Variant report

Variant	nsv984058
Chromosome Location	chr15:41848218-41850246
allele	n/a
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	ARID3A	chr15:41849805-41850122	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:41849792-41850158	K562	blood:	n/a	n/a
3	BACH1	chr15:41849830-41850529	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr15:41849906-41850106	K562	blood:	n/a	n/a
5	BCL11A	chr15:41849859-41850060	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr15:41849900-41850410	GM12878	blood:	n/a	chr15:41849958-41849974 chr15:41849946-41849962
7	BHLHE40	chr15:41849897-41850145	HepG2	liver:	n/a	chr15:41849958-41849974 chr15:41849946-41849962
8	BHLHE40	chr15:41849851-41850299	K562	blood:	n/a	chr15:41849958-41849974 chr15:41849946-41849962
9	BRCA1	chr15:41849895-41850464	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr15:41850027-41850088	HepG2	liver:	n/a	n/a
11	BRCA1	chr15:41849918-41850152	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:41849899-41850123	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPD	chr15:41849894-41850129	HepG2	liver:	n/a	n/a
14	CHD2	chr15:41849997-41850114	HepG2	liver:	n/a	n/a
15	CHD2	chr15:41849872-41850299	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr15:41849880-41850030	HMF	breast:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
17	CTCF	chr15:41849880-41850030	HRE	kidney:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
18	CTCF	chr15:41849764-41850172	K562	blood:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
19	CTCF	chr15:41849805-41850103	LNCaP	prostate:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
20	CTCF	chr15:41849960-41850110	HMEC	breast:	n/a	chr15:41850060-41850073 chr15:41849962-41849975
21	CTCF	chr15:41849860-41850010	AG09309	skin:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
22	CTCF	chr15:41849860-41850010	GM12870	blood:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
23	CTCF	chr15:41849208-41849321	GM13977	blood:	n/a	n/a
24	CTCF	chr15:41849737-41850211	MCF-7	breast:	n/a	chr15:41849950-41849966 chr15:41850174-41850192 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965 chr15:41850180-41850189
25	CTCF	chr15:41849837-41850075	Kidney_OC	kidney:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
26	CTCF	chr15:41849900-41850050	HCFaa	heart:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
27	CTCF	chr15:41849834-41850092	A549	lung:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
28	CTCF	chr15:41849846-41850089	MCF-7	breast:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
29	CTCF	chr15:41849900-41850050	SK-N-SH_RA	brain:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
30	CTCF	chr15:41849819-41850127	GM19240	blood:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
31	CTCF	chr15:41849781-41850126	A549	lung:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
32	CTCF	chr15:41849797-41850102	HepG2	liver:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
33	CTCF	chr15:41849880-41850030	NHDF-neo	bronchial:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
34	CTCF	chr15:41849854-41850075	Fibrobl	skin:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
35	CTCF	chr15:41849830-41850113	Gliobla	brain:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
36	CTCF	chr15:41849920-41850070	HFF-Myc	foreskin:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
37	CTCF	chr15:41849880-41850030	NB4	blood:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
38	CTCF	chr15:41849860-41850010	GM12865	blood:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
39	CTCF	chr15:41849900-41850050	HPAF	blood vessel:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
40	CTCF	chr15:41849726-41851378	A549	lung:	n/a	chr15:41849950-41849966 chr15:41850174-41850192 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41851122-41851135 chr15:41849952-41849965 chr15:41850180-41850189 chr15:41851159-41851172
41	CTCF	chr15:41849880-41850030	HAc	cerebellar:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
42	CTCF	chr15:41849860-41850010	AG10803	skin:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
43	CTCF	chr15:41849785-41850275	K562	blood:	n/a	chr15:41849950-41849966 chr15:41850174-41850192 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965 chr15:41850180-41850189
44	CTCF	chr15:41849786-41850131	K562	blood:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
45	CTCF	chr15:41849940-41850090	HCM	heart:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
46	CTCF	chr15:41849900-41850050	HMEC	breast:	n/a	chr15:41849950-41849966 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
47	CTCF	chr15:41849806-41850116	HUVEC	blood vessel:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
48	CTCF	chr15:41849822-41850104	Lung_OC	lung:	n/a	chr15:41849950-41849966 chr15:41850060-41850073 chr15:41849949-41849962 chr15:41849949-41849967 chr15:41849962-41849975 chr15:41849952-41849965
49	CTCF	chr15:41850120-41850270	HEK293	kidney:	n/a	chr15:41850174-41850192 chr15:41850180-41850189
50	CTCF	chr15:41849297-41849435	GM10248	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41849953-41850003	AG10803	skin:	n/a
2	chr15:41849953-41850003	AG04449	skin:	fetal
3	chr15:41849556-41849606	NB4	blood:	n/a
4	chr15:41849953-41850003	HL-60	blood:	n/a
5	chr15:41849953-41850003	GM12878	blood:	n/a
6	chr15:41849953-41850003	AG09309	skin:	n/a
7	chr15:41849953-41850003	MCF10A-Er-Src	breast:	n/a
