Variant report

Variant	nsv1002903
Chromosome Location	chr1:74831209-74993866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:844)
CpG islands
(count:490)
Chromatin interactive
region (count:19)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:844 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:74934711-74935007	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:74943746-74943751	K562	blood:	n/a	n/a
3	ATF2	chr1:74929255-74929663	GM12878	blood:	n/a	n/a
4	BACH1	chr1:74952507-74952628	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:74862633-74862912	GM12878	blood:	n/a	n/a
6	BATF	chr1:74864921-74865285	GM12878	blood:	n/a	chr1:74865097-74865108
7	BATF	chr1:74929264-74929606	GM12878	blood:	n/a	chr1:74929478-74929489
8	BATF	chr1:74929254-74929656	GM12878	blood:	n/a	chr1:74929478-74929489
9	BATF	chr1:74865039-74865204	GM12878	blood:	n/a	chr1:74865097-74865108
10	BCL11A	chr1:74864896-74865230	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:74929322-74929595	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:74929185-74929684	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:74969965-74970040	K562	blood:	n/a	n/a
14	BHLHE40	chr1:74929307-74929660	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:74969836-74970190	GM12878	blood:	n/a	n/a
16	CEBPB	chr1:74944840-74944920	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:74872165-74872467	A549	lung:	n/a	chr1:74872295-74872306
18	CEBPB	chr1:74889142-74889769	IMR90	lung:	n/a	chr1:74889354-74889367
19	CEBPB	chr1:74929299-74930127	IMR90	lung:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
20	CEBPB	chr1:74933483-74933825	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:74832214-74832457	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:74864001-74864166	H1-hESC	embryonic stem cell:	n/a	chr1:74864058-74864069
23	CEBPB	chr1:74929812-74930102	A549	lung:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
24	CEBPB	chr1:74933510-74933831	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:74872122-74872453	IMR90	lung:	n/a	chr1:74872295-74872306
26	CEBPB	chr1:74863899-74864221	IMR90	lung:	n/a	chr1:74864058-74864069
27	CEBPB	chr1:74933587-74933713	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:74933478-74933842	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr1:74933511-74933815	IMR90	lung:	n/a	n/a
30	CEBPB	chr1:74863934-74864174	A549	lung:	n/a	chr1:74864058-74864069
31	CEBPB	chr1:74863892-74864211	HepG2	liver:	n/a	chr1:74864058-74864069
32	CEBPB	chr1:74859847-74860070	IMR90	lung:	n/a	chr1:74859944-74859957
33	CEBPB	chr1:74969867-74970067	HepG2	liver:	n/a	chr1:74970021-74970032
34	CEBPB	chr1:74929751-74930102	HepG2	liver:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
35	CEBPB	chr1:74933490-74933834	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr1:74872136-74872456	HepG2	liver:	n/a	chr1:74872295-74872306
37	CEBPB	chr1:74933543-74933820	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr1:74929306-74930122	Hela-S3	cervix:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
39	CHD2	chr1:74993857-74993943	HepG2	liver:	n/a	n/a
40	CHD2	chr1:74969973-74970114	GM12878	blood:	n/a	n/a
41	CHD2	chr1:74987849-74988223	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:74934800-74934950	HRE	kidney:	n/a	n/a
43	CTCF	chr1:74934780-74934930	GM06990	blood:	n/a	n/a
44	CTCF	chr1:74969900-74970050	RPTEC	kidney:	n/a	chr1:74970003-74970019
45	CTCF	chr1:74969897-74970161	GM19240	blood:	n/a	chr1:74970003-74970019
46	CTCF	chr1:74934674-74935062	MCF-7	breast:	n/a	n/a
47	CTCF	chr1:74934820-74934970	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr1:74969700-74969850	HepG2	liver:	n/a	n/a
49	CTCF	chr1:74969940-74970090	Hela-S3	cervix:	n/a	chr1:74970003-74970019
50	CTCF	chr1:74969960-74970110	K562	blood:	n/a	chr1:74970003-74970019

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74832752-74832802	HIPEpiC	eye:	n/a
2	chr1:74888995-74889045	Hela-S3	cervix:	n/a
3	chr1:74832752-74832802	HIPEpiC	eye:	n/a
4	chr1:74888995-74889045	Hela-S3	cervix:	n/a
5	chr1:74933557-74933607	SK-N-SH_RA	brain:	n/a
6	chr1:74970626-74970676	ECC-1	luminal epithelium:	n/a
7	chr1:74988194-74988244	HAEpiC	amniotic membrane:	n/a
