Variant report

Variant	nsv1035873
Chromosome Location	chr10:43721143-43873664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3133)
CpG islands
(count:4338)
Chromatin interactive
region (count:211)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3133 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43851352-43851750	K562	blood:	n/a	n/a
2	ARID3A	chr10:43849475-43850040	K562	blood:	n/a	n/a
3	ARID3A	chr10:43872881-43873098	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:43850414-43850703	K562	blood:	n/a	n/a
5	ARID3A	chr10:43843997-43844253	HepG2	liver:	n/a	n/a
6	ATF1	chr10:43782794-43783112	K562	blood:	n/a	n/a
7	ATF1	chr10:43851364-43851733	K562	blood:	n/a	n/a
8	ATF1	chr10:43849742-43850023	K562	blood:	n/a	n/a
9	BACH1	chr10:43725811-43725979	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:43800080-43800440	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:43872802-43873175	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:43769765-43769851	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:43724255-43724899	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr10:43828364-43828380	K562	blood:	n/a	n/a
15	BACH1	chr10:43844047-43844300	K562	blood:	n/a	n/a
16	BACH1	chr10:43857505-43858245	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:43804602-43804617	K562	blood:	n/a	n/a
18	BATF	chr10:43829696-43830134	GM12878	blood:	n/a	chr10:43829882-43829893
19	BCLAF1	chr10:43857783-43858100	GM12878	blood:	n/a	n/a
20	BHLHE40	chr10:43791964-43792071	K562	blood:	n/a	n/a
21	BHLHE40	chr10:43866925-43867233	K562	blood:	n/a	n/a
22	BHLHE40	chr10:43751338-43751539	K562	blood:	n/a	n/a
23	BHLHE40	chr10:43788666-43789060	K562	blood:	n/a	chr10:43788989-43789005
24	BHLHE40	chr10:43843914-43844263	GM12878	blood:	n/a	n/a
25	BHLHE40	chr10:43808198-43808354	K562	blood:	n/a	n/a
26	BHLHE40	chr10:43860859-43861203	K562	blood:	n/a	n/a
27	BHLHE40	chr10:43805103-43805172	K562	blood:	n/a	n/a
28	BHLHE40	chr10:43782768-43783086	K562	blood:	n/a	n/a
29	BHLHE40	chr10:43800241-43800413	K562	blood:	n/a	chr10:43800372-43800388
30	BHLHE40	chr10:43843918-43844290	K562	blood:	n/a	n/a
31	BHLHE40	chr10:43872792-43873232	HepG2	liver:	n/a	n/a
32	BHLHE40	chr10:43857586-43858015	GM12878	blood:	n/a	n/a
33	BHLHE40	chr10:43873542-43873679	K562	blood:	n/a	n/a
34	BHLHE40	chr10:43810301-43810513	K562	blood:	n/a	n/a
35	BHLHE40	chr10:43788740-43788896	GM12878	blood:	n/a	n/a
36	BHLHE40	chr10:43872938-43873008	K562	blood:	n/a	n/a
37	BHLHE40	chr10:43751373-43751579	GM12878	blood:	n/a	n/a
38	BRCA1	chr10:43811217-43811226	HepG2	liver:	n/a	n/a
39	BRCA1	chr10:43865373-43865500	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr10:43782709-43783165	K562	blood:	n/a	n/a
41	CBX3	chr10:43843811-43844299	K562	blood:	n/a	n/a
42	CCNT2	chr10:43849688-43850028	K562	blood:	n/a	n/a
43	CCNT2	chr10:43872902-43873078	K562	blood:	n/a	n/a
44	CCNT2	chr10:43844480-43844680	K562	blood:	n/a	n/a
45	CCNT2	chr10:43800219-43800325	K562	blood:	n/a	n/a
46	CCNT2	chr10:43843970-43844213	K562	blood:	n/a	n/a
47	CCNT2	chr10:43867032-43867212	K562	blood:	n/a	n/a
48	CEBPB	chr10:43869543-43869611	A549	lung:	n/a	n/a
49	CEBPB	chr10:43812007-43812314	K562	blood:	n/a	n/a
50	CEBPB	chr10:43793647-43793803	K562	blood:	n/a	n/a

(count:4338 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43723859-43723909	CMK	blood:	n/a
2	chr10:43834363-43834413	Jurkat	blood:	n/a
3	chr10:43761841-43761891	BE2_C	brain:	n/a
4	chr10:43857904-43857954	CMK	blood:	n/a
5	chr10:43725741-43725791	K562	blood:	n/a
6	chr10:43857301-43857351	AG10803	skin:	n/a
7	chr10:43797263-43797313	PFSK-1	brain:	n/a
8	chr10:43723859-43723909	CMK	blood:	n/a
9	chr10:43834363-43834413	Jurkat	blood:	n/a
10	chr10:43761841-43761891	BE2_C	brain:	n/a
11	chr10:43857904-43857954	CMK	blood:	n/a
12	chr10:43725741-43725791	K562	blood:	n/a
13	chr10:43857301-43857351	AG10803	skin:	n/a
14	chr10:43797263-43797313	PFSK-1	brain:	n/a
15	chr10:43817997-43818047	PrEC	prostate:	n/a
16	chr10:43762680-43762730	GM19239	blood:	n/a
17	chr10:43818695-43818745	AG04449	skin:	fetal
