Variant report

Variant	nsv550696
Chromosome Location	chr10:43695049-43799588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2415)
CpG islands
(count:2018)
Chromatin interactive
region (count:129)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2415 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43697611-43697845	K562	blood:	n/a	n/a
2	ARID3A	chr10:43699107-43699244	K562	blood:	n/a	n/a
3	ARID3A	chr10:43699491-43699537	K562	blood:	n/a	n/a
4	ATF1	chr10:43782794-43783112	K562	blood:	n/a	n/a
5	ATF3	chr10:43699488-43699780	K562	blood:	n/a	n/a
6	BACH1	chr10:43698759-43698935	K562	blood:	n/a	n/a
7	BACH1	chr10:43769765-43769851	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:43698778-43699232	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:43716663-43717089	H1-hESC	embryonic stem cell:	n/a	chr10:43716761-43716775
10	BACH1	chr10:43697668-43698288	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:43724255-43724899	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:43699552-43699682	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:43725811-43725979	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr10:43700455-43700491	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr10:43716620-43716927	GM12878	blood:	n/a	chr10:43716764-43716775
16	BATF	chr10:43716547-43716972	GM12878	blood:	n/a	chr10:43716764-43716775
17	BCL11A	chr10:43716547-43716908	GM12878	blood:	n/a	n/a
18	BHLHE40	chr10:43697640-43697818	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:43751338-43751539	K562	blood:	n/a	n/a
20	BHLHE40	chr10:43700495-43700817	K562	blood:	n/a	n/a
21	BHLHE40	chr10:43697648-43698011	K562	blood:	n/a	n/a
22	BHLHE40	chr10:43700481-43700677	GM12878	blood:	n/a	n/a
23	BHLHE40	chr10:43782768-43783086	K562	blood:	n/a	n/a
24	BHLHE40	chr10:43791964-43792071	K562	blood:	n/a	n/a
25	BHLHE40	chr10:43706244-43706750	K562	blood:	n/a	n/a
26	BHLHE40	chr10:43751373-43751579	GM12878	blood:	n/a	n/a
27	BHLHE40	chr10:43717038-43717110	K562	blood:	n/a	n/a
28	BHLHE40	chr10:43788666-43789060	K562	blood:	n/a	chr10:43788989-43789005
29	BHLHE40	chr10:43788740-43788896	GM12878	blood:	n/a	n/a
30	BHLHE40	chr10:43698653-43699582	K562	blood:	n/a	chr10:43699310-43699326
31	BHLHE40	chr10:43700442-43700768	HepG2	liver:	n/a	n/a
32	BRCA1	chr10:43700460-43700570	H1-hESC	embryonic stem cell:	n/a	chr10:43700460-43700467
33	BRCA1	chr10:43700613-43700784	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr10:43700561-43700665	HepG2	liver:	n/a	n/a
35	CBX3	chr10:43782709-43783165	K562	blood:	n/a	n/a
36	CBX3	chr10:43699037-43699881	K562	blood:	n/a	n/a
37	CBX3	chr10:43697609-43698066	K562	blood:	n/a	n/a
38	CBX3	chr10:43700471-43700906	K562	blood:	n/a	n/a
39	CCNT2	chr10:43697137-43697190	K562	blood:	n/a	n/a
40	CCNT2	chr10:43697705-43698509	K562	blood:	n/a	chr10:43698091-43698100 chr10:43698085-43698094
41	CCNT2	chr10:43698852-43699271	K562	blood:	n/a	n/a
42	CCNT2	chr10:43700527-43700727	K562	blood:	n/a	n/a
43	CEBPB	chr10:43700493-43700977	IMR90	lung:	n/a	n/a
44	CEBPB	chr10:43700613-43700990	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr10:43782785-43783407	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr10:43700524-43700969	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr10:43700660-43700890	K562	blood:	n/a	n/a
48	CEBPB	chr10:43700662-43701007	A549	lung:	n/a	n/a
49	CEBPB	chr10:43742646-43742953	IMR90	lung:	n/a	chr10:43742769-43742780
50	CEBPB	chr10:43767821-43767970	HepG2	liver:	n/a	chr10:43767860-43767871

(count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43701690-43701740	NHBE	bronchial:	n/a
2	chr10:43725275-43725325	H1-hESC	embryonic stem cell:	embryo
3	chr10:43698834-43698884	HUVEC	blood vessel:	n/a
4	chr10:43698931-43698981	Caco-2	colon:	n/a
5	chr10:43725376-43725426	PrEC	prostate:	n/a
6	chr10:43701690-43701740	NHBE	bronchial:	n/a
7	chr10:43725275-43725325	H1-hESC	embryonic stem cell:	embryo
8	chr10:43698834-43698884	HUVEC	blood vessel:	n/a
