Variant report

Variant	nsv572948
Chromosome Location	chr16:70724432-70731870
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:432)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70729555-70729873	K562	blood:	n/a	n/a
2	ATF2	chr16:70727915-70728403	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr16:70729711-70729940	K562	blood:	n/a	n/a
4	BACH1	chr16:70728018-70728457	H1-hESC	embryonic stem cell:	n/a	chr16:70728171-70728185
5	BCL3	chr16:70727687-70728702	A549	lung:	n/a	n/a
6	BHLHE40	chr16:70729308-70729987	K562	blood:	n/a	n/a
7	CBX3	chr16:70729269-70730023	K562	blood:	n/a	n/a
8	CCNT2	chr16:70729500-70730051	K562	blood:	n/a	chr16:70729780-70729800
9	CEBPB	chr16:70725709-70726188	IMR90	lung:	n/a	chr16:70726014-70726026
10	CEBPB	chr16:70726451-70726571	K562	blood:	n/a	n/a
11	CEBPB	chr16:70725829-70726025	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr16:70729629-70729968	K562	blood:	n/a	n/a
13	CEBPB	chr16:70729665-70729925	K562	blood:	n/a	n/a
14	CEBPB	chr16:70730765-70731305	MCF-7	breast:	n/a	n/a
15	CEBPB	chr16:70725922-70725973	HepG2	liver:	n/a	n/a
16	CEBPD	chr16:70729227-70730091	K562	blood:	n/a	n/a
17	CEBPD	chr16:70729486-70730064	K562	blood:	n/a	n/a
18	CHD1	chr16:70725533-70726481	IMR90	lung:	n/a	n/a
19	CHD2	chr16:70729733-70729961	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr16:70729479-70730012	K562	blood:	n/a	n/a
21	CHD2	chr16:70727849-70728310	Hela-S3	cervix:	n/a	n/a
22	CREB1	chr16:70727895-70728685	A549	lung:	n/a	n/a
23	CREB1	chr16:70727965-70728233	A549	lung:	n/a	n/a
24	CTBP2	chr16:70727649-70728345	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr16:70731520-70731670	HMEC	breast:	n/a	n/a
26	CTCF	chr16:70729782-70729910	MCF-7	breast:	n/a	n/a
27	CTCF	chr16:70729392-70729978	K562	blood:	n/a	n/a
28	CTCF	chr16:70729805-70729866	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr16:70729820-70729970	HepG2	liver:	n/a	n/a
30	CTCF	chr16:70728120-70728270	AG10803	skin:	n/a	chr16:70728189-70728202
31	CTCF	chr16:70731420-70731570	HVMF	connective:	n/a	n/a
32	CTCF	chr16:70731540-70731690	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr16:70728000-70728150	AG04449	skin:	n/a	n/a
34	CTCF	chr16:70729780-70729930	MCF-7	breast:	n/a	n/a
35	CTCF	chr16:70729861-70729867	Gliobla	brain:	n/a	n/a
36	CTCF	chr16:70729788-70729909	MCF-7	breast:	n/a	n/a
37	CTCF	chr16:70729840-70729990	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr16:70731558-70731747	GM12878	blood:	n/a	chr16:70731689-70731702
39	CTCF	chr16:70729775-70729925	MCF-7	breast:	n/a	n/a
40	CTCF	chr16:70731580-70731730	NHDF-neo	bronchial:	n/a	chr16:70731689-70731702
41	CTCF	chr16:70729790-70729923	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr16:70729781-70729905	MCF-7	breast:	n/a	n/a
43	CTCF	chr16:70729740-70729890	SAEC	small airway:	n/a	n/a
44	CTCF	chr16:70729760-70729910	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr16:70731620-70731770	NHDF-neo	bronchial:	n/a	chr16:70731689-70731702
46	CTCF	chr16:70729740-70729890	K562	blood:	n/a	n/a
47	CTCF	chr16:70731520-70731670	A549	lung:	n/a	n/a
48	CTCF	chr16:70731560-70731710	SAEC	small airway:	n/a	chr16:70731689-70731702
49	CTCF	chr16:70729740-70729890	BE2_C	brain:	n/a	n/a
50	CTCF	chr16:70731560-70731710	AG09319	gingival:	n/a	chr16:70731689-70731702

