood
21	chr2:55535400-55550200	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr2:55537200-55550200	Strong transcription	HSMM	muscle
23	chr2:55537400-55549600	Strong transcription	Fetal Thymus	thymus
24	chr2:55537600-55550200	Strong transcription	Brain Substantia Nigra	brain
25	chr2:55537800-55554600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr2:55537800-55609400	Weak transcription	Lung	lung
27	chr2:55538000-55549600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr2:55538000-55550000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr2:55538600-55557000	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr2:55539200-55549600	Strong transcription	Osteobl	bone
31	chr2:55539200-55567800	Weak transcription	Colon Smooth Muscle	Colon
32	chr2:55539200-55579000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:55539200-55579000	Weak transcription	NHEK	skin
34	chr2:55539400-55553000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:55539400-55553600	Weak transcription	NHLF	lung
36	chr2:55539800-55549600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr2:55539800-55554400	Weak transcription	Fetal Heart	heart
38	chr2:55541400-55554200	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr2:55541400-55564600	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr2:55541400-55584400	Weak transcription	Spleen	Spleen
41	chr2:55541600-55553000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr2:55541600-55557600	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr2:55541800-55574800	Weak transcription	Ovary	ovary
44	chr2:55542400-55559800	Weak transcription	Fetal Brain Male	brain
45	chr2:55542400-55560400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr2:55542400-55589800	Weak transcription	Fetal Intestine Large	intestine
47	chr2:55542400-55644800	Weak transcription	Primary T cells from cord blood	blood
48	chr2:55542600-55554200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr2:55542600-55563000	Weak transcription	Thymus	Thymus
50	chr2:55542800-55552600	Weak transcription	A549	lung

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