Variant report

Variant	nsv933781
Chromosome Location	chr8:100108619-100160324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:61)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100149959-100150472	K562	blood:	n/a	n/a
2	ARID3A	chr8:100124728-100124858	K562	blood:	n/a	n/a
3	ATF1	chr8:100135547-100135703	K562	blood:	n/a	n/a
4	ATF1	chr8:100150113-100150549	K562	blood:	n/a	n/a
5	ATF3	chr8:100150017-100150481	K562	blood:	n/a	n/a
6	BACH1	chr8:100150185-100150441	K562	blood:	n/a	n/a
7	BHLHE40	chr8:100150155-100150410	K562	blood:	n/a	n/a
8	CBX3	chr8:100150051-100150770	K562	blood:	n/a	n/a
9	CBX3	chr8:100150104-100150431	K562	blood:	n/a	n/a
10	CCNT2	chr8:100150101-100150431	K562	blood:	n/a	n/a
11	CEBPB	chr8:100157064-100157434	IMR90	lung:	n/a	n/a
12	CEBPB	chr8:100117844-100118377	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:100149955-100150424	K562	blood:	n/a	n/a
14	CEBPB	chr8:100150136-100150322	K562	blood:	n/a	n/a
15	CEBPB	chr8:100150009-100150483	K562	blood:	n/a	n/a
16	CEBPB	chr8:100151613-100151750	K562	blood:	n/a	n/a
17	CEBPD	chr8:100150048-100150496	K562	blood:	n/a	n/a
18	CEBPD	chr8:100150011-100150509	K562	blood:	n/a	n/a
19	CHD2	chr8:100150017-100150357	K562	blood:	n/a	n/a
20	CREB1	chr8:100149970-100150550	K562	blood:	n/a	n/a
21	CREB1	chr8:100150031-100150492	K562	blood:	n/a	n/a
22	CTCF	chr8:100112640-100112653	A549	lung:	n/a	n/a
23	CTCF	chr8:100149938-100150334	K562	blood:	n/a	n/a
24	CTCF	chr8:100154002-100154083	GM10248	blood:	n/a	n/a
25	CUX1	chr8:100150076-100150351	K562	blood:	n/a	n/a
26	E2F4	chr8:100157250-100157370	MCF10A-Er-Src	breast:	n/a	n/a
27	EP300	chr8:100149732-100150843	K562	blood:	n/a	chr8:100149765-100149779 chr8:100149760-100149774
28	EP300	chr8:100117811-100118366	T-47D	breast:	n/a	n/a
29	EP300	chr8:100150076-100150439	K562	blood:	n/a	n/a
30	EP300	chr8:100117937-100118290	T-47D	breast:	n/a	n/a
31	EP300	chr8:100135456-100135891	K562	blood:	n/a	n/a
32	EP300	chr8:100150247-100150325	GM12878	blood:	n/a	n/a
33	FOS	chr8:100157035-100157381	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr8:100150079-100150481	K562	blood:	n/a	n/a
35	FOS	chr8:100157044-100157393	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr8:100153642-100153892	MCF10A-Er-Src	breast:	n/a	chr8:100153813-100153821
37	FOS	chr8:100157043-100157393	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr8:100153656-100153936	MCF10A-Er-Src	breast:	n/a	chr8:100153813-100153821
39	FOS	chr8:100157046-100157382	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr8:100153709-100153878	MCF10A-Er-Src	breast:	n/a	chr8:100153813-100153821
41	FOSL1	chr8:100150082-100150484	K562	blood:	n/a	n/a
42	FOSL1	chr8:100150101-100150401	K562	blood:	n/a	n/a
43	FOSL2	chr8:100117934-100118354	MCF-7	breast:	n/a	n/a
44	FOSL2	chr8:100117801-100118291	MCF-7	breast:	n/a	n/a
45	FOXA1	chr8:100110338-100110584	T-47D	breast:	n/a	chr8:100110489-100110504
46	FOXA1	chr8:100117943-100118249	T-47D	breast:	n/a	n/a
47	FOXA1	chr8:100117911-100118342	T-47D	breast:	n/a	n/a
48	FOXA1	chr8:100116163-100116738	T-47D	breast:	n/a	chr8:100116539-100116554
49	FOXA1	chr8:100119732-100120011	T-47D	breast:	n/a	n/a
50	FOXA1	chr8:100124125-100124548	T-47D	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100157208-100157258	GM12891	blood:	n/a
2	chr8:100157208-100157258	ovcar-3	ovarian:	n/a
3	chr8:100157208-100157258	SK-N-MC	brain:	n/a
4	chr8:100157208-100157258	ECC-1	luminal epithelium:	n/a
5	chr8:100157208-100157258	HRCEpiC	kidney:	n/a
6	chr8:100157208-100157258	CMK	blood:	n/a
7	chr8:100157208-100157258	SAEC	small airway:	n/a
8	chr8:100157208-100157258	HCM	heart:	n/a
9	chr8:100157208-100157258	AG09309	skin:	n/a
10	chr8:100157208-100157258	HNPCEpiC	eye:	n/a
11	chr8:100157208-100157258	U87	brain:	n/a
12	chr8:100157208-100157258	Hela-S3	cervix:	n/a
13	chr8:100157208-100157258	Hepatocyte	liver:	n/a
14	chr8:100157208-100157258	HIPEpiC	eye:	n/a
15	chr8:100157208-100157258	HL-60	blood:	n/a
16	chr8:100157208-100157258	HCT-116	colon:	n/a
17	chr8:100157208-100157258	SK-N-SH_RA	brain:	n/a
18	chr8:100157208-100157258	HRE	kidney:	n/a
19	chr8:100157208-100157258	AoSMC	blood vessel:	n/a
20	chr8:100157208-100157258	LNCaP	prostate:	n/a
21	chr8:100157208-100157258	HRPEpiC	eye:	n/a
22	chr8:100157208-100157258	NHDF-neo	bronchial:	n/a
23	chr8:100157208-100157258	SK-N-SH	brain:	n/a
24	chr8:100157208-100157258	HMEC	breast:	n/a
25	chr8:100157208-100157258	GM12878	blood:	n/a
26	chr8:100157208-100157258	ProgFib	skin:	n/a
27	chr8:100157208-100157258	BE2_C	brain:	n/a
28	chr8:100157208-100157258	HCF	heart:	n/a
29	chr8:100157208-100157258	GM19239	blood:	n/a
30	chr8:100157208-100157258	MCF-7	breast:	n/a
31	chr8:100157208-100157258	T-47D	breast:	n/a
32	chr8:100157208-100157258	HCPEpiC	choroid plexus:	n/a
33	chr8:100157208-100157258	HEK293	kidney:	embryo
34	chr8:100157208-100157258	Caco-2	colon:	n/a
35	chr8:100157208-100157258	GM12892	blood:	n/a
36	chr8:100157208-100157258	RPTEC	kidney:	n/a
37	chr8:100157208-100157258	AG04449	skin:	fetal
38	chr8:100157208-100157258	H1-hESC	embryonic stem cell:	embryo
39	chr8:100157208-100157258	PANC-1	pancreas:	n/a
40	chr8:100157208-100157258	NH-A	brain:	n/a
41	chr8:100157208-100157258	HEEpiC	esophagus:	n/a
42	chr8:100157208-100157258	HepG2	liver:	n/a
43	chr8:100157208-100157258	NHBE	bronchial:	n/a
44	chr8:100157208-100157258	AG04450	lung:	fetal
