Variant report

Variant	nsv872481
Chromosome Location	chr1:158625789-158712510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:673)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:158702324-158702669	K562	blood:	n/a	n/a
2	ARID3A	chr1:158698592-158698924	K562	blood:	n/a	n/a
3	ARID3A	chr1:158656270-158657331	K562	blood:	n/a	n/a
4	ARID3A	chr1:158709982-158710193	K562	blood:	n/a	n/a
5	ARID3A	chr1:158654761-158655083	K562	blood:	n/a	n/a
6	ARID3A	chr1:158652878-158653020	K562	blood:	n/a	n/a
7	ARID3A	chr1:158699545-158699797	K562	blood:	n/a	n/a
8	ARID3A	chr1:158704604-158704729	K562	blood:	n/a	n/a
9	ARID3A	chr1:158661717-158663024	K562	blood:	n/a	n/a
10	ARID3A	chr1:158658785-158659538	K562	blood:	n/a	n/a
11	ATF1	chr1:158656332-158656676	K562	blood:	n/a	n/a
12	ATF2	chr1:158685997-158686610	GM12878	blood:	n/a	n/a
13	ATF2	chr1:158685985-158686572	GM12878	blood:	n/a	n/a
14	ATF3	chr1:158656295-158656679	K562	blood:	n/a	n/a
15	BACH1	chr1:158655817-158657137	K562	blood:	n/a	n/a
16	BACH1	chr1:158701798-158702048	K562	blood:	n/a	n/a
17	BACH1	chr1:158656378-158656622	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr1:158686205-158686468	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:158686138-158686476	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
20	BCLAF1	chr1:158686191-158686569	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
21	BHLHE40	chr1:158652798-158652801	K562	blood:	n/a	n/a
22	BHLHE40	chr1:158627499-158627501	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:158664562-158664735	K562	blood:	n/a	n/a
24	BHLHE40	chr1:158701588-158702091	K562	blood:	n/a	n/a
25	CCNT2	chr1:158658982-158659203	K562	blood:	n/a	n/a
26	CCNT2	chr1:158656386-158656746	K562	blood:	n/a	n/a
27	CCNT2	chr1:158661758-158662042	K562	blood:	n/a	n/a
28	CEBPB	chr1:158656281-158656794	K562	blood:	n/a	n/a
29	CEBPB	chr1:158705115-158705187	K562	blood:	n/a	n/a
30	CEBPB	chr1:158680686-158680988	A549	lung:	n/a	chr1:158680816-158680827
31	CEBPB	chr1:158711092-158711357	K562	blood:	n/a	n/a
32	CEBPB	chr1:158654746-158655057	K562	blood:	n/a	n/a
33	CEBPB	chr1:158664592-158664615	K562	blood:	n/a	n/a
34	CEBPB	chr1:158680689-158680944	IMR90	lung:	n/a	chr1:158680816-158680827
35	CEBPB	chr1:158662771-158663096	K562	blood:	n/a	n/a
36	CEBPB	chr1:158689483-158689802	K562	blood:	n/a	n/a
37	CEBPB	chr1:158680693-158680923	K562	blood:	n/a	chr1:158680816-158680827
38	CEBPB	chr1:158659026-158659223	K562	blood:	n/a	n/a
39	CEBPB	chr1:158661727-158662494	K562	blood:	n/a	n/a
40	CEBPB	chr1:158654365-158654493	A549	lung:	n/a	n/a
41	CEBPB	chr1:158680660-158680979	HepG2	liver:	n/a	chr1:158680816-158680827
42	CEBPB	chr1:158662761-158663125	K562	blood:	n/a	n/a
43	CEBPB	chr1:158656117-158657013	K562	blood:	n/a	n/a
44	CEBPD	chr1:158658949-158659382	K562	blood:	n/a	n/a
45	CEBPD	chr1:158656224-158656767	K562	blood:	n/a	n/a
46	CEBPD	chr1:158661650-158662098	K562	blood:	n/a	n/a
47	CEBPD	chr1:158658939-158659356	K562	blood:	n/a	n/a
48	CEBPD	chr1:158702247-158702768	K562	blood:	n/a	n/a
49	CEBPD	chr1:158661791-158662138	K562	blood:	n/a	n/a
50	CEBPD	chr1:158702210-158702773	K562	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158687431-158687481	Hepatocyte	liver:	n/a
2	chr1:158688804-158688854	Jurkat	blood:	n/a
3	chr1:158687431-158687481	Hepatocyte	liver:	n/a
4	chr1:158688804-158688854	Jurkat	blood:	n/a
5	chr1:158670397-158670447	HNPCEpiC	eye:	n/a
6	chr1:158656718-158656768	H1-hESC	embryonic stem cell:	embryo
7	chr1:158688775-158688825	AG10803	skin:	n/a
8	chr1:158687431-158687481	HMEC	breast:	n/a
9	chr1:158670124-158670174	AG10803	skin:	n/a
10	chr1:158689263-158689313	K562	blood:	n/a
11	chr1:158670397-158670447	AG04450	lung:	fetal
12	chr1:158689141-158689191	HCPEpiC	choroid plexus:	n/a
13	chr1:158656718-158656768	NH-A	brain:	n/a
14	chr1:158670124-158670174	ovcar-3	ovarian:	n/a
15	chr1:158688804-158688854	Hepatocyte	liver:	n/a
16	chr1:158671873-158671923	SK-N-MC	brain:	n/a
17	chr1:158689263-158689313	Jurkat	blood:	n/a
18	chr1:158688926-158688976	PFSK-1	brain:	n/a
19	chr1:158687431-158687481	RPTEC	kidney:	n/a
20	chr1:158670397-158670447	BE2_C	brain:	n/a
21	chr1:158689263-158689313	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:158670397-158670447	GM12892	blood:	n/a
23	chr1:158687431-158687481	HUVEC	blood vessel:	n/a
24	chr1:158671873-158671923	Caco-2	colon:	n/a
25	chr1:158670617-158670667	LNCaP	prostate:	n/a
