Variant report

Variant	nsv999069
Chromosome Location	chr3:178979923-179013281
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:613)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:178993888-178994286	K562	blood:	n/a	n/a
2	ARID3A	chr3:178983613-178984080	K562	blood:	n/a	n/a
3	ARID3A	chr3:179006631-179007354	K562	blood:	n/a	n/a
4	ATF1	chr3:178986214-178986617	K562	blood:	n/a	n/a
5	ATF1	chr3:178983638-178984053	K562	blood:	n/a	n/a
6	ATF1	chr3:179000897-179000910	K562	blood:	n/a	n/a
7	ATF1	chr3:179006645-179006997	K562	blood:	n/a	n/a
8	ATF3	chr3:178983652-178983974	K562	blood:	n/a	n/a
9	BACH1	chr3:179006689-179007145	K562	blood:	n/a	n/a
10	BACH1	chr3:178987077-178987078	K562	blood:	n/a	n/a
11	BACH1	chr3:179006710-179007097	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:179010504-179010769	GM12878	blood:	n/a	chr3:179010640-179010651
13	BCL3	chr3:179011763-179011979	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:178986255-178987459	K562	blood:	n/a	n/a
15	BHLHE40	chr3:178984424-178984499	K562	blood:	n/a	n/a
16	CBX3	chr3:178983532-178984798	K562	blood:	n/a	n/a
17	CBX3	chr3:178980796-178981437	K562	blood:	n/a	n/a
18	CBX3	chr3:178981009-178981374	K562	blood:	n/a	n/a
19	CBX3	chr3:178986133-178986678	K562	blood:	n/a	n/a
20	CBX3	chr3:178979973-178980745	K562	blood:	n/a	n/a
21	CBX3	chr3:178983630-178984029	K562	blood:	n/a	n/a
22	CBX3	chr3:178982877-178983293	K562	blood:	n/a	n/a
23	CCNT2	chr3:179006635-179007092	K562	blood:	n/a	n/a
24	CCNT2	chr3:178987051-178987382	K562	blood:	n/a	n/a
25	CCNT2	chr3:178994600-178994913	K562	blood:	n/a	n/a
26	CCNT2	chr3:179012385-179012644	K562	blood:	n/a	n/a
27	CEBPB	chr3:178983676-178984090	K562	blood:	n/a	n/a
28	CEBPB	chr3:178998230-178998568	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:178994573-178994802	K562	blood:	n/a	n/a
30	CEBPB	chr3:178998358-178998526	K562	blood:	n/a	n/a
31	CEBPB	chr3:178994504-178994816	K562	blood:	n/a	n/a
32	CEBPB	chr3:179004544-179004744	HepG2	liver:	n/a	chr3:179004668-179004679 chr3:179004628-179004639
33	CEBPB	chr3:178983665-178984167	K562	blood:	n/a	n/a
34	CEBPD	chr3:178983613-178984135	K562	blood:	n/a	chr3:178984105-178984116
35	CEBPD	chr3:178994423-178994935	K562	blood:	n/a	n/a
36	CEBPD	chr3:178982874-178983214	K562	blood:	n/a	n/a
37	CTCF	chr3:178990348-178990449	K562	blood:	n/a	n/a
38	CTCF	chr3:178990240-178990390	AG04450	lung:	n/a	n/a
39	CTCF	chr3:178990263-178990453	GM12878	blood:	n/a	n/a
40	CTCF	chr3:178999202-178999206	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:178990277-178990449	A549	lung:	n/a	n/a
42	CTCF	chr3:178990298-178990381	Lung_OC	lung:	n/a	n/a
43	CTCF	chr3:178990240-178990390	HL-60	blood:	n/a	n/a
44	CTCF	chr3:178999100-178999250	BJ	skin:	n/a	n/a
45	CTCF	chr3:178990240-178990390	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr3:178990280-178990430	AG09309	skin:	n/a	n/a
47	CTCF	chr3:178990240-178990390	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr3:178990280-178990430	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr3:178999100-178999250	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:178999196-178999291	HUVEC	blood vessel:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:178984973-178985023	A549	lung:	n/a
2	chr3:178984747-178984797	CMK	blood:	n/a
3	chr3:178984841-178984891	SK-N-SH	brain:	n/a
4	chr3:178984973-178985023	A549	lung:	n/a
5	chr3:178984747-178984797	CMK	blood:	n/a
6	chr3:178984841-178984891	SK-N-SH	brain:	n/a
7	chr3:178984910-178984960	PANC-1	pancreas:	n/a
8	chr3:178986203-178986253	GM06990	blood:	n/a
9	chr3:178984973-178985023	K562	blood:	n/a
10	chr3:178984841-178984891	Jurkat	blood:	n/a
11	chr3:178986203-178986253	AG09309	skin:	n/a
12	chr3:178984841-178984891	HCF	heart:	n/a
13	chr3:178984841-178984891	CMK	blood:	n/a
14	chr3:178984910-178984960	HCF	heart:	n/a
15	chr3:178984858-178984908	HEEpiC	esophagus:	n/a
16	chr3:178983283-178983333	HRE	kidney:	n/a
17	chr3:178983283-178983333	HEEpiC	esophagus:	n/a
18	chr3:178984858-178984908	SK-N-SH_RA	brain:	n/a
19	chr3:178986203-178986253	ProgFib	skin:	n/a
20	chr3:178980938-178980988	PrEC	prostate:	n/a
21	chr3:178984747-178984797	GM12892	blood:	n/a
22	chr3:178980938-178980988	HCM	heart:	n/a
23	chr3:178986203-178986253	HEK293	kidney:	embryo
24	chr3:178984747-178984797	U87	brain:	n/a
25	chr3:178980938-178980988	NH-A	brain:	n/a
26	chr3:178981100-178981150	HCPEpiC	choroid plexus:	n/a
27	chr3:178986203-178986253	PANC-1	pancreas:	n/a
28	chr3:178984910-178984960	SKMC	muscle:	n/a