18	chr10:43818603-43818653	GM19239	blood:	n/a
19	chr10:43817997-43818047	Hela-S3	cervix:	n/a
20	chr10:43723859-43723909	SK-N-SH	brain:	n/a
21	chr10:43802881-43802931	T-47D	breast:	n/a
22	chr10:43844651-43844701	HAEpiC	amniotic membrane:	n/a
23	chr10:43838627-43838677	HAEpiC	amniotic membrane:	n/a
24	chr10:43815780-43815830	HUVEC	blood vessel:	n/a
25	chr10:43728230-43728280	PANC-1	pancreas:	n/a
26	chr10:43846539-43846589	SKMC	muscle:	n/a
27	chr10:43857301-43857351	HRE	kidney:	n/a
28	chr10:43866966-43867016	AoSMC	blood vessel:	n/a
29	chr10:43800227-43800277	HCM	heart:	n/a
30	chr10:43728230-43728280	AG04450	lung:	fetal
31	chr10:43849970-43850020	HL-60	blood:	n/a
32	chr10:43839193-43839243	AG10803	skin:	n/a
33	chr10:43800227-43800277	A549	lung:	n/a
34	chr10:43800478-43800528	T-47D	breast:	n/a
35	chr10:43857641-43857691	HEEpiC	esophagus:	n/a
36	chr10:43721445-43721495	HEEpiC	esophagus:	n/a
37	chr10:43739117-43739167	K562	blood:	n/a
38	chr10:43818243-43818293	SK-N-SH_RA	brain:	n/a
39	chr10:43857301-43857351	RPTEC	kidney:	n/a
40	chr10:43800154-43800204	AoSMC	blood vessel:	n/a
41	chr10:43724742-43724792	HCF	heart:	n/a
42	chr10:43800313-43800363	HCM	heart:	n/a
43	chr10:43800133-43800183	HCPEpiC	choroid plexus:	n/a
44	chr10:43846705-43846755	MCF-7	breast:	n/a
45	chr10:43857904-43857954	RPTEC	kidney:	n/a
46	chr10:43725612-43725662	Hepatocyte	liver:	n/a
47	chr10:43811183-43811233	ovcar-3	ovarian:	n/a
48	chr10:43800478-43800528	NHBE	bronchial:	n/a
49	chr10:43818365-43818415	PrEC	prostate:	n/a
50	chr10:43857301-43857351	CMK	blood:	n/a

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr10:43748329..43751092-chr10:43758387..43762104,3	MCF-7	breast:
2	chr10:43848751..43853953-chr10:43869065..43873618,8	MCF-7	breast:
3	chr10:43785328..43787796-chr10:43843270..43845965,2	MCF-7	breast:
4	chr10:43860960..43862469-chr10:43868449..43871286,2	MCF-7	breast:
5	chr10:43791107..43791656-chr10:43844974..43845746,2	MCF-7	breast:
6	chr10:43853906..43856900-chr10:43857802..43860629,2	MCF-7	breast:
7	chr10:43855555..43859405-chr10:43889416..43893889,5	MCF-7	breast:
8	chr10:43717975..43720515-chr10:43721363..43724311,2	MCF-7	breast:
9	chr10:43858596..43860755-chr10:43865023..43867031,2	K562	blood:
10	chr10:43860521..43863338-chr10:43914398..43916785,2	MCF-7	breast:
11	chr10:43812264..43813765-chr10:43817090..43818832,2	K562	blood:
12	chr10:43873108..43875014-chr10:43949897..43951449,2	MCF-7	breast:
13	chr10:43798662..43800539-chr10:43858079..43860696,2	MCF-7	breast:
14	chr10:43851891..43853491-chr10:43856042..43858143,2	MCF-7	breast:
15	chr10:43771552..43773988-chr10:43789349..43792291,2	K562	blood:
16	chr10:43784148..43786640-chr10:43904010..43906183,2	K562	blood:
17	chr10:43624978..43626803-chr10:43789083..43792063,2	K562	blood:
18	chr10:43822305..43824647-chr10:43844072..43845599,2	K562	blood:
19	chr10:43844277..43845840-chr10:43851755..43853493,2	MCF-7	breast:
20	chr10:43811335..43814194-chr10:43855788..43859216,3	MCF-7	breast:
21	chr10:43856477..43861777-chr10:43890250..43893117,4	MCF-7	breast:
22	chr10:43843617..43844600-chr10:43950622..43951351,3	K562	blood:
23	chr10:43787258..43789990-chr10:43857247..43859004,2	MCF-7	breast:
24	chr10:43844606..43847679-chr10:43848074..43851632,6	MCF-7	breast:
25	chr10:43780568..43784623-chr10:43788000..43790414,4	MCF-7	breast:
26	chr10:43760886..43761922-chr10:43843561..43844509,10	MCF-7	breast:
27	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:
28	chr10:43721241..43722992-chr10:43727167..43730117,3	MCF-7	breast:
29	chr10:43853521..43859723-chr10:43870896..43875408,11	MCF-7	breast:
30	chr10:43812264..43813765-chr10:43817090..43818832,2	K562	blood:
31	chr10:43845683..43851518-chr10:43853877..43859694,14	MCF-7	breast:
32	chr10:43849709..43851969-chr10:43889837..43893145,4	MCF-7	breast:
33	chr10:43842333..43853034-chr10:43900806..43908178,21	MCF-7	breast:
34	chr10:43782797..43785398-chr10:43889783..43892550,2	MCF-7	breast:
35	chr10:43853521..43859723-chr10:43870896..43875408,11	MCF-7	breast:
