Variant report

Variant	nsv547989
Chromosome Location	chr1:158685036-158852953
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:782)
CpG islands
(count:1407)
Chromatin interactive
region (count:57)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:158709982-158710193	K562	blood:	n/a	n/a
2	ARID3A	chr1:158825932-158825957	K562	blood:	n/a	n/a
3	ARID3A	chr1:158769460-158770024	K562	blood:	n/a	n/a
4	ARID3A	chr1:158704604-158704729	K562	blood:	n/a	n/a
5	ARID3A	chr1:158702324-158702669	K562	blood:	n/a	n/a
6	ARID3A	chr1:158788979-158789707	K562	blood:	n/a	n/a
7	ARID3A	chr1:158699545-158699797	K562	blood:	n/a	n/a
8	ARID3A	chr1:158698592-158698924	K562	blood:	n/a	n/a
9	ATF1	chr1:158769556-158769886	K562	blood:	n/a	n/a
10	ATF1	chr1:158789343-158789721	K562	blood:	n/a	n/a
11	ATF2	chr1:158789360-158789737	GM12878	blood:	n/a	n/a
12	ATF2	chr1:158800669-158801400	GM12878	blood:	n/a	n/a
13	ATF2	chr1:158685997-158686610	GM12878	blood:	n/a	n/a
14	ATF2	chr1:158685985-158686572	GM12878	blood:	n/a	n/a
15	ATF2	chr1:158800775-158801330	GM12878	blood:	n/a	n/a
16	ATF3	chr1:158769474-158769844	K562	blood:	n/a	n/a
17	ATF3	chr1:158789352-158789686	K562	blood:	n/a	n/a
18	BACH1	chr1:158805878-158806042	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:158805801-158806172	K562	blood:	n/a	n/a
20	BACH1	chr1:158701798-158702048	K562	blood:	n/a	n/a
21	BACH1	chr1:158737227-158737232	K562	blood:	n/a	n/a
22	BATF	chr1:158686205-158686468	GM12878	blood:	n/a	n/a
23	BCL11A	chr1:158686138-158686476	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
24	BCLAF1	chr1:158800861-158801338	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:158686191-158686569	GM12878	blood:	n/a	chr1:158686264-158686273 chr1:158686265-158686274
26	BHLHE40	chr1:158701588-158702091	K562	blood:	n/a	n/a
27	BHLHE40	chr1:158788081-158788271	K562	blood:	n/a	n/a
28	BHLHE40	chr1:158726549-158726678	K562	blood:	n/a	chr1:158726580-158726593 chr1:158726576-158726597
29	BHLHE40	chr1:158788978-158789714	K562	blood:	n/a	n/a
30	BHLHE40	chr1:158800659-158801366	GM12878	blood:	n/a	n/a
31	CBX3	chr1:158769307-158769963	K562	blood:	n/a	n/a
32	CBX3	chr1:158798388-158798797	K562	blood:	n/a	n/a
33	CBX3	chr1:158788999-158790050	K562	blood:	n/a	n/a
34	CBX3	chr1:158797558-158797934	K562	blood:	n/a	n/a
35	CBX3	chr1:158808439-158808799	K562	blood:	n/a	n/a
36	CBX3	chr1:158808484-158808794	K562	blood:	n/a	n/a
37	CCNT2	chr1:158789159-158789743	K562	blood:	n/a	n/a
38	CCNT2	chr1:158769560-158769964	K562	blood:	n/a	n/a
39	CEBPB	chr1:158803107-158803362	K562	blood:	n/a	chr1:158803197-158803208
40	CEBPB	chr1:158754063-158754299	A549	lung:	n/a	chr1:158754205-158754216
41	CEBPB	chr1:158789116-158789734	K562	blood:	n/a	n/a
42	CEBPB	chr1:158722945-158723184	H1-hESC	embryonic stem cell:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
43	CEBPB	chr1:158722864-158723064	A549	lung:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
44	CEBPB	chr1:158787677-158787924	K562	blood:	n/a	n/a
45	CEBPB	chr1:158711092-158711357	K562	blood:	n/a	n/a
46	CEBPB	chr1:158722931-158723169	IMR90	lung:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
47	CEBPB	chr1:158719103-158719306	A549	lung:	n/a	chr1:158719183-158719196 chr1:158719183-158719194
48	CEBPB	chr1:158776989-158777341	IMR90	lung:	n/a	chr1:158777157-158777168 chr1:158777157-158777168
49	CEBPB	chr1:158722871-158723208	K562	blood:	n/a	chr1:158723040-158723051 chr1:158723037-158723054 chr1:158723040-158723053
50	CEBPB	chr1:158754057-158754293	HepG2	liver:	n/a	chr1:158754205-158754216

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158723939-158723989	BE2_C	brain:	n/a
2	chr1:158736312-158736362	A549	lung:	n/a
3	chr1:158747277-158747327	SK-N-SH	brain:	n/a
4	chr1:158736112-158736162	CMK	blood:	n/a
5	chr1:158723939-158723989	BE2_C	brain:	n/a
6	chr1:158736312-158736362	A549	lung:	n/a
7	chr1:158747277-158747327	SK-N-SH	brain:	n/a
8	chr1:158736112-158736162	CMK	blood:	n/a
9	chr1:158799935-158799985	AG10803	skin:	n/a
10	chr1:158688926-158688976	SAEC	small airway:	n/a
11	chr1:158687431-158687481	RPTEC	kidney:	n/a
12	chr1:158809049-158809099	HCT-116	colon:	n/a
13	chr1:158688775-158688825	HRCEpiC	kidney:	n/a
14	chr1:158736112-158736162	GM12891	blood:	n/a
15	chr1:158724362-158724412	AG04449	skin:	fetal
16	chr1:158800024-158800074	AG04450	lung:	fetal
17	chr1:158799935-158799985	GM19239	blood:	n/a
18	chr1:158724794-158724844	Jurkat	blood:	n/a
19	chr1:158689141-158689191	HL-60	blood:	n/a
20	chr1:158736112-158736162	Jurkat	blood:	n/a
21	chr1:158736112-158736162	Hela-S3	cervix:	n/a
22	chr1:158724362-158724412	Hepatocyte	liver:	n/a
