Variant report

Variant	nsv535002
Chromosome Location	chr1:74726454-74976335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1050)
CpG islands
(count:427)
Chromatin interactive
region (count:27)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1050 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr1:74822262-74822579	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:74943746-74943751	K562	blood:	n/a	n/a
4	ATF2	chr1:74929255-74929663	GM12878	blood:	n/a	n/a
5	BACH1	chr1:74952507-74952628	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr1:74929264-74929606	GM12878	blood:	n/a	chr1:74929478-74929489
7	BATF	chr1:74865039-74865204	GM12878	blood:	n/a	chr1:74865097-74865108
8	BATF	chr1:74862633-74862912	GM12878	blood:	n/a	n/a
9	BATF	chr1:74929254-74929656	GM12878	blood:	n/a	chr1:74929478-74929489
10	BATF	chr1:74864921-74865285	GM12878	blood:	n/a	chr1:74865097-74865108
11	BCL11A	chr1:74864896-74865230	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:74929185-74929684	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:74929322-74929595	GM12878	blood:	n/a	n/a
14	BCL3	chr1:74822171-74822614	A549	lung:	n/a	n/a
15	BHLHE40	chr1:74929307-74929660	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:74969965-74970040	K562	blood:	n/a	n/a
17	BHLHE40	chr1:74746472-74746612	K562	blood:	n/a	n/a
18	BHLHE40	chr1:74969836-74970190	GM12878	blood:	n/a	n/a
19	CEBPB	chr1:74969867-74970067	HepG2	liver:	n/a	chr1:74970021-74970032
20	CEBPB	chr1:74929299-74930127	IMR90	lung:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
21	CEBPB	chr1:74864001-74864166	H1-hESC	embryonic stem cell:	n/a	chr1:74864058-74864069
22	CEBPB	chr1:74780245-74780491	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr1:74768320-74768669	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr1:74933490-74933834	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr1:74863934-74864174	A549	lung:	n/a	chr1:74864058-74864069
27	CEBPB	chr1:74929751-74930102	HepG2	liver:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939
28	CEBPB	chr1:74771504-74771688	HepG2	liver:	n/a	chr1:74771612-74771623
29	CEBPB	chr1:74863892-74864211	HepG2	liver:	n/a	chr1:74864058-74864069
30	CEBPB	chr1:74933483-74933825	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr1:74808826-74809251	IMR90	lung:	n/a	chr1:74808957-74808968
32	CEBPB	chr1:74933511-74933815	IMR90	lung:	n/a	n/a
33	CEBPB	chr1:74859847-74860070	IMR90	lung:	n/a	chr1:74859944-74859957
34	CEBPB	chr1:74872136-74872456	HepG2	liver:	n/a	chr1:74872295-74872306
35	CEBPB	chr1:74728463-74728579	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:74944840-74944920	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr1:74808794-74809122	HepG2	liver:	n/a	chr1:74808957-74808968
38	CEBPB	chr1:74889142-74889769	IMR90	lung:	n/a	chr1:74889354-74889367
39	CEBPB	chr1:74780146-74780463	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:74822239-74822574	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:74872122-74872453	IMR90	lung:	n/a	chr1:74872295-74872306
42	CEBPB	chr1:74822142-74822758	IMR90	lung:	n/a	chr1:74822623-74822634
43	CEBPB	chr1:74933543-74933820	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr1:74729369-74729404	H1-hESC	embryonic stem cell:	n/a	chr1:74729392-74729403
45	CEBPB	chr1:74783362-74783693	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:74777395-74777659	HepG2	liver:	n/a	chr1:74777540-74777553 chr1:74777541-74777552
47	CEBPB	chr1:74808794-74809117	H1-hESC	embryonic stem cell:	n/a	chr1:74808957-74808968
48	CEBPB	chr1:74783464-74783590	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:74872165-74872467	A549	lung:	n/a	chr1:74872295-74872306
50	CEBPB	chr1:74929306-74930122	Hela-S3	cervix:	n/a	chr1:74929930-74929941 chr1:74929928-74929941 chr1:74929928-74929941 chr1:74929930-74929939 chr1:74929928-74929939

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:74941958-74942008	NB4	blood:	n/a
2	chr1:74891564-74891614	NH-A	brain:	n/a
3	chr1:74888995-74889045	GM12891	blood:	n/a
4	chr1:74941958-74942008	PFSK-1	brain:	n/a
5	chr1:74945347-74945397	PANC-1	pancreas:	n/a
6	chr1:74945347-74945397	NT2-D1	testis:	n/a
7	chr1:74832752-74832802	HCPEpiC	choroid plexus:	n/a
8	chr1:74970626-74970676	HUVEC	blood vessel:	n/a