26	chr1:158689141-158689191	IMR90	lung:	fetal
27	chr1:158670124-158670174	AG09319	gingival:	n/a
28	chr1:158656718-158656768	ProgFib	skin:	n/a
29	chr1:158688775-158688825	MCF-7	breast:	n/a
30	chr1:158689263-158689313	AG10803	skin:	n/a
31	chr1:158688926-158688976	GM12891	blood:	n/a
32	chr1:158689141-158689191	GM06990	blood:	n/a
33	chr1:158689263-158689313	LNCaP	prostate:	n/a
34	chr1:158670397-158670447	HPAEpiC	pulmonary alveolar:	n/a
35	chr1:158671873-158671923	SKMC	muscle:	n/a
36	chr1:158689263-158689313	Hela-S3	cervix:	n/a
37	chr1:158670124-158670174	HIPEpiC	eye:	n/a
38	chr1:158688804-158688854	AoSMC	blood vessel:	n/a
39	chr1:158688926-158688976	SAEC	small airway:	n/a
40	chr1:158688926-158688976	AG09309	skin:	n/a
41	chr1:158689263-158689313	SAEC	small airway:	n/a
42	chr1:158688804-158688854	AG04450	lung:	fetal
43	chr1:158689263-158689313	CMK	blood:	n/a
44	chr1:158688775-158688825	SK-N-SH	brain:	n/a
45	chr1:158671873-158671923	GM12878	blood:	n/a
46	chr1:158670617-158670667	HAEpiC	amniotic membrane:	n/a
47	chr1:158688775-158688825	GM19239	blood:	n/a
48	chr1:158688926-158688976	HMEC	breast:	n/a
49	chr1:158687431-158687481	GM19239	blood:	n/a
50	chr1:158671873-158671923	T-47D	breast:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:
2	chr1:158684463..158686914-chr1:158687743..158690259,2	K562	blood:
3	chr1:158674913..158677154-chr1:158686436..158687990,2	K562	blood:
4	chr1:158625997..158628686-chr1:158631738..158634479,2	K562	blood:
5	chr1:158647173..158649566-chr1:158944147..158946933,2	K562	blood:
6	chr1:158618865..158621818-chr1:158624025..158625964,2	K562	blood:
7	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
8	chr1:158659639..158662606-chr1:158667652..158670080,3	K562	blood:
9	chr1:158701358..158703864-chr1:158711036..158713684,2	K562	blood:
10	chr1:158651218..158653402-chr1:158664730..158667068,2	K562	blood:
11	chr1:158651585..158653705-chr1:158746762..158749250,2	K562	blood:
12	chr1:158659297..158661841-chr1:158675200..158677714,2	K562	blood:
13	chr1:158651114..158653909-chr1:158727740..158729801,2	K562	blood:
14	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
15	chr1:158704822..158706927-chr1:158777581..158780196,2	K562	blood:
16	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
17	chr1:158649920..158652819-chr1:158694905..158696838,2	K562	blood:
18	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
19	chr1:158661667..158663696-chr1:158666950..158669041,2	K562	blood:
20	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
21	chr1:158639659..158640479-chr1:158747413..158748380,2	K562	blood:
22	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
23	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
24	chr1:158631479..158633632-chr1:158637060..158639879,2	K562	blood:
25	chr1:158669887..158672800-chr1:158674715..158677591,2	K562	blood:
26	chr1:158649920..158652819-chr1:158694905..158696838,2	K562	blood:
27	chr1:158656464..158659384-chr1:159045094..159048407,3	K562	blood:
28	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
29	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
30	chr1:158625997..158628686-chr1:158631738..158634479,2	K562	blood:
31	chr1:158624243..158625903-chr1:158627434..158629466,2	K562	blood:
32	chr1:158659639..158662606-chr1:158667652..158670080,3	K562	blood:
33	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
34	chr1:158653549..158656527-chr1:158701529..158703994,2	K562	blood:
35	chr1:158595061..158598004-chr1:158625327..158626951,2	K562	blood:
36	chr1:158619384..158624051-chr1:158626769..158630364,5	K562	blood:
37	chr1:158661667..158663696-chr1:158666950..158669041,2	K562	blood:
38	chr1:158631479..158633632-chr1:158637060..158639879,2	K562	blood:
39	chr1:158653068..158653568-chr17:41445238..41445752,2	Hela-S3	cervix:
40	chr1:158659297..158661841-chr1:158675200..158677714,2	K562	blood:
41	chr1:158624243..158625903-chr1:158627434..158629466,2	K562	blood:
42	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
43	chr1:158640177..158642154-chr1:158966970..158969167,2	K562	blood:
44	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
45	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
46	chr1:158653068..158654068-chr17:41445126..41445769,2	HCT-116	colon:
47	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:

No data

Variant related genes	Relation type
