Variant report

Variant	nsv611759
Chromosome Location	chr8:96221122-96247835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:733)
CpG islands
(count:61)
Chromatin interactive
region (count:108)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:96237312-96237625	K562	blood:	n/a	n/a
2	ARID3A	chr8:96224165-96224531	K562	blood:	n/a	n/a
3	ARID3A	chr8:96237680-96238075	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:96222407-96222791	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:96237833-96237936	K562	blood:	n/a	n/a
6	ARID3A	chr8:96223744-96224151	HepG2	liver:	n/a	chr8:96223906-96223922 chr8:96223905-96223921
7	ARID3A	chr8:96238736-96239118	K562	blood:	n/a	n/a
8	ARID3A	chr8:96235911-96236248	K562	blood:	n/a	n/a
9	ATF1	chr8:96238705-96239049	K562	blood:	n/a	n/a
10	ATF1	chr8:96221867-96222148	K562	blood:	n/a	n/a
11	ATF1	chr8:96241079-96241401	K562	blood:	n/a	n/a
12	ATF1	chr8:96235725-96236095	K562	blood:	n/a	n/a
13	ATF2	chr8:96240355-96240989	GM12878	blood:	n/a	n/a
14	ATF2	chr8:96226054-96226497	GM12878	blood:	n/a	n/a
15	ATF2	chr8:96240481-96240886	GM12878	blood:	n/a	n/a
16	ATF3	chr8:96241722-96242193	GM12878	blood:	n/a	n/a
17	ATF3	chr8:96238640-96239042	K562	blood:	n/a	n/a
18	ATF3	chr8:96241002-96241334	K562	blood:	n/a	n/a
19	ATF3	chr8:96241832-96242128	K562	blood:	n/a	n/a
20	ATF3	chr8:96241845-96242061	GM12878	blood:	n/a	n/a
21	BACH1	chr8:96238683-96239045	K562	blood:	n/a	n/a
22	BACH1	chr8:96237741-96238307	K562	blood:	n/a	n/a
23	BACH1	chr8:96237898-96237955	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr8:96240535-96240805	GM12878	blood:	n/a	n/a
25	BCL11A	chr8:96240489-96240847	GM12878	blood:	n/a	n/a
26	BCL11A	chr8:96240502-96240757	GM12878	blood:	n/a	n/a
27	BCL3	chr8:96229221-96229625	GM12878	blood:	n/a	n/a
28	BCLAF1	chr8:96240458-96241034	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:96238650-96239057	K562	blood:	n/a	n/a
30	BHLHE40	chr8:96224599-96224903	K562	blood:	n/a	n/a
31	BHLHE40	chr8:96237572-96238122	K562	blood:	n/a	n/a
32	BHLHE40	chr8:96241057-96241691	K562	blood:	n/a	n/a
33	BHLHE40	chr8:96240570-96240977	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:96226960-96227142	K562	blood:	n/a	n/a
35	BHLHE40	chr8:96235734-96236401	K562	blood:	n/a	n/a
36	BHLHE40	chr8:96243632-96243648	K562	blood:	n/a	n/a
37	BRCA1	chr8:96237889-96238027	HepG2	liver:	n/a	n/a
38	BRCA1	chr8:96238870-96238884	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr8:96241028-96242353	K562	blood:	n/a	n/a
40	CBX3	chr8:96238613-96239203	K562	blood:	n/a	n/a
41	CCNT2	chr8:96238569-96239100	K562	blood:	n/a	chr8:96238680-96238689
42	CCNT2	chr8:96235761-96236074	K562	blood:	n/a	n/a
43	CCNT2	chr8:96241063-96241528	K562	blood:	n/a	chr8:96241245-96241265
44	CCNT2	chr8:96237723-96238100	K562	blood:	n/a	n/a
45	CCNT2	chr8:96224640-96225068	K562	blood:	n/a	chr8:96224871-96224891 chr8:96224829-96224849 chr8:96224778-96224787
46	CEBPB	chr8:96247830-96248298	K562	blood:	n/a	chr8:96248025-96248036
47	CEBPB	chr8:96224693-96225097	K562	blood:	n/a	n/a
48	CEBPB	chr8:96247821-96248257	MCF-7	breast:	n/a	chr8:96248025-96248036
49	CEBPB	chr8:96223769-96224133	HepG2	liver:	n/a	chr8:96223935-96223952
50	CEBPB	chr8:96223739-96224039	HepG2	liver:	n/a	chr8:96223935-96223952

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:96226844-96226894	HRCEpiC	kidney:	n/a
2	chr8:96226844-96226894	BE2_C	brain:	n/a
3	chr8:96226844-96226894	CMK	blood:	n/a
4	chr8:96226844-96226894	HRPEpiC	eye:	n/a
5	chr8:96226844-96226894	AG04450	lung:	fetal
6	chr8:96226844-96226894	BJ	skin:	n/a
7	chr8:96226844-96226894	MCF10A-Er-Src	breast:	n/a
8	chr8:96226844-96226894	K562	blood:	n/a
9	chr8:96226844-96226894	AG04449	skin:	fetal
10	chr8:96226844-96226894	HMEC	breast:	n/a
11	chr8:96226844-96226894	ECC-1	luminal epithelium:	n/a
12	chr8:96226844-96226894	Caco-2	colon:	n/a
13	chr8:96226844-96226894	PANC-1	pancreas:	n/a
14	chr8:96226844-96226894	NH-A	brain:	n/a
15	chr8:96226844-96226894	RPTEC	kidney:	n/a
16	chr8:96226844-96226894	HPAEpiC	pulmonary alveolar:	n/a
17	chr8:96226844-96226894	GM12892	blood:	n/a
18	chr8:96226844-96226894	H1-hESC	embryonic stem cell:	embryo
19	chr8:96226844-96226894	ovcar-3	ovarian:	n/a
20	chr8:96226844-96226894	HIPEpiC	eye:	n/a
21	chr8:96226844-96226894	PrEC	prostate:	n/a
22	chr8:96226844-96226894	HUVEC	blood vessel:	n/a
23	chr8:96226844-96226894	SK-N-SH_RA	brain:	n/a
