Variant report

Variant	nsv531881
Chromosome Location	chr1:94937444-95053785
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1936)
CpG islands
(count:1592)
Chromatin interactive
region (count:34)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1936 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:95045656-95045854	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:95007441-95007657	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94979757-94979966	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:95006245-95006874	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:94980945-94981143	K562	blood:	n/a	n/a
6	ATF3	chr1:95007406-95007641	HepG2	liver:	n/a	n/a
7	ATF3	chr1:95007409-95007615	K562	blood:	n/a	n/a
8	ATF3	chr1:95007381-95007616	K562	blood:	n/a	n/a
9	BACH1	chr1:95010637-95011052	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:95006990-95008182	H1-hESC	embryonic stem cell:	n/a	chr1:95007515-95007529
11	BACH1	chr1:95046483-95046614	K562	blood:	n/a	n/a
12	BACH1	chr1:95010661-95011027	K562	blood:	n/a	n/a
13	BACH1	chr1:95045344-95045736	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr1:95006511-95006916	HepG2	liver:	n/a	n/a
15	BHLHE40	chr1:94981123-94981297	K562	blood:	n/a	n/a
16	BHLHE40	chr1:94979694-94979963	K562	blood:	n/a	n/a
17	BHLHE40	chr1:95028019-95028678	HepG2	liver:	n/a	n/a
18	BRCA1	chr1:94985616-94985642	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr1:95045221-95045801	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr1:95007079-95007218	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:95046209-95046570	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr1:95038360-95038684	K562	blood:	n/a	n/a
23	CBX3	chr1:95033783-95034080	K562	blood:	n/a	n/a
24	CBX3	chr1:95038362-95038802	HCT-116	colon:	n/a	n/a
25	CBX3	chr1:95033759-95034127	K562	blood:	n/a	n/a
26	CBX3	chr1:95038307-95038792	HCT-116	colon:	n/a	n/a
27	CBX3	chr1:95038385-95038614	K562	blood:	n/a	n/a
28	CCNT2	chr1:95007075-95007604	K562	blood:	n/a	n/a
29	CEBPB	chr1:95012648-95012712	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr1:95006661-95006947	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:94986257-94986544	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:94979729-94980040	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:94979701-94980026	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr1:95008575-95009059	Hela-S3	cervix:	n/a	chr1:95008723-95008734
35	CEBPB	chr1:94979787-94979988	MCF-7	breast:	n/a	n/a
36	CEBPB	chr1:94993012-94993538	Hela-S3	cervix:	n/a	chr1:94993111-94993123
37	CEBPB	chr1:95047899-95048402	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:94937794-94938064	IMR90	lung:	n/a	chr1:94937930-94937943
39	CEBPB	chr1:95006439-95008044	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr1:95007459-95007657	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:95044467-95044783	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:94986346-94986444	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:95034556-95034578	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr1:95044520-95044760	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:95009497-95010147	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:95007389-95007702	IMR90	lung:	n/a	n/a
47	CEBPB	chr1:95025538-95025963	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:94979723-94980021	K562	blood:	n/a	n/a
49	CEBPB	chr1:95008570-95008904	IMR90	lung:	n/a	chr1:95008723-95008734
50	CEBPB	chr1:95045398-95045901	Hela-S3	cervix:	n/a	n/a

(count:1592 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:95007489-95007539	BE2_C	brain:	n/a
2	chr1:95008050-95008100	U87	brain:	n/a
3	chr1:95008041-95008091	LNCaP	prostate:	n/a
4	chr1:94995935-94995985	AG09319	gingival:	n/a
5	chr1:95007541-95007591	HUVEC	blood vessel:	n/a
6	chr1:95006322-95006372	HRE	kidney:	n/a
7	chr1:95007489-95007539	BE2_C	brain:	n/a
8	chr1:95008050-95008100	U87	brain:	n/a
9	chr1:95008041-95008091	LNCaP	prostate:	n/a
10	chr1:94995935-94995985	AG09319	gingival:	n/a
11	chr1:95007541-95007591	HUVEC	blood vessel:	n/a
12	chr1:95006322-95006372	HRE	kidney:	n/a
13	chr1:94995935-94995985	SK-N-MC	brain:	n/a
14	chr1:95008041-95008091	AoSMC	blood vessel:	n/a
15	chr1:95007543-95007593	NHBE	bronchial:	n/a
16	chr1:95007489-95007539	NB4	blood:	n/a
