Variant report

Variant	nsv891182
Chromosome Location	chr8:90785685-90888786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1295)
CpG islands
(count:306)
Chromatin interactive
region (count:211)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1295 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90860445-90860888	K562	blood:	n/a	n/a
2	ARID3A	chr8:90838811-90838957	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:90809181-90809566	K562	blood:	n/a	n/a
4	ARID3A	chr8:90860399-90860818	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:90813191-90814432	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:90811318-90811856	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:90864780-90864855	K562	blood:	n/a	n/a
8	ATF1	chr8:90809195-90809942	K562	blood:	n/a	n/a
9	ATF1	chr8:90796935-90797378	K562	blood:	n/a	n/a
10	ATF1	chr8:90851185-90851416	K562	blood:	n/a	n/a
11	ATF1	chr8:90817504-90817686	K562	blood:	n/a	n/a
12	ATF1	chr8:90814000-90814251	K562	blood:	n/a	n/a
13	ATF2	chr8:90849017-90849522	GM12878	blood:	n/a	n/a
14	ATF2	chr8:90848887-90849536	GM12878	blood:	n/a	n/a
15	ATF3	chr8:90851178-90851424	K562	blood:	n/a	n/a
16	ATF3	chr8:90880968-90881353	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:90835853-90835861	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr8:90849099-90849357	GM12878	blood:	n/a	n/a
19	BATF	chr8:90849053-90849348	GM12878	blood:	n/a	n/a
20	BATF	chr8:90813846-90814319	GM12878	blood:	n/a	chr8:90814102-90814113
21	BATF	chr8:90846770-90847078	GM12878	blood:	n/a	n/a
22	BATF	chr8:90813945-90814232	GM12878	blood:	n/a	chr8:90814102-90814113
23	BATF	chr8:90794451-90794806	GM12878	blood:	n/a	n/a
24	BCL11A	chr8:90845928-90846150	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:90849030-90849412	GM12878	blood:	n/a	chr8:90849336-90849345
26	BCL3	chr8:90811477-90812336	A549	lung:	n/a	n/a
27	BCL3	chr8:90813484-90813869	GM12878	blood:	n/a	n/a
28	BCLAF1	chr8:90848930-90849556	GM12878	blood:	n/a	chr8:90849336-90849345
29	BCLAF1	chr8:90813916-90814267	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:90860355-90860838	GM12878	blood:	n/a	chr8:90860523-90860532 chr8:90860752-90860761
31	BCLAF1	chr8:90848961-90849387	GM12878	blood:	n/a	chr8:90849336-90849345
32	BHLHE40	chr8:90848633-90848775	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:90795025-90795124	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:90797159-90797330	K562	blood:	n/a	n/a
35	BHLHE40	chr8:90849020-90849429	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:90827609-90827779	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:90814010-90814135	GM12878	blood:	n/a	n/a
38	BHLHE40	chr8:90813978-90814173	K562	blood:	n/a	n/a
39	BHLHE40	chr8:90838425-90838937	GM12878	blood:	n/a	n/a
40	BHLHE40	chr8:90811542-90812093	GM12878	blood:	n/a	n/a
41	BHLHE40	chr8:90871027-90871284	K562	blood:	n/a	n/a
42	BHLHE40	chr8:90809804-90810011	K562	blood:	n/a	n/a
43	BHLHE40	chr8:90847723-90847926	GM12878	blood:	n/a	n/a
44	BRCA1	chr8:90838179-90838327	GM12878	blood:	n/a	n/a
45	CBX3	chr8:90827039-90827515	HCT-116	colon:	n/a	n/a
46	CBX3	chr8:90813454-90814572	HCT-116	colon:	n/a	n/a
47	CBX3	chr8:90813375-90814640	HCT-116	colon:	n/a	n/a
48	CEBPB	chr8:90854445-90854729	K562	blood:	n/a	n/a
49	CEBPB	chr8:90860402-90860796	Hela-S3	cervix:	n/a	chr8:90860571-90860582 chr8:90860569-90860580 chr8:90860571-90860582
50	CEBPB	chr8:90851097-90851459	HepG2	liver:	n/a	chr8:90851263-90851274