24	chr8:96226844-96226894	HAEpiC	amniotic membrane:	n/a
25	chr8:96226844-96226894	NT2-D1	testis:	n/a
26	chr8:96226844-96226894	SK-N-SH	brain:	n/a
27	chr8:96226844-96226894	HCPEpiC	choroid plexus:	n/a
28	chr8:96226844-96226894	SAEC	small airway:	n/a
29	chr8:96226844-96226894	HepG2	liver:	n/a
30	chr8:96226844-96226894	HEK293	kidney:	embryo
31	chr8:96226844-96226894	NB4	blood:	n/a
32	chr8:96226844-96226894	T-47D	breast:	n/a
33	chr8:96226844-96226894	LNCaP	prostate:	n/a
34	chr8:96226844-96226894	HL-60	blood:	n/a
35	chr8:96226844-96226894	U87	brain:	n/a
36	chr8:96226844-96226894	PFSK-1	brain:	n/a
37	chr8:96226844-96226894	GM12878	blood:	n/a
38	chr8:96226844-96226894	HCT-116	colon:	n/a
39	chr8:96226844-96226894	GM19239	blood:	n/a
40	chr8:96226844-96226894	GM06990	blood:	n/a
41	chr8:96226844-96226894	AG10803	skin:	n/a
42	chr8:96226844-96226894	A549	lung:	n/a
43	chr8:96226844-96226894	NHDF-neo	bronchial:	n/a
44	chr8:96226844-96226894	GM12891	blood:	n/a
45	chr8:96226844-96226894	ProgFib	skin:	n/a
46	chr8:96226844-96226894	AG09309	skin:	n/a
47	chr8:96226844-96226894	Hela-S3	cervix:	n/a
48	chr8:96226844-96226894	HRE	kidney:	n/a
49	chr8:96226844-96226894	SKMC	muscle:	n/a
50	chr8:96226844-96226894	AG09319	gingival:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:96039022..96041365-chr8:96246280..96249199,2	K562	blood:
2	chr8:96245615..96247830-chr8:96279996..96282391,2	MCF-7	breast:
3	chr8:96204194..96207440-chr8:96236906..96239736,3	MCF-7	breast:
4	chr8:96111749..96114066-chr8:96234612..96236782,2	K562	blood:
5	chr8:96078172..96080522-chr8:96236324..96239006,2	MCF-7	breast:
6	chr8:96229120..96231629-chr8:96232251..96235212,3	MCF-7	breast:
7	chr8:96232323..96234888-chr8:96235835..96240054,4	MCF-7	breast:
8	chr8:96236593..96238582-chr8:96243971..96246452,2	K562	blood:
9	chr8:96215901..96218694-chr8:96226457..96227957,2	MCF-7	breast:
10	chr8:96229389..96231464-chr8:96247771..96249721,2	K562	blood:
11	chr8:96232022..96234358-chr8:96242400..96245249,2	K562	blood:
12	chr8:96183340..96184864-chr8:96221923..96223784,2	MCF-7	breast:
13	chr8:96145188..96147654-chr8:96237767..96240393,2	K562	blood:
14	chr8:96230420..96235229-chr8:96280327..96282960,4	MCF-7	breast:
15	chr8:96214009..96217041-chr8:96227079..96229399,3	K562	blood:
16	chr8:96145223..96147405-chr8:96242438..96245086,2	MCF-7	breast:
17	chr8:96244866..96247715-chr8:96248127..96251735,3	K562	blood:
18	chr8:96192843..96194703-chr8:96238022..96240558,2	K562	blood:
19	chr8:96222002..96228732-chr8:96228964..96237755,16	MCF-7	breast:
20	chr8:96143545..96145795-chr8:96241070..96242615,2	K562	blood:
21	chr8:96241648..96244611-chr8:96247721..96251221,3	K562	blood:
22	chr8:96218170..96221837-chr8:96222580..96225075,3	MCF-7	breast:
23	chr8:96224814..96227323-chr8:96239460..96241166,3	MCF-7	breast:
24	chr8:96228560..96230239-chr8:96242060..96244919,2	MCF-7	breast:
25	chr8:96239016..96241801-chr8:96243185..96245921,2	MCF-7	breast:
26	chr8:96234462..96239842-chr8:96279058..96283088,6	K562	blood:
27	chr8:96232022..96234358-chr8:96242400..96245249,2	K562	blood:
28	chr8:96229120..96231629-chr8:96232251..96235212,3	MCF-7	breast:
29	chr8:96124242..96126154-chr8:96223005..96225325,2	MCF-7	breast:
30	chr8:96037192..96039493-chr8:96242564..96245463,2	MCF-7	breast:
31	chr8:96039470..96042211-chr8:96236701..96239677,2	K562	blood:
32	chr8:96201546..96203086-chr8:96222450..96224514,2	MCF-7	breast:
33	chr8:96148386..96151549-chr8:96224432..96227854,3	MCF-7	breast:
34	chr8:96241997..96243931-chr8:96244182..96247053,2	MCF-7	breast:
35	chr8:96233041..96235359-chr8:96238288..96241007,3	K562	blood:
36	chr8:96239240..96241215-chr8:96244914..96248459,3	K562	blood:
37	chr8:96215833..96219585-chr8:96222855..96225579,4	K562	blood:
38	chr8:96238086..96240049-chr8:96241356..96243074,2	K562	blood:
39	chr8:96077808..96080245-chr8:96234205..96235808,2	MCF-7	breast:
40	chr8:96204685..96206421-chr8:96234538..96236078,2	MCF-7	breast:
41	chr8:96148421..96149927-chr8:96235607..96238590,2	K562	blood:
42	chr8:96220160..96222982-chr8:96225240..96226907,2	K562	blood:
43	chr8:96143360..96148175-chr8:96235522..96240876,10	MCF-7	breast:
44	chr8:96241648..96244611-chr8:96247721..96251221,3	K562	blood:
45	chr8:96214177..96216026-chr8:96245562..96248226,2	MCF-7	breast:
46	chr8:96224254..96224982-chr8:96236085..96236596,2	MCF-7	breast:
47	chr8:96239351..96241151-chr8:96247805..96249381,2	MCF-7	breast:
48	chr8:96219891..96220818-chr8:96235921..96236731,3	MCF-7	breast:
49	chr8:96124552..96125363-chr8:96224111..96224757,2	MCF-7	breast:
50	chr8:96228952..96231247-chr8:96237951..96240683,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf37-1	chr8:96228546-96228602	ENSG00000253351
2	lnc-C8orf37-1	chr8:96228546-96228743	NONHSAT127827

No data

Variant related genes	Relation type
ENSG00000253351	TF binding region
ENSG00000253351	CpG island
ENSG00000175895	chromatin interactions
ENSG00000156471	chromatin interactions
ENSG00000156469	chromatin interactions
ENSG00000253351	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000245080	chromatin interactions
ENSG00000253773	chromatin interactions
ENSG00000156172	chromatin interactions
ENSG00000254248	chromatin interactions

Extended variants
information (count: 940 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs734666	chr8:96221122-96221123	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570098239	chr8:96221140-96221141	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375681995	chr8:96221160-96221161	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376197681	chr8:96221184-96221185	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145806672	chr8:96221185-96221186	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs880642	chr8:96221214-96221215	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs533850883	chr8:96221222-96221223	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs113178081	chr8:96221251-96221252	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs61463017	chr8:96221437-96221438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372789129	chr8:96221469-96221470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs553685706	chr8:96221581-96221582	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573278763	chr8:96221634-96221635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576238496	chr8:96221637-96221638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs556212410	chr8:96221686-96221687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576065349	chr8:96221742-96221743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545534460	chr8:96221758-96221759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565357696	chr8:96221767-96221768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2439642	chr8:96221825-96221826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541727423	chr8:96221846-96221847	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs372243747	chr8:96221851-96221852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs148543725	chr8:96221852-96221853	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561617887	chr8:96221865-96221866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs11267335	chr8:96221867-96221868	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530110453	chr8:96221894-96221895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs549917797	chr8:96221896-96221897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563757048	chr8:96221897-96221898	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532522606	chr8:96221900-96221901	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76020428	chr8:96221994-96221995	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs2514567	chr8:96222002-96222003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533765589	chr8:96222005-96222006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190088268	chr8:96222020-96222021	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181672092	chr8:96222139-96222140	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535805188	chr8:96222150-96222151	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs555888035	chr8:96222162-96222163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554698920	chr8:96222242-96222243	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576057950	chr8:96222265-96222266	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs62522644	chr8:96222321-96222322	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs543676876	chr8:96222345-96222346	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs545252325	chr8:96222367-96222368	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558651578	chr8:96222438-96222439	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs572675774	