17	chr1:95003968-95004018	U87	brain:	n/a
18	chr1:95018889-95018939	AG09319	gingival:	n/a
19	chr1:95007593-95007643	HCM	heart:	n/a
20	chr1:95007356-95007406	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:95007502-95007552	Hela-S3	cervix:	n/a
22	chr1:95006838-95006888	SAEC	small airway:	n/a
23	chr1:95001236-95001286	HUVEC	blood vessel:	n/a
24	chr1:95007331-95007381	HRPEpiC	eye:	n/a
25	chr1:95045763-95045813	MCF-7	breast:	n/a
26	chr1:95018889-95018939	GM12878	blood:	n/a
27	chr1:95003968-95004018	HL-60	blood:	n/a
28	chr1:95003968-95004018	MCF10A-Er-Src	breast:	n/a
29	chr1:95003968-95004018	SKMC	muscle:	n/a
30	chr1:95027075-95027125	BJ	skin:	n/a
31	chr1:95003968-95004018	ovcar-3	ovarian:	n/a
32	chr1:95003968-95004018	HRPEpiC	eye:	n/a
33	chr1:95010070-95010120	HL-60	blood:	n/a
34	chr1:95027075-95027125	HL-60	blood:	n/a
35	chr1:95006322-95006372	PANC-1	pancreas:	n/a
36	chr1:95027075-95027125	GM06990	blood:	n/a
37	chr1:95001236-95001286	HEEpiC	esophagus:	n/a
38	chr1:95008050-95008100	AG10803	skin:	n/a
39	chr1:95007573-95007623	RPTEC	kidney:	n/a
40	chr1:95007489-95007539	RPTEC	kidney:	n/a
41	chr1:94995935-94995985	HAEpiC	amniotic membrane:	n/a
42	chr1:95006729-95006779	BE2_C	brain:	n/a
43	chr1:95007573-95007623	AG09309	skin:	n/a
44	chr1:95009677-95009727	ovcar-3	ovarian:	n/a
45	chr1:94995935-94995985	U87	brain:	n/a
46	chr1:95007331-95007381	HCF	heart:	n/a
47	chr1:95006729-95006779	Jurkat	blood:	n/a
48	chr1:95007356-95007406	GM19239	blood:	n/a
49	chr1:95007331-95007381	SK-N-SH_RA	brain:	n/a
50	chr1:95045763-95045813	HMEC	breast:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:95043796..95046993-chr1:95048870..95051582,3	K562	blood:
2	chr1:95044965..95045519-chr1:95065172..95065776,2	MCF-7	breast:
3	chr1:95005939..95010305-chr1:95012395..95021281,11	MCF-7	breast:
4	chr1:95043796..95046691-chr1:95048870..95051582,2	K562	blood:
5	chr1:95044875..95047288-chr1:95048137..95050937,2	MCF-7	breast:
6	chr1:95006436..95008771-chr1:95043871..95046807,3	MCF-7	breast:
7	chr1:95043796..95046993-chr1:95048870..95051582,3	K562	blood:
8	chr1:95043796..95046691-chr1:95048870..95051582,2	K562	blood:
9	chr1:95011302..95013095-chr1:95017503..95019363,2	MCF-7	breast:
10	chr1:94941332..94943153-chr1:94956990..94959761,2	MCF-7	breast:
11	chr1:94965266..94968110-chr1:94970843..94972625,2	MCF-7	breast:
12	chr1:95015461..95017197-chr1:95086412..95088142,2	K562	blood:
13	chr1:94997172..94998108-chr1:95064305..95065624,5	MCF-7	breast:
14	chr1:95002334..95004389-chr1:95062847..95065293,3	MCF-7	breast:
15	chr1:95001173..95003691-chr1:95006398..95009153,2	MCF-7	breast:
16	chr1:95007807..95010270-chr1:95025313..95026976,2	MCF-7	breast:
17	chr1:94965266..94968110-chr1:94970843..94972625,2	MCF-7	breast:
18	chr1:94947212..94947799-chr1:95319643..95320515,2	K562	blood:
19	chr1:94946963..94948709-chr1:95581027..95583387,2	K562	blood:
20	chr1:94941332..94943153-chr1:94956990..94959761,2	MCF-7	breast:
21	chr1:94987984..94988512-chr1:95267242..95268185,2	MCF-7	breast:
22	chr1:95044875..95047288-chr1:95048137..95050937,2	MCF-7	breast:
23	chr1:95007066..95011283-chr1:95013175..95017472,7	MCF-7	breast:
24	chr1:94997312..94997997-chr1:95271190..95272030,3	MCF-7	breast:
25	chr1:94987992..94988549-chr1:95064767..95065433,2	MCF-7	breast:
26	chr1:94992707..94993493-chr1:95064769..95065395,2	MCF-7	breast:
27	chr1:95004605..95005274-chr18:74502570..74503410,2	MCF-7	breast:
28	chr1:95004121..95007110-chr1:95017554..95021316,3	MCF-7	breast:
29	chr1:95007807..95010270-chr1:95025313..95026976,2	MCF-7	breast:
30	chr1:95004121..95007110-chr1:95017554..95021316,3	MCF-7	breast:
31	chr1:95006856..95007717-chr15:75932354..75933289,2	NB4	blood:
32	chr1:95001173..95003691-chr1:95006398..95009153,2	MCF-7	breast:
33	chr1:95011302..95013095-chr1:95017503..95019363,2	MCF-7	breast:
34	chr1:95007807..95010747-chr1:95056056..95057592,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F3-1	chr1:95051112-95052318	XLOC_000921
2	lnc-F3-3	chr1:94970402-94970548	l_89_chr1:94917575-94970548_76bGuttman_hLF
3	lnc-ABCD3-1	chr1:95007516-95008786	NONHSAT004594
4	lnc-ABCD3-1	chr1:95008015-95008571	XLOC_000302
5	lnc-ABCD3-1	chr1:95007608-95007649	XLOC_000302
6	lnc-F3-3	chr1:94943583-94943687	l_89_chr1:94917575-94970548_76bGuttman_hLF