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90847772-90847822	NH-A	brain:	n/a
2	chr8:90847772-90847822	NH-A	brain:	n/a
3	chr8:90794647-90794697	IMR90	lung:	fetal
4	chr8:90847772-90847822	K562	blood:	n/a
5	chr8:90847772-90847822	BJ	skin:	n/a
6	chr8:90837663-90837713	AG04450	lung:	fetal
7	chr8:90847772-90847822	MCF-7	breast:	n/a
8	chr8:90847772-90847822	SK-N-MC	brain:	n/a
9	chr8:90860821-90860871	IMR90	lung:	fetal
10	chr8:90794647-90794697	AoSMC	blood vessel:	n/a
11	chr8:90847772-90847822	NT2-D1	testis:	n/a
12	chr8:90847772-90847822	HRPEpiC	eye:	n/a
13	chr8:90860821-90860871	AG10803	skin:	n/a
14	chr8:90847772-90847822	AG10803	skin:	n/a
15	chr8:90794647-90794697	PANC-1	pancreas:	n/a
16	chr8:90849014-90849064	HRE	kidney:	n/a
17	chr8:90849014-90849064	SKMC	muscle:	n/a
18	chr8:90849014-90849064	HCPEpiC	choroid plexus:	n/a
19	chr8:90849014-90849064	SK-N-SH_RA	brain:	n/a
20	chr8:90847772-90847822	HEK293	kidney:	embryo
21	chr8:90849014-90849064	GM12878	blood:	n/a
22	chr8:90849014-90849064	HRCEpiC	kidney:	n/a
23	chr8:90847772-90847822	SKMC	muscle:	n/a
24	chr8:90794647-90794697	PFSK-1	brain:	n/a
25	chr8:90837663-90837713	PANC-1	pancreas:	n/a
26	chr8:90860821-90860871	AG09319	gingival:	n/a
27	chr8:90849014-90849064	SK-N-SH	brain:	n/a
28	chr8:90849014-90849064	LNCaP	prostate:	n/a
29	chr8:90794647-90794697	AG10803	skin:	n/a
30	chr8:90847772-90847822	AG09319	gingival:	n/a
31	chr8:90794647-90794697	LNCaP	prostate:	n/a
32	chr8:90837663-90837713	ProgFib	skin:	n/a
33	chr8:90837663-90837713	K562	blood:	n/a
34	chr8:90847772-90847822	U87	brain:	n/a
35	chr8:90860821-90860871	BE2_C	brain:	n/a
36	chr8:90860821-90860871	HMEC	breast:	n/a
37	chr8:90837663-90837713	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:90837663-90837713	Caco-2	colon:	n/a
39	chr8:90847772-90847822	HepG2	liver:	n/a
40	chr8:90847772-90847822	GM12878	blood:	n/a
41	chr8:90837663-90837713	HepG2	liver:	n/a
42	chr8:90860821-90860871	ProgFib	skin:	n/a
43	chr8:90860821-90860871	Jurkat	blood:	n/a
44	chr8:90849014-90849064	Hepatocyte	liver:	n/a
45	chr8:90847772-90847822	HCF	heart:	n/a
46	chr8:90849014-90849064	ProgFib	skin:	n/a
47	chr8:90849014-90849064	GM06990	blood:	n/a
48	chr8:90837663-90837713	AG09319	gingival:	n/a
49	chr8:90794647-90794697	A549	lung:	n/a
50	chr8:90837663-90837713	SK-N-MC	brain:	n/a