chr8:96222452-96222453	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs541688763	chr8:96222464-96222465	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149077947	chr8:96222517-96222518	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs530685163	chr8:96222615-96222616	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs575215450	chr8:96222616-96222617	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143194429	chr8:96222621-96222622	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs148269060	chr8:96222678-96222679	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs75362267	chr8:96222719-96222720	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs552369332	chr8:96222743-96222744	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559465985	chr8:96222820-96222821	Enhancers Weak transcription Active TSS	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
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
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96214200-96226400	Weak transcription	Right Atrium	heart
2	chr8:96214400-96233400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:96218800-96227000	Enhancers	Pancreas	Pancrea
4	chr8:96219400-96221400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr8:96219400-96222400	Enhancers	Placenta	Placenta
6	chr8:96219400-96229600	Enhancers	Fetal Thymus	thymus
7	chr8:96219800-96225600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr8:96219800-96251800	Enhancers	Primary B cells from peripheral blood	blood
9	chr8:96220000-96221400	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chr8:96220000-96221600	Enhancers	Left Ventricle	heart
11	chr8:96220000-96221800	Enhancers	Fetal Muscle Trunk	muscle
12	chr8:96220000-96223200	Enhancers	Fetal Muscle Leg	muscle
13	chr8:96220000-96224200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr8:96220000-96227200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr8:96220200-96223000	Weak transcription	Spleen	Spleen
16	chr8:96220200-96225600	Enhancers	K562	blood
17	chr8:96220600-96221800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr8:96220600-96222400	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr8:96220600-96222800	Enhancers	Lung	lung
20	chr8:96220600-96223400	Weak transcription	HMEC	breast
21	chr8:96220600-96229400	Enhancers	Primary hematopoietic stem cells	blood
22	chr8:96220800-96221400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:96220800-96221400	Weak transcription	Gastric	stomach
24	chr8:96220800-96224600	Weak transcription	Esophagus	oesophagus
25	chr8:96220800-96226000	Weak transcription	Right Ventricle	heart
26	chr8:96220800-96226400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr8:96220800-96228000	Enhancers	Thymus	Thymus
28	chr8:96220800-96229600	Enhancers	Primary B cells from cord blood	blood
29	chr8:96221000-96221200	Flanking Bivalent TSS/Enh	HepG2	liver
30	chr8:96221000-96222600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:96221000-96228400	Enhancers	Primary T cells fromperipheralblood	blood
32	chr8:96221200-96221400	Bivalent Enhancer	HepG2	liver
33	chr8:96221200-96222000	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr8:96221200-96224800	Enhancers	Liver	Liver
35	chr8:96221200-96228800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr8:96221400-96221600	Enhancers	GM12878-XiMat	blood
37	chr8:96221400-96222200	Enhancers	HepG2	liver
38	chr8:96221400-96223400	Enhancers	Gastric	stomach
39	chr8:96221400-96223600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr8:96221400-96226000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr8:96221400-96226200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:96221600-96222600	Weak transcription	Left Ventricle	heart
43	chr8:96221600-96224200	Weak transcription	GM12878-XiMat	blood
44	chr8:96221800-96224000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr8:96221800-96225200	Enhancers	Stomach Mucosa	stomach
46	chr8:96221800-96226200	Weak transcription	Fetal Muscle Trunk	muscle
47	chr8:96222000-96222200	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr8:96222000-96223600	Enhancers	Fetal Intestine Small	intestine
49	chr8:96222000-96223800	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr8:96222000-96224200	Enhancers	Rectal Mucosa Donor 31	rectum

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