Variant report

Variant	nsv516035
Chromosome Location	chr8:96208726-96235451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:184)
Chromatin interactive
region (count:78)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:96212521-96212598	K562	blood:	n/a	n/a
2	ARID3A	chr8:96212726-96212965	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:96222407-96222791	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:96224165-96224531	K562	blood:	n/a	n/a
5	ARID3A	chr8:96223744-96224151	HepG2	liver:	n/a	chr8:96223906-96223922 chr8:96223905-96223921
6	ATF1	chr8:96221867-96222148	K562	blood:	n/a	n/a
7	ATF1	chr8:96211938-96212282	K562	blood:	n/a	n/a
8	ATF2	chr8:96226054-96226497	GM12878	blood:	n/a	n/a
9	BCL3	chr8:96229221-96229625	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:96226960-96227142	K562	blood:	n/a	n/a
11	BHLHE40	chr8:96224599-96224903	K562	blood:	n/a	n/a
12	BRCA1	chr8:96214094-96214463	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr8:96210432-96210870	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr8:96211922-96212232	K562	blood:	n/a	n/a
15	CCNT2	chr8:96224640-96225068	K562	blood:	n/a	chr8:96224871-96224891 chr8:96224829-96224849 chr8:96224778-96224787
16	CEBPB	chr8:96223796-96224102	IMR90	lung:	n/a	chr8:96223935-96223952
17	CEBPB	chr8:96212677-96212998	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:96224407-96225092	K562	blood:	n/a	n/a
19	CEBPB	chr8:96223743-96224742	Hela-S3	cervix:	n/a	chr8:96223935-96223952
20	CEBPB	chr8:96228265-96228279	K562	blood:	n/a	n/a
21	CEBPB	chr8:96223745-96225224	MCF-7	breast:	n/a	chr8:96223935-96223952
22	CEBPB	chr8:96210323-96210849	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:96226206-96226424	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:96224693-96225097	K562	blood:	n/a	n/a
25	CEBPB	chr8:96223776-96224140	K562	blood:	n/a	chr8:96223935-96223952
26	CEBPB	chr8:96227022-96227160	K562	blood:	n/a	n/a
27	CEBPB	chr8:96212635-96213057	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr8:96223769-96224133	HepG2	liver:	n/a	chr8:96223935-96223952
29	CEBPB	chr8:96223821-96224049	HepG2	liver:	n/a	chr8:96223935-96223952
30	CEBPB	chr8:96223712-96224175	MCF-7	breast:	n/a	chr8:96223935-96223952
31	CEBPB	chr8:96223739-96224039	HepG2	liver:	n/a	chr8:96223935-96223952
32	CEBPB	chr8:96224262-96224811	MCF-7	breast:	n/a	n/a
33	CEBPD	chr8:96224628-96225111	K562	blood:	n/a	n/a
34	CHD2	chr8:96231359-96231390	HepG2	liver:	n/a	n/a
35	CHD2	chr8:96212913-96212929	HepG2	liver:	n/a	n/a
36	CHD2	chr8:96214105-96214300	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr8:96233732-96233773	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr8:96215243-96215387	HepG2	liver:	n/a	n/a
39	CHD2	chr8:96210312-96210689	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr8:96212781-96213059	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr8:96215260-96215410	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr8:96215340-96215490	HVMF	connective:	n/a	n/a
43	CTCF	chr8:96216040-96216190	GM06990	blood:	n/a	n/a
44	CTCF	chr8:96215097-96215499	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:96215260-96215410	GM12867	blood:	n/a	n/a
46	CTCF	chr8:96215260-96215410	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr8:96213559-96213642	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:96231360-96231510	HepG2	liver:	n/a	n/a
49	CTCF	chr8:96213580-96213730	NHEK	skin:	n/a	n/a
50	CTCF	chr8:96215240-96215390	GM12872	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96213626-96213676	SK-N-MC	brain:	n/a
2	chr8:96213626-96213676	SK-N-MC	brain:	n/a
3	chr8:96213626-96213676	IMR90	lung:	fetal
4	chr8:96213626-96213676	U87	brain:	n/a
5	chr8:96213626-96213676	T-47D	breast:	n/a
6	chr8:96214079-96214129	IMR90	lung:	fetal
7	chr8:96226844-96226894	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:96214079-96214129	GM12892	blood:	n/a
9	chr8:96213626-96213676	GM12892	blood:	n/a
10	chr8:96214079-96214129	SK-N-SH	brain:	n/a
11	chr8:96226844-96226894	Hepatocyte	liver:	n/a
12	chr8:96214079-96214129	K562	blood:	n/a
13	chr8:96214079-96214129	HCT-116	colon:	n/a
14	chr8:96214079-96214129	ProgFib	skin:	n/a
15	chr8:96214079-96214129	HAEpiC	amniotic membrane:	n/a
16	chr8:96213626-96213676	ovcar-3	ovarian:	n/a
17	chr8:96213626-96213676	NH-A	brain:	n/a
18	chr8:96214079-96214129	A549	lung:	n/a
19	chr8:96226844-96226894	NT2-D1	testis:	n/a
20	chr8:96213626-96213676	HNPCEpiC	eye:	n/a
21	chr8:96214079-96214129	RPTEC	kidney:	n/a