36	chr10:43787068..43788733-chr10:43871356..43873584,2	MCF-7	breast:
37	chr10:43705829..43707653-chr10:43720065..43721565,2	K562	blood:
38	chr10:43846613..43849361-chr10:43890166..43892037,2	MCF-7	breast:
39	chr10:43798662..43800539-chr10:43858079..43860696,2	MCF-7	breast:
40	chr10:43859399..43861070-chr10:43862861..43865041,2	MCF-7	breast:
41	chr10:43700022..43701253-chr10:43750988..43751917,9	MCF-7	breast:
42	chr10:43845581..43847759-chr10:43871473..43872986,2	MCF-7	breast:
43	chr10:43873117..43874743-chr10:43887091..43889680,2	MCF-7	breast:
44	chr10:43844606..43847679-chr10:43848074..43851632,6	MCF-7	breast:
45	chr10:43847056..43849483-chr10:43852032..43853812,3	MCF-7	breast:
46	chr10:43816783..43818713-chr10:43838155..43841036,2	MCF-7	breast:
47	chr10:43844277..43845840-chr10:43851755..43853493,2	MCF-7	breast:
48	chr10:43843618..43844595-chr10:43957020..43957977,4	K562	blood:
49	chr10:43788712..43789316-chr10:43957074..43958273,3	K562	blood:
50	chr10:43855647..43857752-chr10:43878006..43881075,3	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF487P-6	chr10:43870061-43870087	NONHSAT012958
2	lnc-ZNF487P-6	chr10:43871595-43871783	NONHSAT012958
3	lnc-CSGALNACT2-2	chr10:43780837-43781139	l_304_chr10:43724730-43729936_testes
4	lnc-FXYD4-1	chr10:43822819-43822910	XLOC_008466
5	lnc-HNRNPF-3	chr10:43727747-43727780	NONHSAT012945
6	lnc-CSGALNACT2-2	chr10:43729213-43729690	NONHSAT012946
7	lnc-CSGALNACT2-2	chr10:43759816-43759920	NONHSAT012948
8	lnc-CSGALNACT2-2	chr10:43724848-43725231	l_304_chr10:43724730-43729936_testes
9	lnc-CSGALNACT2-2	chr10:43727803-43727932	l_304_chr10:43724730-43729936_testes
10	lnc-FXYD4-1	chr10:43822000-43822045	NONHSAT012949
11	lnc-FXYD4-1	chr10:43819113-43819148	XLOC_008466
12	lnc-CSGALNACT2-2	chr10:43754457-43755996	NONHSAT012948
13	lnc-FXYD4-5	chr10:43795908-43798196	l_305_chr10:43781931-43798196_testes
14	lnc-FXYD4-5	chr10:43781932-43782168	l_305_chr10:43781931-43798196_testes
15	lnc-CSGALNACT2-2	chr10:43724731-43724847	l_304_chr10:43724730-43729936_testes
16	lnc-ZNF487P-6	chr10:43869917-43869950	NONHSAT012958
17	lnc-CSGALNACT2-2	chr10:43729213-43729936	l_304_chr10:43724730-43729936_testes
18	lnc-HNRNPF-2	chr10:43729353-43729460	NONHSAT012947
19	lnc-FXYD4-1	chr10:43822819-43823417	XLOC_008466
20	lnc-FXYD4-2	chr10:43845685-43847096	NONHSAT012954
21	lnc-CSGALNACT2-2	chr10:43759311-43759487	l_304_chr10:43724730-43729936_testes
22	lnc-HNRNPF-2	chr10:43729604-43729960	NONHSAT012947
23	lnc-FXYD4-1	chr10:43823118-43823380	XLOC_008466
24	lnc-ZNF487P-6	chr10:43871143-43871182	NONHSAT012958
25	lnc-CSGALNACT2-2	chr10:43759311-43759445	NONHSAT012948
26	lnc-CSGALNACT2-2	chr10:43727898-43727932	NONHSAT012946
27	lnc-HNRNPF-3	chr10:43727747-43727797	l_303_chr10:43716824-43727797_testes
28	lnc-FXYD4-1	chr10:43818459-43819148	XLOC_008466
29	lnc-CSGALNACT2-2	chr10:43758646-43758735	NONHSAT012948
30	lnc-FXYD4-3	chr10:43840353-43840576	NONHSAT012953
31	lnc-CSGALNACT2-2	chr10:43756176-43756431	NONHSAT012948
32	lnc-FXYD4-1	chr10:43818459-43819148	NONHSAT012949
33	lnc-CSGALNACT2-2	chr10:43758646-43758735	l_304_chr10:43724730-43729936_testes
34	lnc-ZNF487P-6	chr10:43871480-43871517	NONHSAT012958

No data

Variant related genes	Relation type
FXYD4	TF binding region
RNU6ATAC11P	TF binding region
RASGEF1A	TF binding region
ENSG00000224265	TF binding region
FXYD4	CpG island
RNU6ATAC11P	CpG island
RASGEF1A	CpG island
ENSG00000224265	CpG island
ENSG00000273008	chromatin interactions
ENSG00000221468	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000198915	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000230555	chromatin interactions
ENSG00000150201	chromatin interactions
ENSG00000252532	chromatin interactions
ENSG00000243660	chromatin interactions
ENSG00000165731	chromatin interactions
RIOK3	miRNA target sites
RLF	miRNA target sites

Extended variants