7	lnc-F3-3	chr1:95031090-95031132	l_89_chr1:94917575-94970548_76bGuttman_hLF

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	F3	hsa-miR-130b-3p	chr1:94995114-94995135
2	ABCD3	hsa-miR-21-5p	chr1:94983826-94983845
3	F3	hsa-miR-26b-5p	chr1:94994895-94994916
4	F3	hsa-miR-93-5p	chr1:94995118-94995111
5	F3	hsa-miR-93-5p	chr1:94995112-94995134
6	F3	hsa-miR-130b-3p	chr1:94995974-94995995

Variant related genes	Relation type
ABCD3	TF binding region
F3	TF binding region
ABCD3	CpG island
F3	CpG island
ENSG00000177971	chromatin interactions
ENSG00000152078	chromatin interactions
ENSG00000117525	chromatin interactions
ERBB2IP	miRNA target sites
ERBB3	miRNA target sites

Extended variants
information (count: 4357 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4357 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576132267	chr1:94937512-94937513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141260585	chr1:94937618-94937619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs972360	chr1:94937670-94937671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572111628	chr1:94937671-94937672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192663732	chr1:94937680-94937681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560766872	chr1:94937686-94937687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574362108	chr1:94937731-94937732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543341940	chr1:94937732-94937733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562177816	chr1:94937750-94937751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563327936	chr1:94937797-94937798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559502593	chr1:94937821-94937822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370761072	chr1:94937854-94937855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532440852	chr1:94937904-94937905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552636248	chr1:94937915-94937916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184456668	chr1:94937968-94937969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528595586	chr1:94937971-94937972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113837716	chr1:94938002-94938003	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs367975621	chr1:94938011-94938012	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77674803	chr1:94938023-94938024	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs397980870	chr1:94938024-94938025	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373196864	chr1:94938027-94938028	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548456336	chr1:94938028-94938029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568689402	chr1:94938055-94938056	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537715713	chr1:94938073-94938074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539121706	chr1:94938154-94938155	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1158254	chr1:94938269-94938270	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs569668200	chr1:94938270-94938271	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs77027811	chr1:94938357-94938358	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542110813	chr1:94938454-94938455	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558534919	chr1:94938465-94938466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138880536	chr1:94938478-94938479	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534737142	chr1:94938501-94938502	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186873803	chr1:94938549-94938550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142076993	chr1:94938687-94938688	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146296035	chr1:94938688-94938689	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139566629	chr1:94938716-94938717	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192399871	chr1:94938721-94938722	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577069684	chr1:94938764-94938765	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs545837410	chr1:94938770-94938771	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559712558	chr1:94938805-94938806	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528546410	chr1:94938837-94938838	