9	chr10:43698931-43698981	Caco-2	colon:	n/a
10	chr10:43725376-43725426	PrEC	prostate:	n/a
11	chr10:43697849-43697899	ECC-1	luminal epithelium:	n/a
12	chr10:43697849-43697899	NHDF-neo	bronchial:	n/a
13	chr10:43701731-43701781	GM12891	blood:	n/a
14	chr10:43763042-43763092	HRCEpiC	kidney:	n/a
15	chr10:43725741-43725791	BE2_C	brain:	n/a
16	chr10:43763042-43763092	PFSK-1	brain:	n/a
17	chr10:43697521-43697571	GM12878	blood:	n/a
18	chr10:43797263-43797313	Hepatocyte	liver:	n/a
19	chr10:43762670-43762720	GM06990	blood:	n/a
20	chr10:43699070-43699120	PANC-1	pancreas:	n/a
21	chr10:43700652-43700702	H1-hESC	embryonic stem cell:	embryo
22	chr10:43699070-43699120	Caco-2	colon:	n/a
23	chr10:43725612-43725662	SKMC	muscle:	n/a
24	chr10:43698141-43698191	PFSK-1	brain:	n/a
25	chr10:43698008-43698058	SKMC	muscle:	n/a
26	chr10:43724742-43724792	SKMC	muscle:	n/a
27	chr10:43725612-43725662	SK-N-MC	brain:	n/a
28	chr10:43721445-43721495	RPTEC	kidney:	n/a
29	chr10:43701731-43701781	HNPCEpiC	eye:	n/a
30	chr10:43697918-43697968	AoSMC	blood vessel:	n/a
31	chr10:43763042-43763092	GM12891	blood:	n/a
32	chr10:43725411-43725461	HCT-116	colon:	n/a
33	chr10:43725275-43725325	PFSK-1	brain:	n/a
34	chr10:43697817-43697867	NHDF-neo	bronchial:	n/a
35	chr10:43725411-43725461	GM12892	blood:	n/a
36	chr10:43725411-43725461	HCF	heart:	n/a
37	chr10:43728230-43728280	PrEC	prostate:	n/a
38	chr10:43725277-43725327	A549	lung:	n/a
39	chr10:43697849-43697899	GM19239	blood:	n/a
40	chr10:43701690-43701740	NH-A	brain:	n/a
41	chr10:43725376-43725426	HRE	kidney:	n/a
42	chr10:43725741-43725791	T-47D	breast:	n/a
43	chr10:43698931-43698981	SK-N-MC	brain:	n/a
44	chr10:43697521-43697571	HCPEpiC	choroid plexus:	n/a
45	chr10:43761841-43761891	AG04450	lung:	fetal
46	chr10:43704423-43704473	RPTEC	kidney:	n/a
47	chr10:43725275-43725325	AG04449	skin:	fetal
48	chr10:43761841-43761891	GM19239	blood:	n/a
49	chr10:43698008-43698058	PFSK-1	brain:	n/a
50	chr10:43698931-43698981	AG09309	skin:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:43741068..43743342-chr10:43744213..43745801,2	K562	blood:
2	chr10:43788353..43788943-chr10:43843731..43844609,2	MCF-7	breast:
3	chr10:43720076..43721666-chr10:43723376..43725809,2	K562	blood:
4	chr10:43624629..43626379-chr10:43749891..43752180,2	K562	blood:
5	chr10:43750362..43752659-chr10:43753450..43755922,3	K562	blood:
6	chr10:43780568..43784623-chr10:43788000..43790414,4	MCF-7	breast:
7	chr10:43788453..43789259-chr10:43957179..43957947,3	MCF-7	breast:
8	chr10:43746978..43749423-chr10:43756169..43758679,2	K562	blood:
9	chr10:43771948..43774253-chr10:43775459..43778308,3	K562	blood:
10	chr10:43788559..43789114-chr10:43875906..43876735,2	K562	blood:
11	chr10:43745055..43746859-chr10:43757087..43758973,2	MCF-7	breast:
12	chr10:43716570..43717454-chr10:43751032..43752428,7	MCF-7	breast:
13	chr10:43787979..43788967-chr10:43843516..43844636,5	K562	blood:
14	chr10:43717975..43720515-chr10:43721363..43724311,2	MCF-7	breast:
15	chr10:43717975..43720515-chr10:43721363..43724311,2	MCF-7	breast:
16	chr10:43716570..43717454-chr10:43751032..43752428,7	MCF-7	breast:
17	chr10:43696369..43700743-chr10:43891529..43894634,3	K562	blood:
18	chr10:43772713..43774253-chr10:43775459..43778308,2	K562	blood:
19	chr10:43757038..43760449-chr10:43762640..43764974,3	K562	blood:
20	chr10:43689923..43692438-chr10:43693060..43695471,2	MCF-7	breast:
21	chr10:43729621..43731654-chr10:43739921..43741494,2	MCF-7	breast:
22	chr10:43781689..43785378-chr10:43787938..43790513,4	MCF-7	breast:
23	chr10:43786873..43787506-chr10:43843726..43844460,2	MCF-7	breast:
24	chr10:43633619..43635410-chr10:43761017..43763266,2	MCF-7	breast:
25	chr10:43721241..43722992-chr10:43727167..43730117,3	MCF-7	breast:
26	chr10:43700022..43701253-chr10:43750988..43751917,9	MCF-7	breast:
27	chr10:43722360..43723991-chr10:43726752..43728958,3	K562	blood:
28	chr10:43782797..43785398-chr10:43889783..43892550,2	MCF-7	breast:
