Variant report

Variant	nsv515898
Chromosome Location	chr8:10530037-10557407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:411)
CpG islands
(count:427)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:411 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:10556072-10556385	K562	blood:	n/a	n/a
2	ATF1	chr8:10534198-10534697	K562	blood:	n/a	n/a
3	ATF1	chr8:10547285-10547485	K562	blood:	n/a	n/a
4	ATF3	chr8:10534277-10534710	K562	blood:	n/a	n/a
5	ATF3	chr8:10538386-10538728	A549	lung:	n/a	n/a
6	ATF3	chr8:10556054-10556401	K562	blood:	n/a	n/a
7	ATF3	chr8:10534373-10534559	K562	blood:	n/a	n/a
8	BCL3	chr8:10538290-10538870	A549	lung:	n/a	n/a
9	BCL3	chr8:10538308-10538830	A549	lung:	n/a	n/a
10	BHLHE40	chr8:10534348-10534720	K562	blood:	n/a	n/a
11	BHLHE40	chr8:10537101-10537120	K562	blood:	n/a	n/a
12	BHLHE40	chr8:10547066-10547446	K562	blood:	n/a	n/a
13	BHLHE40	chr8:10556120-10556373	K562	blood:	n/a	n/a
14	BHLHE40	chr8:10548293-10549087	K562	blood:	n/a	chr8:10548805-10548821 chr8:10548940-10548956
15	BRCA1	chr8:10548322-10549104	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:10537000-10537113	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr8:10538366-10538794	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr8:10534312-10534703	K562	blood:	n/a	n/a
19	CBX3	chr8:10548378-10548714	K562	blood:	n/a	n/a
20	CCNT2	chr8:10534254-10534702	K562	blood:	n/a	chr8:10534536-10534556
21	CEBPB	chr8:10534313-10534550	K562	blood:	n/a	n/a
22	CEBPB	chr8:10534301-10534559	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:10538263-10538912	A549	lung:	n/a	n/a
24	CEBPB	chr8:10556061-10556406	A549	lung:	n/a	chr8:10556221-10556232
25	CEBPB	chr8:10532907-10532950	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:10557100-10557263	K562	blood:	n/a	n/a
27	CEBPB	chr8:10556051-10556400	IMR90	lung:	n/a	chr8:10556221-10556232
28	CEBPB	chr8:10544799-10544897	HepG2	liver:	n/a	chr8:10544848-10544859
29	CEBPB	chr8:10556056-10556388	HepG2	liver:	n/a	chr8:10556221-10556232
30	CEBPB	chr8:10532514-10533090	MCF-7	breast:	n/a	n/a
31	CEBPB	chr8:10556072-10556406	Hela-S3	cervix:	n/a	chr8:10556221-10556232
32	CEBPB	chr8:10556053-10556413	K562	blood:	n/a	chr8:10556221-10556232
33	CEBPB	chr8:10538372-10538912	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr8:10556133-10556276	K562	blood:	n/a	chr8:10556221-10556232
35	CEBPB	chr8:10548379-10549212	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr8:10534289-10534684	K562	blood:	n/a	n/a
37	CEBPB	chr8:10556073-10556387	K562	blood:	n/a	chr8:10556221-10556232
38	CEBPB	chr8:10534261-10534649	K562	blood:	n/a	n/a
39	CEBPD	chr8:10534293-10534745	K562	blood:	n/a	n/a
40	CHD1	chr8:10547388-10547392	GM12878	blood:	n/a	n/a
41	CHD2	chr8:10538401-10538873	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr8:10548267-10549252	Hela-S3	cervix:	n/a	n/a
43	CREB1	chr8:10538427-10538870	A549	lung:	n/a	n/a
44	CTCF	chr8:10539460-10539610	NHEK	skin:	n/a	chr8:10539477-10539490
45	CTCF	chr8:10540020-10540170	GM12868	blood:	n/a	n/a
46	CTCF	chr8:10538680-10538830	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr8:10552860-10553010	NHEK	skin:	n/a	chr8:10552951-10552969 chr8:10552957-10552966
48	CTCF	chr8:10539220-10539370	HMEC	breast:	n/a	n/a
49	CTCF	chr8:10534313-10534513	K562	blood:	n/a	chr8:10534389-10534402
50	CTCF	chr8:10539340-10539490	GM12873	blood:	n/a	chr8:10539477-10539490

