Variant report

Variant	nsv520773
Chromosome Location	chr1:159922959-159935569
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:133)
CpG islands
(count:366)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:133 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:159927422-159927876	K562	blood:	n/a	n/a
2	ARID3A	chr1:159934747-159934786	K562	blood:	n/a	n/a
3	ATF1	chr1:159930887-159931113	K562	blood:	n/a	n/a
4	ATF1	chr1:159927611-159928120	K562	blood:	n/a	n/a
5	ATF1	chr1:159923940-159924205	K562	blood:	n/a	n/a
6	ATF2	chr1:159928474-159928886	GM12878	blood:	n/a	n/a
7	BATF	chr1:159928452-159929056	GM12878	blood:	n/a	n/a
8	BATF	chr1:159928491-159928876	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:159927651-159928083	K562	blood:	n/a	n/a
10	BHLHE40	chr1:159923808-159923890	K562	blood:	n/a	n/a
11	CCNT2	chr1:159927634-159928259	K562	blood:	n/a	n/a
12	CEBPB	chr1:159930576-159931175	IMR90	lung:	n/a	chr1:159930982-159930990
13	CEBPB	chr1:159930842-159931171	Hela-S3	cervix:	n/a	chr1:159930982-159930990
14	CEBPB	chr1:159930867-159931186	K562	blood:	n/a	chr1:159930982-159930990
15	CEBPD	chr1:159927455-159927975	K562	blood:	n/a	n/a
16	CEBPD	chr1:159927467-159927887	K562	blood:	n/a	n/a
17	CTCF	chr1:159927940-159928090	NHEK	skin:	n/a	n/a
18	CTCF	chr1:159923044-159923074	GM20000	blood:	n/a	n/a
19	CTCF	chr1:159927880-159928030	SAEC	small airway:	n/a	n/a
20	CTCF	chr1:159927662-159927731	K562	blood:	n/a	n/a
21	CTCF	chr1:159927982-159928062	LNCaP	prostate:	n/a	n/a
22	CTCF	chr1:159928012-159928081	Pancreas_OC	pancreas:	n/a	n/a
23	CUX1	chr1:159930716-159930845	K562	blood:	n/a	n/a
24	ELF1	chr1:159927672-159927830	K562	blood:	n/a	n/a
25	EP300	chr1:159927750-159928248	T-47D	breast:	n/a	n/a
26	EP300	chr1:159927514-159928183	K562	blood:	n/a	chr1:159927607-159927621
27	EP300	chr1:159924189-159924556	K562	blood:	n/a	chr1:159924404-159924418
28	EP300	chr1:159927770-159928185	T-47D	breast:	n/a	n/a
29	EP300	chr1:159927675-159928282	ECC-1	luminal epithelium:	n/a	n/a
30	FAM48A	chr1:159930891-159931046	GM12878	blood:	n/a	n/a
31	FOS	chr1:159925447-159925494	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:159932923-159933009	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:159924026-159924146	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:159930386-159931090	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
35	FOS	chr1:159930399-159931180	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
36	FOS	chr1:159932941-159933093	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:159923925-159924350	MCF10A-Er-Src	breast:	n/a	chr1:159924165-159924173 chr1:159924163-159924174
38	FOS	chr1:159930362-159931187	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
39	FOS	chr1:159923994-159924234	MCF10A-Er-Src	breast:	n/a	chr1:159924165-159924173 chr1:159924163-159924174
40	FOS	chr1:159930369-159931123	MCF10A-Er-Src	breast:	n/a	chr1:159930983-159930992
41	FOS	chr1:159923923-159924324	MCF10A-Er-Src	breast:	n/a	chr1:159924165-159924173 chr1:159924163-159924174
42	FOS	chr1:159929360-159929540	MCF10A-Er-Src	breast:	n/a	n/a
43	FOXA1	chr1:159927824-159928092	ECC-1	luminal epithelium:	n/a	chr1:159928020-159928035
44	FOXA1	chr1:159929265-159929579	T-47D	breast:	n/a	n/a
45	FOXA1	chr1:159927777-159928165	T-47D	breast:	n/a	chr1:159928020-159928035
46	FOXA1	chr1:159927828-159928147	T-47D	breast:	n/a	chr1:159928020-159928035
47	FOXA1	chr1:159929234-159929633	T-47D	breast:	n/a	n/a
48	FOXA1	chr1:159927852-159928150	ECC-1	luminal epithelium:	n/a	chr1:159928020-159928035
49	FOXA2	chr1:159926522-159927000	A549	lung:	n/a	n/a
50	GATA1	chr1:159930531-159931402	PBDE	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:159923725-159923775	BJ	skin:	n/a
2	chr1:159925272-159925322	RPTEC	kidney:	n/a
3	chr1:159925272-159925322	HEEpiC	esophagus:	n/a
4	chr1:159925272-159925322	AG10803	skin:	n/a
5	chr1:159925416-159925466	AG10803	skin:	n/a
6	chr1:159923525-159923575	IMR90	lung:	fetal
7	chr1:159925416-159925466	K562	blood:	n/a
8	chr1:159923725-159923775	ovcar-3	ovarian:	n/a
9	chr1:159925416-159925466	AG09319	gingival:	n/a
10	chr1:159925272-159925322	GM19239	blood:	n/a
11	chr1:159924541-159924591	HMEC	breast:	n/a
12	chr1:159925416-159925466	PrEC	prostate:	n/a
13	chr1:159923525-159923575	AG04450	lung:	fetal
14	chr1:159923525-159923575	HEK293	kidney:	embryo
15	chr1:159923861-159923911	NB4	blood:	n/a
16	chr1:159925272-159925322	GM12892	blood:	n/a
17	chr1:159923725-159923775	NHDF-neo	bronchial:	n/a
18	chr1:159925272-159925322	SKMC	muscle:	n/a
19	chr1:159923525-159923575	K562	blood:	n/a
20	chr1:159923525-159923575	HCPEpiC	choroid plexus:	n/a
21	chr1:159923725-159923775	GM12891	blood:	n/a
22	chr1:159925272-159925322	H1-hESC	embryonic stem cell:	embryo
23	chr1:159925416-159925466	HCPEpiC	choroid plexus:	n/a
24	chr1:159923861-159923911	AoSMC	blood vessel:	n/a
25	chr1:159925272-159925322	IMR90	lung:	fetal
26	chr1:159925272-159925322	HCPEpiC	choroid plexus:	n/a
27	chr1:159923525-159923575	MCF10A-Er-Src	breast:	n/a
28	chr1:159923525-159923575	LNCaP	prostate:	n/a
29	chr1:159924541-159924591	HRE	kidney:	n/a
30	chr1:159924541-159924591	GM12892	blood:	n/a
31	chr1:159924541-159924591	Hepatocyte	liver:	n/a
32	chr1:159925416-159925466	HepG2	liver:	n/a
33	chr1:159923525-159923575	NH-A	brain:	n/a
34	chr1:159923861-159923911	BE2_C	brain:	n/a
35	chr1:159923725-159923775	HRPEpiC	eye:	n/a
36	chr1:159923861-159923911	NT2-D1	testis:	n/a
