Variant report

Variant	nsv520425
Chromosome Location	chr1:150669952-150673684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:279)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150669458-150670246	K562	blood:	n/a	n/a
2	ARID3A	chr1:150669521-150670181	HepG2	liver:	n/a	n/a
3	ATF1	chr1:150669547-150670029	K562	blood:	n/a	n/a
4	BCL3	chr1:150669301-150670144	A549	lung:	n/a	n/a
5	BHLHE40	chr1:150669725-150669999	GM12878	blood:	n/a	n/a
6	BRCA1	chr1:150669458-150670063	Hela-S3	cervix:	n/a	chr1:150669751-150669758
7	CBX3	chr1:150669327-150670139	K562	blood:	n/a	n/a
8	CEBPB	chr1:150669483-150670066	Hela-S3	cervix:	n/a	chr1:150669882-150669890
9	CEBPB	chr1:150669362-150670126	MCF-7	breast:	n/a	chr1:150669882-150669890 chr1:150669436-150669449
10	CEBPB	chr1:150669545-150669987	IMR90	lung:	n/a	chr1:150669882-150669890
11	CEBPZ	chr1:150669516-150670046	HepG2	liver:	n/a	n/a
12	CHD2	chr1:150669499-150670016	HepG2	liver:	n/a	n/a
13	CHD2	chr1:150669410-150670300	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr1:150669083-150670112	Hela-S3	cervix:	n/a	chr1:150669266-150669276
15	CHD2	chr1:150669396-150670144	GM12878	blood:	n/a	n/a
16	CHD2	chr1:150669452-150670078	K562	blood:	n/a	n/a
17	CREB1	chr1:150669420-150670149	GM12878	blood:	n/a	n/a
18	CREB1	chr1:150669444-150669989	A549	lung:	n/a	n/a
19	CREB1	chr1:150669353-150670238	GM12878	blood:	n/a	n/a
20	CREB1	chr1:150669435-150669965	A549	lung:	n/a	n/a
21	CREB1	chr1:150669424-150670110	ECC-1	luminal epithelium:	n/a	n/a
22	CREB1	chr1:150669355-150670153	HepG2	liver:	n/a	n/a
23	CREB1	chr1:150669321-150670121	HepG2	liver:	n/a	n/a
24	CREB1	chr1:150669423-150670041	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr1:150669900-150670050	HCM	heart:	n/a	n/a
26	CTCF	chr1:150669820-150669970	HMEC	breast:	n/a	n/a
27	CTCF	chr1:150669900-150670050	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr1:150669644-150669964	IMR90	lung:	n/a	n/a
29	CUX1	chr1:150669413-150670177	GM12878	blood:	n/a	n/a
30	CUX1	chr1:150669430-150670020	K562	blood:	n/a	n/a
31	E2F4	chr1:150668646-150670023	MCF10A-Er-Src	breast:	n/a	chr1:150669881-150669890
32	EBF1	chr1:150669475-150670211	GM12878	blood:	n/a	n/a
33	ELF1	chr1:150669298-150670140	SK-N-SH	brain:	n/a	n/a
34	ELF1	chr1:150669333-150669988	K562	blood:	n/a	n/a
35	ELF1	chr1:150669367-150670029	HepG2	liver:	n/a	n/a
36	ELF1	chr1:150669261-150670339	MCF-7	breast:	n/a	n/a
37	ELF1	chr1:150669409-150670017	SK-N-SH	brain:	n/a	n/a
38	ELF1	chr1:150669395-150669976	HepG2	liver:	n/a	n/a
39	ELF1	chr1:150669397-150670189	MCF-7	breast:	n/a	n/a
40	ELF1	chr1:150669375-150669961	GM12878	blood:	n/a	n/a
41	ELF1	chr1:150669429-150670000	A549	lung:	n/a	n/a
42	ELK1	chr1:150669458-150670153	GM12878	blood:	n/a	n/a
43	EP300	chr1:150669483-150670065	K562	blood:	n/a	n/a
44	EP300	chr1:150669521-150669971	GM12878	blood:	n/a	n/a
45	EP300	chr1:150669472-150669977	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr1:150669399-150670313	GM12878	blood:	n/a	n/a
47	EP300	chr1:150669508-150669953	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr1:150669723-150669975	GM12878	blood:	n/a	n/a
49	FOS	chr1:150669489-150670027	MCF10A-Er-Src	breast:	n/a	chr1:150669883-150669892 chr1:150669712-150669721 chr1:150669682-150669691
50	FOS	chr1:150669529-150670038	Hela-S3	cervix:	n/a	chr1:150669883-150669892 chr1:150669712-150669721 chr1:150669682-150669691

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150672619-150672669	A549	lung:	n/a
2	chr1:150672619-150672669	U87	brain:	n/a
3	chr1:150672619-150672669	HL-60	blood:	n/a
4	chr1:150670422-150670472	A549	lung:	n/a
5	chr1:150672619-150672669	SKMC	muscle:	n/a
6	chr1:150672619-150672669	Hela-S3	cervix:	n/a
7	chr1:150670422-150670472	BJ	skin:	n/a
8	chr1:150672619-150672669	NT2-D1	testis:	n/a
9	chr1:150670422-150670472	GM06990	blood:	n/a
10	chr1:150669977-150670027	MCF10A-Er-Src	breast:	n/a