8	chr1:74945347-74945397	HepG2	liver:	n/a
9	chr1:74941958-74942008	H1-hESC	embryonic stem cell:	embryo
10	chr1:74832752-74832802	PANC-1	pancreas:	n/a
11	chr1:74988194-74988244	SKMC	muscle:	n/a
12	chr1:74832752-74832802	HRPEpiC	eye:	n/a
13	chr1:74832752-74832802	GM12891	blood:	n/a
14	chr1:74933557-74933607	NT2-D1	testis:	n/a
15	chr1:74988194-74988244	ProgFib	skin:	n/a
16	chr1:74945347-74945397	HAEpiC	amniotic membrane:	n/a
17	chr1:74933557-74933607	Hela-S3	cervix:	n/a
18	chr1:74832752-74832802	HEK293	kidney:	embryo
19	chr1:74970626-74970676	SKMC	muscle:	n/a
20	chr1:74941958-74942008	CMK	blood:	n/a
21	chr1:74832752-74832802	HCM	heart:	n/a
22	chr1:74933557-74933607	HNPCEpiC	eye:	n/a
23	chr1:74945347-74945397	ProgFib	skin:	n/a
24	chr1:74988194-74988244	GM19239	blood:	n/a
25	chr1:74891564-74891614	HRCEpiC	kidney:	n/a
26	chr1:74888995-74889045	IMR90	lung:	fetal
27	chr1:74888995-74889045	MCF-7	breast:	n/a
28	chr1:74988194-74988244	HCT-116	colon:	n/a
29	chr1:74970626-74970676	AG04449	skin:	fetal
30	chr1:74891564-74891614	HRPEpiC	eye:	n/a
31	chr1:74970626-74970676	HCF	heart:	n/a
32	chr1:74945347-74945397	NHDF-neo	bronchial:	n/a
33	chr1:74941958-74942008	MCF-7	breast:	n/a
34	chr1:74945347-74945397	SK-N-MC	brain:	n/a
35	chr1:74891564-74891614	NT2-D1	testis:	n/a
36	chr1:74891564-74891614	AG09309	skin:	n/a
37	chr1:74933557-74933607	HUVEC	blood vessel:	n/a
38	chr1:74945347-74945397	Jurkat	blood:	n/a
39	chr1:74988194-74988244	HCPEpiC	choroid plexus:	n/a
40	chr1:74891564-74891614	ECC-1	luminal epithelium:	n/a
41	chr1:74933557-74933607	GM12892	blood:	n/a
42	chr1:74888995-74889045	HCF	heart:	n/a
43	chr1:74941958-74942008	HepG2	liver:	n/a
44	chr1:74970626-74970676	HEEpiC	esophagus:	n/a
45	chr1:74945347-74945397	AG10803	skin:	n/a
46	chr1:74988194-74988244	HRCEpiC	kidney:	n/a
47	chr1:74891564-74891614	PFSK-1	brain:	n/a
48	chr1:74832752-74832802	T-47D	breast:	n/a
49	chr1:74888995-74889045	HIPEpiC	eye:	n/a
50	chr1:74888995-74889045	A549	lung:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74949493..74951450-chr1:74951854..74954172,2	MCF-7	breast:
2	chr1:74934779..74936281-chr1:74938303..74940454,2	K562	blood:
3	chr1:74868917..74870654-chr1:74871411..74874146,2	K562	blood:
4	chr1:74934779..74936281-chr1:74938303..74940454,2	K562	blood:
5	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
6	chr1:74921227..74923766-chr1:74925738..74927601,2	K562	blood:
7	chr1:74921227..74923766-chr1:74925738..74927601,2	K562	blood:
8	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
9	chr1:74949493..74951450-chr1:74951854..74954172,2	MCF-7	breast:
10	chr1:74977554..74979985-chr1:75198825..75201036,2	K562	blood:
11	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:
12	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
13	chr1:74990321..74992157-chr1:75009741..75011754,2	K562	blood:
14	chr1:74971580..74976038-chr1:74977181..74980046,4	K562	blood:
15	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
16	chr1:74867146..74867864-chr13:25216133..25216958,2	MCF-7	breast:
17	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:
18	chr1:74868917..74870654-chr1:74871411..74874146,2	K562	blood:
19	chr1:74969628..74970367-chr1:75199475..75200023,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003961
2	lnc-FPGT-1	chr1:74941196-74941236	NONHSAT003961
3	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003962
4	lnc-FPGT-1	chr1:74949131-74949200	NONHSAT003963
5	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003960
6	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003963
7	lnc-FPGT-1	chr1:74934667-74934715	NONHSAT003962
8	lnc-FPGT-1	chr1:74934820-74934979	NONHSAT003960
9	lnc-FPGT-1	chr1:74934667-74934808	ENSG00000233894.1
10	lnc-FPGT-1	chr1:74934197-74934233	ENSG00000233894.1
11	lnc-LRRC53-1	chr1:74844380-74844486	ENSG00000237324.2
12	lnc-LRRC53-1	chr1:74834673-74834803	ENSG00000237324.2
13	lnc-FPGT-7	chr1:74853478-74853568	ucscGeneNc_uc001dgh_2
14	lnc-LRRC53-1	chr1:74832267-74832410	ENSG00000237324.2
15	lnc-FPGT-7	chr1:74859668-74864369	ucscGeneNc_uc001dgh_2
16	lnc-FPGT-1	chr1:74934820-74935227	ENSG00000233894.1
17	lnc-FPGT-1	chr1:74933879-74934233	ENSG00000233894.1

No data

Variant related genes	Relation type