37	chr1:159923861-159923911	SK-N-MC	brain:	n/a
38	chr1:159924541-159924591	HCF	heart:	n/a
39	chr1:159925416-159925466	GM12891	blood:	n/a
40	chr1:159924541-159924591	MCF-7	breast:	n/a
41	chr1:159925416-159925466	BE2_C	brain:	n/a
42	chr1:159925272-159925322	AoSMC	blood vessel:	n/a
43	chr1:159924541-159924591	ECC-1	luminal epithelium:	n/a
44	chr1:159925416-159925466	HRE	kidney:	n/a
45	chr1:159923725-159923775	PANC-1	pancreas:	n/a
46	chr1:159923861-159923911	ProgFib	skin:	n/a
47	chr1:159924541-159924591	PrEC	prostate:	n/a
48	chr1:159924541-159924591	HRPEpiC	eye:	n/a
49	chr1:159924541-159924591	U87	brain:	n/a
50	chr1:159923525-159923575	HMEC	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:159914406..159916851-chr1:159926521..159929440,2	MCF-7	breast:
2	chr1:159913973..159917644-chr1:159927852..159934070,11	MCF-7	breast:
3	chr1:159913231..159916078-chr1:159934626..159937390,2	MCF-7	breast:
4	chr1:159894586..159896290-chr1:159926599..159929253,2	K562	blood:
5	chr1:159922806..159924393-chr1:159927902..159929423,2	MCF-7	breast:
6	chr1:159907235..159909524-chr1:159933511..159935771,2	MCF-7	breast:
7	chr1:159914809..159917137-chr1:159930388..159932667,2	K562	blood:
8	chr1:159925103..159927154-chr1:159928753..159930871,2	MCF-7	breast:
9	chr1:159893947..159895991-chr1:159928260..159930233,2	MCF-7	breast:
10	chr1:159893768..159896638-chr1:159931610..159934083,3	K562	blood:
11	chr1:159934579..159937237-chr1:159944112..159946274,2	K562	blood:
12	chr1:159926244..159929298-chr1:159931208..159934136,4	K562	blood:
13	chr1:159907782..159910427-chr1:159933319..159935593,2	MCF-7	breast:
14	chr1:159925103..159927154-chr1:159928753..159930871,2	MCF-7	breast:
15	chr1:159892760..159896965-chr1:159922291..159925141,4	K562	blood:
16	chr1:159915177..159916048-chr1:159924751..159925565,2	K562	blood:
17	chr1:159921624..159923917-chr1:159925948..159927812,2	K562	blood:
18	chr1:159926244..159929298-chr1:159931208..159934136,4	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNJ9-2	chr1:159931014-159931195	NONHSAT007033
2	lnc-KCNJ9-2	chr1:159935289-159935435	NONHSAT007031
3	lnc-KCNJ9-2	chr1:159930965-159931195	NONHSAT007031
4	lnc-KCNJ9-2	chr1:159935289-159935435	ENSG00000224259
5	lnc-KCNJ9-2	chr1:159931008-159931195	ENSG00000224259
6	lnc-KCNJ9-2	chr1:159931014-159931195	ENSG00000224259

No data

Variant related genes	Relation type
SLAMF9	TF binding region
LINC01133	TF binding region
SLAMF9	CpG island
LINC01133	CpG island
ENSG00000158710	chromatin interactions
ENSG00000162723	chromatin interactions
ENSG00000085552	chromatin interactions

Extended variants
information (count: 502 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2249707	chr1:159922959-159922960	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368481860	chr1:159923028-159923029	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs540644973	chr1:159923035-159923036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565312061	chr1:159923038-159923039	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368920026	chr1:159923051-159923052	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs148625770	chr1:159923057-159923058	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550943661	chr1:159923083-159923084	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374371894	chr1:159923098-159923099	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199677431	chr1:159923104-159923105	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2789417	chr1:159923111-159923112	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs182565844	chr1:159923131-159923132	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142119593	chr1:159923141-159923142	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140698454	chr1:159923148-159923149	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs146654789	chr1:159923201-159923202	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143559532	chr1:159923223-159923224	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34540580	chr1:159923234-159923235	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs570157487	chr1:159923247-159923248	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375812784	chr1:159923263-159923264	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375532203	chr1:159923294-159923295	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370201078	chr1:159923301-159923302	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201668987	chr1:159923330-159923331	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138732277	chr1:159923350-159923351	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373318679	chr1:159923370-159923371	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375866089	chr1:159923383-159923384	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs61732670	chr1:159923395-159923396	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575847451	chr1:159923400-159923401	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140245593	chr1:159923409-159923410	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs555109259	chr1:159923414-159923415	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573458236	chr1:159923470-159923471	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs1344028	chr1:159923475-159923476	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs565377410	chr1:159923493-159923494	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577353726	chr1:159923503-159923504	