Variant report

Variant	nsv872765
Chromosome Location	chr1:190418653-190464647
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	chr1:190422723-190422890	HepG2	liver:	n/a	n/a
2	BACH1	chr1:190444539-190444919	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr1:190448178-190448180	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr1:190444585-190445212	IMR90	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
5	CEBPB	chr1:190444800-190445186	HepG2	liver:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
6	CEBPB	chr1:190444814-190445176	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
7	CEBPB	chr1:190463528-190463986	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:190444799-190445222	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
9	CEBPB	chr1:190444837-190445233	MCF-7	breast:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
10	CEBPB	chr1:190444781-190445213	MCF-7	breast:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
11	CEBPB	chr1:190444847-190445175	K562	blood:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
12	CEBPB	chr1:190448377-190448519	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:190444708-190445343	A549	lung:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
14	CEBPB	chr1:190444631-190445184	H1-hESC	embryonic stem cell:	n/a	chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005 chr1:190444996-190445005
15	CEBPB	chr1:190447237-190447354	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr1:190448119-190448317	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr1:190447111-190447248	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr1:190444232-190444267	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr1:190444200-190444215	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr1:190447252-190447284	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:190448095-190448332	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr1:190447174-190448394	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:190460620-190460770	HCT-116	colon:	n/a	n/a
24	CTCF	chr1:190447360-190447510	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr1:190422539-190423132	A549	lung:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
26	CTCF	chr1:190422700-190422850	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr1:190447320-190447470	HRE	kidney:	n/a	n/a
28	CTCF	chr1:190422760-190422910	HMEC	breast:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
29	CTCF	chr1:190422740-190422890	GM12874	blood:	n/a	n/a
30	CTCF	chr1:190422780-190422930	HCM	heart:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
31	CTCF	chr1:190447380-190447530	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr1:190447360-190447510	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr1:190447360-190447510	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr1:190460580-190460730	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr1:190448845-190448930	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:190423720-190423870	HRE	kidney:	n/a	n/a
37	CTCF	chr1:190422820-190422970	HMF	breast:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
38	CTCF	chr1:190447522-190447524	Gliobla	brain:	n/a	n/a
39	CTCF	chr1:190422862-190422880	LNCaP	prostate:	n/a	n/a
40	CTCF	chr1:190422711-190423073	IMR90	lung:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
41	CTCF	chr1:190460637-190460740	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr1:190460640-190460790	BE2_C	brain:	n/a	n/a
43	CTCF	chr1:190447460-190447610	AG04450	lung:	n/a	n/a
44	CTCF	chr1:190422815-190422919	Hela-S3	cervix:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
45	CTCF	chr1:190447520-190447670	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr1:190422740-190422890	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr1:190422760-190422910	HCPEpiC	choroid plexus:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
48	CTCF	chr1:190447278-190447521	Gliobla	brain:	n/a	n/a
49	CTCF	chr1:190422800-190422950	HPF	lung:	n/a	chr1:190422882-190422892 chr1:190422874-190422895 chr1:190422881-190422894 chr1:190422880-190422896 chr1:190422879-190422897
50	CTCF	chr1:190422720-190422870	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:190444825-190444875	HAEpiC	amniotic membrane:	n/a