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562045698	chr1:94938862-94938863	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542368674	chr1:94938885-94938886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113536600	chr1:94938933-94938934	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113130328	chr1:94938962-94938963	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111319989	chr1:94938968-94938969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372365316	chr1:94938994-94938995	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149638782	chr1:94939011-94939012	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531167769	chr1:94939035-94939036	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551200049	chr1:94939066-94939067	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2603 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94913800-94974200	Weak transcription	Psoas Muscle	Psoas
2	chr1:94914200-94951800	Weak transcription	Brain Angular Gyrus	brain
3	chr1:94914800-94985800	Weak transcription	NHLF	lung
4	chr1:94915400-94993200	Weak transcription	HSMMtube	muscle
5	chr1:94915800-94955400	Weak transcription	NHDF-Ad	bronchial
6	chr1:94915800-94956600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr1:94916000-94941800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr1:94916000-94957200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:94916000-94969600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:94916000-94970000	Weak transcription	Ovary	ovary
11	chr1:94916000-94970000	Weak transcription	Spleen	Spleen
12	chr1:94916000-94973800	Weak transcription	Pancreas	Pancrea
13	chr1:94916000-94993000	Weak transcription	Esophagus	oesophagus
14	chr1:94916200-94968400	Weak transcription	Gastric	stomach
15	chr1:94916200-94971600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:94916200-94974200	Weak transcription	Lung	lung
17	chr1:94917200-94964400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr1:94917800-94971800	Weak transcription	NHEK	skin
19	chr1:94917800-95000800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:94918000-94942000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr1:94918000-94957000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr1:94918800-94941600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr1:94919000-94942800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr1:94920600-94948400	Weak transcription	Small Intestine	intestine
25	chr1:94921000-94957800	Weak transcription	Brain Germinal Matrix	brain
26	chr1:94923200-94942000	Weak transcription	Right Ventricle	heart
27	chr1:94923600-94956400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr1:94923600-94956600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr1:94923800-94941800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr1:94923800-94948000	Weak transcription	NH-A	brain
31	chr1:94923800-95000400	Weak transcription	Aorta	Aorta
32	chr1:94924000-94947000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr1:94924000-94964400	Weak transcription	GM12878-XiMat	blood
34	chr1:94924800-94968400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:94926600-94950400	Weak transcription	Primary B cells from cord blood	blood
36	chr1:94929000-94938600	Weak transcription	Brain Substantia Nigra	brain
37	chr1:94929000-94954200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr1:94929000-94957200	Weak transcription	Colonic Mucosa	Colon
39	chr1:94929200-94938200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr1:94929200-94941800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr1:94929400-94941600	Weak transcription	HUVEC	blood vessel
42	chr1:94929400-94947000	Weak transcription	Brain Cingulate Gyrus	brain
43	chr1:94929400-94980200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr1:94929600-94938800	Strong transcription	HepG2	liver
45	chr1:94929600-94942000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr1:94929600-94955400	Weak transcription	Fetal Heart	heart
47	chr1:94929600-94985400	Weak transcription	Fetal Brain Female	brain
48	chr1:94929800-94944800	Weak transcription	A549	lung
49	chr1:94929800-94945200	Weak transcription	Stomach Mucosa	stomach
50	chr1:94930000-94938000	Strong transcription	Liver	Liver

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