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70728425-70728475	HIPEpiC	eye:	n/a
2	chr16:70728001-70728051	PrEC	prostate:	n/a
3	chr16:70728425-70728475	HCF	heart:	n/a
4	chr16:70728425-70728475	NB4	blood:	n/a
5	chr16:70728425-70728475	HEK293	kidney:	embryo
6	chr16:70728001-70728051	AG09319	gingival:	n/a
7	chr16:70728001-70728051	HMEC	breast:	n/a
8	chr16:70728001-70728051	AoSMC	blood vessel:	n/a
9	chr16:70728001-70728051	HEEpiC	esophagus:	n/a
10	chr16:70728001-70728051	HNPCEpiC	eye:	n/a
11	chr16:70728001-70728051	ECC-1	luminal epithelium:	n/a
12	chr16:70728001-70728051	HUVEC	blood vessel:	n/a
13	chr16:70728425-70728475	MCF-7	breast:	n/a
14	chr16:70728425-70728475	GM06990	blood:	n/a
15	chr16:70728001-70728051	NHDF-neo	bronchial:	n/a
16	chr16:70728001-70728051	HCT-116	colon:	n/a
17	chr16:70728001-70728051	HRPEpiC	eye:	n/a
18	chr16:70728001-70728051	HL-60	blood:	n/a
19	chr16:70728001-70728051	GM19239	blood:	n/a
20	chr16:70728001-70728051	HCPEpiC	choroid plexus:	n/a
21	chr16:70728001-70728051	Hepatocyte	liver:	n/a
22	chr16:70728425-70728475	NH-A	brain:	n/a
23	chr16:70728001-70728051	BE2_C	brain:	n/a
24	chr16:70728001-70728051	H1-hESC	embryonic stem cell:	embryo
25	chr16:70728001-70728051	HIPEpiC	eye:	n/a
26	chr16:70728425-70728475	ECC-1	luminal epithelium:	n/a
27	chr16:70728425-70728475	BE2_C	brain:	n/a
28	chr16:70728425-70728475	ovcar-3	ovarian:	n/a
29	chr16:70728001-70728051	SK-N-SH_RA	brain:	n/a
30	chr16:70728001-70728051	HepG2	liver:	n/a
31	chr16:70728425-70728475	RPTEC	kidney:	n/a
32	chr16:70728425-70728475	A549	lung:	n/a
33	chr16:70728425-70728475	SK-N-SH_RA	brain:	n/a
34	chr16:70728001-70728051	GM06990	blood:	n/a
35	chr16:70728425-70728475	GM12891	blood:	n/a
36	chr16:70728001-70728051	CMK	blood:	n/a
37	chr16:70728001-70728051	AG04449	skin:	fetal
38	chr16:70728001-70728051	ovcar-3	ovarian:	n/a
39	chr16:70728001-70728051	T-47D	breast:	n/a
40	chr16:70728425-70728475	ProgFib	skin:	n/a
41	chr16:70728001-70728051	AG10803	skin:	n/a
42	chr16:70728001-70728051	BJ	skin:	n/a
43	chr16:70728425-70728475	AG04450	lung:	fetal
44	chr16:70728425-70728475	PFSK-1	brain:	n/a
45	chr16:70728001-70728051	GM12892	blood:	n/a
46	chr16:70728001-70728051	HCM	heart:	n/a
47	chr16:70728425-70728475	PrEC	prostate:	n/a
48	chr16:70728425-70728475	GM19239	blood:	n/a
49	chr16:70728001-70728051	A549	lung:	n/a
50	chr16:70728425-70728475	NHDF-neo	bronchial:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70726776..70729774-chr16:70778926..70781727,2	K562	blood:
2	chr16:70728125..70734937-chr16:70778355..70783574,11	MCF-7	breast:
3	chr16:70731234..70732060-chr16:70804672..70805218,2	MCF-7	breast:
4	chr16:70694604..70697183-chr16:70727406..70729893,2	K562	blood:
5	chr16:70731211..70733556-chr16:70795711..70798621,2	MCF-7	breast:
6	chr16:70557802..70559378-chr16:70727499..70729855,2	MCF-7	breast:
7	chr16:70725942..70727688-chr16:70759419..70762080,2	K562	blood:
8	chr16:70731044..70733238-chr16:70775632..70778039,2	MCF-7	breast:
9	chr16:70555851..70557474-chr16:70727939..70730719,2	MCF-7	breast:
10	chr16:70728939..70732766-chr16:70778342..70782420,7	MCF-7	breast:
11	chr16:70731581..70732230-chr16:70771694..70772666,3	MCF-7	breast:
12	chr16:70730415..70732560-chr16:70741033..70742955,2	K562	blood:
13	chr16:69758592..69760994-chr16:70729394..70731021,2	K562	blood:
14	chr16:70724785..70727476-chr16:70778008..70779690,2	MCF-7	breast:
15	chr16:70710502..70716221-chr16:70726302..70731102,7	K562	blood:
16	chr16:70729813..70732672-chr16:70787716..70789495,2	MCF-7	breast:

No data

Variant related genes	Relation type
MTSS1L	TF binding region
VAC14	TF binding region
MTSS1L	CpG island
VAC14	CpG island
ENSG00000103051	chromatin interactions
ENSG00000132613	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000181019	chromatin interactions
ENSG00000268927	chromatin interactions
ENSG00000262136	chromatin interactions
ENSG00000260156	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000214353	chromatin interactions