2	chr1:190447640-190447690	AG09319	gingival:	n/a
3	chr1:190444761-190444811	CMK	blood:	n/a
4	chr1:190444825-190444875	RPTEC	kidney:	n/a
5	chr1:190447603-190447653	A549	lung:	n/a
6	chr1:190444825-190444875	HNPCEpiC	eye:	n/a
7	chr1:190446829-190446879	MCF10A-Er-Src	breast:	n/a
8	chr1:190444761-190444811	HRCEpiC	kidney:	n/a
9	chr1:190444825-190444875	GM12891	blood:	n/a
10	chr1:190444761-190444811	Hepatocyte	liver:	n/a
11	chr1:190447640-190447690	AG10803	skin:	n/a
12	chr1:190448126-190448176	NH-A	brain:	n/a
13	chr1:190447232-190447282	HCM	heart:	n/a
14	chr1:190444825-190444875	HEEpiC	esophagus:	n/a
15	chr1:190444387-190444437	HIPEpiC	eye:	n/a
16	chr1:190444776-190444826	BE2_C	brain:	n/a
17	chr1:190448126-190448176	HEK293	kidney:	embryo
18	chr1:190446829-190446879	AoSMC	blood vessel:	n/a
19	chr1:190444761-190444811	IMR90	lung:	fetal
20	chr1:190445197-190445247	LNCaP	prostate:	n/a
21	chr1:190444761-190444811	K562	blood:	n/a
22	chr1:190446829-190446879	PANC-1	pancreas:	n/a
23	chr1:190444825-190444875	SK-N-SH	brain:	n/a
24	chr1:190445197-190445247	HMEC	breast:	n/a
25	chr1:190444666-190444716	Hepatocyte	liver:	n/a
26	chr1:190448126-190448176	GM12892	blood:	n/a
27	chr1:190447640-190447690	HL-60	blood:	n/a
28	chr1:190447232-190447282	AG04450	lung:	fetal
29	chr1:190444761-190444811	HCPEpiC	choroid plexus:	n/a
30	chr1:190446756-190446806	MCF10A-Er-Src	breast:	n/a
31	chr1:190444776-190444826	AG09309	skin:	n/a
32	chr1:190444776-190444826	Jurkat	blood:	n/a
33	chr1:190447421-190447471	H1-hESC	embryonic stem cell:	embryo
34	chr1:190447603-190447653	HRE	kidney:	n/a
35	chr1:190446756-190446806	BJ	skin:	n/a
36	chr1:190447603-190447653	Hela-S3	cervix:	n/a
37	chr1:190444387-190444437	NHBE	bronchial:	n/a
38	chr1:190444387-190444437	HRE	kidney:	n/a
39	chr1:190447421-190447471	HMEC	breast:	n/a
40	chr1:190447290-190447340	NT2-D1	testis:	n/a
41	chr1:190447290-190447340	HEK293	kidney:	embryo
42	chr1:190444761-190444811	H1-hESC	embryonic stem cell:	embryo
43	chr1:190444825-190444875	NT2-D1	testis:	n/a
44	chr1:190446756-190446806	NH-A	brain:	n/a
45	chr1:190444776-190444826	HNPCEpiC	eye:	n/a
46	chr1:190444761-190444811	GM06990	blood:	n/a
47	chr1:190444387-190444437	T-47D	breast:	n/a
48	chr1:190447421-190447471	AG10803	skin:	n/a
49	chr1:190446829-190446879	Hela-S3	cervix:	n/a
50	chr1:190445197-190445247	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:190456328..190457105-chr20:42218949..42219566,2	Hela-S3	cervix:
2	chr1:190405958..190408213-chr1:190432999..190435234,2	K562	blood:
3	chr1:190443878..190446178-chr1:190461343..190463264,2	K562	blood:
4	chr1:190438085..190440650-chr1:190553313..190555425,2	K562	blood:
5	chr1:187382637..187383516-chr1:190422637..190423274,2	MCF-7	breast:
6	chr1:190429891..190431427-chr1:190443822..190445349,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-5	chr1:190446965-190447761	NONHSAT008497
2	lnc-RGS18-5	chr1:190444703-190444884	NONHSAT008495
3	lnc-RGS18-5	chr1:190449475-190449704	XLOC_000505
4	lnc-RGS18-5	chr1:190449475-190449865	XLOC_000505
5	lnc-RGS18-5	chr1:190449475-190449779	NONHSAT008496
6	lnc-RGS18-5	chr1:190449475-190450669	XLOC_000505
7	lnc-RGS18-5	chr1:190449509-190449554	ENSG00000241505
8	lnc-RGS18-5	chr1:190448212-190448255	NONHSAT008497
9	lnc-RGS18-5	chr1:190449475-190449865	XLOC_000505
10	lnc-RGS18-5	chr1:190448171-190448270	XLOC_000505
11	lnc-RGS18-5	chr1:190462968-190463427	ENSG00000241505
12	lnc-RGS18-5	chr1:190444999-190445131	NONHSAT008496
13	lnc-RGS18-5	chr1:190447329-190447761	NONHSAT008498
14	lnc-RGS18-5	chr1:190448136-190448270	XLOC_000505
15	lnc-RGS18-5	chr1:190447888-190448066	NONHSAT008498
16	lnc-RGS18-5	chr1:190447939-190447943	XLOC_000505
17	lnc-RGS18-5	chr1:190447390-190447622	XLOC_000505
18	lnc-RGS18-5	chr1:190447681-190447761	XLOC_000505
19	lnc-RGS18-5	chr1:190447611-190447761	XLOC_000505
20	lnc-RGS18-5	chr1:190448171-190448270	XLOC_000505
21	lnc-RGS18-5	chr1:190448212-190448270	XLOC_000505
22	lnc-RGS18-5	chr1:190462968-190463251	XLOC_000505
23	lnc-RGS18-5	chr1:190445011-190445157	NONHSAT008495
24	lnc-RGS18-5	chr1:190447356-190447622	XLOC_000505
25	lnc-RGS18-5	chr1:190447753-190447761	XLOC_000505
26	lnc-RGS18-5	chr1:190448171-190448271	XLOC_000505
27	lnc-RGS18-5	chr1:190449475-190450669	XLOC_000505