29	chr10:43693302..43696158-chr10:43696913..43699983,3	MCF-7	breast:
30	chr10:43665667..43666593-chr10:43751227..43751730,2	K562	blood:
31	chr10:43729621..43731654-chr10:43739921..43741494,2	MCF-7	breast:
32	chr10:43781454..43785014-chr10:43786070..43790387,3	K562	blood:
33	chr10:43779843..43782753-chr10:43889684..43893625,3	K562	blood:
34	chr10:43760886..43761922-chr10:43843561..43844509,10	MCF-7	breast:
35	chr10:43788412..43790350-chr10:43892794..43895604,2	K562	blood:
36	chr10:43679135..43682088-chr10:43694226..43696696,2	MCF-7	breast:
37	chr10:43768711..43770698-chr10:43777235..43780048,2	K562	blood:
38	chr10:43700964..43703905-chr10:43902812..43905482,2	K562	blood:
39	chr10:43721241..43722992-chr10:43727167..43730117,3	MCF-7	breast:
40	chr10:43720964..43723652-chr10:43803043..43805548,2	K562	blood:
41	chr10:43780568..43784623-chr10:43788000..43790414,4	MCF-7	breast:
42	chr10:43748329..43751092-chr10:43758387..43762104,3	MCF-7	breast:
43	chr10:43746978..43749423-chr10:43756169..43758679,2	K562	blood:
44	chr10:43748329..43751092-chr10:43758387..43762104,3	MCF-7	breast:
45	chr10:43781454..43785014-chr10:43786070..43790387,3	K562	blood:
46	chr10:43716710..43720339-chr10:43755141..43758566,3	K562	blood:
47	chr10:43750917..43751578-chr10:43813067..43813837,2	K562	blood:
48	chr10:43698957..43702295-chr10:43702554..43706038,5	K562	blood:
49	chr10:43788331..43789347-chr10:43843553..43844589,11	MCF-7	breast:
50	chr10:43749564..43751225-chr10:43756675..43758831,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPF-3	chr10:43716825-43717277	l_303_chr10:43716824-43727797_testes
2	lnc-HNRNPF-2	chr10:43729353-43729460	NONHSAT012947
3	lnc-CSGALNACT2-2	chr10:43759311-43759487	l_304_chr10:43724730-43729936_testes
4	lnc-CSGALNACT2-2	chr10:43754457-43755996	NONHSAT012948
5	lnc-CSGALNACT2-2	chr10:43729213-43729690	NONHSAT012946
6	lnc-CSGALNACT2-2	chr10:43758646-43758735	NONHSAT012948
7	lnc-HNRNPF-3	chr10:43716819-43717277	NONHSAT012945
8	lnc-HNRNPF-3	chr10:43727747-43727797	l_303_chr10:43716824-43727797_testes
9	lnc-CSGALNACT2-2	chr10:43727803-43727932	l_304_chr10:43724730-43729936_testes
10	lnc-HNRNPF-3	chr10:43718876-43719043	l_303_chr10:43716824-43727797_testes
11	lnc-CSGALNACT2-2	chr10:43729213-43729936	l_304_chr10:43724730-43729936_testes
12	lnc-CSGALNACT2-2	chr10:43724848-43725231	l_304_chr10:43724730-43729936_testes
13	lnc-FXYD4-5	chr10:43781932-43782168	l_305_chr10:43781931-43798196_testes
14	lnc-CSGALNACT2-2	chr10:43756176-43756431	NONHSAT012948
15	lnc-HNRNPF-3	chr10:43727747-43727780	NONHSAT012945
16	lnc-CSGALNACT2-2	chr10:43759311-43759445	NONHSAT012948
17	lnc-HNRNPF-2	chr10:43729604-43729960	NONHSAT012947
18	lnc-CSGALNACT2-2	chr10:43758646-43758735	l_304_chr10:43724730-43729936_testes
19	lnc-CSGALNACT2-2	chr10:43727898-43727932	NONHSAT012946
20	lnc-FXYD4-5	chr10:43795908-43798196	l_305_chr10:43781931-43798196_testes
21	lnc-CSGALNACT2-2	chr10:43759816-43759920	NONHSAT012948
22	lnc-CSGALNACT2-2	chr10:43724731-43724847	l_304_chr10:43724730-43729936_testes
23	lnc-CSGALNACT2-2	chr10:43780837-43781139	l_304_chr10:43724730-43729936_testes
24	lnc-CSGALNACT2-1	chr10:43710319-43710887	NONHSAT012944

No data

Variant related genes	Relation type
RASGEF1A	TF binding region
RASGEF1A	CpG island
ENSG00000169813	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000243660	chromatin interactions
ENSG00000198915	chromatin interactions
ENSG00000169826	chromatin interactions

Extended variants