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10555466-10555516	RPTEC	kidney:	n/a
2	chr8:10530053-10530103	HNPCEpiC	eye:	n/a
3	chr8:10530123-10530173	HAEpiC	amniotic membrane:	n/a
4	chr8:10555382-10555432	HepG2	liver:	n/a
5	chr8:10555466-10555516	HIPEpiC	eye:	n/a
6	chr8:10530053-10530103	GM19239	blood:	n/a
7	chr8:10536539-10536589	GM12891	blood:	n/a
8	chr8:10555466-10555516	LNCaP	prostate:	n/a
9	chr8:10553728-10553778	K562	blood:	n/a
10	chr8:10530053-10530103	RPTEC	kidney:	n/a
11	chr8:10555466-10555516	AG09309	skin:	n/a
12	chr8:10530148-10530198	Hela-S3	cervix:	n/a
13	chr8:10536539-10536589	MCF-7	breast:	n/a
14	chr8:10536539-10536589	Hela-S3	cervix:	n/a
15	chr8:10553728-10553778	HL-60	blood:	n/a
16	chr8:10530123-10530173	HepG2	liver:	n/a
17	chr8:10553728-10553778	AoSMC	blood vessel:	n/a
18	chr8:10530053-10530103	K562	blood:	n/a
19	chr8:10530053-10530103	NHBE	bronchial:	n/a
20	chr8:10555382-10555432	HCT-116	colon:	n/a
21	chr8:10530123-10530173	SK-N-MC	brain:	n/a
22	chr8:10555466-10555516	HL-60	blood:	n/a
23	chr8:10530148-10530198	RPTEC	kidney:	n/a
24	chr8:10530148-10530198	HCT-116	colon:	n/a
25	chr8:10530053-10530103	AG04449	skin:	fetal
26	chr8:10555466-10555516	SAEC	small airway:	n/a
27	chr8:10530123-10530173	CMK	blood:	n/a
28	chr8:10555382-10555432	HCF	heart:	n/a
29	chr8:10555466-10555516	Caco-2	colon:	n/a
30	chr8:10530123-10530173	GM12891	blood:	n/a
31	chr8:10530148-10530198	GM06990	blood:	n/a
32	chr8:10530053-10530103	HUVEC	blood vessel:	n/a
33	chr8:10530053-10530103	HCPEpiC	choroid plexus:	n/a
34	chr8:10530123-10530173	Hepatocyte	liver:	n/a
35	chr8:10536539-10536589	U87	brain:	n/a
36	chr8:10553728-10553778	HUVEC	blood vessel:	n/a
37	chr8:10536539-10536589	CMK	blood:	n/a
38	chr8:10536539-10536589	HRPEpiC	eye:	n/a
39	chr8:10553728-10553778	HMEC	breast:	n/a
40	chr8:10553728-10553778	NHBE	bronchial:	n/a
41	chr8:10536539-10536589	AG04449	skin:	fetal
42	chr8:10530148-10530198	AG09309	skin:	n/a
43	chr8:10555466-10555516	HEEpiC	esophagus:	n/a
44	chr8:10530123-10530173	MCF-7	breast:	n/a
45	chr8:10555466-10555516	NB4	blood:	n/a
46	chr8:10555466-10555516	ProgFib	skin:	n/a
47	chr8:10536539-10536589	MCF10A-Er-Src	breast:	n/a
48	chr8:10530148-10530198	GM12891	blood:	n/a
49	chr8:10555382-10555432	HUVEC	blood vessel:	n/a
50	chr8:10555382-10555432	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:10553813..10555777-chr8:10556607..10558383,2	K562	blood:
2	chr8:10555796..10558370-chr8:10558494..10560524,2	K562	blood:
3	chr8:10537022..10539383-chr8:10695484..10697412,2	K562	blood:
4	chr8:10535340..10537589-chr8:10540581..10542267,2	K562	blood:
5	chr8:10527187..10529394-chr8:10534040..10536905,2	K562	blood:
6	chr8:10539212..10541927-chr8:10542466..10544181,2	K562	blood:
7	chr19:16180029..16180673-chr8:10548540..10549342,2	Hela-S3	cervix:
8	chr8:10516980..10519109-chr8:10534324..10536494,2	K562	blood:
9	chr8:10556318..10558383-chr8:10558421..10560305,2	MCF-7	breast:
10	chr8:10553523..10556097-chr8:10561265..10564003,2	K562	blood:
11	chr8:10553813..10555777-chr8:10556607..10558383,2	K562	blood:
12	chr8:10556097..10559916-chr8:10561605..10564138,3	K562	blood:
13	chr8:10528112..10530692-chr8:10696880..10699073,2	K562	blood:
14	chr8:10549207..10552160-chr8:10577938..10579847,2	K562	blood:
15	chr8:10539212..10540819-chr8:10542466..10545338,2	K562	blood:
16	chr8:10534702..10537389-chr8:10561883..10564793,2	K562	blood:
17	chr8:10535340..10537589-chr8:10540581..10542267,2	K562	blood:
18	chr8:10533955..10536464-chr8:10664070..10665725,2	K562	blood:

No data

Variant related genes	Relation type
C8orf74	TF binding region
RNA5SP252	TF binding region
C8orf74	CpG island
RNA5SP252	CpG island
ENSG00000212433	chromatin interactions
ENSG00000258724	chromatin interactions
ENSG00000254093	chromatin interactions
ENSG00000253695	chromatin interactions