8	chr15:41849556-41849606	PFSK-1	brain:	n/a
9	chr15:41849953-41850003	GM19239	blood:	n/a
10	chr15:41849556-41849606	HEK293	kidney:	embryo
11	chr15:41849953-41850003	GM06990	blood:	n/a
12	chr15:41849953-41850003	AG04450	lung:	fetal
13	chr15:41849953-41850003	NB4	blood:	n/a
14	chr15:41849953-41850003	RPTEC	kidney:	n/a
15	chr15:41849556-41849606	Hepatocyte	liver:	n/a
16	chr15:41849953-41850003	GM12892	blood:	n/a
17	chr15:41849953-41850003	ovcar-3	ovarian:	n/a
18	chr15:41849953-41850003	AG09319	gingival:	n/a
19	chr15:41849953-41850003	ECC-1	luminal epithelium:	n/a
20	chr15:41849556-41849606	HRE	kidney:	n/a
21	chr15:41849556-41849606	U87	brain:	n/a
22	chr15:41849953-41850003	BE2_C	brain:	n/a
23	chr15:41849556-41849606	Hela-S3	cervix:	n/a
24	chr15:41849556-41849606	T-47D	breast:	n/a
25	chr15:41849556-41849606	HCPEpiC	choroid plexus:	n/a
26	chr15:41849556-41849606	AG09319	gingival:	n/a
27	chr15:41849953-41850003	SK-N-MC	brain:	n/a
28	chr15:41849953-41850003	Caco-2	colon:	n/a
29	chr15:41849556-41849606	GM12892	blood:	n/a
30	chr15:41849953-41850003	HCM	heart:	n/a
31	chr15:41849953-41850003	GM12891	blood:	n/a
32	chr15:41849953-41850003	NHBE	bronchial:	n/a
33	chr15:41849953-41850003	ProgFib	skin:	n/a
34	chr15:41849556-41849606	K562	blood:	n/a
35	chr15:41849556-41849606	GM12891	blood:	n/a
36	chr15:41849556-41849606	HCF	heart:	n/a
37	chr15:41849556-41849606	ProgFib	skin:	n/a
38	chr15:41849953-41850003	SK-N-SH	brain:	n/a
39	chr15:41849953-41850003	SAEC	small airway:	n/a
40	chr15:41849556-41849606	NHBE	bronchial:	n/a
41	chr15:41849556-41849606	GM06990	blood:	n/a
42	chr15:41849556-41849606	MCF-7	breast:	n/a
43	chr15:41849556-41849606	SAEC	small airway:	n/a
44	chr15:41849556-41849606	NT2-D1	testis:	n/a
45	chr15:41849556-41849606	RPTEC	kidney:	n/a
46	chr15:41849556-41849606	PrEC	prostate:	n/a
47	chr15:41849953-41850003	HRE	kidney:	n/a
48	chr15:41849953-41850003	HCF	heart:	n/a
49	chr15:41849556-41849606	HNPCEpiC	eye:	n/a
50	chr15:41849556-41849606	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:41849860..41852803-chr15:41858013..41860929,2	MCF-7	breast:
2	chr15:41784400..41789772-chr15:41847283..41854059,7	K562	blood:
3	chr15:41834571..41836708-chr15:41849262..41851156,2	K562	blood:
4	chr15:41847317..41853712-chr15:41951201..41955578,8	K562	blood:
5	chr15:41845325..41848797-chr15:41849286..41852428,6	MCF-7	breast:
6	chr15:41849370..41852913-chr15:41951069..41953769,6	K562	blood:
7	chr15:41841534..41844151-chr15:41845202..41848536,3	K562	blood:
8	chr15:41849459..41853162-chr15:41854225..41857161,4	MCF-7	breast:

Variant related genes	Relation type
TYRO3	TF binding region
TCEB1P2	TF binding region
TYRO3	CpG island
TCEB1P2	CpG island
ENSG00000092445	chromatin interactions
ENSG00000103932	chromatin interactions
ENSG00000137825	chromatin interactions
ENSG00000174197	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12593245	chr15:41848230-41848231	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs140491757	chr15:41848296-41848297	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs8040005	chr15:41848310-41848311	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs576791432	chr15:41848365-41848366	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs190771601	chr15:41848427-41848428	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs550751119	chr15:41848459-41848460	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs150017204	chr15:41848520-41848521	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs372637206	chr15:41848549-41848550	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs181969202	chr15:41848573-41848574	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs147699306	chr15:41848588-41848589	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs373727176	chr15:41848589-41848590	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs372654204	chr15:41848593-41848594	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs142325071	chr15:41848614-41848615	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs538640314	chr15:41848654-41848655	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs186341035	chr15:41848686-41848687	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs376879494	chr15:41848695-41848696	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs567136851	chr15:41848699-41848700	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs569372780	chr15:41848721-41848722	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs570906700	chr15:41848749-41848750	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs537284627	chr15:41848795-41848796	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs12593920	chr15:41848796-41848797	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs573707827	chr15:41848845-41848846	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs542932437	chr15:41848891-41848892	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs34004332	chr15:41848895-41848896	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs570099927	chr15:41848945-41848946	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs552960233	chr15:41848952-41848953	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs572832845	chr15:41849021-41849022	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs116264307	chr15:41849026-41849027	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs62001443	chr15:41849033-41849034	