Extended variants
information (count: 330 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4985560	chr16:70724432-70724433	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs374807708	chr16:70724457-70724458	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs527749422	chr16:70724459-70724460	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs566520078	chr16:70724491-70724492	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs533757916	chr16:70724521-70724522	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs371349080	chr16:70724559-70724560	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546849994	chr16:70724571-70724572	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs374876244	chr16:70724610-70724611	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544892793	chr16:70724644-70724645	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs563092919	chr16:70724757-70724758	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs115754951	chr16:70724844-70724845	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs542372999	chr16:70724874-70724875	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs369295470	chr16:70724972-70724973	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs150390500	chr16:70725001-70725002	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs552541373	chr16:70725010-70725011	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535428675	chr16:70725013-70725014	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570727120	chr16:70725026-70725027	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143897528	chr16:70725054-70725055	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs550444099	chr16:70725082-70725083	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs568737580	chr16:70725112-70725113	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs113929080	chr16:70725120-70725121	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs57682106	chr16:70725124-70725125	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146600890	chr16:70725136-70725137	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533605205	chr16:70725137-70725138	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs3826272	chr16:70725141-70725142	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs537870294	chr16:70725156-70725157	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576875187	chr16:70725164-70725165	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544957823	chr16:70725198-70725199	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs572517276	chr16:70725264-70725265	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs373894378	chr16:70725307-70725308	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs557297407	chr16:70725309-70725310	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs78557852	chr16:70725310-70725311	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs115021889	chr16:70725317-70725318	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs4985561	chr16:70725326-70725327	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs3837791	chr16:70725367-70725368	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs397841296	chr16:70725368-70725369	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368297321	chr16:70725372-70725373	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs545941468	chr16:70725373-70725374	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs539800399	chr16:70725383-70725384	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185843892	chr16:70725429-70725430	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs117791015	chr16:70725452-70725453	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574169801	chr16:70725461-70725462	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568800875	chr16:70725486-70725487	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs529897488	chr16:70725518-70725519	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs548367488	chr16:70725546-70725547	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs3826271	chr16:70725589-70725590	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs533904799	chr16:70725630-70725631	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs558355564	chr16:70725666-70725667	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs570491730	chr16:70725685-70725686	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs112009880	chr16:70725707-70725708	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:510 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70719400-70727800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr16:70719400-70729200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr16:70719400-70729400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr16:70719800-70732400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr16:70720000-70732200	Enhancers	Fetal Brain Male	brain
6	chr16:70720200-70728200	Enhancers	Fetal Heart	heart
7	chr16:70720400-70725400	Enhancers	Esophagus	oesophagus
8	chr16:70720400-70725400	Enhancers	Lung	lung
9	chr16:70720400-70727000	Enhancers	Colonic Mucosa	Colon
10	chr16:70720400-70729200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr16:70720400-70729600	Enhancers	Right Atrium	heart
12	chr16:70720400-70732400	Enhancers	Right Ventricle	heart
13	chr16:70720400-70733400	Enhancers	Left Ventricle	heart
14	chr16:70720400-70753200	Weak transcription	Primary B cells from cord blood	blood
15	chr16:70720600-70726200	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr16:70720600-70726800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr16:70720600-70728200	Weak transcription	Primary hematopoietic stem cells	blood
18	chr16:70720600-70728600	Enhancers	Placenta	Placenta
19	chr16:70720600-70728800	Weak transcription	Primary T cells from cord blood	blood
20	chr16:70720600-70729000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr16:70720600-70729200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr16:70720600-70729600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr16:70720600-70729600	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr16:70720600-70729800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr16:70720600-70730000	Enhancers	Psoas Muscle	Psoas
26	chr16:70720600-70731800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr16:70720800-70726600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr16:70720800-70727600	Enhancers	Brain Substantia Nigra	brain
29	chr16:70720800-70727600	Weak transcription	Dnd41	blood
30	chr16:70720800-70729800	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr16:70720800-70730200	Enhancers	Adipose Nuclei	Adipose
32	chr16:70720800-70731800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr16:70720800-70732400	Genic enhancers	Fetal Stomach	stomach
34	chr16:70721000-70725400	Enhancers	NHLF	lung
35	chr16:70721000-70727200	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr16:70721000-70728800	Enhancers	Fetal Muscle Trunk	muscle
37	chr16:70721000-70732400	Genic enhancers	Fetal Intestine Small	intestine
38	chr16:70721200-70724600	Enhancers	Fetal Thymus	thymus
39	chr16:70721200-70725800	Enhancers	Fetal Muscle Leg	muscle
40	chr16:70721200-70726400	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chr16:70721200-70727400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr16:70721200-70728000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr16:70721200-70728200	Enhancers	Fetal Lung	lung
44	chr16:70721200-70730000	Enhancers	Brain Anterior Caudate	brain
45	chr16:70721200-70730200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr16:70721200-70730200	Enhancers	NHDF-Ad	bronchial
47	chr16:70721400-70726200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr16:70721400-70728000	Weak transcription	K562	blood
49	chr16:70721600-70724600	Weak transcription	Hela-S3	cervix
50	chr16:70721600-70727600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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