Extended variants
information (count: 1664 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11250057	chr8:10530037-10530038	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs375158169	chr8:10530054-10530055	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs73666403	chr8:10530055-10530056	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562921614	chr8:10530081-10530082	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs531714196	chr8:10530088-10530089	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs184676748	chr8:10530093-10530094	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs568124719	chr8:10530149-10530150	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs368483018	chr8:10530180-10530181	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs373780439	chr8:10530185-10530186	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs374988450	chr8:10530197-10530198	Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs369257053	chr8:10530212-10530213	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs11250058	chr8:10530218-10530219	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547463597	chr8:10530299-10530300	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs570757720	chr8:10530332-10530333	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs80181543	chr8:10530351-10530352	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs371927159	chr8:10530361-10530362	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs576267834	chr8:10530371-10530372	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs535551785	chr8:10530373-10530374	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs116144810	chr8:10530389-10530390	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs572167445	chr8:10530444-10530445	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs541064064	chr8:10530468-10530469	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs536836036	chr8:10530471-10530472	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs527811329	chr8:10530481-10530482	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs577496962	chr8:10530492-10530493	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs34271040	chr8:10530506-10530507	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs546154820	chr8:10530508-10530509	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs562758356	chr8:10530517-10530518	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs75276654	chr8:10530531-10530532	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs548281319	chr8:10530547-10530548	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs561885472	chr8:10530549-10530550	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs527766627	chr8:10530594-10530595	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs547797580	chr8:10530624-10530625	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs570729061	chr8:10530649-10530650	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs73200713	chr8:10530664-10530665	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs374814186	chr8:10530692-10530693	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs73666404	chr8:10530712-10530713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535693411	chr8:10530738-10530739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11778725	chr8:10530750-10530751	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572208352	chr8:10530793-10530794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534401200	chr8:10530808-10530809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113247593	chr8:10530828-10530829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577531721	chr8:10530845-10530846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76677929	chr8:10530880-10530881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556394068	chr8:10530885-10530886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372447623	chr8:10530889-10530890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181715410	chr8:10530925-10530926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs62492310	chr8:10530933-10530934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376455988	chr8:10530940-10530941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542051285	chr8:10530977-10530978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375199012	chr8:10530995-10530996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10526800-10537600	Weak transcription	Gastric	stomach
2	chr8:10528600-10531000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:10529000-10530600	Enhancers	Spleen	Spleen
4	chr8:10529000-10531000	Enhancers	HUVEC	blood vessel
5	chr8:10529200-10530600	Enhancers	Esophagus	oesophagus
6	chr8:10529200-10530600	Enhancers	HMEC	breast
7	chr8:10529400-10530800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:10529400-10530800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:10529600-10530600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:10529600-10530600	Enhancers	Brain Anterior Caudate	brain
11	chr8:10529600-10530800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:10529600-10530800	Enhancers	Lung	lung
13	chr8:10529600-10532800	Weak transcription	K562	blood
14	chr8:10529800-10530400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:10529800-10530400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:10529800-10530400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
17	chr8:10529800-10530400	Enhancers	NHEK	skin
18	chr8:10529800-10530600	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr8:10529800-10531000	Enhancers	Hela-S3	cervix
20	chr8:10530000-10530200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr8:10530000-10530400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:10530000-10530400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:10530000-10530400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:10530000-10530600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr8:10530000-10530600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:10530000-10530800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:10530000-10532600	Weak transcription	A549	lung
28	chr8:10530200-10530600	Enhancers	NH-A	brain
29	chr8:10530200-10530800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:10530600-10532200	Weak transcription	Esophagus	oesophagus
31	chr8:10530600-10532800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:10530600-10536800	Weak transcription	Spleen	Spleen
33	chr8:10530800-10537200	Weak transcription	Lung	lung
34	chr8:10531000-10532200	Weak transcription	Hela-S3	cervix
35	chr8:10531000-10534200	Weak transcription	HUVEC	blood vessel
36	chr8:10532200-10532600	Enhancers	Esophagus	oesophagus
37	chr8:10532200-10533200	Enhancers	Hela-S3	cervix
38	chr8:10532400-10532600	Enhancers	Pancreas	Pancrea
39	chr8:10532400-10532600	Enhancers	Stomach Mucosa	stomach
40	chr8:10532600-10534000	Enhancers	A549	lung
41	chr8:10532600-10534200	Weak transcription	Esophagus	oesophagus
42	chr8:10532800-10533000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:10532800-10534200	Weak transcription	Stomach Mucosa	stomach
44	chr8:10532800-10535800	Enhancers	K562	blood
45	chr8:10533000-10533400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr8:10533200-10536200	Weak transcription	Hela-S3	cervix
47	chr8:10533200-10538200	Weak transcription	Pancreas	Pancrea
48	chr8:10534000-10534400	Bivalent Enhancer	A549	lung
49	chr8:10534200-10534800	Enhancers	Esophagus	oesophagus
50	chr8:10534200-10534800	Enhancers	Stomach Mucosa	stomach

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