information (count: 4261 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4261 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1254964	chr10:43695049-43695050	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373617588	chr10:43695074-43695075	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs549159403	chr10:43695082-43695083	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs185837886	chr10:43695083-43695084	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368852111	chr10:43695100-43695101	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs376128525	chr10:43695105-43695106	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs374472625	chr10:43695106-43695107	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs41301581	chr10:43695112-43695113	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs76306135	chr10:43695113-43695114	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs139262265	chr10:43695145-43695146	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs201765175	chr10:43695193-43695194	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs374403441	chr10:43695208-43695209	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs189494581	chr10:43695235-43695236	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs575901432	chr10:43695279-43695280	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs138086250	chr10:43695280-43695281	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs555013287	chr10:43695322-43695323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs573524937	chr10:43695341-43695342	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs540807592	chr10:43695342-43695343	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs552886057	chr10:43695348-43695349	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs577857260	chr10:43695482-43695483	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs1272142	chr10:43695484-43695485	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs191232348	chr10:43695523-43695524	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs530769819	chr10:43695524-43695525	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs183870080	chr10:43695529-43695530	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116260578	chr10:43695538-43695539	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs528722615	chr10:43695539-43695540	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547199632	chr10:43695560-43695561	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs149358205	chr10:43695568-43695569	Weak transcription Strong transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs41301583	chr10:43695616-43695617	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77077330	chr10:43695662-43695663	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371709436	chr10:43695663-43695664	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149633919	chr10:43695675-43695676	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544272873	chr10:43695704-43695705	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571838913	chr10:43695776-43695777	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs569649610	chr10:43695782-43695783	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536616926	chr10:43695791-43695792	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181531046	chr10:43695802-43695803	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567009977	chr10:43695813-43695814	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs77562345	chr10:43695861-43695862	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs117675731	chr10:43695866-43695867	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs116333666	chr10:43695923-43695924	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545295289	chr10:43695927-43695928	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376930583	chr10:43695959-43695960	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575615802	chr10:43695960-43695961	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543021327	chr10:43695963-43695964	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs111950946	chr10:43696003-43696004	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs142878700	chr10:43696004-43696005	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs528594662	chr10:43696007-43696008	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115380536	chr10:43696038-43696039	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs61843255	chr10:43696045-43696046	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	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	21293372	CNVD