11	chr1:150669977-150670027	T-47D	breast:	n/a
12	chr1:150670196-150670246	AG04449	skin:	fetal
13	chr1:150670422-150670472	AG10803	skin:	n/a
14	chr1:150669977-150670027	MCF-7	breast:	n/a
15	chr1:150672619-150672669	HCF	heart:	n/a
16	chr1:150670196-150670246	SAEC	small airway:	n/a
17	chr1:150670422-150670472	HEK293	kidney:	embryo
18	chr1:150670422-150670472	HL-60	blood:	n/a
19	chr1:150672619-150672669	MCF-7	breast:	n/a
20	chr1:150670422-150670472	T-47D	breast:	n/a
21	chr1:150670422-150670472	HAEpiC	amniotic membrane:	n/a
22	chr1:150670422-150670472	Hela-S3	cervix:	n/a
23	chr1:150670196-150670246	GM19239	blood:	n/a
24	chr1:150670422-150670472	K562	blood:	n/a
25	chr1:150672619-150672669	GM12878	blood:	n/a
26	chr1:150672619-150672669	AG09309	skin:	n/a
27	chr1:150672619-150672669	AG10803	skin:	n/a
28	chr1:150670196-150670246	IMR90	lung:	fetal
29	chr1:150669977-150670027	PANC-1	pancreas:	n/a
30	chr1:150672619-150672669	HCT-116	colon:	n/a
31	chr1:150669977-150670027	H1-hESC	embryonic stem cell:	embryo
32	chr1:150670422-150670472	HRCEpiC	kidney:	n/a
33	chr1:150669977-150670027	BE2_C	brain:	n/a
34	chr1:150669977-150670027	HIPEpiC	eye:	n/a
35	chr1:150670422-150670472	RPTEC	kidney:	n/a
36	chr1:150670196-150670246	A549	lung:	n/a
37	chr1:150670422-150670472	AG04449	skin:	fetal
38	chr1:150669977-150670027	GM12878	blood:	n/a
39	chr1:150670196-150670246	ECC-1	luminal epithelium:	n/a
40	chr1:150669977-150670027	NT2-D1	testis:	n/a
41	chr1:150670196-150670246	MCF10A-Er-Src	breast:	n/a
42	chr1:150672619-150672669	HEEpiC	esophagus:	n/a
43	chr1:150670422-150670472	SKMC	muscle:	n/a
44	chr1:150670196-150670246	PrEC	prostate:	n/a
45	chr1:150669977-150670027	NHDF-neo	bronchial:	n/a
46	chr1:150669977-150670027	Hela-S3	cervix:	n/a
47	chr1:150670196-150670246	HIPEpiC	eye:	n/a
48	chr1:150672619-150672669	SK-N-SH	brain:	n/a
49	chr1:150670422-150670472	NB4	blood:	n/a
50	chr1:150670422-150670472	HRPEpiC	eye:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150600620..150604710-chr1:150667156..150670884,6	K562	blood:
2	chr1:150668347..150671201-chr1:150671621..150673676,2	MCF-7	breast:
3	chr1:150669609..150671897-chr1:150782631..150785278,2	K562	blood:
4	chr1:150668066..150670256-chr1:150778150..150780706,2	K562	blood:
5	chr1:150600649..150603708-chr1:150666872..150671304,5	K562	blood:
6	chr1:150667811..150671175-chr1:150944483..150949055,4	MCF-7	breast:
7	chr1:150670046..150672281-chr1:150847927..150849937,2	MCF-7	breast:
8	chr1:150551078..150552936-chr1:150667990..150671349,4	K562	blood:
9	chr1:150668066..150670376-chr1:150778150..150781017,2	K562	blood:
10	chr1:150533613..150535919-chr1:150668275..150670992,2	MCF-7	breast:
11	chr1:150672673..150675324-chr1:150676637..150678852,2	K562	blood:
12	chr1:150600957..150603301-chr1:150669104..150670860,3	MCF-7	breast:
13	chr1:150551507..150553628-chr1:150668472..150670953,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLPH3L-2	chr1:150671330-150671441	NONHSAT006324
2	lnc-GOLPH3L-2	chr1:150672588-150672659	NONHSAT006324
3	lnc-GOLPH3L-2	chr1:150670867-150671210	NONHSAT006324

No data

Variant related genes	Relation type
GOLPH3L	TF binding region
RNU6-1042P	TF binding region
GOLPH3L	CpG island
RNU6-1042P	CpG island
ENSG00000143452	chromatin interactions
ENSG00000200175	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000203804	chromatin interactions
ENSG00000143418	chromatin interactions
ENSG00000143437	chromatin interactions
ENSG00000143387	chromatin interactions
ENSG00000143420	chromatin interactions
ENSG00000231073	chromatin interactions