LRRC53	TF binding region
ENSG00000237324	TF binding region
TNNI3K	TF binding region
ENSG00000233894	TF binding region
LRRC53	CpG island
ENSG00000237324	CpG island
TNNI3K	CpG island
ENSG00000233894	CpG island
ENSG00000116791	chromatin interactions
ENSG00000162623	chromatin interactions
ENSG00000162621	chromatin interactions
TARBP2	miRNA target sites
IP6K2	miRNA target sites

Extended variants
information (count: 6291 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:6291 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186085011	chr1:74831226-74831227	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529143372	chr1:74831239-74831240	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80027694	chr1:74831257-74831258	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1935126	chr1:74831440-74831441	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12121557	chr1:74831446-74831447	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17095200	chr1:74831533-74831534	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs386632451	chr1:74831543-74831544	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146891710	chr1:74831544-74831545	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570029209	chr1:74831556-74831557	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537585619	chr1:74831646-74831647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555787561	chr1:74831652-74831653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs539710293	chr1:74831686-74831687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190217851	chr1:74831690-74831691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12136497	chr1:74831756-74831757	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs78164420	chr1:74831803-74831804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs578099817	chr1:74831809-74831810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182442995	chr1:74831822-74831823	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs1358375	chr1:74831823-74831824	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs141248265	chr1:74831837-74831838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115558389	chr1:74831877-74831878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561345151	chr1:74831960-74831961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1527682	chr1:74832001-74832002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs540887213	chr1:74832002-74832003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150780965	chr1:74832017-74832018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533285494	chr1:74832031-74832032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11803631	chr1:74832032-74832033	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs573370636	chr1:74832068-74832069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114738810	chr1:74832161-74832162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530904742	chr1:74832168-74832169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543831998	chr1:74832173-74832174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143938344	chr1:74832213-74832214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs151136292	chr1:74832245-74832246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs567620961	chr1:74832250-74832251	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs61776224	chr1:74832273-74832274	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs186017151	chr1:74832330-74832331	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs45481095	chr1:74832335-74832336	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs539355445	chr1:74832402-74832403	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs557265735	chr1:74832433-74832434	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575843226	chr1:74832460-74832461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536702318	chr1:74832498-74832499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555053339	chr1:74832500-74832501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190779124	chr1:74832503-74832504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147273218	