22	chr8:96214079-96214129	HepG2	liver:	n/a
23	chr8:96214079-96214129	HUVEC	blood vessel:	n/a
24	chr8:96214079-96214129	MCF10A-Er-Src	breast:	n/a
25	chr8:96213626-96213676	AoSMC	blood vessel:	n/a
26	chr8:96214079-96214129	MCF-7	breast:	n/a
27	chr8:96214079-96214129	HNPCEpiC	eye:	n/a
28	chr8:96213626-96213676	HUVEC	blood vessel:	n/a
29	chr8:96226844-96226894	HAEpiC	amniotic membrane:	n/a
30	chr8:96213626-96213676	HL-60	blood:	n/a
31	chr8:96214079-96214129	SK-N-SH_RA	brain:	n/a
32	chr8:96213626-96213676	PANC-1	pancreas:	n/a
33	chr8:96214079-96214129	NB4	blood:	n/a
34	chr8:96214079-96214129	GM06990	blood:	n/a
35	chr8:96213626-96213676	GM12891	blood:	n/a
36	chr8:96213626-96213676	Jurkat	blood:	n/a
37	chr8:96226844-96226894	CMK	blood:	n/a
38	chr8:96213626-96213676	Hepatocyte	liver:	n/a
39	chr8:96214079-96214129	PANC-1	pancreas:	n/a
40	chr8:96226844-96226894	NHDF-neo	bronchial:	n/a
41	chr8:96226844-96226894	SK-N-SH_RA	brain:	n/a
42	chr8:96226844-96226894	ProgFib	skin:	n/a
43	chr8:96226844-96226894	BE2_C	brain:	n/a
44	chr8:96226844-96226894	RPTEC	kidney:	n/a
45	chr8:96214079-96214129	AG10803	skin:	n/a
46	chr8:96213626-96213676	AG04449	skin:	fetal
47	chr8:96213626-96213676	GM19239	blood:	n/a
48	chr8:96213626-96213676	HCPEpiC	choroid plexus:	n/a
49	chr8:96214079-96214129	GM19239	blood:	n/a
50	chr8:96226844-96226894	AG09309	skin:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:96222030..96225621-chr8:96235538..96238037,4	MCF-7	breast:
2	chr8:96220160..96222982-chr8:96225240..96226907,2	K562	blood:
3	chr8:96234462..96239842-chr8:96279058..96283088,6	K562	blood:
4	chr8:96201546..96203086-chr8:96222450..96224514,2	MCF-7	breast:
5	chr8:96206048..96207695-chr8:96222331..96224850,2	MCF-7	breast:
6	chr8:96202933..96207621-chr8:96217016..96224905,7	MCF-7	breast:
7	chr8:96224814..96227323-chr8:96239460..96241166,3	MCF-7	breast:
8	chr8:96221181..96226002-chr8:96248062..96252220,6	MCF-7	breast:
9	chr8:96233041..96235359-chr8:96238288..96241007,3	K562	blood:
10	chr8:96109979..96112421-chr8:96207106..96209124,2	MCF-7	breast:
11	chr8:96111749..96114066-chr8:96234612..96236782,2	K562	blood:
12	chr8:96203164..96205455-chr8:96217318..96219508,3	MCF-7	breast:
13	chr8:96145311..96147896-chr8:96222063..96224775,3	MCF-7	breast:
14	chr8:96114675..96115219-chr8:96215202..96216074,2	MCF-7	breast:
15	chr8:96201649..96205216-chr8:96206550..96209721,4	MCF-7	breast:
16	chr8:96222260..96224188-chr8:96237998..96239656,2	MCF-7	breast:
17	chr8:96124552..96125363-chr8:96224111..96224757,2	MCF-7	breast:
18	chr8:96214009..96217041-chr8:96227079..96229399,3	K562	blood:
19	chr8:96203613..96205936-chr8:96222642..96224693,2	MCF-7	breast:
20	chr8:96229389..96231464-chr8:96247771..96249721,2	K562	blood:
21	chr8:96222002..96228732-chr8:96228964..96237755,16	MCF-7	breast:
22	chr8:96078403..96080929-chr8:96218241..96220291,2	MCF-7	breast:
23	chr8:96215901..96218694-chr8:96226457..96227957,2	MCF-7	breast:
24	chr8:96234981..96237972-chr8:97273758..97275615,2	MCF-7	breast:
25	chr8:96202506..96205446-chr8:96207707..96209234,2	K562	blood:
26	chr8:96147448..96150087-chr8:96233164..96235373,2	MCF-7	breast:
27	chr8:96139078..96141526-chr8:96207452..96210065,2	MCF-7	breast:
28	chr8:96205065..96207467-chr8:96211843..96213815,3	MCF-7	breast:
29	chr8:96232022..96234358-chr8:96242400..96245249,2	K562	blood:
30	chr8:96218874..96220553-chr8:96227342..96228870,2	MCF-7	breast:
31	chr8:96100067..96101759-chr8:96219152..96221642,2	MCF-7	breast:
32	chr8:96144879..96147244-chr8:96226350..96228191,2	MCF-7	breast:
33	chr8:96210411..96214534-chr8:96214869..96218158,4	K562	blood:
34	chr8:96214177..96216026-chr8:96245562..96248226,2	MCF-7	breast:
35	chr8:96221874..96223119-chr8:96235797..96236697,5	MCF-7	breast:
36	chr8:96212357..96216108-chr8:96221721..96225402,5	MCF-7	breast:
37	chr8:96214009..96217041-chr8:96227079..96229399,3	K562	blood:
38	chr8:96145520..96147593-chr8:96211677..96214625,3	MCF-7	breast:
39	chr8:96232323..96234888-chr8:96235835..96240054,4	MCF-7	breast:
40	chr8:96221802..96225274-chr8:96226379..96230011,4	K562	blood:
41	chr8:96212357..96216108-chr8:96221721..96225402,5	MCF-7	breast:
42	chr8:96204685..96206421-chr8:96234538..96236078,2	MCF-7	breast:
43	chr8:96205463..96207920-chr8:96210246..96213783,6	MCF-7	breast:
44	chr8:96230420..96235229-chr8:96280327..96282960,4	MCF-7	breast:
45	chr8:96217038..96220399-chr8:96221117..96225068,5	MCF-7	breast:
46	chr8:96217038..96220399-chr8:96221117..96225068,5	MCF-7	breast:
