Variant report

Variant	esv3356004
Chromosome Location	chr6:166719787-166722335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:173)
CpG islands
(count:856)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:173 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:166719692-166720195	HepG2	liver:	n/a	n/a
2	BACH1	chr6:166720441-166720971	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:166721825-166721891	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:166721222-166721264	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr6:166721858-166722322	GM12878	blood:	n/a	n/a
6	BCLAF1	chr6:166721860-166722417	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:166720543-166720920	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:166721775-166722393	GM12878	blood:	n/a	chr6:166722082-166722098
9	CCNT2	chr6:166720752-166720895	K562	blood:	n/a	n/a
10	CEBPB	chr6:166719805-166720185	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:166719901-166720100	HepG2	liver:	n/a	n/a
12	CHD1	chr6:166721944-166722338	GM12878	blood:	n/a	n/a
13	CHD2	chr6:166720755-166720759	GM12878	blood:	n/a	n/a
14	CHD2	chr6:166721801-166721879	HepG2	liver:	n/a	chr6:166721862-166721872
15	CTCF	chr6:166720795-166720805	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr6:166722000-166722150	SK-N-SH_RA	brain:	n/a	chr6:166722081-166722094 chr6:166722141-166722150
17	CTCF	chr6:166720821-166720945	GM19239	blood:	n/a	n/a
18	CTCF	chr6:166720720-166720870	GM12869	blood:	n/a	n/a
19	CTCF	chr6:166720480-166720630	GM06990	blood:	n/a	n/a
20	CTCF	chr6:166720620-166720770	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr6:166720859-166720925	NHEK	skin:	n/a	n/a
22	CTCF	chr6:166720466-166720742	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr6:166721991-166722140	GM12892	blood:	n/a	chr6:166722081-166722094
24	CTCF	chr6:166720578-166720701	GM19238	blood:	n/a	n/a
25	CTCF	chr6:166722080-166722230	HepG2	liver:	n/a	chr6:166722081-166722094 chr6:166722141-166722150
26	CTCF	chr6:166720860-166721010	GM12866	blood:	n/a	n/a
27	CTCF	chr6:166720400-166720550	GM12869	blood:	n/a	n/a
28	CTCF	chr6:166721920-166722070	Caco-2	colon:	n/a	chr6:166721932-166721945
29	CTCF	chr6:166720760-166720910	GM12864	blood:	n/a	n/a
30	CTCF	chr6:166720660-166720810	GM12865	blood:	n/a	n/a
31	CTCF	chr6:166720680-166720830	GM12874	blood:	n/a	n/a
32	CTCF	chr6:166720825-166720967	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr6:166721960-166722110	GM12871	blood:	n/a	chr6:166722081-166722094
34	CTCF	chr6:166721933-166722276	GM12878	blood:	n/a	chr6:166722081-166722094 chr6:166722141-166722150
35	CTCF	chr6:166720500-166720650	GM12864	blood:	n/a	n/a
36	CTCF	chr6:166721860-166722010	GM12866	blood:	n/a	chr6:166721896-166721906 chr6:166721932-166721945
37	CTCF	chr6:166720560-166720710	GM12870	blood:	n/a	n/a
38	CTCF	chr6:166720904-166720922	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr6:166720888-166720948	GM10248	blood:	n/a	n/a
40	CTCF	chr6:166720500-166720650	GM12866	blood:	n/a	n/a
41	CTCF	chr6:166720560-166720710	GM12871	blood:	n/a	n/a
42	CTCF	chr6:166720854-166721006	GM19238	blood:	n/a	n/a