28	lnc-RGS18-5	chr1:190449475-190450667	XLOC_000505
29	lnc-RGS18-5	chr1:190449475-190450523	XLOC_000505
30	lnc-RGS18-5	chr1:190447593-190447761	XLOC_000505

Variant related genes	Relation type
ENSG00000237457	TF binding region
ENSG00000241505	TF binding region
BRINP3	TF binding region
ENSG00000237457	CpG island
ENSG00000241505	CpG island
BRINP3	CpG island
ENSG00000162670	chromatin interactions
FECH	miRNA target sites
PRNP	miRNA target sites
PDLIM5	miRNA target sites
NRAS	miRNA target sites

Extended variants
information (count: 1526 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1171023	chr1:190418653-190418654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76751759	chr1:190418655-190418656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199559182	chr1:190418691-190418692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34335384	chr1:190418693-190418694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537004224	chr1:190418694-190418695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556425388	chr1:190418695-190418696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs398039060	chr1:190418706-190418707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370543201	chr1:190418707-190418708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374582612	chr1:190418709-190418710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181648075	chr1:190418718-190418719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185928759	chr1:190418730-190418731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535300893	chr1:190418741-190418742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555120690	chr1:190418758-190418759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116118705	chr1:190418772-190418773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541135544	chr1:190418836-190418837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557525600	chr1:190418855-190418856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577567819	chr1:190418856-190418857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376686997	chr1:190418867-190418868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564008986	chr1:190418918-190418919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574374705	chr1:190418940-190418941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1171024	chr1:190418961-190418962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs117282909	chr1:190419008-190419009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577828301	chr1:190419054-190419055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528665004	chr1:190419075-190419076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557361437	chr1:190419116-190419117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191042901	chr1:190419126-190419127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182583257	chr1:190419239-190419240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187145761	chr1:190419322-190419323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539854709	chr1:190419371-190419372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550683805	chr1:190419409-190419410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs80209499	chr1:190419417-190419418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573401019	chr1:190419464-190419465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191151929	chr1:190419547-190419548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548829421	chr1:190419563-190419564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565545797	chr1:190419569-190419570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182497997	chr1:190419590-190419591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12042770	chr1:190419635-190419636	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs35783738	chr1:190419639-190419640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs577652653	chr1:190419647-190419648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78540358	chr1:190419761-190419762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188359915	chr1:190419773-190419774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556977123	chr1:190419861-190419862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189981349	