Variant report

Variant	rs4765817
Chromosome Location	chr12:1027036-1027037
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:1027012-1027353	IMR90	lung:	n/a	n/a
2	CEBPB	chr12:1027014-1027374	HepG2	liver:	n/a	n/a
3	CEBPB	chr12:1027022-1027402	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:1022033..1023631-chr12:1025919..1029696,3	K562	blood:
2	chr12:1026662..1028225-chr12:1041093..1043045,2	K562	blood:

Variant related genes	Relation type
RAD52	TF binding region
ENSG00000002016	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10744728	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10774475	1.00[AMR][1000 genomes]
rs10849591	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10849597	1.00[AMR][1000 genomes]
rs10849606	1.00[AMR][1000 genomes]
rs12298816	1.00[AMR][1000 genomes]
rs1344442	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1833096	1.00[AMR][1000 genomes]
rs2023944	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4765861	1.00[AMR][1000 genomes]
rs4766334	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4766369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4987206	1.00[AMR][1000 genomes]
rs6489762	1.00[AMR][1000 genomes]
rs6489763	1.00[AMR][1000 genomes]
rs6489772	1.00[AMR][1000 genomes]
rs7135192	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7295127	1.00[AMR][1000 genomes]
rs7308582	1.00[AMR][1000 genomes]
rs7312247	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7955371	1.00[AMR][1000 genomes]
rs7960055	1.00[AMR][1000 genomes]
rs7968475	1.00[AMR][1000 genomes]
rs7971205	1.00[AMR][1000 genomes]
rs7972168	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7973061	1.00[AMR][1000 genomes]
rs9919750	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869390	chr12:282465-1045994	Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats 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	80 gene(s)	inside rSNPs	diseases
3	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv1044433	chr12:321619-1065402	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv541323	chr12:321619-1065402	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh 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
6	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	nsv556890	chr12:662448-1100555	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
8	nsv556892	chr12:673515-1210884	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
9	nsv898576	chr12:813411-1553450	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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 miRNA target site	56 gene(s)	inside rSNPs	diseases
10	nsv948760	chr12:863833-1542875	Active TSS Enhancers Weak transcription Strong transcription Flanking 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 miRNA target site	42 gene(s)	inside rSNPs	diseases
11	nsv1042333	chr12:907975-1081509	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv1052589	chr12:910460-1421493	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
13	nsv1045278	chr12:920251-1697030	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
14	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
15	nsv468960	chr12:975276-1455106	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
16	nsv556941	chr12:975276-1455106	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers 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	33 gene(s)	inside rSNPs	diseases
17	nsv1044329	chr12:985144-1403020	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
18	nsv541340	chr12:985144-1403020	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
19	nsv1053198	chr12:993822-1034603	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
20	nsv541341	chr12:993822-1034603	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
21	nsv1041675	chr12:993822-1091354	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
22	nsv470256	chr12:998365-1438761	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
23	nsv492321	chr12:1011692-1388512	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
24	nsv898579	chr12:1013176-1510505	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
25	nsv898580	chr12:1024688-1569097	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers 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	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:964400-1042200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:964600-1027200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr12:965800-1028400	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr12:986200-1042200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr12:986800-1028400	Strong transcription	Placenta	Placenta
6	chr12:987000-1028400	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr12:987000-1028800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr12:987000-1041200	Strong transcription	Fetal Intestine Large	intestine
9	chr12:988600-1029400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr12:989200-1042200	Strong transcription	Fetal Muscle Leg	muscle
11	chr12:989400-1028400	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr12:1001800-1028200	Strong transcription	HepG2	liver
13	chr12:1003600-1028000	Strong transcription	Duodenum Smooth Muscle	Duodenum
14	chr12:1003600-1028200	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr12:1003600-1028400	Strong transcription	NHDF-Ad	bronchial
16	chr12:1004200-1027200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr12:1004400-1041200	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr12:1004800-1037400	Strong transcription	Fetal Lung	lung
19	chr12:1005000-1028000	Strong transcription	Sigmoid Colon	Sigmoid Colon
20	chr12:1005200-1028800	Strong transcription	Rectal Smooth Muscle	rectum
21	chr12:1006600-1028200	Strong transcription	HSMMtube	muscle
22	chr12:1007000-1028400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr12:1008000-1028000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:1008200-1028800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:1009400-1027200	Strong transcription	Colonic Mucosa	Colon
26	chr12:1014600-1028200	Strong transcription	Primary T cells from cord blood	blood
27	chr12:1015200-1028000	Strong transcription	Brain Cingulate Gyrus	brain
28	chr12:1015200-1028200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr12:1015200-1028400	Strong transcription	GM12878-XiMat	blood
30	chr12:1015200-1029200	Strong transcription	Brain Anterior Caudate	brain
31	chr12:1015200-1038800	Weak transcription	Fetal Brain Male	brain
32	chr12:1015400-1028400	Strong transcription	Duodenum Mucosa	Duodenum
33	chr12:1015600-1030800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr12:1015800-1028600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr12:1019200-1028200	Strong transcription	A549	lung
36	chr12:1020800-1054600	Strong transcription	Fetal Intestine Small	intestine
37	chr12:1021200-1028200	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr12:1021600-1033800	Weak transcription	Fetal Heart	heart
39	chr12:1021800-1028600	Strong transcription	Lung	lung
40	chr12:1022000-1027200	Strong transcription	NHLF	lung
41	chr12:1022000-1028400	Strong transcription	Right Ventricle	heart
42	chr12:1022200-1027200	Strong transcription	Colon Smooth Muscle	Colon
43	chr12:1023200-1038800	Weak transcription	Psoas Muscle	Psoas
44	chr12:1023600-1028800	Strong transcription	HSMM	muscle
45	chr12:1023800-1028400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:1023800-1029200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr12:1023800-1029400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr12:1023800-1041000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:1024000-1027400	Strong transcription	Osteobl	bone
50	chr12:1024000-1028400	Strong transcription	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links