45	chr8:100157208-100157258	NB4	blood:	n/a
46	chr8:100157208-100157258	SKMC	muscle:	n/a
47	chr8:100157208-100157258	MCF10A-Er-Src	breast:	n/a
48	chr8:100157208-100157258	AG09319	gingival:	n/a
49	chr8:100157208-100157258	K562	blood:	n/a
50	chr8:100157208-100157258	PrEC	prostate:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:100136650..100138168-chr8:100240298..100242917,2	K562	blood:
2	chr8:100115261..100117016-chr8:100117428..100119133,2	K562	blood:
3	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
4	chr8:99955457..99958039-chr8:100115422..100117482,3	MCF-7	breast:
5	chr8:100023955..100026746-chr8:100146269..100148393,2	K562	blood:
6	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
7	chr8:100130524..100132088-chr8:100135733..100138707,2	K562	blood:
8	chr8:99995141..99996042-chr8:100118104..100118628,2	MCF-7	breast:
9	chr17:59467368..59468208-chr8:100108099..100109078,2	MCF-7	breast:
10	chr8:100109070..100113299-chr8:100115182..100118080,5	MCF-7	breast:
11	chr8:100012703..100016134-chr8:100151109..100154697,3	MCF-7	breast:
12	chr8:100024034..100025700-chr8:100109623..100113452,3	MCF-7	breast:
13	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:
14	chr8:99956376..99957970-chr8:100136435..100137944,2	MCF-7	breast:
15	chr8:100144557..100146496-chr8:100147591..100149372,3	MCF-7	breast:
16	chr8:100109729..100112333-chr8:100147157..100149231,2	K562	blood:
17	chr8:100101168..100103542-chr8:100111717..100113562,2	K562	blood:
18	chr8:100125265..100128114-chr8:100129986..100133353,3	K562	blood:
19	chr8:100103552..100105106-chr8:100109674..100111736,2	K562	blood:
20	chr8:100024762..100026893-chr8:100106816..100109546,3	MCF-7	breast:
21	chr8:100023368..100025355-chr8:100122244..100124287,2	MCF-7	breast:
22	chr8:100024284..100027084-chr8:100113982..100120280,5	MCF-7	breast:
23	chr8:100043379..100045451-chr8:100150795..100153462,2	MCF-7	breast:
24	chr8:100145698..100148364-chr8:100156045..100158193,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-2	chr8:100132332-100132809	ENSG00000253532.1
2	lnc-OSR2-2	chr8:100131580-100131696	ENSG00000253532.1

No data

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000253562	TF binding region
ENSG00000253532	TF binding region
VPS13B	CpG island
ENSG00000253562	CpG island
ENSG00000253532	CpG island
ENSG00000253532	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000253180	chromatin interactions

Extended variants
information (count: 1728 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1728 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571633913	chr8:100108652-100108653	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544866134	chr8:100108687-100108688	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs146475623	chr8:100108696-100108697	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370748247	chr8:100108705-100108706	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs567552880	chr8:100108733-100108734	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs564757590	chr8:100108743-100108744	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs536187840	chr8:100108755-100108756	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs572157755	chr8:100108836-100108837	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs141308505	chr8:100108841-100108842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs575662526	chr8:100108850-100108851	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs376816903	chr8:100108918-100108919	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373747854	chr8:100108947-100108948	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571248059	chr8:100108948-100108949	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558246483	chr8:100108977-100108978	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs56378823	chr8:100108984-100108985	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs398009005	chr8:100109001-100109002	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs541174895	chr8:100109033-100109034	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540825095	chr8:100109056-100109057	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs560442162	chr8:100109067-100109068	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs574165926	chr8:100109097-100109098	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs561432620	chr8:100109105-100109106	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543387888	chr8:100109108-100109109	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs563152747	chr8:100109109-100109110	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530069585	chr8:100109117-100109118	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs369824084	chr8:100109143-100109144	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531774425	chr8:100109184-100109185	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188246082	chr8:100109257-100109258	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565397628	chr8:100109309-100109310	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs6999263	chr8:100109311-100109312	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs547576519	chr8:100109358-100109359	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs181033939	chr8:100109384-100109385	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112713765	chr8:100109418-100109419	