chr1:74832513-74832514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371183071	chr1:74832514-74832515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558956971	chr1:74832526-74832527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577849934	chr1:74832546-74832547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140670860	chr1:74832556-74832557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182658241	chr1:74832587-74832588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144632508	chr1:74832590-74832591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549461942	chr1:74832672-74832673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
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
Melanoma	17363583	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
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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74821200-74844400	Weak transcription	Right Ventricle	heart
2	chr1:74823600-74834200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:74823800-74832600	Weak transcription	Fetal Brain Male	brain
4	chr1:74829400-74847800	Weak transcription	Aorta	Aorta
5	chr1:74829600-74832000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr1:74829600-74832200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:74830200-74831600	Genic enhancers	Fetal Heart	heart
8	chr1:74830600-74834200	Weak transcription	Left Ventricle	heart
9	chr1:74830600-74840800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:74831600-74833400	Enhancers	Fetal Heart	heart
11	chr1:74832000-74832800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr1:74832200-74833000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:74832200-74841200	Weak transcription	Psoas Muscle	Psoas
14	chr1:74832400-74833000	Enhancers	Stomach Smooth Muscle	stomach
15	chr1:74832600-74832800	Enhancers	Fetal Brain Male	brain
16	chr1:74833400-74835000	Weak transcription	Fetal Heart	heart
17	chr1:74833800-74834400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr1:74833800-74837400	Weak transcription	Ovary	ovary
19	chr1:74834000-74834400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr1:74834000-74834400	Enhancers	NH-A	brain
21	chr1:74834000-74836400	Weak transcription	Liver	Liver
22	chr1:74834200-74834600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:74834200-74834600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr1:74834200-74834600	Enhancers	NHLF	lung
25	chr1:74834200-74834800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:74834200-74835400	Strong transcription	Left Ventricle	heart
27	chr1:74835000-74836800	Strong transcription	Fetal Heart	heart
28	chr1:74835400-74846000	Weak transcription	Left Ventricle	heart
29	chr1:74836600-74837200	Enhancers	Placenta Amnion	Placenta Amnion
30	chr1:74836800-74838600	Weak transcription	Fetal Heart	heart
31	chr1:74837200-74837600	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr1:74837600-74837800	Enhancers	Placenta Amnion	Placenta Amnion
33	chr1:74837800-74841400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr1:74838600-74838800	Enhancers	Fetal Heart	heart
35	chr1:74838800-74839200	Weak transcription	Fetal Heart	heart
36	chr1:74839200-74840200	Enhancers	Fetal Heart	heart
37	chr1:74840200-74841200	Genic enhancers	Fetal Heart	heart
38	chr1:74840800-74841400	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr1:74841200-74841400	Enhancers	Psoas Muscle	Psoas
40	chr1:74841200-74844400	Weak transcription	Fetal Heart	heart
41	chr1:74841400-74841600	Enhancers	Placenta Amnion	Placenta Amnion
42	chr1:74844400-74844600	Enhancers	Right Ventricle	heart
43	chr1:74844400-74846200	Enhancers	Fetal Heart	heart
44	chr1:74844600-74845000	Weak transcription	Right Ventricle	heart
45	chr1:74845000-74845200	Enhancers	Right Ventricle	heart
46	chr1:74845200-74846400	Enhancers	Right Atrium	heart
47	chr1:74845200-74851000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr1:74845200-74860800	Weak transcription	Right Ventricle	heart
49	chr1:74845600-74846600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr1:74845600-74846600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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