23	chr1:158817808-158817858	IMR90	lung:	fetal
24	chr1:158689263-158689313	HPAEpiC	pulmonary alveolar:	n/a
25	chr1:158724057-158724107	HepG2	liver:	n/a
26	chr1:158800024-158800074	AG10803	skin:	n/a
27	chr1:158737599-158737649	GM19239	blood:	n/a
28	chr1:158689141-158689191	AG04450	lung:	fetal
29	chr1:158736112-158736162	IMR90	lung:	fetal
30	chr1:158724794-158724844	HEK293	kidney:	embryo
31	chr1:158723939-158723989	HNPCEpiC	eye:	n/a
32	chr1:158723939-158723989	GM06990	blood:	n/a
33	chr1:158724057-158724107	K562	blood:	n/a
34	chr1:158817808-158817858	HCT-116	colon:	n/a
35	chr1:158737599-158737649	SK-N-SH_RA	brain:	n/a
36	chr1:158688926-158688976	HCF	heart:	n/a
37	chr1:158723939-158723989	IMR90	lung:	fetal
38	chr1:158689141-158689191	AoSMC	blood vessel:	n/a
39	chr1:158689263-158689313	AG09309	skin:	n/a
40	chr1:158737599-158737649	HCPEpiC	choroid plexus:	n/a
41	chr1:158725300-158725350	U87	brain:	n/a
42	chr1:158736112-158736162	HCM	heart:	n/a
43	chr1:158688775-158688825	U87	brain:	n/a
44	chr1:158746611-158746661	CMK	blood:	n/a
45	chr1:158746611-158746661	LNCaP	prostate:	n/a
46	chr1:158800024-158800074	HRPEpiC	eye:	n/a
47	chr1:158687431-158687481	Hela-S3	cervix:	n/a
48	chr1:158724362-158724412	SKMC	muscle:	n/a
49	chr1:158736112-158736162	HRPEpiC	eye:	n/a
50	chr1:158688804-158688854	AG09309	skin:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:158722697..158725195-chr1:158729520..158731092,2	K562	blood:
2	chr1:158770831..158772373-chr1:158787697..158790487,2	K562	blood:
3	chr1:158653549..158656527-chr1:158701529..158703994,2	K562	blood:
4	chr1:158821520..158824176-chr1:158832622..158835555,2	K562	blood:
5	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
6	chr1:158821520..158824176-chr1:158832622..158835555,2	K562	blood:
7	chr1:158733358..158736133-chr1:158736433..158738088,2	K562	blood:
8	chr1:158820836..158822483-chr1:158829667..158831273,2	K562	blood:
9	chr1:158757057..158758976-chr1:158767246..158769366,2	K562	blood:
10	chr1:158770831..158772373-chr1:158787697..158790487,2	K562	blood:
11	chr1:158704822..158706927-chr1:158777581..158780196,2	K562	blood:
12	chr1:158812214..158814009-chr1:158818009..158819946,2	K562	blood:
13	chr1:158812790..158814752-chr1:158826099..158828358,2	K562	blood:
14	chr1:158649920..158652819-chr1:158694905..158696838,2	K562	blood:
15	chr1:158812214..158814009-chr1:158818009..158819946,2	K562	blood:
16	chr1:158768206..158768907-chr1:158968540..158969106,3	MCF-7	breast:
17	chr1:158779601..158781616-chr1:158791201..158793222,2	K562	blood:
18	chr1:158779601..158781616-chr1:158791201..158793222,2	K562	blood:
19	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
20	chr1:158843130..158845633-chr1:158846139..158848183,2	K562	blood:
21	chr1:158691383..158694379-chr1:158696049..158697811,2	K562	blood:
22	chr1:158684463..158686914-chr1:158687743..158690259,2	K562	blood:
23	chr1:158735490..158738266-chr1:158739766..158741760,2	K562	blood:
24	chr1:158691573..158694598-chr1:158696049..158698060,3	K562	blood:
25	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
26	chr1:158842732..158844535-chr1:158852060..158853613,2	MCF-7	breast:
27	chr1:158757287..158759072-chr1:158760688..158763230,2	K562	blood:
28	chr1:158696982..158701883-chr1:158702210..158705771,7	K562	blood:
29	chr1:158763178..158764363-chr1:158967947..158968721,3	MCF-7	breast:
30	chr1:158843130..158845633-chr1:158845939..158848183,3	K562	blood:
31	chr1:158701358..158703864-chr1:158711036..158713684,2	K562	blood:
32	chr1:158801901..158804321-chr1:158817913..158819439,2	K562	blood:
33	chr1:158812790..158814752-chr1:158826099..158828358,2	K562	blood:
34	chr1:158843130..158845633-chr1:158846139..158848183,2	K562	blood:
35	chr1:158701755..158705583-chr1:158706296..158709041,3	K562	blood:
36	chr1:158801901..158804321-chr1:158817913..158819439,2	K562	blood:
37	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
38	chr1:158748328..158750308-chr1:158751698..158753611,2	K562	blood:
39	chr1:158843130..158845633-chr1:158845939..158848183,3	K562	blood:
40	chr1:158820836..158822483-chr1:158829667..158831273,2	K562	blood:
41	chr1:158676105..158677828-chr1:158684515..158686089,2	K562	blood:
42	chr1:158757287..158759072-chr1:158760688..158763230,2	K562	blood:
43	chr1:158697116..158699497-chr1:158702619..158704927,2	K562	blood:
44	chr1:158715265..158717778-chr1:158778694..158781362,2	K562	blood:
45	chr1:158699118..158701949-chr1:158709331..158711984,2	K562	blood:
46	chr1:158748328..158750308-chr1:158751698..158753611,2	K562	blood:
47	chr1:158842732..158844535-chr1:158852060..158853613,2	MCF-7	breast:
48	chr1:158702009..158703945-chr1:158717255..158718973,2	K562	blood:
49	chr1:158651114..158653909-chr1:158727740..158729801,2	K562	blood:
50	chr1:158771201..158773385-chr1:158776168..158777671,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MNDA-1	chr1:158848536-158848798	NONHSAT006992
2	lnc-MNDA-1	chr1:158850520-158850686	NONHSAT006992
3	lnc-MNDA-1	chr1:158849834-158849979	NONHSAT006992

No data

Variant related genes	Relation type
OR6N2	TF binding region
OR2AQ1P	TF binding region
OR6K5P	TF binding region
OR10AA1P	TF binding region
ENSG00000229849	TF binding region
OR6N1	TF binding region
MNDA	TF binding region
OR6K6	TF binding region
OR6K4P	TF binding region
OR6K3	TF binding region
OR6N2	CpG island
OR2AQ1P	CpG island
OR6K5P	CpG island
OR10AA1P	CpG island
ENSG00000229849	CpG island
OR6N1	CpG island
MNDA	CpG island
OR6K6	CpG island
OR6K4P	CpG island
OR6K3	CpG island
ENSG00000203757	chromatin interactions
ENSG00000180409	chromatin interactions
ENSG00000197403	chromatin interactions
ENSG00000226949	chromatin interactions
ENSG00000163554	chromatin interactions
ENSG00000229849	chromatin interactions
ENSG00000180433	chromatin interactions

Extended variants
information (count: 5242 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:5242 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs451851	chr1:158685036-158685037	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537057739	chr1:158685063-158685064	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs148827272	chr1:158685083-158685084	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs36013655	chr1:158685103-158685104	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554312630	chr1:158685156-158685157	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572688756	chr1:158685174-158685175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540079612	chr1:158685204-158685205	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs189082779	chr1:158685264-158685265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143428737	chr1:158685335-158685336	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544152634	chr1:158685347-158685348	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556720501	chr1:158685355-158685356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs413543	chr1:158685363-158685364	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529784916	chr1:158685392-158685393	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548320576	chr1:158685437-158685438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181832455	chr1:158685450-158685451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150963966	chr1:158685476-158685477	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111543836	chr1:158685484-158685485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs546918718	chr1:158685499-158685500	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571870427	chr1:158685510-158685511	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539308037	chr1:158685565-158685566	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112803058	chr1:158685572-158685573	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186483045	chr1:158685603-158685604	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146023022	chr1:158685658-158685659	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189778477	chr1:158685670-158685671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs6682506	chr1:158685672-158685673	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112236082	chr1:158685693-158685694	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552816160	chr1:158685717-158685718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554623693	chr1:158685727-158685728	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573300635	chr1:158685760-158685761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533978377	chr1:158685766-158685767	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs562933462	chr1:158685817-158685818	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs202033159	chr1:158685832-158685833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372905193	chr1:158685841-158685842	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558479697	chr1:158685846-158685847	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6682713	chr1:158685854-158685855	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577018584	chr1:158685878-158685879	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569908296	chr1:158685891-158685892	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556159628	chr1:158685919-158685920	