47	chr8:96124242..96126154-chr8:96223005..96225325,2	MCF-7	breast:
48	chr21:41758888..41761339-chr8:96214084..96215888,2	MCF-7	breast:
49	chr8:96231573..96233965-chr8:96249378..96252236,2	K562	blood:
50	chr8:96148386..96151549-chr8:96224432..96227854,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLEKHF2-2	chr8:96217488-96217540	ENSG00000253773.1
2	lnc-C8orf37-1	chr8:96228546-96228602	ENSG00000253351
3	lnc-PLEKHF2-2	chr8:96216684-96217151	ENSG00000253773.1
4	lnc-C8orf37-1	chr8:96220647-96220806	ENSG00000253351
5	lnc-C8orf37-1	chr8:96219235-96219536	ENSG00000253351
6	lnc-C8orf37-1	chr8:96228546-96228743	NONHSAT127827
7	lnc-C8orf37-1	chr8:96220713-96220767	NONHSAT127827

No data

Variant related genes	Relation type
ENSG00000253351	TF binding region
ENSG00000253773	TF binding region
ENSG00000253351	CpG island
ENSG00000253773	CpG island
ENSG00000156469	chromatin interactions
ENSG00000156172	chromatin interactions
ENSG00000254248	chromatin interactions
ENSG00000253351	chromatin interactions
ENSG00000156471	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000175895	chromatin interactions
ENSG00000253773	chromatin interactions

Extended variants
information (count: 1041 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4484658	chr8:96208726-96208727	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185809640	chr8:96208729-96208730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142391097	chr8:96208734-96208735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190281558	chr8:96208748-96208749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556535478	chr8:96208789-96208790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs576575937	chr8:96208821-96208822	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537876279	chr8:96208822-96208823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375012446	chr8:96208837-96208838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56832812	chr8:96208841-96208842	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577902604	chr8:96208855-96208856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141846876	chr8:96208868-96208869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529614737	chr8:96208888-96208889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560165222	chr8:96208919-96208920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376758879	chr8:96208942-96208943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182050951	chr8:96208985-96208986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542225313	chr8:96208986-96208987	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147103279	chr8:96209026-96209027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4734300	chr8:96209033-96209034	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs77090709	chr8:96209045-96209046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138665786	chr8:96209063-96209064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35302103	chr8:96209159-96209160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527878456	chr8:96209178-96209179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548000717	chr8:96209183-96209184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184350826	chr8:96209242-96209243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13259025	chr8:96209272-96209273	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs189053303	chr8:96209310-96209311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs141096535	chr8:96209325-96209326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181391881	chr8:96209357-96209358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559091097	chr8:96209368-96209369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547927467	chr8:96209402-96209403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566178013	chr8:96209446-96209447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs142545917	chr8:96209449-96209450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185633941	chr8:96209475-96209476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570619538	chr8:96209505-96209506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553949172	chr8:96209543-96209544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1561713	chr8:96209551-96209552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542911780	chr8:96209575-96209576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562104345	