ENSG00000143457	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2275236	chr1:150669952-150669953	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587606593	chr1:150669957-150669958	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs587661013	chr1:150669972-150669973	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs147466307	chr1:150670176-150670177	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs587613679	chr1:150670246-150670247	Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs587697626	chr1:150670266-150670267	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs148502617	chr1:150670298-150670299	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs190093656	chr1:150670300-150670301	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
9	rs587711168	chr1:150670442-150670443	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs34152646	chr1:150670448-150670449	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs6700022	chr1:150670484-150670485	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs142232678	chr1:150670539-150670540	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs587719572	chr1:150670618-150670619	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs587750552	chr1:150670675-150670676	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs587642074	chr1:150670720-150670721	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs587714044	chr1:150670750-150670751	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs587753019	chr1:150670753-150670754	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs587650971	chr1:150670761-150670762	Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs587707973	chr1:150670907-150670908	Weak transcription Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
20	rs587606524	chr1:150670909-150670910	Weak transcription Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
21	rs587660963	chr1:150670941-150670942	Weak transcription Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
22	rs56078201	chr1:150670943-150670944	Weak transcription Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
23	rs587599567	chr1:150670978-150670979	Weak transcription Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
24	rs587678125	chr1:150671038-150671039	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs185895111	chr1:150671072-150671073	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
26	rs374185460	chr1:150671136-150671137	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
27	rs149543711	chr1:150671154-150671155	Weak transcription Enhancers	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
28	rs200664192	chr1:150671179-150671180	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs200370965	chr1:150671209-150671210	Weak transcription Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs202000008	chr1:150671220-150671221	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs139837908	chr1:150671244-150671245	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs371260657	chr1:150671250-150671251	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs587766240	chr1:150671300-150671301	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs61817597	chr1:150671316-150671317	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs587639484	chr1:150671372-150671373	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs190308214	chr1:150671393-150671394	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs16839888	chr1:150671398-150671399	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs12120459	chr1:150671414-150671415	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs587694477	chr1:150671437-150671438	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs6688430	chr1:150671444-150671445	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs587650748	chr1:150671445-150671446	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs111487999	chr1:150671449-150671450	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs12058220	chr1:150671462-150671463	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs587704344	chr1:150671598-150671599	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs587763784	chr1:150671601-150671602	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs11204704	chr1:150671630-150671631	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs151213476	chr1:150671683-150671684	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs74124973	chr1:150671814-150671815	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188647074	chr1:150671817-150671818	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs139152781	chr1:150671873-150671874	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150667600-150670200	Active TSS	Rectal Mucosa Donor 29	rectum