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182953713	chr1:158685933-158685934	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs541874547	chr1:158685969-158685970	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560280333	chr1:158686039-158686040	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527404241	chr1:158686046-158686047	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs142389297	chr1:158686079-158686080	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572723896	chr1:158686090-158686091	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs540775920	chr1:158686104-158686105	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs565361462	chr1:158686174-158686175	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532807518	chr1:158686192-158686193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs12062148	chr1:158686254-158686255	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs399848	chr1:158686269-158686270	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs530030826	chr1:158686319-158686320	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	17440070	CNVD
Diabetes mellitus	21357537	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158686600-158687600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:158687000-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:158687000-158687600	Enhancers	HMEC	breast
4	chr1:158687200-158687600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:158692600-158735200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr1:158698600-158701800	Enhancers	K562	blood
7	chr1:158699200-158700400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr1:158699600-158699800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr1:158700200-158700600	Flanking Active TSS	Liver	Liver
10	chr1:158700400-158700600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr1:158700600-158701000	Enhancers	Liver	Liver
12	chr1:158701800-158702000	Flanking Active TSS	K562	blood
13	chr1:158701800-158702200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:158702000-158702400	Enhancers	K562	blood
15	chr1:158702400-158702800	Flanking Active TSS	K562	blood
16	chr1:158702800-158706200	Enhancers	K562	blood
17	chr1:158705600-158705800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:158705600-158706000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr1:158706200-158708000	Weak transcription	K562	blood
20	chr1:158708000-158708800	Enhancers	K562	blood
21	chr1:158708800-158709600	Weak transcription	K562	blood
22	chr1:158709600-158709800	Active TSS	K562	blood
23	chr1:158709800-158710000	Flanking Active TSS	K562	blood
24	chr1:158710000-158710200	Enhancers	K562	blood
25	chr1:158721800-158722200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:158722400-158724800	Enhancers	Fetal Heart	heart
27	chr1:158735200-158737800	Strong transcription	Primary neutrophils fromperipheralblood	blood
28	chr1:158735400-158735800	Enhancers	Fetal Stomach	stomach
29	chr1:158737800-158740000	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr1:158739800-158740600	Enhancers	Fetal Heart	heart
31	chr1:158740000-158741800	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr1:158740400-158741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:158740600-158740800	Flanking Active TSS	Fetal Heart	heart
34	chr1:158740800-158741000	Enhancers	Fetal Heart	heart
35	chr1:158741000-158741200	Flanking Active TSS	Fetal Heart	heart
36	chr1:158741200-158744400	Enhancers	Fetal Heart	heart
37	chr1:158741800-158742000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
38	chr1:158742000-158742600	Enhancers	K562	blood
39	chr1:158742000-158746000	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr1:158746000-158747400	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr1:158747400-158752200	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr1:158748400-158748800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr1:158751000-158751200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr1:158752200-158753200	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr1:158752600-158753400	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr1:158752800-158753000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr1:158752800-158753200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr1:158753000-158753200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr1:158763000-158763600	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr1:158763200-158763600	Enhancers	Monocytes-CD14+_RO01746	blood

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