OR6K1P	TF binding region
OR6K2	TF binding region
SPTA1	TF binding region
OR6K4P	TF binding region
OR6K3	TF binding region
OR6K1P	CpG island
OR6K2	CpG island
SPTA1	CpG island
OR6K4P	CpG island
OR6K3	CpG island
ENSG00000226949	chromatin interactions
ENSG00000163554	chromatin interactions
ENSG00000196171	chromatin interactions
ENSG00000188340	chromatin interactions
ENSG00000163568	chromatin interactions
ENSG00000231237	chromatin interactions
ENSG00000180409	chromatin interactions
ENSG00000203757	chromatin interactions

Extended variants
information (count: 3136 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3136 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16840445	chr1:158625789-158625790	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539787776	chr1:158625790-158625791	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183935245	chr1:158625801-158625802	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569768563	chr1:158625895-158625896	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537157713	chr1:158625914-158625915	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16840446	chr1:158625938-158625939	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573776316	chr1:158625945-158625946	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534543711	chr1:158625992-158625993	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553216505	chr1:158626002-158626003	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34782304	chr1:158626026-158626027	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs60240422	chr1:158626058-158626059	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs544990651	chr1:158626073-158626074	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs563274781	chr1:158626105-158626106	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374482780	chr1:158626115-158626116	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575367457	chr1:158626118-158626119	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142901870	chr1:158626142-158626143	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558819094	chr1:158626143-158626144	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150642166	chr1:158626191-158626192	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186672227	chr1:158626214-158626215	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191428827	chr1:158626218-158626219	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533461111	chr1:158626243-158626244	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551322104	chr1:158626263-158626264	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368476702	chr1:158626281-158626282	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372615791	chr1:158626283-158626284	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371239036	chr1:158626301-158626302	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375001730	chr1:158626313-158626314	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369269751	chr1:158626337-158626338	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371639635	chr1:158626363-158626364	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567687301	chr1:158626377-158626378	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs857691	chr1:158626378-158626379	Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs34706737	chr1:158626382-158626383	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183996341	chr1:158626390-158626391	Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576741169	chr1:158626406-158626407	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374168455	chr1:158626417-158626418	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377688677	chr1:158626421-158626422	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs36109350	chr1:158626440-158626441	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372976600	chr1:158626465-158626466	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376113424	chr1:158626487-158626488	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547908010	chr1:158626518-158626519	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs557330832	chr1:158626530-158626531	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575293361	chr1:158626541-158626542	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542682024	chr1:158626574-158626575	