information (count: 6232 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:6232 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544270530	chr10:43721229-43721230	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs186037271	chr10:43721239-43721240	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557843251	chr10:43721249-43721250	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149223820	chr10:43721260-43721261	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143368013	chr10:43721267-43721268	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112450803	chr10:43721272-43721273	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540627731	chr10:43721324-43721325	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140229344	chr10:43721342-43721343	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72783237	chr10:43721347-43721348	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs549276695	chr10:43721348-43721349	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145395129	chr10:43721351-43721352	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs137924192	chr10:43721359-43721360	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs61268333	chr10:43721370-43721371	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs60627376	chr10:43721378-43721379	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs113195386	chr10:43721396-43721397	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189545402	chr10:43721397-43721398	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557546882	chr10:43721418-43721419	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs543379424	chr10:43721452-43721453	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs116999365	chr10:43721453-43721454	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs60845448	chr10:43721462-43721463	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs7915431	chr10:43721481-43721482	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs138791244	chr10:43721489-43721490	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115343025	chr10:43721552-43721553	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs577682230	chr10:43721705-43721706	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs544664536	chr10:43721747-43721748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs182222756	chr10:43721812-43721813	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs534504501	chr10:43721824-43721825	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs75277515	chr10:43721909-43721910	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs75729584	chr10:43721910-43721911	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs77287957	chr10:43721951-43721952	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs542984335	chr10:43721957-43721958	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs186911520	chr10:43721992-43721993	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs141751787	chr10:43722013-43722014	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs150566829	chr10:43722071-43722072	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs138573201	chr10:43722091-43722092	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs79009967	chr10:43722099-43722100	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs111655680	chr10:43722138-43722139	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs571321205	chr10:43722159-43722160	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs527441053	chr10:43722183-43722184	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs569144892	chr10:43722225-43722226	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs536442002	chr10:43722264-43722265	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs371242699	chr10:43722315-43722316	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs566830002	chr10:43722372-43722373	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs11238482	chr10:43722382-43722383	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs552953163	chr10:43722392-43722393	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs117657945	chr10:43722411-43722412	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs117414926	chr10:43722421-43722422	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs527543421	chr10:43722429-43722430	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs556771627	chr10:43722435-43722436	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs372486709	chr10:43722446-43722447	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3282 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43698000-43722800	Weak transcription	Gastric	stomach
