Variant report

Variant	rs12487702
Chromosome Location	chr3:195775991-195775992
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195775087..195781112-chr3:195806132..195810328,7	K562	blood:
2	chr3:195751254..195754207-chr3:195773192..195776278,3	K562	blood:
3	chr3:195774592..195777044-chr3:195910665..195912937,2	K562	blood:
4	chr3:195774337..195776699-chr3:195790526..195792198,2	K562	blood:
5	chr3:195774978..195780765-chr3:195803293..195810200,8	K562	blood:
6	chr3:195774337..195780265-chr3:195790698..195793878,6	K562	blood:
7	chr3:195774699..195776571-chr3:195794634..195796757,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000072274	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs1004860	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1004992	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12490842	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12491771	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12493933	0.95[ASN][1000 genomes]
rs2300779	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34906439	1.00[ASN][1000 genomes]
rs366268	0.80[ASN][1000 genomes]
rs3761716	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3804138	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3804141	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3827556	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3933	1.00[ASN][1000 genomes]
rs406271	0.96[ASN][1000 genomes]
rs41259844	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41297523	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41298087	1.00[ASN][1000 genomes]
rs41298097	1.00[ASN][1000 genomes]
rs41299394	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41300427	0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41301353	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs419059	0.96[ASN][1000 genomes]
rs492288	1.00[ASN][1000 genomes]
rs492349	1.00[ASN][1000 genomes]
rs539816	1.00[ASN][1000 genomes]
rs557527	1.00[ASN][1000 genomes]
rs570	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60148746	0.89[ASN][1000 genomes]
rs62284053	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62285381	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62285382	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62285387	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62285392	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62285393	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6763092	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7645812	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759213	chr3:195102787-196071593	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
2	nsv428102	chr3:195201080-195829426	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv428430	chr3:195201080-195829426	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
4	esv2757913	chr3:195379484-196071593	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS 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 miRNA target site	108 gene(s)	inside rSNPs	diseases
5	nsv1006165	chr3:195383130-195777211	Bivalent Enhancer Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
6	nsv471621	chr3:195417664-195795474	Flanking Active TSS Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	nsv469518	chr3:195623722-195795474	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
8	nsv482784	chr3:195623722-195795474	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1010395	chr3:195641908-195848264	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv532213	chr3:195643944-196063636	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
11	esv1822059	chr3:195651349-195776737	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
12	esv1844691	chr3:195651349-195776737	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
13	esv1820982	chr3:195651349-195835519	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv997797	chr3:195658360-196212958	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
15	nsv878170	chr3:195677895-195871388	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
16	nsv878171	chr3:195677895-195959924	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
17	nsv1008512	chr3:195709662-195974936	Strong transcription Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
18	nsv1004940	chr3:195734933-195777211	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
19	nsv1002584	chr3:195734933-195910772	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
20	nsv432543	chr3:195746690-196015690	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
21	nsv878172	chr3:195751853-195831098	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
22	nsv532214	chr3:195762648-195916068	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
23	nsv1002065	chr3:195769609-195877692	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
24	nsv1009105	chr3:195769609-195984388	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
25	nsv820015	chr3:195770699-195776215	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
26	esv3461301	chr3:195772155-195776753	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195762800-195780200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:195768400-195781600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:195768600-195778800	Weak transcription	Fetal Stomach	stomach
4	chr3:195769200-195776000	Weak transcription	K562	blood
5	chr3:195769800-195776400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr3:195770000-195778800	Weak transcription	Gastric	stomach
7	chr3:195770200-195778000	Weak transcription	Ovary	ovary
8	chr3:195770200-195778800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:195770400-195776800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:195770400-195778200	Weak transcription	Fetal Kidney	kidney
11	chr3:195770800-195776000	Weak transcription	Brain Germinal Matrix	brain
12	chr3:195771000-195776600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr3:195771400-195804000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:195771600-195776400	Weak transcription	Stomach Smooth Muscle	stomach
15	chr3:195771800-195776400	Weak transcription	Colonic Mucosa	Colon
16	chr3:195771800-195778800	Weak transcription	Lung	lung
17	chr3:195772400-195781000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:195772800-195776000	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:195772800-195776400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr3:195773000-195776400	Weak transcription	Brain Cingulate Gyrus	brain
21	chr3:195773000-195802000	Strong transcription	Dnd41	blood
22	chr3:195773200-195776600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr3:195773200-195805200	Strong transcription	Fetal Thymus	thymus
24	chr3:195773400-195800400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:195773600-195776000	Weak transcription	HUVEC	blood vessel
26	chr3:195773600-195776400	Weak transcription	Right Ventricle	heart
27	chr3:195773600-195776600	Weak transcription	Psoas Muscle	Psoas
28	chr3:195773600-195778200	Weak transcription	Pancreas	Pancrea
29	chr3:195773600-195782000	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr3:195773600-195790200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr3:195774200-195785600	Strong transcription	A549	lung
32	chr3:195774200-195791400	Strong transcription	Primary B cells from cord blood	blood
33	chr3:195774200-195800200	Strong transcription	Placenta	Placenta
34	chr3:195774200-195803800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:195774200-195804800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr3:195774400-195776400	Weak transcription	Fetal Heart	heart
37	chr3:195774400-195777000	Strong transcription	Cortex derived primary cultured neurospheres	brain
38	chr3:195774400-195778000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr3:195774400-195784400	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr3:195774400-195800200	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr3:195774400-195803800	Strong transcription	Duodenum Mucosa	Duodenum
42	chr3:195774600-195776200	Weak transcription	NHLF	lung
43	chr3:195774600-195776400	Weak transcription	HSMMtube	muscle
44	chr3:195774600-195778000	Weak transcription	Fetal Brain Male	brain
45	chr3:195774600-195778200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr3:195774600-195778600	Weak transcription	NHDF-Ad	bronchial
47	chr3:195774600-195783200	Strong transcription	HMEC	breast
48	chr3:195774600-195789600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr3:195774600-195803800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr3:195774600-195805400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links