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116126552	chr1:159923515-159923516	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs77280868	chr1:159923600-159923601	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529974159	chr1:159923623-159923624	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2789416	chr1:159923628-159923629	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs560330943	chr1:159923725-159923726	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs527463685	chr1:159923726-159923727	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs551892335	chr1:159923727-159923728	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570171644	chr1:159923746-159923747	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs35681757	chr1:159923852-159923853	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201908862	chr1:159923861-159923862	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557558805	chr1:159923881-159923882	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs145274502	chr1:159923904-159923905	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs569464243	chr1:159923923-159923924	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs147539315	chr1:159923926-159923927	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573973237	chr1:159923952-159923953	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs536984854	chr1:159923960-159923961	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554941223	chr1:159924019-159924020	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567119299	chr1:159924021-159924022	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
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
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	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19602461	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159916200-159930600	Weak transcription	Right Atrium	heart
2	chr1:159916800-159923600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:159917000-159923400	Weak transcription	NHEK	skin
4	chr1:159919400-159923600	Weak transcription	K562	blood
5	chr1:159919600-159923000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:159919600-159923400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:159919800-159923600	Weak transcription	Esophagus	oesophagus
8	chr1:159919800-159923800	Weak transcription	Fetal Intestine Small	intestine
9	chr1:159919800-159930400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr1:159920000-159923800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:159920200-159923200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr1:159920200-159923200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr1:159921800-159923400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr1:159922800-159924000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:159922800-159924200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr1:159923000-159923200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:159923000-159926200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:159923200-159924200	Enhancers	Stomach Mucosa	stomach
19	chr1:159923200-159924400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:159923200-159924400	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr1:159923200-159924600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr1:159923400-159924000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:159923400-159924400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr1:159923400-159926400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:159923400-159926400	Enhancers	NHEK	skin
26	chr1:159923600-159923800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr1:159923600-159924000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:159923600-159924000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:159923600-159924000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
30	chr1:159923600-159924000	Enhancers	Esophagus	oesophagus
31	chr1:159923600-159924000	Bivalent Enhancer	Placenta	Placenta
32	chr1:159923600-159924000	Enhancers	HSMMtube	muscle
33	chr1:159923600-159924400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:159923600-159924400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:159923600-159924400	Enhancers	HSMM	muscle
36	chr1:159923600-159924400	Enhancers	K562	blood
37	chr1:159923600-159924400	Enhancers	Osteobl	bone
38	chr1:159923600-159925400	Enhancers	HMEC	breast
39	chr1:159923600-159925600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:159923800-159924000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr1:159923800-159924000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr1:159923800-159924000	Bivalent Enhancer	Fetal Muscle Leg	muscle
43	chr1:159923800-159924000	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr1:159923800-159924000	Enhancers	NHDF-Ad	bronchial
45	chr1:159923800-159924200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr1:159923800-159924400	Enhancers	Fetal Intestine Small	intestine
47	chr1:159924000-159924200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr1:159924000-159924200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr1:159924000-159924400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr1:159924000-159927800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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