43	CTCF	chr6:166720631-166720658	GM12878	blood:	n/a	n/a
44	CTCF	chr6:166720900-166721050	GM12871	blood:	n/a	n/a
45	CTCF	chr6:166720880-166721030	GM12870	blood:	n/a	n/a
46	CTCF	chr6:166720540-166720690	GM12864	blood:	n/a	n/a
47	CTCF	chr6:166720540-166720690	GM12866	blood:	n/a	n/a
48	CTCF	chr6:166720507-166721020	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr6:166720560-166720710	GM12865	blood:	n/a	n/a
50	CTCF	chr6:166720820-166720970	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166720997-166721047	HIPEpiC	eye:	n/a
2	chr6:166722062-166722112	H1-hESC	embryonic stem cell:	embryo
3	chr6:166720997-166721047	HIPEpiC	eye:	n/a
4	chr6:166722062-166722112	H1-hESC	embryonic stem cell:	embryo
5	chr6:166722058-166722108	Caco-2	colon:	n/a
6	chr6:166722248-166722298	ProgFib	skin:	n/a
7	chr6:166722060-166722110	NB4	blood:	n/a
8	chr6:166720092-166720142	HNPCEpiC	eye:	n/a
9	chr6:166722165-166722215	Jurkat	blood:	n/a
10	chr6:166722058-166722108	Hela-S3	cervix:	n/a
11	chr6:166721759-166721809	HIPEpiC	eye:	n/a
12	chr6:166720114-166720164	HCM	heart:	n/a
13	chr6:166722053-166722103	SK-N-MC	brain:	n/a
14	chr6:166722062-166722112	HRPEpiC	eye:	n/a
15	chr6:166721644-166721694	AG09319	gingival:	n/a
16	chr6:166722060-166722110	SAEC	small airway:	n/a
17	chr6:166720749-166720799	ProgFib	skin:	n/a
18	chr6:166722058-166722108	SK-N-SH_RA	brain:	n/a
19	chr6:166721759-166721809	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:166720092-166720142	HCF	heart:	n/a
21	chr6:166720092-166720142	SAEC	small airway:	n/a
22	chr6:166722248-166722298	GM06990	blood:	n/a
23	chr6:166722060-166722110	GM12878	blood:	n/a
24	chr6:166722060-166722110	AG04450	lung:	fetal
25	chr6:166722053-166722103	NHBE	bronchial:	n/a
26	chr6:166722062-166722112	BJ	skin:	n/a
27	chr6:166721759-166721809	NHBE	bronchial:	n/a
28	chr6:166720092-166720142	SK-N-SH	brain:	n/a
29	chr6:166720114-166720164	H1-hESC	embryonic stem cell:	embryo
30	chr6:166722060-166722110	GM19239	blood:	n/a
31	chr6:166722053-166722103	Hepatocyte	liver:	n/a
32	chr6:166721644-166721694	GM12892	blood:	n/a
33	chr6:166720114-166720164	HNPCEpiC	eye:	n/a
34	chr6:166722058-166722108	Jurkat	blood:	n/a
35	chr6:166721644-166721694	AoSMC	blood vessel:	n/a
36	chr6:166722060-166722110	AG04449	skin:	fetal
37	chr6:166721155-166721205	Hela-S3	cervix:	n/a
38	chr6:166721644-166721694	PrEC	prostate:	n/a
39	chr6:166722058-166722108	HEEpiC	esophagus:	n/a
40	chr6:166721644-166721694	GM12878	blood:	n/a
41	chr6:166720114-166720164	PrEC	prostate:	n/a
42	chr6:166722060-166722110	RPTEC	kidney:	n/a
43	chr6:166722165-166722215	AoSMC	blood vessel:	n/a
44	chr6:166722165-166722215	HAEpiC	amniotic membrane:	n/a
45	chr6:166720997-166721047	HCT-116	colon:	n/a
46	chr6:166722053-166722103	HIPEpiC	eye:	n/a
47	chr6:166720114-166720164	PANC-1	pancreas:	n/a
48	chr6:166721759-166721809	AoSMC	blood vessel:	n/a
49	chr6:166722058-166722108	PANC-1	pancreas:	n/a
50	chr6:166722053-166722103	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:166722256..166724406-chr6:166752301..166754007,2	MCF-7	breast:
2	chr6:166719852..166722547-chr6:166755922..166758056,2	K562	blood:

No data

Variant related genes	Relation type
PRR18	TF binding region
PRR18	CpG island
ENSG00000198818	chromatin interactions

Extended variants
information (count: 116 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:116 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537278107	chr6:166719856-166719857	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs557175209	chr6:166719874-166719875	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs141617764	chr6:166719974-166719975	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1108821	chr6:166720005-166720006	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs149273819	chr6:166720032-166720033	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs397692234	chr6:166720038-166720039	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539933281	chr6:166720044-166720045	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs76163453	chr6:166720074-166720075	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541465412	chr6:166720110-166720111	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573191357	chr6:166720115-166720116	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs56919691	chr6:166720166-166720167	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142299154	chr6:166720241-166720242	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs573977446	chr6:166720245-166720246	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs544430796	chr6:166720246-166720247	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs562739645	chr6:166720279-166720280	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs530559791	chr6:166720281-166720282	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552257939	chr6:166720285-166720286	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559766878	chr6:166720301-166720302	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528104889	chr6:166720304-166720305	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376492732	chr6:166720315-166720316	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182353237	chr6:166720363-166720364	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568392884	chr6:166720365-166720366	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs535747339	chr6:166720390-166720391	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550837397	chr6:166720396-166720397	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs569084254	chr6:166720426-166720427	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs546331655	chr6:166720462-166720463	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369623036	chr6:166720466-166720467	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564662775	chr6:166720476-166720477	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143023200	chr6:166720480-166720481	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374732308	chr6:166720516-166720517	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs73788227	chr6:166720520-166720521	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs558251611	chr6:166720553-166720554	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10946152	chr6:166720557-166720558	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs534229967	chr6:166720574-166720575	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555453879	chr6:166720576-166720577	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574041090	chr6:166720593-166720594	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9348117	chr6:166720614-166720615	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs562800402	chr6:166720628-166720629	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs577840069	chr6:166720633-166720634	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545237707	chr6:166720663-166720664	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368508545	chr6:166720685-166720686	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564242411	chr6:166720687-166720688	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528153364	chr6:166720706-166720707	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374644887	chr6:166720725-166720726	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs561661162	chr6:166720789-166720790	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528855362	chr6:166720797-166720798	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368146277	chr6:166720802-166720803	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs911203	chr6:166720806-166720807	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs199941091	chr6:166720807-166720808	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs569143466	chr6:166720823-166720824	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166717000-166720200	Weak transcription	Pancreas	Pancrea
2	chr6:166718800-166722600	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr6:166719000-166720000	Bivalent Enhancer	Fetal Intestine Small	intestine
4	chr6:166719000-166720200	Bivalent Enhancer	Fetal Intestine Large	intestine
5	chr6:166719200-166720000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:166719200-166720000	Enhancers	GM12878-XiMat	blood
7	chr6:166719200-166722400	Active TSS	Brain Substantia Nigra	brain
8	chr6:166719400-166719800	Weak transcription	Liver	Liver
9	chr6:166719400-166720200	Active TSS	Brain Anterior Caudate	brain
10	chr6:166719400-166720200	Active TSS	Brain Hippocampus Middle	brain
11	chr6:166719400-166720200	Bivalent Enhancer	HepG2	liver
12	chr6:166719400-166720400	Bivalent Enhancer	Adipose Nuclei	Adipose
13	chr6:166719400-166720400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
14	chr6:166719400-166720400	Active TSS	Brain Inferior Temporal Lobe	brain
15	chr6:166719400-166722400	Active TSS	Brain Cingulate Gyrus	brain
16	chr6:166719600-166719800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:166719800-166720600	Enhancers	Liver	Liver
18	chr6:166719800-166720800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
19	chr6:166719800-166722400	Bivalent Enhancer	Fetal Brain Male	brain
20	chr6:166720000-166720200	Enhancers	Gastric	stomach
21	chr6:166720000-166720200	Flanking Active TSS	GM12878-XiMat	blood
22	chr6:166720000-166720600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
23	chr6:166720000-166720600	Bivalent Enhancer	Fetal Brain Female	brain
24	chr6:166720000-166720800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:166720000-166720800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
26	chr6:166720000-166720800	Bivalent Enhancer	Fetal Lung	lung
27	chr6:166720200-166720400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
28	chr6:166720200-166720400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
29	chr6:166720200-166720400	Flanking Active TSS	Gastric	stomach
30	chr6:166720200-166720400	Flanking Bivalent TSS/Enh	HepG2	liver
31	chr6:166720200-166720600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:166720200-166720600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:166720200-166720600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
34	chr6:166720200-166720600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
35	chr6:166720200-166720600	Bivalent Enhancer	Colonic Mucosa	Colon
36	chr6:166720200-166720600	Enhancers	Pancreas	Pancrea
37	chr6:166720200-166720800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
38	chr6:166720200-166720800	Bivalent Enhancer	Lung	lung
39	chr6:166720200-166721000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
40	chr6:166720200-166721000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
41	chr6:166720200-166722000	Active TSS	GM12878-XiMat	blood
42	chr6:166720200-166722200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
43	chr6:166720200-166722400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:166720400-166720600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr6:166720400-166720600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:166720400-166720600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:166720400-166720600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
48	chr6:166720400-166720600	Bivalent Enhancer	Primary B cells from cord blood	blood
49	chr6:166720400-166720600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
50	chr6:166720400-166720600	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood

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