(count:211 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:90791423..90793075-chr8:90800712..90802481,2	MCF-7	breast:
2	chr8:90884964..90887444-chr8:90889188..90890987,3	K562	blood:
3	chr8:90787120..90788718-chr8:90790537..90792123,2	K562	blood:
4	chr8:90858673..90862372-chr8:90995003..90998670,3	K562	blood:
5	chr8:90859127..90860639-chr8:90860686..90863094,2	MCF-7	breast:
6	chr8:90801418..90803391-chr8:90808526..90811319,2	MCF-7	breast:
7	chr8:90801418..90803391-chr8:90808526..90811319,2	MCF-7	breast:
8	chr8:90801184..90803292-chr8:90992105..90995010,2	MCF-7	breast:
9	chr8:90869094..90872518-chr8:90873810..90876034,4	MCF-7	breast:
10	chr8:90882781..90884744-chr8:90914063..90915962,2	MCF-7	breast:
11	chr8:90776459..90778873-chr8:90786925..90789865,2	K562	blood:
12	chr8:90812521..90814949-chr8:90913581..90915961,2	MCF-7	breast:
13	chr8:90858582..90866507-chr8:90866541..90873248,10	MCF-7	breast:
14	chr8:90808879..90811361-chr8:90813296..90815805,3	K562	blood:
15	chr8:90801163..90803261-chr8:90961126..90962760,2	MCF-7	breast:
16	chr8:90836699..90839189-chr8:90853198..90855476,2	MCF-7	breast:
17	chr8:90767178..90772166-chr8:90803183..90807118,5	MCF-7	breast:
18	chr8:90874955..90877119-chr8:90913162..90914813,2	MCF-7	breast:
19	chr8:90800083..90802743-chr8:90803621..90807196,3	MCF-7	breast:
20	chr8:90819524..90821279-chr8:90821317..90823717,2	MCF-7	breast:
21	chr8:90844734..90847246-chr8:90847760..90849982,2	MCF-7	breast:
22	chr8:90767933..90770718-chr8:90788442..90790406,2	K562	blood:
23	chr8:90860679..90862898-chr8:90864045..90867127,3	K562	blood:
24	chr8:90843753..90846365-chr8:90914514..90916042,2	MCF-7	breast:
25	chr8:90868769..90874649-chr8:90891359..90894975,5	MCF-7	breast:
26	chr8:90859420..90866965-chr8:90912674..90917180,23	MCF-7	breast:
27	chr8:90875884..90877610-chr8:90879120..90881443,2	MCF-7	breast:
28	chr8:90835014..90836804-chr8:90836875..90838600,2	K562	blood:
29	chr8:90817275..90817869-chr8:91013652..91014304,2	MCF-7	breast:
30	chr8:90873270..90875909-chr8:90879908..90881482,2	K562	blood:
31	chr8:90873270..90875909-chr8:90879908..90881482,2	K562	blood:
32	chr8:90806351..90809015-chr8:90995258..90997957,2	MCF-7	breast:
33	chr8:90885956..90887593-chr8:90995530..90997918,2	MCF-7	breast:
34	chr8:90810531..90814020-chr8:90816566..90819944,3	MCF-7	breast:
35	chr8:90794527..90798218-chr8:90801291..90805045,3	K562	blood:
36	chr8:90860679..90862898-chr8:90864045..90867127,3	K562	blood:
37	chr8:90861358..90862876-chr8:90877013..90879435,2	MCF-7	breast:
38	chr8:90852614..90855258-chr8:90856891..90858844,2	MCF-7	breast:
39	chr8:90737986..90738708-chr8:90849422..90850036,2	MCF-7	breast:
40	chr8:90733869..90736282-chr8:90859813..90862694,2	K562	blood:
41	chr8:90860020..90861677-chr8:90894087..90895653,8	MCF-7	breast:
42	chr8:90876426..90880425-chr8:90881590..90883827,5	MCF-7	breast:
43	chr8:90769536..90771377-chr8:90858098..90861015,2	MCF-7	breast:
44	chr8:90860109..90861127-chr8:90996276..90997394,6	K562	blood:
45	chr8:90788699..90792573-chr8:90996217..90998925,4	MCF-7	breast:
46	chr8:90852614..90855258-chr8:90856891..90858844,2	MCF-7	breast:
47	chr8:90860127..90861878-chr8:90995834..90997368,12	MCF-7	breast:
48	chr8:90800222..90801982-chr8:90840675..90842723,2	MCF-7	breast:
49	chr8:90788241..90790215-chr8:90796193..90798741,2	K562	blood:
50	chr8:90884877..90887679-chr8:90895518..90898177,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBN-5	chr8:90806868-90806991	ucscGeneNc_uc003yed_1
2	lnc-OSGIN2-3	chr8:90792599-90793006	NONHSAT127627
3	lnc-NBN-5	chr8:90803365-90803506	ucscGeneNc_uc003yed_1
4	lnc-NBN-5	chr8:90838399-90839074	ucscGeneNc_uc003yed_1
5	lnc-NBN-4	chr8:90835776-90836030	NONHSAT127628
6	lnc-NBN-5	chr8:90805979-90806316	ucscGeneNc_uc003yed_1
7	lnc-OSGIN2-3	chr8:90792316-90792388	NONHSAT127627
8	lnc-NBN-5	chr8:90798778-90799078	ucscGeneNc_uc003yed_1

No data

Variant related genes	Relation type
COX6B1P6	TF binding region
RIPK2	TF binding region
COX6B1P6	CpG island
RIPK2	CpG island
ENSG00000253349	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000104312	chromatin interactions
ENSG00000104320	chromatin interactions
ENSG00000256316	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000164823	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000160741	chromatin interactions
GPD2	miRNA target sites
GPD1L	miRNA target sites

