Variant report

Variant	rs10933345
Chromosome Location	chr2:231447718-231447719
allele	A/C
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	ATF2	chr2:231447466-231448294	GM12878	blood:	n/a	n/a
2	POLR2A	chr2:231447478-231449216	GM12878	blood:	n/a	n/a
3	POLR2A	chr2:231447503-231448186	GM12891	blood:	n/a	n/a
4	FOXM1	chr2:231447041-231448305	GM12878	blood:	n/a	n/a
5	POLR2A	chr2:231447455-231449128	GM12892	blood:	n/a	n/a
6	MTA3	chr2:231447140-231448977	GM12878	blood:	n/a	n/a
7	CHD1	chr2:231447550-231448627	GM12878	blood:	n/a	n/a
8	PML	chr2:231447286-231449090	GM12878	blood:	n/a	chr2:231448813-231448821
9	TBP	chr2:231447600-231448097	GM12878	blood:	n/a	n/a
10	EP300	chr2:231447549-231448078	GM12878	blood:	n/a	chr2:231447804-231447818
11	BCL3	chr2:231447555-231448071	GM12878	blood:	n/a	chr2:231447804-231447813
12	POU2F2	chr2:231447587-231448162	GM12878	blood:	n/a	chr2:231447906-231447920 chr2:231447908-231447921 chr2:231447908-231447921
13	TCF12	chr2:231447621-231448012	GM12878	blood:	n/a	n/a
14	BCLAF1	chr2:231447303-231448937	GM12878	blood:	n/a	chr2:231448477-231448486 chr2:231447804-231447813 chr2:231448763-231448772
15	BCL11A	chr2:231447590-231447988	GM12878	blood:	n/a	chr2:231447804-231447813
16	RELA	chr2:231447615-231448711	GM19099	blood:	n/a	n/a
17	YY1	chr2:231447533-231448213	GM12891	blood:	n/a	n/a
18	STAT5A	chr2:231447432-231448811	GM12878	blood:	n/a	chr2:231448358-231448366 chr2:231447822-231447830 chr2:231447802-231447813
19	NFATC1	chr2:231447359-231448688	GM12878	blood:	n/a	n/a
20	MEF2A	chr2:231447550-231448079	GM12878	blood:	n/a	chr2:231447775-231447786 chr2:231447831-231447846 chr2:231447773-231447788 chr2:231447831-231447846 chr2:231447775-231447790
21	BHLHE40	chr2:231447643-231448041	GM12878	blood:	n/a	n/a
22	MEF2A	chr2:231447416-231448141	GM12878	blood:	n/a	chr2:231447775-231447786 chr2:231447831-231447846 chr2:231447773-231447788 chr2:231447831-231447846 chr2:231447775-231447790
23	YY1	chr2:231447507-231447866	SK-N-SH	brain:	n/a	n/a
24	NFATC1	chr2:231447384-231448213	GM12878	blood:	n/a	n/a
25	POLR2A	chr2:231447291-231449074	GM12878	blood:	n/a	n/a
26	JUND	chr2:231447672-231448092	GM12878	blood:	n/a	chr2:231447886-231447898 chr2:231447902-231447914
27	STAT1	chr2:231447601-231447941	GM12878	blood:	n/a	chr2:231447822-231447830 chr2:231447802-231447813
28	RCOR1	chr2:231447120-231447949	GM12878	blood:	n/a	n/a
29	EP300	chr2:231447554-231448102	GM12878	blood:	n/a	chr2:231447804-231447818
30	SPI1	chr2:231447582-231448002	GM12891	blood:	n/a	chr2:231447804-231447813
31	YY1	chr2:231447527-231448087	GM12892	blood:	n/a	n/a
32	RUNX3	chr2:231447405-231448926	GM12878	blood:	n/a	n/a
33	IKZF1	chr2:231447588-231448862	GM12878	blood:	n/a	n/a
34	POLR2A	chr2:231447492-231449219	GM12891	blood:	n/a	n/a
35	RUNX3	chr2:231447421-231448746	GM12878	blood:	n/a	n/a
36	CREB1	chr2:231447396-231448790	GM12878	blood:	n/a	n/a
37	NFIC	chr2:231447287-231449123	GM12878	blood:	n/a	n/a
38	STAT3	chr2:231447475-231448649	GM12878	blood:	n/a	chr2:231448358-231448366 chr2:231447822-231447830 chr2:231447802-231447813
39	CEBPB	chr2:231447055-231448245	GM12878	blood:	n/a	n/a
40	POLR2A	chr2:231447486-231448114	GM12891	blood:	n/a	n/a
41	YY1	chr2:231447534-231448147	GM12892	blood:	n/a	n/a
42	SPI1	chr2:231447675-231447907	GM12878	blood:	n/a	chr2:231447804-231447813
43	EP300	chr2:231447421-231448100	GM12878	blood:	n/a	chr2:231447804-231447818
44	TCF3	chr2:231447594-231447923	GM12878	blood:	n/a	n/a
45	YY1	chr2:231447560-231448069	K562	blood:	n/a	n/a
46	RELA	chr2:231447543-231448953	GM12891	blood:	n/a	n/a
47	RELA	chr2:231447604-231448140	GM18951	blood:	n/a	n/a
48	POU2F2	chr2:231447586-231448143	GM12891	blood:	n/a	chr2:231447906-231447920 chr2:231447908-231447921 chr2:231447908-231447921
49	TCF12	chr2:231447579-231448126	SK-N-SH	brain:	n/a	n/a
50	CREB1	chr2:231447616-231448134	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
RNU6-451P	TF binding region
ENSG00000235419	TF binding region

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10167135	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11674658	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12477212	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12611446	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12615477	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35028536	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6736679	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73106818	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv18000	chr2:231072978-231467847	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv875953	chr2:231415189-231457819	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv875955	chr2:231440555-231500805	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv961010	chr2:231446732-231451285	Flanking Active TSS Enhancers Weak transcription	TF binding region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:231443400-231451000	Weak transcription	Primary T cells from cord blood	blood
2	chr2:231443400-231453800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr2:231443400-231454400	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr2:231443400-231454600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr2:231446800-231449000	Enhancers	Primary B cells from peripheral blood	blood
6	chr2:231447200-231448200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr2:231447200-231448600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr2:231447200-231449000	Flanking Active TSS	GM12878-XiMat	blood
9	chr2:231447400-231448400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr2:231447400-231448400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr2:231447600-231447800	Weak transcription	Primary B cells from cord blood	blood
12	chr2:231447600-231448200	Enhancers	Primary T cells fromperipheralblood	blood

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