9	chr1:74970626-74970676	GM19239	blood:	n/a
10	chr1:74891564-74891614	Caco-2	colon:	n/a
11	chr1:74891564-74891614	HIPEpiC	eye:	n/a
12	chr1:74945347-74945397	AG09319	gingival:	n/a
13	chr1:74933557-74933607	ProgFib	skin:	n/a
14	chr1:74945347-74945397	HNPCEpiC	eye:	n/a
15	chr1:74832752-74832802	IMR90	lung:	fetal
16	chr1:74832752-74832802	NB4	blood:	n/a
17	chr1:74891564-74891614	H1-hESC	embryonic stem cell:	embryo
18	chr1:74933557-74933607	AG09309	skin:	n/a
19	chr1:74970626-74970676	NHBE	bronchial:	n/a
20	chr1:74941958-74942008	HEK293	kidney:	embryo
21	chr1:74970626-74970676	Jurkat	blood:	n/a
22	chr1:74888995-74889045	NHBE	bronchial:	n/a
23	chr1:74970626-74970676	HPAEpiC	pulmonary alveolar:	n/a
24	chr1:74945347-74945397	HAEpiC	amniotic membrane:	n/a
25	chr1:74970626-74970676	PANC-1	pancreas:	n/a
26	chr1:74945347-74945397	AG04450	lung:	fetal
27	chr1:74891564-74891614	AoSMC	blood vessel:	n/a
28	chr1:74970626-74970676	GM12892	blood:	n/a
29	chr1:74888995-74889045	HRE	kidney:	n/a
30	chr1:74945347-74945397	HRCEpiC	kidney:	n/a
31	chr1:74970626-74970676	SAEC	small airway:	n/a
32	chr1:74941958-74942008	U87	brain:	n/a
33	chr1:74945347-74945397	BE2_C	brain:	n/a
34	chr1:74891564-74891614	HCT-116	colon:	n/a
35	chr1:74933557-74933607	HCF	heart:	n/a
36	chr1:74933557-74933607	CMK	blood:	n/a
37	chr1:74941958-74942008	K562	blood:	n/a
38	chr1:74891564-74891614	BE2_C	brain:	n/a
39	chr1:74888995-74889045	PrEC	prostate:	n/a
40	chr1:74832752-74832802	HEK293	kidney:	embryo
41	chr1:74891564-74891614	HAEpiC	amniotic membrane:	n/a
42	chr1:74891564-74891614	AG04449	skin:	fetal
43	chr1:74970626-74970676	HEEpiC	esophagus:	n/a
44	chr1:74888995-74889045	HRCEpiC	kidney:	n/a
45	chr1:74941958-74942008	HRCEpiC	kidney:	n/a
46	chr1:74970626-74970676	T-47D	breast:	n/a
47	chr1:74933557-74933607	HEK293	kidney:	embryo
48	chr1:74832752-74832802	GM06990	blood:	n/a
49	chr1:74933557-74933607	GM06990	blood:	n/a
50	chr1:74832752-74832802	HCT-116	colon:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:74622416..74625063-chr1:74764779..74767346,2	K562	blood:
2	chr1:74867146..74867864-chr13:25216133..25216958,2	MCF-7	breast:
3	chr1:74868917..74870654-chr1:74871411..74874146,2	K562	blood:
4	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
5	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:
6	chr1:74868917..74870654-chr1:74871411..74874146,2	K562	blood:
7	chr1:74949493..74951450-chr1:74951854..74954172,2	MCF-7	breast:
8	chr1:74921227..74923766-chr1:74925738..74927601,2	K562	blood:
9	chr1:74921227..74923766-chr1:74925738..74927601,2	K562	blood:
10	chr1:74701198..74703916-chr1:74780316..74782785,2	K562	blood:
11	chr1:74969628..74970367-chr1:75199475..75200023,2	MCF-7	breast:
12	chr1:74799781..74801961-chr1:74805527..74808251,2	MCF-7	breast:
13	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
14	chr1:74835693..74838448-chr1:74838770..74840795,2	K562	blood:
15	chr1:74641537..74643099-chr1:74809509..74811733,2	K562	blood:
16	chr1:74934779..74936281-chr1:74938303..74940454,2	K562	blood:
17	chr1:74949493..74951450-chr1:74951854..74954172,2	MCF-7	breast:
18	chr1:74847175..74848707-chr1:74848769..74850609,2	MCF-7	breast:
19	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:
20	chr1:74934779..74936281-chr1:74938303..74940454,2	K562	blood:
21	chr1:74971580..74976038-chr1:74977181..74980046,4	K562	blood:
22	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
23	chr1:74835693..74838448-chr1:74838770..74840805,3	K562	blood:
24	chr1:74725032..74727117-chr1:74729630..74732086,2	K562	blood:
25	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
26	chr1:74725032..74727513-chr1:74728453..74731130,2	K562	blood:
27	chr1:74789903..74792042-chr1:74796412..74799113,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FPGT-1	chr1:74934667-74934808	ENSG00000233894.1
2	lnc-FPGT-1	chr1:74934820-74934979	NONHSAT003960
3	lnc-LRRC53-1	chr1:74834673-74834803	ENSG00000237324.2
4	lnc-FPGT-1	chr1:74934667-74934715	NONHSAT003962
5	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003960
6	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003963
7	lnc-FPGT-1	chr1:74941196-74941236	NONHSAT003961
8	lnc-FPGT-1	chr1:74949131-74949200	NONHSAT003963
9	lnc-FPGT-7	chr1:74815702-74815781	ucscGeneNc_uc001dgh_2