29	chr3:178984973-178985023	GM12878	blood:	n/a
30	chr3:178984910-178984960	AG04449	skin:	fetal
31	chr3:178984747-178984797	GM06990	blood:	n/a
32	chr3:178984747-178984797	HCPEpiC	choroid plexus:	n/a
33	chr3:178984858-178984908	HNPCEpiC	eye:	n/a
34	chr3:178984841-178984891	HCPEpiC	choroid plexus:	n/a
35	chr3:178984973-178985023	HIPEpiC	eye:	n/a
36	chr3:178984747-178984797	BE2_C	brain:	n/a
37	chr3:178986203-178986253	PrEC	prostate:	n/a
38	chr3:178980938-178980988	HRCEpiC	kidney:	n/a
39	chr3:178986203-178986253	BJ	skin:	n/a
40	chr3:178984858-178984908	SK-N-MC	brain:	n/a
41	chr3:178985975-178986025	AG09309	skin:	n/a
42	chr3:178985975-178986025	Hela-S3	cervix:	n/a
43	chr3:178983283-178983333	NHBE	bronchial:	n/a
44	chr3:178985975-178986025	AG04449	skin:	fetal
45	chr3:178981100-178981150	GM06990	blood:	n/a
46	chr3:178984841-178984891	GM12878	blood:	n/a
47	chr3:178984910-178984960	BJ	skin:	n/a
48	chr3:178981100-178981150	PANC-1	pancreas:	n/a
49	chr3:178984910-178984960	HMEC	breast:	n/a
50	chr3:178984747-178984797	NHDF-neo	bronchial:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:178977469..178980839-chr3:179038593..179042214,6	K562	blood:
2	chr3:178991613..178994425-chr3:179013219..179014781,2	K562	blood:
3	chr3:178898456..178900555-chr3:179010797..179013245,2	K562	blood:
4	chr3:178977696..178979251-chr3:179000554..179002401,2	K562	blood:
5	chr3:178987126..178990060-chr3:179028963..179031707,2	K562	blood:
6	chr3:178978041..178980864-chr3:179039699..179042008,3	K562	blood:
7	chr3:178977127..178979109-chr3:178982574..178984293,2	MCF-7	breast:
8	chr3:178822936..178823520-chr3:178989911..178990654,3	MCF-7	breast:
9	chr3:178985215..178988061-chr3:178992622..178994393,3	K562	blood:
10	chr3:178971723..178977145-chr3:178977567..178980865,6	K562	blood:
11	chr3:178976479..178980556-chr3:178981755..178985679,10	K562	blood:
12	chr3:179002404..179004252-chr3:179036373..179038873,2	K562	blood:
13	chr3:178977694..178979388-chr3:178980882..178983068,3	MCF-7	breast:
14	chr3:178976479..178980556-chr3:178981755..178985679,10	K562	blood:
15	chr3:179006501..179008935-chr3:179014327..179018161,3	K562	blood:
16	chr3:178992829..178995798-chr3:178996277..178997929,2	K562	blood:
17	chr3:178977549..178980456-chr3:179006646..179008470,2	MCF-7	breast:
18	chr3:178987261..178990114-chr3:179041227..179043942,2	MCF-7	breast:
19	chr3:178996544..178999289-chr3:179003469..179005765,2	K562	blood:
20	chr3:178985215..178988061-chr3:178992622..178994393,3	K562	blood:
21	chr3:178992829..178995758-chr3:178995882..178997777,2	K562	blood:
22	chr3:178986328..178988905-chr3:179009647..179011944,2	K562	blood:
23	chr3:178988379..178990812-chr3:178994556..178996288,2	K562	blood:
24	chr3:178866345..178868537-chr3:178986255..178987859,2	K562	blood:
25	chr3:178976102..178980828-chr3:178981002..178985885,12	K562	blood:
26	chr3:178992829..178995798-chr3:178996277..178997929,2	K562	blood:
27	chr3:178788152..178789762-chr3:179013021..179015401,2	K562	blood:
28	chr3:178995091..178997695-chr3:179278725..179280840,2	K562	blood:
29	chr3:178989886..178991481-chr3:179014093..179016741,2	MCF-7	breast:
30	chr3:178976102..178980828-chr3:178981002..178985885,12	K562	blood:
31	chr3:178991613..178994425-chr3:179013219..179014781,2	K562	blood:
32	chr3:178977755..178980061-chr3:178993976..178996284,3	K562	blood:
33	chr3:178978959..178980541-chr3:178987188..178990133,3	K562	blood:
34	chr3:178997889..179000034-chr3:179007138..179009372,2	K562	blood:
35	chr3:178994652..178998436-chr3:179003323..179005765,4	K562	blood:
36	chr3:179004788..179007511-chr3:179040770..179043675,3	K562	blood:
37	chr3:178986328..178988905-chr3:179009647..179011944,2	K562	blood:
38	chr3:179006501..179009380-chr3:179014327..179018161,4	K562	blood:
39	chr3:178976762..178980101-chr3:178998298..179001669,3	MCF-7	breast:
40	chr3:178994652..178998436-chr3:179003323..179005765,4	K562	blood:
41	chr3:178988379..178990812-chr3:178994556..178996288,2	K562	blood:
42	chr3:179009053..179011621-chr3:179014043..179016990,3	K562	blood:
43	chr3:178977742..178980061-chr3:178992823..178996284,4	K562	blood:
44	chr3:178863877..178868371-chr3:178977065..178980370,6	K562	blood:
45	chr3:178992829..178995758-chr3:178995882..178997777,2	K562	blood:
46	chr3:178787922..178790661-chr3:179007166..179008700,2	K562	blood:
47	chr3:179004788..179007511-chr3:179041633..179043675,2	K562	blood:
48	chr3:178989881..178990650-chr3:179033690..179034572,2	MCF-7	breast:
49	chr3:178978959..178980523-chr3:178987188..178990133,2	K562	blood:
50	chr3:178864784..178866579-chr3:179010384..179012137,2	MCF-7	breast:

No data

Variant related genes	Relation type
LRRFIP1P1	TF binding region
KCNMB3	TF binding region
LRRFIP1P1	CpG island
KCNMB3	CpG island
ENSG00000171121	chromatin interactions
ENSG00000121864	chromatin interactions
ENSG00000229102	chromatin interactions
ENSG00000121879	chromatin interactions
ENSG00000240429	chromatin interactions
ENSG00000136518	chromatin interactions
ENSG00000172667	chromatin interactions

Extended variants
information (count: 1430 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1430 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577128737	chr3:178979992-178979993	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs147665081	chr3:178979998-178979999	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs562769933	chr3:178980060-178980061	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs576464762	chr3:178980074-178980075	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs542383013	chr3:178980078-178980079	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs7619599	chr3:178980107-178980108	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs143174733	chr3:178980125-178980126	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs534597613	chr3:178980128-178980129	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs547680867	chr3:178980136-178980137	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs564428651	chr3:178980149-178980150	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs533104796	chr3:178980164-178980165	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs549736441	chr3:178980170-178980171	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs569593126	chr3:178980189-178980190	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs556454773	chr3:178980190-178980191	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs151231322	chr3:178980194-178980195	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs565376569	chr3:178980198-178980199	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs7619835	chr3:178980217-178980218	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186716684	chr3:178980238-178980239	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs554014506	chr3:178980267-178980268	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs6773405	chr3:178980268-178980269	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs138029909	chr3:178980279-178980280	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs373935748	chr3:178980282-178980283	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs142417230	chr3:178980283-178980284	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs576406692	chr3:178980324-178980325	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs542296979	chr3:178980328-178980329	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs6443631	chr3:178980333-178980334	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs191162160	chr3:178980347-178980348	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs541206816	chr3:178980353-178980354	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs564161362	chr3:178980395-178980396	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs113000836	chr3:178980404-178980405	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs182953434	chr3:178980425-178980426	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs187544987	chr3:178980433-178980434	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs138515861	chr3:178980437-178980438	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs548630699	chr3:178980442-178980443	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs149253378	chr3:178980476-178980477	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs7619958	chr3:178980499-178980500	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs148789256	chr3:178980500-178980501	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs570996821	chr3:178980563-178980564	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs540122359	chr3:178980573-178980574	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs7622256	chr3:178980577-178980578	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs192562969	chr3:178980590-178980591	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs141576872	chr3:178980617-178980618	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs147498671	chr3:178980621-178980622	