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs376250023	chr8:100109492-100109493	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549701887	chr8:100109535-100109536	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569582266	chr8:100109536-100109537	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs186271085	chr8:100109596-100109597	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143643758	chr8:100109599-100109600	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572117616	chr8:100109650-100109651	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs145714998	chr8:100109701-100109702	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189733639	chr8:100109763-100109764	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs372770076	chr8:100109768-100109769	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574311382	chr8:100109808-100109809	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs532878766	chr8:100109850-100109851	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181334169	chr8:100109879-100109880	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs117110942	chr8:100109886-100109887	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545422863	chr8:100109887-100109888	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs76123556	chr8:100109900-100109901	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs527684053	chr8:100109901-100109902	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs536355694	chr8:100109953-100109954	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143655583	chr8:100109967-100109968	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:690 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100089800-100115400	Weak transcription	Left Ventricle	heart
2	chr8:100090000-100115000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:100090000-100115400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr8:100090200-100118600	Weak transcription	Primary T cells from cord blood	blood
5	chr8:100090800-100126600	Weak transcription	Fetal Lung	lung
6	chr8:100091200-100115600	Weak transcription	Thymus	Thymus
7	chr8:100091200-100137000	Weak transcription	Pancreas	Pancrea
8	chr8:100091400-100116200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr8:100093000-100109200	Weak transcription	Primary B cells from cord blood	blood
10	chr8:100093600-100111800	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr8:100099200-100160200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr8:100099600-100131400	Weak transcription	Lung	lung
13	chr8:100099600-100161000	Weak transcription	Spleen	Spleen
14	chr8:100099800-100115200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:100100000-100128200	Weak transcription	Fetal Stomach	stomach
16	chr8:100100400-100147400	Weak transcription	Brain Hippocampus Middle	brain
17	chr8:100100400-100161000	Weak transcription	Esophagus	oesophagus
18	chr8:100100800-100133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:100101800-100115200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr8:100101800-100125400	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr8:100101800-100160800	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr8:100102200-100116000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr8:100102200-100162600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr8:100102400-100109600	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr8:100102400-100129600	Weak transcription	Small Intestine	intestine
26	chr8:100102800-100109000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr8:100102800-100110000	Weak transcription	Fetal Intestine Large	intestine
28	chr8:100102800-100112600	Weak transcription	Fetal Intestine Small	intestine
29	chr8:100103000-100151400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr8:100103200-100109000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr8:100103200-100110200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:100103400-100175600	Weak transcription	NHEK	skin
33	chr8:100103600-100160200	Weak transcription	A549	lung
34	chr8:100104000-100160200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr8:100104200-100116000	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr8:100104200-100121600	Weak transcription	Gastric	stomach
37	chr8:100104200-100121600	Weak transcription	Psoas Muscle	Psoas
38	chr8:100104200-100121600	Weak transcription	Right Ventricle	heart
39	chr8:100104200-100141600	Weak transcription	Ovary	ovary
40	chr8:100104400-100109200	Weak transcription	HSMM	muscle
41	chr8:100104400-100111600	Weak transcription	Adipose Nuclei	Adipose
42	chr8:100104400-100115400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr8:100104400-100124800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr8:100104400-100133400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr8:100104400-100155200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr8:100104400-100160800	Weak transcription	HSMMtube	muscle
47	chr8:100104600-100109400	Weak transcription	GM12878-XiMat	blood
48	chr8:100104600-100114800	Weak transcription	Osteobl	bone
49	chr8:100104600-100115200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:100104600-100121600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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