10	lnc-LRRC53-1	chr1:74807263-74807671	ENSG00000237324.2
11	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003961
12	lnc-FPGT-1	chr1:74934820-74935227	ENSG00000233894.1
13	lnc-FPGT-7	chr1:74859668-74864369	ucscGeneNc_uc001dgh_2
14	lnc-FPGT-1	chr1:74934197-74934233	ENSG00000233894.1
15	lnc-LRRC53-1	chr1:74832267-74832410	ENSG00000237324.2
16	lnc-LRRC53-1	chr1:74844380-74844486	ENSG00000237324.2
17	lnc-FPGT-1	chr1:74933879-74934233	ENSG00000233894.1
18	lnc-FPGT-7	chr1:74853478-74853568	ucscGeneNc_uc001dgh_2
19	lnc-FPGT-1	chr1:74933443-74934233	NONHSAT003962

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
ENSG00000162621	chromatin interactions
ENSG00000116783	chromatin interactions
IP6K2	miRNA target sites
TARBP2	miRNA target sites

Extended variants
information (count: 9432 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:9432 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578251720	chr1:74726470-74726471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545722334	chr1:74726507-74726508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77109844	chr1:74726508-74726509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548149336	chr1:74726576-74726577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570856906	chr1:74726689-74726690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538666546	chr1:74726728-74726729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561463890	chr1:74726762-74726763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367883391	chr1:74726765-74726766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528831773	chr1:74726822-74726823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554090696	chr1:74726876-74726877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553594	chr1:74726903-74726904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565598665	chr1:74726915-74726916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572033327	chr1:74726917-74726918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539849310	chr1:74726941-74726942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191636117	chr1:74726942-74726943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565269862	chr1:74726959-74726960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs45600031	chr1:74726960-74726961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542481855	chr1:74727040-74727041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371354175	chr1:74727044-74727045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537265746	chr1:74727074-74727075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183201074	chr1:74727089-74727090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567763070	chr1:74727100-74727101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534972972	chr1:74727145-74727146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553391456	chr1:74727165-74727166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs45510604	chr1:74727172-74727173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545358478	chr1:74727208-74727209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs509849	chr1:74727221-74727222	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs575717088	chr1:74727343-74727344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs45562841	chr1:74727413-74727414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561400996	chr1:74727421-74727422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12043716	chr1:74727458-74727459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
32	rs540768649	chr1:74727465-74727466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558901461	chr1:74727466-74727467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs45580141	chr1:74727484-74727485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147514757	chr1:74727529-74727530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569954957	chr1:74727544-74727545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530571549	chr1:74727552-74727553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556366625	chr1:74727576-74727577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549207314	chr1:74727607-74727608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188079995	