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs541581651	chr3:178980636-178980637	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs140126520	chr3:178980639-178980640	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs183282477	chr3:178980644-178980645	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs187523787	chr3:178980657-178980658	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs563448121	chr3:178980678-178980679	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs528827752	chr3:178980690-178980691	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs115360484	chr3:178980734-178980735	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Prostate cancer	18632612	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178978400-178980000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr3:178978600-178980000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:178978800-178980000	Active TSS	K562	blood
4	chr3:178979000-178980400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr3:178979400-178980000	Flanking Active TSS	Primary T cells from cord blood	blood
6	chr3:178979400-178980000	Flanking Active TSS	Hela-S3	cervix
7	chr3:178979400-178984400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr3:178979600-178980000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr3:178979600-178980000	Enhancers	Brain Substantia Nigra	brain
10	chr3:178979600-178980200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr3:178979600-178980200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
12	chr3:178979600-178980400	Enhancers	Primary B cells from peripheral blood	blood
13	chr3:178979600-178980800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr3:178979600-178981000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:178979600-178984000	Weak transcription	Right Ventricle	heart
16	chr3:178979600-178984400	Weak transcription	Fetal Muscle Leg	muscle
17	chr3:178979800-178980000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr3:178979800-178980000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr3:178979800-178980000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr3:178979800-178980000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr3:178979800-178980000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:178979800-178980000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:178979800-178980000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr3:178979800-178980000	Active TSS	GM12878-XiMat	blood
25	chr3:178979800-178980200	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr3:178979800-178980200	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr3:178979800-178980200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr3:178979800-178980200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr3:178979800-178980400	Enhancers	Primary B cells from cord blood	blood
30	chr3:178979800-178980400	Enhancers	Primary T cells fromperipheralblood	blood
31	chr3:178979800-178981800	Weak transcription	Thymus	Thymus
32	chr3:178979800-178983800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr3:178979800-178984200	Weak transcription	Fetal Muscle Trunk	muscle
34	chr3:178979800-178984200	Weak transcription	HUVEC	blood vessel
35	chr3:178980000-178980200	Enhancers	Primary T cells from cord blood	blood
36	chr3:178980000-178980200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:178980000-178980200	Flanking Active TSS	GM12878-XiMat	blood
38	chr3:178980000-178980200	Active TSS	Hela-S3	cervix
39	chr3:178980000-178980800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:178980000-178982200	Weak transcription	K562	blood
41	chr3:178980000-178983600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:178980200-178981200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr3:178980200-178986400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:178980400-178983000	Weak transcription	Primary B cells from cord blood	blood
45	chr3:178980400-178983000	Weak transcription	Primary B cells from peripheral blood	blood
46	chr3:178980800-178981200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr3:178981000-178981200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr3:178981200-178981400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr3:178981200-178981800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr3:178981200-178986200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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