Chromatin state (count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43652600-43697200	Weak transcription	Pancreas	Pancrea
2	chr10:43662200-43697600	Weak transcription	NHEK	skin
3	chr10:43674400-43697800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr10:43675600-43700600	Weak transcription	A549	lung
5	chr10:43675800-43697000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:43678800-43696800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr10:43679400-43697400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr10:43680000-43697600	Weak transcription	NH-A	brain
9	chr10:43682000-43697400	Weak transcription	Liver	Liver
10	chr10:43682600-43697400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr10:43682600-43697400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr10:43683000-43696000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr10:43683000-43697000	Weak transcription	Primary hematopoietic stem cells	blood
14	chr10:43683000-43697200	Weak transcription	Primary B cells from cord blood	blood
15	chr10:43683000-43697400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr10:43683000-43697400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr10:43683000-43697400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr10:43683200-43697000	Weak transcription	Fetal Brain Male	brain
19	chr10:43683200-43697200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr10:43683200-43697200	Weak transcription	Duodenum Mucosa	Duodenum
21	chr10:43683400-43695200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr10:43683400-43697000	Weak transcription	Fetal Intestine Small	intestine
23	chr10:43683800-43696600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr10:43683800-43697000	Weak transcription	Fetal Lung	lung
25	chr10:43684400-43697200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr10:43684400-43697200	Weak transcription	Ovary	ovary
27	chr10:43684400-43697400	Weak transcription	Primary T cells from cord blood	blood
28	chr10:43686800-43697000	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr10:43688600-43697000	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr10:43688600-43697800	Weak transcription	Aorta	Aorta
31	chr10:43688800-43696000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr10:43688800-43697600	Weak transcription	NHLF	lung
33	chr10:43689000-43696800	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr10:43689000-43697800	Weak transcription	HSMM	muscle
35	chr10:43689200-43697200	Weak transcription	Thymus	Thymus
36	chr10:43689200-43697400	Weak transcription	Esophagus	oesophagus
37	chr10:43690000-43696800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr10:43690000-43697000	Strong transcription	H9 Cell Line	embryonic stem cell
39	chr10:43690000-43697400	Weak transcription	Fetal Brain Female	brain
40	chr10:43690400-43696600	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chr10:43690400-43696600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
42	chr10:43690400-43696600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr10:43690600-43695800	Weak transcription	Gastric	stomach
44	chr10:43690600-43696000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr10:43690600-43696200	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr10:43690600-43696200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr10:43690600-43696600	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr10:43690600-43696800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
49	chr10:43690600-43697400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr10:43690800-43696800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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