chr8:96209611-96209612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575625704	chr8:96209793-96209794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs12056575	chr8:96209862-96209863	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564618524	chr8:96209865-96209866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527418673	chr8:96209892-96209893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547644998	chr8:96209900-96209901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs59851845	chr8:96209937-96209938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs66735518	chr8:96209938-96209939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551629738	chr8:96209966-96209967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs397762263	chr8:96209973-96209974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367916347	chr8:96210011-96210012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550437462	chr8:96210024-96210025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191137810	chr8:96210025-96210026	Weak transcription Enhancers	n/a	n/a	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
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD

Chromatin state (count:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96204600-96212400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:96205000-96213400	Weak transcription	Lung	lung
3	chr8:96205600-96210200	Weak transcription	HMEC	breast
4	chr8:96205600-96213800	Weak transcription	Thymus	Thymus
5	chr8:96206200-96210000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:96206400-96215000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr8:96206800-96208800	Enhancers	Hela-S3	cervix
8	chr8:96207000-96209200	Enhancers	Esophagus	oesophagus
9	chr8:96207400-96212800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:96208200-96209000	Enhancers	Placenta	Placenta
11	chr8:96208200-96209000	Enhancers	Right Ventricle	heart
12	chr8:96208200-96209000	Enhancers	Stomach Mucosa	stomach
13	chr8:96208200-96209200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr8:96208200-96211000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:96208200-96211200	Enhancers	NHEK	skin
16	chr8:96208400-96209000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:96208400-96209200	Enhancers	Pancreas	Pancrea
18	chr8:96208400-96212000	Weak transcription	Primary B cells from peripheral blood	blood
19	chr8:96208600-96211800	Weak transcription	Right Atrium	heart
20	chr8:96208600-96216400	Weak transcription	Gastric	stomach
21	chr8:96208800-96210200	Weak transcription	Hela-S3	cervix
22	chr8:96209000-96210000	Weak transcription	Placenta	Placenta
23	chr8:96209000-96210200	Weak transcription	Stomach Mucosa	stomach
24	chr8:96209000-96211800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr8:96209000-96220000	Weak transcription	Right Ventricle	heart
26	chr8:96209200-96209600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:96209200-96209600	Weak transcription	Esophagus	oesophagus
28	chr8:96209200-96209600	Weak transcription	Pancreas	Pancrea
29	chr8:96209600-96210200	Enhancers	Pancreas	Pancrea
30	chr8:96209600-96210400	Enhancers	Esophagus	oesophagus
31	chr8:96209600-96211400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr8:96209800-96210400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:96210000-96210800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:96210000-96210800	Enhancers	Placenta	Placenta
35	chr8:96210200-96211000	Enhancers	HMEC	breast
36	chr8:96210200-96211200	Enhancers	Stomach Mucosa	stomach
37	chr8:96210200-96212600	Weak transcription	Pancreas	Pancrea
38	chr8:96210200-96214600	Enhancers	Hela-S3	cervix
39	chr8:96210400-96210600	Enhancers	HepG2	liver
40	chr8:96210400-96210800	Enhancers	Fetal Heart	heart
41	chr8:96210400-96210800	Enhancers	A549	lung
42	chr8:96210400-96211000	Enhancers	HSMMtube	muscle
43	chr8:96210400-96212600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr8:96210400-96212600	Weak transcription	Esophagus	oesophagus
45	chr8:96210800-96211600	Weak transcription	HepG2	liver
46	chr8:96210800-96212600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:96210800-96212600	Weak transcription	A549	lung
48	chr8:96210800-96214000	Weak transcription	Placenta	Placenta
49	chr8:96211000-96212400	Weak transcription	HMEC	breast
50	chr8:96211000-96212800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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