chr1:190419889-190419890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543783079	chr1:190419958-190419959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543360903	chr1:190420005-190420006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114556298	chr1:190420025-190420026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573389384	chr1:190420060-190420061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28712328	chr1:190420086-190420087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550019843	chr1:190420087-190420088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565419202	chr1:190420104-190420105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:190379400-190420000	Weak transcription	Fetal Intestine Large	intestine
2	chr1:190411000-190425600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:190414000-190419200	Weak transcription	Fetal Intestine Small	intestine
4	chr1:190419200-190419400	Enhancers	Fetal Intestine Small	intestine
5	chr1:190419200-190420800	Enhancers	Duodenum Mucosa	Duodenum
6	chr1:190419400-190419800	Weak transcription	Fetal Intestine Small	intestine
7	chr1:190419800-190420800	Enhancers	Fetal Intestine Small	intestine
8	chr1:190420000-190422000	Enhancers	Fetal Intestine Large	intestine
9	chr1:190420400-190421000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:190420800-190421600	Weak transcription	Fetal Intestine Small	intestine
11	chr1:190421400-190422200	Enhancers	HepG2	liver
12	chr1:190421400-190424200	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr1:190421600-190422800	Strong transcription	Fetal Intestine Small	intestine
14	chr1:190421800-190422200	Enhancers	Placenta	Placenta
15	chr1:190422000-190438400	Weak transcription	Fetal Intestine Large	intestine
16	chr1:190422800-190438800	Weak transcription	Fetal Intestine Small	intestine
17	chr1:190423800-190424000	Enhancers	Fetal Heart	heart
18	chr1:190436200-190436600	Enhancers	Fetal Heart	heart
19	chr1:190438400-190439000	Active TSS	Fetal Intestine Large	intestine
20	chr1:190438800-190439400	Enhancers	Fetal Intestine Small	intestine
21	chr1:190439000-190440200	Weak transcription	Fetal Intestine Large	intestine
22	chr1:190439400-190441200	Weak transcription	Fetal Intestine Small	intestine
23	chr1:190440000-190440200	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr1:190440000-190448800	Active TSS	Duodenum Mucosa	Duodenum
25	chr1:190440200-190448800	Active TSS	Fetal Intestine Large	intestine
26	chr1:190440600-190441000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr1:190440800-190448600	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr1:190440800-190448800	Active TSS	Rectal Mucosa Donor 29	rectum
29	chr1:190441000-190445800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:190441200-190441800	Active TSS	Brain Germinal Matrix	brain
31	chr1:190441200-190443600	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr1:190441200-190448600	Active TSS	Fetal Intestine Small	intestine
33	chr1:190441200-190448600	Active TSS	Right Atrium	heart
34	chr1:190441400-190444600	Active TSS	Brain Angular Gyrus	brain
35	chr1:190441400-190445600	Active TSS	Brain Anterior Caudate	brain
36	chr1:190441800-190442200	Active TSS	Fetal Lung	lung
37	chr1:190441800-190442600	Weak transcription	Brain Germinal Matrix	brain
38	chr1:190442200-190442400	Bivalent/Poised TSS	Fetal Lung	lung
39	chr1:190442600-190443800	Active TSS	Fetal Stomach	stomach
40	chr1:190442600-190445000	Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr1:190442600-190445200	Active TSS	Brain Germinal Matrix	brain
42	chr1:190442800-190444200	Active TSS	Fetal Brain Female	brain
43	chr1:190443000-190443800	Active TSS	Brain Cingulate Gyrus	brain
44	chr1:190443000-190445600	Active TSS	Colonic Mucosa	Colon
45	chr1:190443000-190449600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr1:190443200-190443400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
47	chr1:190443200-190443400	Active TSS	Fetal Brain Male	brain
48	chr1:190443200-190445600	Bivalent/Poised TSS	Fetal Lung	lung
49	chr1:190443200-190445800	Active TSS	Fetal Heart	heart
50	chr1:190443400-190443600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

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