Extended variants
information (count: 3664 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3664 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs447618	chr8:90785685-90785686	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73694484	chr8:90785705-90785706	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs144522304	chr8:90785706-90785707	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs575006205	chr8:90785886-90785887	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs191064647	chr8:90785968-90785969	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs532098749	chr8:90785970-90785971	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs547155445	chr8:90785991-90785992	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs183567845	chr8:90786048-90786049	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs189026180	chr8:90786105-90786106	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs192466894	chr8:90786108-90786109	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548463429	chr8:90786124-90786125	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs569894681	chr8:90786249-90786250	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs538230082	chr8:90786271-90786272	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs556626083	chr8:90786284-90786285	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs571738946	chr8:90786297-90786298	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs182746449	chr8:90786339-90786340	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs188077991	chr8:90786372-90786373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs76773876	chr8:90786373-90786374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs565624718	chr8:90786438-90786439	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs572602416	chr8:90786451-90786452	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs191549267	chr8:90786495-90786496	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs146652553	chr8:90786542-90786543	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs139096894	chr8:90786602-90786603	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs117598005	chr8:90786656-90786657	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs564555320	chr8:90786661-90786662	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs184376285	chr8:90786666-90786667	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs187219034	chr8:90786677-90786678	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs555990950	chr8:90786696-90786697	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs559232098	chr8:90786716-90786717	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs529891666	chr8:90786773-90786774	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs373332496	chr8:90786857-90786858	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs116868490	chr8:90786900-90786901	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs149890706	chr8:90786919-90786920	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs377458306	chr8:90786948-90786949	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs192074554	chr8:90786980-90786981	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538195853	chr8:90787005-90787006	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs556330355	chr8:90787027-90787028	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs571675959	chr8:90787065-90787066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs539086961	chr8:90787164-90787165	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs144940404	chr8:90787165-90787166	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs149067740	chr8:90787200-90787201	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs13250876	chr8:90787227-90787228	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201478294	chr8:90787332-90787333	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs116059951	chr8:90787387-90787388	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs371192021	chr8:90787400-90787401	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545436930	chr8:90787467-90787468	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554892381	chr8:90787508-90787509	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143119055	chr8:90787520-90787521	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs147829388	chr8:90787521-90787522	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs141397488	chr8:90787530-90787531	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Autism	22495311	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Acute lymphoblastic leukemia	18458336	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
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1724 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90771000-90797000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:90771600-90803800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr8:90771800-90805000	Weak transcription	Esophagus	oesophagus
4	chr8:90772000-90796800	Weak transcription	Lung	lung
5	chr8:90772000-90797000	Weak transcription	Ovary	ovary
6	chr8:90772200-90802000	Weak transcription	Colonic Mucosa	Colon
7	chr8:90772200-90802400	Weak transcription	Spleen	Spleen
8	chr8:90772200-90805200	Weak transcription	Fetal Brain Male	brain
9	chr8:90772200-90807200	Weak transcription	Pancreas	Pancrea
10	chr8:90772200-90809400	Weak transcription	Small Intestine	intestine
11	chr8:90772400-90787200	Weak transcription	Fetal Stomach	stomach
12	chr8:90772400-90790600	Weak transcription	NHEK	skin
13	chr8:90772400-90802200	Weak transcription	Colon Smooth Muscle	Colon
14	chr8:90773000-90806800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr8:90773000-90812400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr8:90773200-90799000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:90774200-90803600	Weak transcription	Fetal Heart	heart
18	chr8:90774400-90793600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:90775800-90807200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:90776400-90793800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr8:90776400-90799800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:90777000-90786200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:90777200-90787200	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr8:90777200-90787400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr8:90777400-90789400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr8:90778800-90786200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr8:90779000-90801200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr8:90779200-90786600	Weak transcription	NHLF	lung
29	chr8:90779200-90793200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr8:90779200-90793400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr8:90779200-90793800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr8:90779600-90802200	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr8:90781200-90786400	Strong transcription	NHDF-Ad	bronchial
34	chr8:90781400-90789800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr8:90781400-90806600	Weak transcription	Right Ventricle	heart
36	chr8:90781600-90788800	Strong transcription	Primary B cells from peripheral blood	blood
37	chr8:90781600-90790000	Strong transcription	Liver	Liver
38	chr8:90781600-90790200	Strong transcription	Placenta	Placenta
39	chr8:90781800-90805600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr8:90782000-90787600	Strong transcription	Primary hematopoietic stem cells	blood
41	chr8:90782000-90788200	Strong transcription	Osteobl	bone
42	chr8:90782000-90788800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr8:90782000-90789200	Strong transcription	Primary T helper cells fromperipheralblood	blood
44	chr8:90782000-90789600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:90782000-90789600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:90782200-90786800	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr8:90782200-90787800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:90782200-90790200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr8:90782600-90789600	Strong transcription	NH-A	brain
50	chr8:90783200-90786000	Strong transcription	GM12878-XiMat	blood

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