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs62001444	chr15:41849035-41849036	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs62001445	chr15:41849037-41849038	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs62001446	chr15:41849044-41849045	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs112671461	chr15:41849048-41849049	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs369512825	chr15:41849049-41849050	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs374641346	chr15:41849062-41849063	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs58922499	chr15:41849063-41849064	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs200668293	chr15:41849066-41849067	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs111861161	chr15:41849069-41849070	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs76227053	chr15:41849076-41849077	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs74918081	chr15:41849078-41849079	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs543854396	chr15:41849095-41849096	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs561165692	chr15:41849097-41849098	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs571825198	chr15:41849142-41849143	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs530200026	chr15:41849146-41849147	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs542429633	chr15:41849201-41849202	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs61748808	chr15:41849226-41849227	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs371326471	chr15:41849282-41849283	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs180704819	chr15:41849285-41849286	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs61748807	chr15:41849290-41849291	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs567030975	chr15:41849331-41849332	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41837200-41850000	Weak transcription	Brain Anterior Caudate	brain
2	chr15:41837200-41850200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:41845800-41850600	Enhancers	HUVEC	blood vessel
4	chr15:41846000-41850000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr15:41846200-41850000	Weak transcription	Osteobl	bone
6	chr15:41846400-41850000	Weak transcription	HSMMtube	muscle
7	chr15:41847000-41850000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:41847000-41850000	Weak transcription	Left Ventricle	heart
9	chr15:41847200-41849600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:41847200-41850000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr15:41847200-41850000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr15:41847200-41850000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr15:41847200-41850000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr15:41847200-41850000	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr15:41847400-41849600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr15:41847400-41849800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr15:41847400-41850000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:41847400-41850000	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr15:41847400-41850000	Weak transcription	Fetal Kidney	kidney
20	chr15:41847400-41850000	Weak transcription	Placenta	Placenta
21	chr15:41847400-41850000	Weak transcription	HSMM	muscle
22	chr15:41847600-41848400	Weak transcription	Adipose Nuclei	Adipose
23	chr15:41847600-41848400	Weak transcription	Right Atrium	heart
24	chr15:41847600-41850000	Weak transcription	Brain Angular Gyrus	brain
25	chr15:41847600-41850000	Weak transcription	Fetal Intestine Large	intestine
26	chr15:41847600-41850000	Weak transcription	Fetal Intestine Small	intestine
27	chr15:41847600-41850000	Weak transcription	Spleen	Spleen
28	chr15:41848200-41848400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr15:41848200-41848400	Enhancers	Fetal Muscle Leg	muscle
30	chr15:41848200-41848400	Enhancers	Psoas Muscle	Psoas
31	chr15:41848200-41848800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr15:41848200-41849000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:41848200-41849400	Enhancers	K562	blood
34	chr15:41848200-41850400	Enhancers	Primary B cells from peripheral blood	blood
35	chr15:41848400-41848600	Enhancers	Adipose Nuclei	Adipose
36	chr15:41848400-41848600	Enhancers	Lung	lung
37	chr15:41848400-41848800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr15:41848400-41848800	Enhancers	Right Atrium	heart
39	chr15:41848400-41850000	Weak transcription	Psoas Muscle	Psoas
40	chr15:41848600-41849000	Weak transcription	Adipose Nuclei	Adipose
41	chr15:41848600-41849200	Enhancers	Primary B cells from cord blood	blood
42	chr15:41848800-41850000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr15:41848800-41850000	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr15:41848800-41850000	Weak transcription	Lung	lung
45	chr15:41848800-41850000	Weak transcription	Right Atrium	heart
46	chr15:41849000-41849400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:41849000-41850000	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr15:41849000-41850000	Enhancers	Adipose Nuclei	Adipose
49	chr15:41849000-41850000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr15:41849200-41849600	Weak transcription	Primary B cells from cord blood	blood

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