2	chr1:150667600-150670200	Active TSS	GM12878-XiMat	blood
3	chr1:150667800-150670400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:150668000-150670200	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr1:150668000-150670200	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr1:150668000-150670400	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr1:150668000-150670400	Active TSS	Duodenum Mucosa	Duodenum
8	chr1:150668000-150670600	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr1:150668000-150670600	Active TSS	K562	blood
10	chr1:150668200-150670000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr1:150668200-150670000	Active TSS	NHEK	skin
12	chr1:150668200-150670200	Active TSS	Colonic Mucosa	Colon
13	chr1:150668200-150670400	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr1:150668200-150670600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr1:150668400-150670200	Active TSS	Fetal Intestine Large	intestine
16	chr1:150668400-150670200	Active TSS	Fetal Stomach	stomach
17	chr1:150668400-150670400	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr1:150668400-150670600	Active TSS	Ovary	ovary
19	chr1:150668600-150670000	Active TSS	HSMMtube	muscle
20	chr1:150668600-150670200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:150668600-150670200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:150668600-150670200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
23	chr1:150668600-150670200	Active TSS	Stomach Mucosa	stomach
24	chr1:150668600-150670400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr1:150668600-150670400	Active TSS	H1 Cell Line	embryonic stem cell
26	chr1:150668600-150670400	Active TSS	H9 Cell Line	embryonic stem cell
27	chr1:150668600-150670400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:150668600-150670400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:150668600-150670400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr1:150668600-150670400	Active TSS	Brain Germinal Matrix	brain
31	chr1:150668600-150670400	Active TSS	Fetal Muscle Trunk	muscle
32	chr1:150668600-150670400	Active TSS	HSMM	muscle
33	chr1:150668600-150670600	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr1:150668600-150670600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr1:150668600-150670600	Active TSS	Right Atrium	heart
36	chr1:150668800-150670000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr1:150668800-150670000	Active TSS	HMEC	breast
38	chr1:150668800-150670200	Active TSS	Fetal Intestine Small	intestine
39	chr1:150668800-150670200	Active TSS	Fetal Muscle Leg	muscle
40	chr1:150668800-150670200	Active TSS	Fetal Thymus	thymus
41	chr1:150668800-150670200	Active TSS	Skeletal Muscle Male	skeletal muscle
42	chr1:150668800-150670200	Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr1:150668800-150670200	Active TSS	A549	lung
44	chr1:150668800-150670200	Active TSS	NH-A	brain
45	chr1:150668800-150670400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:150668800-150670400	Active TSS	Fetal Brain Female	brain
47	chr1:150668800-150670400	Active TSS	Fetal Lung	lung
48	chr1:150668800-150670400	Active TSS	Psoas Muscle	Psoas
49	chr1:150668800-150670400	Active TSS	HepG2	liver
50	chr1:150668800-150670600	Active TSS	Brain Angular Gyrus	brain

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