chr1:74727610-74727611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375845218	chr1:74727674-74727675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200528370	chr1:74727743-74727744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533128288	chr1:74727744-74727745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs45539540	chr1:74727783-74727784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559356909	chr1:74727862-74727863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs12750181	chr1:74727864-74727865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs571538245	chr1:74727868-74727869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370228218	chr1:74727873-74727874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140385605	chr1:74727894-74727895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12080871	chr1:74727913-74727914	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:74671400-74751800	Weak transcription	Ovary	ovary
2	chr1:74717000-74751800	Weak transcription	Aorta	Aorta
3	chr1:74718600-74727400	Weak transcription	Fetal Heart	heart
4	chr1:74719600-74753800	Weak transcription	Right Ventricle	heart
5	chr1:74723800-74731800	Weak transcription	Gastric	stomach
6	chr1:74724200-74746400	Weak transcription	Left Ventricle	heart
7	chr1:74727400-74728000	Enhancers	Fetal Heart	heart
8	chr1:74728000-74730800	Weak transcription	Fetal Heart	heart
9	chr1:74730800-74731800	Genic enhancers	Fetal Heart	heart
10	chr1:74730800-74733200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:74731400-74731800	Enhancers	Brain Hippocampus Middle	brain
12	chr1:74731400-74732200	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr1:74731600-74732200	Enhancers	Brain Angular Gyrus	brain
14	chr1:74731800-74732000	Enhancers	Gastric	stomach
15	chr1:74731800-74732800	Enhancers	Brain Anterior Caudate	brain
16	chr1:74731800-74735200	Enhancers	Fetal Heart	heart
17	chr1:74731800-74743800	Weak transcription	Brain Hippocampus Middle	brain
18	chr1:74733200-74735400	Enhancers	Fetal Intestine Large	intestine
19	chr1:74734000-74734400	Enhancers	Fetal Intestine Small	intestine
20	chr1:74734000-74734600	Enhancers	Fetal Stomach	stomach
21	chr1:74735200-74742200	Weak transcription	Fetal Heart	heart
22	chr1:74735800-74751400	Weak transcription	Psoas Muscle	Psoas
23	chr1:74736600-74740400	Weak transcription	Brain Substantia Nigra	brain
24	chr1:74736800-74751600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr1:74742200-74743200	Enhancers	Fetal Heart	heart
26	chr1:74743200-74746400	Weak transcription	Fetal Heart	heart
27	chr1:74746400-74746800	Genic enhancers	Left Ventricle	heart
28	chr1:74746400-74747400	Enhancers	Fetal Heart	heart
29	chr1:74746800-74748400	Strong transcription	Left Ventricle	heart
30	chr1:74747400-74747800	Weak transcription	Fetal Heart	heart
31	chr1:74747600-74752000	Weak transcription	Gastric	stomach
32	chr1:74747800-74748000	Enhancers	Fetal Heart	heart
33	chr1:74748000-74769200	Weak transcription	Fetal Heart	heart
34	chr1:74748400-74751800	Weak transcription	Left Ventricle	heart
35	chr1:74750800-74751200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr1:74751800-74752200	ZNF genes & repeats	Aorta	Aorta
37	chr1:74751800-74752600	ZNF genes & repeats	Left Ventricle	heart
38	chr1:74751800-74752600	ZNF genes & repeats	Ovary	ovary
39	chr1:74752000-74752200	ZNF genes & repeats	Gastric	stomach
40	chr1:74752600-74753200	Weak transcription	Left Ventricle	heart
41	chr1:74764000-74771000	Weak transcription	Left Ventricle	heart
42	chr1:74766000-74771000	Weak transcription	Brain Hippocampus Middle	brain
43	chr1:74768000-74768800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:74768000-74769200	Weak transcription	Adipose Nuclei	Adipose
45	chr1:74768200-74768600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr1:74769200-74769400	ZNF genes & repeats	Adipose Nuclei	Adipose
47	chr1:74769200-74773200	Strong transcription	Fetal Heart	heart
48	chr1:74769400-74771000	Weak transcription	Adipose Nuclei	Adipose
49	chr1:74769400-74772000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr1:74771000-74771400	Enhancers	Adipose Nuclei	Adipose

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