Variant report

Variant	rs12321532
Chromosome Location	chr12:388245-388246
allele	C/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	POLR2A	chr12:387987-388386	GM12891	blood:	n/a	n/a
2	POLR2A	chr12:386112-390163	K562	blood:	n/a	n/a
3	POLR2A	chr12:387584-389215	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:381899..385111-chr12:386819..388918,3	K562	blood:
2	chr12:381899..384416-chr12:386819..388918,2	K562	blood:

Variant related genes	Relation type
ENSG00000261799	TF binding region

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1017162	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.87[AMR][1000 genomes]
rs11062187	1.00[CEU][hapmap]
rs11062211	0.94[ASN][1000 genomes]
rs11062212	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11062328	0.87[AMR][1000 genomes]
rs11062353	0.87[AMR][1000 genomes]
rs11062355	0.87[AMR][1000 genomes]
rs11062465	0.91[AMR][1000 genomes]
rs11062616	0.91[AMR][1000 genomes]
rs11062659	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes]
rs11834271	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes]
rs12298836	0.91[AMR][1000 genomes]
rs12299740	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12301464	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12303118	0.87[AMR][1000 genomes]
rs12303378	0.87[AMR][1000 genomes]
rs12304242	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes]
rs12306188	0.87[AMR][1000 genomes]
rs12312809	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12314514	1.00[CEU][hapmap];0.86[CHB][hapmap];0.81[JPT][hapmap];0.91[AMR][1000 genomes]
rs12315694	0.91[AMR][1000 genomes]
rs12317640	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12317905	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12321487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12321513	0.91[AMR][1000 genomes]
rs12321546	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1541584	0.87[AMR][1000 genomes]
rs16929048	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16929851	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.91[AMR][1000 genomes]
rs16930401	1.00[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap]
rs2053736	0.87[AMR][1000 genomes]
rs2267987	0.91[AMR][1000 genomes]
rs2284335	0.87[AMR][1000 genomes]
rs2284336	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.80[YRI][hapmap];0.89[AMR][1000 genomes]
rs2300128	0.91[CHB][hapmap];0.82[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2300130	0.95[CHB][hapmap];0.90[JPT][hapmap];0.91[AMR][1000 genomes]
rs2305164	1.00[CEU][hapmap]
rs28880686	0.87[AMR][1000 genomes]
rs3753160	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes]
rs3759370	0.91[AMR][1000 genomes]
rs3782854	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3815557	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes]
rs4980812	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4980870	0.89[AMR][1000 genomes]
rs4980873	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.96[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4980887	0.91[AMR][1000 genomes]
rs4980890	0.85[AMR][1000 genomes]
rs4980893	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs57139014	0.85[AMR][1000 genomes]
rs57580513	0.85[AMR][1000 genomes]
rs58979246	0.87[AMR][1000 genomes]
rs61349553	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs720127	0.91[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes]
rs74057642	0.83[AMR][1000 genomes]
rs74057643	0.89[AMR][1000 genomes]
rs74057646	0.89[AMR][1000 genomes]
rs74057651	0.87[AMR][1000 genomes]
rs74057652	0.89[AMR][1000 genomes]
rs74057660	0.89[AMR][1000 genomes]
rs7487555	0.91[AMR][1000 genomes]
rs7488483	0.86[AMR][1000 genomes]
rs7954487	1.00[CEU][hapmap];0.82[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7970562	0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv983433	chr12:145740-400932	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1046121	chr12:282465-416134	Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv531957	chr12:282465-465789	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1049579	chr12:282465-471163	Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv949498	chr12:282465-493900	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv1051726	chr12:282465-511843	Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	nsv541304	chr12:282465-635505	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv1042991	chr12:282465-666255	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
9	nsv1041574	chr12:282465-812000	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
10	nsv541305	chr12:282465-1016828	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	nsv1054973	chr12:296179-464439	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
15	nsv541321	chr12:296179-464439	Weak transcription Strong transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	nsv1050781	chr12:321353-783899	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
17	nsv1040849	chr12:321619-771493	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
18	nsv541322	chr12:321619-771493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
19	nsv1035679	chr12:321619-781558	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
20	nsv1053519	chr12:321619-828175	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
21	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
22	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
23	nsv898563	chr12:332860-493900	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	esv2757484	chr12:335010-543206	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
25	esv2759875	chr12:335010-990544	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
26	nsv1045638	chr12:349031-893536	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
27	nsv541325	chr12:349031-893536	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
28	nsv1050646	chr12:362398-658665	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
29	nsv541326	chr12:362398-658665	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
30	nsv570	chr12:366791-395823	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
31	nsv898564	chr12:368476-415056	Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
32	nsv1050912	chr12:371410-402148	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
33	esv34939	chr12:371786-433151	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
34	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

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:372400-393600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:373200-391200	Weak transcription	Lung	lung
3	chr12:373200-393600	Weak transcription	A549	lung
4	chr12:373200-401400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:373800-393000	Weak transcription	Thymus	Thymus
6	chr12:374200-389800	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr12:376600-391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:376800-393800	Weak transcription	Fetal Kidney	kidney
9	chr12:377200-392400	Weak transcription	Osteobl	bone
10	chr12:377400-391200	Weak transcription	Adipose Nuclei	Adipose
11	chr12:377400-393800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:377800-391600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:378000-388400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr12:378000-392000	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr12:378000-393600	Weak transcription	Brain Substantia Nigra	brain
16	chr12:378000-393600	Weak transcription	Fetal Brain Female	brain
17	chr12:378000-393600	Weak transcription	Pancreas	Pancrea
18	chr12:378800-393600	Weak transcription	Esophagus	oesophagus
19	chr12:379200-389200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr12:379200-391400	Weak transcription	Placenta	Placenta
21	chr12:380400-393600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr12:380400-393800	Weak transcription	Fetal Lung	lung
23	chr12:380600-392400	Weak transcription	NHDF-Ad	bronchial
24	chr12:380600-393600	Weak transcription	Aorta	Aorta
25	chr12:380600-393600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr12:380600-393600	Weak transcription	HSMMtube	muscle
27	chr12:380600-401600	Weak transcription	Fetal Brain Male	brain
28	chr12:380800-391400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr12:381000-392000	Weak transcription	Dnd41	blood
30	chr12:381000-393600	Weak transcription	Fetal Stomach	stomach
31	chr12:381400-391200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr12:381400-391600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr12:381600-391600	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr12:381800-393600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr12:382200-391200	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr12:382400-401000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:382400-401000	Weak transcription	Small Intestine	intestine
38	chr12:382600-391200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr12:382600-393600	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr12:382600-393600	Weak transcription	Ovary	ovary
41	chr12:382800-388400	Weak transcription	Duodenum Mucosa	Duodenum
42	chr12:382800-388800	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr12:382800-389600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:382800-392000	Weak transcription	HUVEC	blood vessel
45	chr12:382800-392600	Weak transcription	Left Ventricle	heart
46	chr12:382800-393600	Weak transcription	Brain Angular Gyrus	brain
47	chr12:382800-393600	Weak transcription	Gastric	stomach
48	chr12:382800-393600	Weak transcription	Spleen	Spleen
49	chr12:382800-394000	Weak transcription	Brain Hippocampus Middle	brain
50	chr12:383200-394000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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