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188834378	chr1:158626595-158626596	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561006300	chr1:158626617-158626618	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114530502	chr1:158626643-158626644	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541567998	chr1:158626660-158626661	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567786849	chr1:158626677-158626678	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533389808	chr1:158626684-158626685	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551655651	chr1:158626710-158626711	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139734970	chr1:158626757-158626758	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	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
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
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
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
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158612200-158628800	Strong transcription	K562	blood
2	chr1:158624800-158625800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:158625000-158626400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:158628800-158629800	Weak transcription	K562	blood
5	chr1:158629800-158633600	Strong transcription	K562	blood
6	chr1:158631000-158631200	Enhancers	Pancreas	Pancrea
7	chr1:158633600-158634400	Weak transcription	K562	blood
8	chr1:158634400-158652800	Strong transcription	K562	blood
9	chr1:158641000-158642000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr1:158644400-158645400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
11	chr1:158644400-158645400	Enhancers	Primary hematopoietic stem cells	blood
12	chr1:158644400-158645400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
13	chr1:158644400-158646800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:158644600-158646600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr1:158644800-158646200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr1:158645200-158646600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr1:158645800-158646200	Enhancers	Fetal Thymus	thymus
18	chr1:158651000-158652200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr1:158651200-158652200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:158652200-158656200	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr1:158652800-158655200	Transcr. at gene 5' and 3'	K562	blood
22	chr1:158655200-158655400	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
23	chr1:158655200-158657000	Active TSS	K562	blood
24	chr1:158655800-158656200	Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr1:158655800-158657000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:158656000-158656600	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:158656000-158656800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:158656200-158656400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr1:158656200-158656400	Enhancers	A549	lung
30	chr1:158656200-158656600	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:158656200-158656800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:158656200-158657000	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr1:158656400-158657200	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr1:158657000-158657400	Flanking Active TSS	K562	blood
35	chr1:158657400-158657800	Enhancers	K562	blood
36	chr1:158657800-158658800	Weak transcription	K562	blood
37	chr1:158658800-158659000	Active TSS	K562	blood
38	chr1:158659000-158660000	Flanking Active TSS	K562	blood
39	chr1:158660000-158660800	Enhancers	K562	blood
40	chr1:158660800-158661600	Weak transcription	K562	blood
41	chr1:158661600-158661800	Active TSS	K562	blood
42	chr1:158661800-158662000	Flanking Active TSS	K562	blood
43	chr1:158662000-158662200	Active TSS	K562	blood
44	chr1:158662200-158662400	Flanking Active TSS	K562	blood
45	chr1:158662400-158665000	Enhancers	K562	blood
46	chr1:158665000-158667200	Weak transcription	K562	blood
47	chr1:158669800-158670000	ZNF genes & repeats	Pancreas	Pancrea
48	chr1:158676800-158677200	Enhancers	K562	blood
49	chr1:158686600-158687600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr1:158687000-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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