2	chr10:43699400-43724600	Weak transcription	Right Atrium	heart
3	chr10:43714800-43722000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:43717000-43724000	Weak transcription	A549	lung
5	chr10:43717600-43724000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr10:43720400-43721200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr10:43720400-43721200	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr10:43720400-43721800	Enhancers	Brain Anterior Caudate	brain
9	chr10:43720400-43722200	Enhancers	Primary T cells fromperipheralblood	blood
10	chr10:43720400-43722200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:43720400-43722200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr10:43720600-43721400	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr10:43720600-43724400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr10:43720800-43721200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr10:43720800-43721800	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr10:43720800-43721800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr10:43720800-43724000	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr10:43720800-43724200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr10:43720800-43724600	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr10:43721000-43721600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr10:43721000-43721600	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr10:43721000-43722200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr10:43721000-43724200	Weak transcription	Pancreas	Pancrea
24	chr10:43721000-43724600	Enhancers	Spleen	Spleen
25	chr10:43721200-43721600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:43721200-43721600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:43721200-43721600	Bivalent Enhancer	Placenta	Placenta
28	chr10:43721200-43722000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr10:43721400-43721800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr10:43721600-43722000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr10:43721600-43722400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr10:43721600-43723800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr10:43721800-43722200	Weak transcription	Brain Anterior Caudate	brain
34	chr10:43721800-43722400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr10:43721800-43724000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr10:43722000-43722200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:43722000-43722200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr10:43722000-43722400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr10:43722200-43722400	Enhancers	Brain Anterior Caudate	brain
40	chr10:43722200-43723800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr10:43722200-43724000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr10:43722400-43722600	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr10:43722400-43723000	Weak transcription	Brain Anterior Caudate	brain
44	chr10:43722400-43724000	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr10:43722600-43722800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr10:43722800-43723000	Bivalent Enhancer	Placenta	Placenta
47	chr10:43722800-43723000	Enhancers	Gastric	stomach
48	chr10:43723000-43724000	Weak transcription	Gastric	stomach
49	chr10:43723000-43724200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr10:43723000-43724200	Enhancers	Brain Anterior Caudate	brain

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