Variant report

Variant	esv3421182
Chromosome Location	chr6:166720387-166722935
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:217)
CpG islands
(count:796)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:217 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:166721825-166721891	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:166721222-166721264	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:166720441-166720971	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr6:166721858-166722322	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:166721860-166722417	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:166721775-166722393	GM12878	blood:	n/a	chr6:166722082-166722098
7	BHLHE40	chr6:166720543-166720920	GM12878	blood:	n/a	n/a
8	CCNT2	chr6:166720752-166720895	K562	blood:	n/a	n/a
9	CHD1	chr6:166721944-166722338	GM12878	blood:	n/a	n/a
10	CHD2	chr6:166720755-166720759	GM12878	blood:	n/a	n/a
11	CHD2	chr6:166722786-166722894	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr6:166721801-166721879	HepG2	liver:	n/a	chr6:166721862-166721872
13	CTCF	chr6:166720480-166720630	GM06990	blood:	n/a	n/a
14	CTCF	chr6:166720800-166721003	GM12891	blood:	n/a	n/a
15	CTCF	chr6:166720560-166720710	GM12870	blood:	n/a	n/a
16	CTCF	chr6:166720578-166720701	GM19238	blood:	n/a	n/a
17	CTCF	chr6:166720580-166720730	GM12878	blood:	n/a	n/a
18	CTCF	chr6:166720560-166720710	GM12871	blood:	n/a	n/a
19	CTCF	chr6:166722780-166722930	HepG2	liver:	n/a	n/a
20	CTCF	chr6:166720820-166720970	GM12878	blood:	n/a	n/a
21	CTCF	chr6:166720720-166720870	GM12869	blood:	n/a	n/a
22	CTCF	chr6:166720795-166720805	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr6:166720904-166720922	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr6:166720540-166720690	GM12866	blood:	n/a	n/a
25	CTCF	chr6:166722817-166722958	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:166720760-166720910	GM12864	blood:	n/a	n/a
27	CTCF	chr6:166720620-166720770	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr6:166720560-166720710	GM12865	blood:	n/a	n/a
29	CTCF	chr6:166722047-166722145	GM12891	blood:	n/a	chr6:166722081-166722094
30	CTCF	chr6:166720860-166721010	GM12867	blood:	n/a	n/a
31	CTCF	chr6:166720888-166720948	GM10248	blood:	n/a	n/a
32	CTCF	chr6:166720662-166720682	GM12891	blood:	n/a	n/a
33	CTCF	chr6:166721991-166722140	GM12892	blood:	n/a	chr6:166722081-166722094
34	CTCF	chr6:166720660-166720810	GM12865	blood:	n/a	n/a
35	CTCF	chr6:166721960-166722110	GM12871	blood:	n/a	chr6:166722081-166722094
36	CTCF	chr6:166720900-166721050	GM12871	blood:	n/a	n/a
37	CTCF	chr6:166720520-166720670	GM12867	blood:	n/a	n/a
38	CTCF	chr6:166720547-166721057	GM12878	blood:	n/a	n/a
39	CTCF	chr6:166720880-166721030	GM12870	blood:	n/a	n/a
40	CTCF	chr6:166720631-166720658	GM12878	blood:	n/a	n/a
41	CTCF	chr6:166720466-166720742	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:166720500-166720650	GM12866	blood:	n/a	n/a
43	CTCF	chr6:166722808-166722997	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:166720854-166721006	GM19238	blood:	n/a	n/a
45	CTCF	chr6:166722065-166722107	GM19238	blood:	n/a	chr6:166722081-166722094
46	CTCF	chr6:166720860-166721010	GM12866	blood:	n/a	n/a
47	CTCF	chr6:166720680-166720830	GM12874	blood:	n/a	n/a
48	CTCF	chr6:166720825-166720967	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr6:166720580-166720730	GM12871	blood:	n/a	n/a
50	CTCF	chr6:166722820-166722970	HUVEC	blood vessel:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166720433-166720483	HepG2	liver:	n/a
2	chr6:166722165-166722215	HCF	heart:	n/a
3	chr6:166722062-166722112	SK-N-SH_RA	brain:	n/a
4	chr6:166720433-166720483	HepG2	liver:	n/a
5	chr6:166722165-166722215	HCF	heart:	n/a
6	chr6:166722062-166722112	SK-N-SH_RA	brain:	n/a
7	chr6:166721759-166721809	HRE	kidney:	n/a
8	chr6:166721155-166721205	HRPEpiC	eye:	n/a
9	chr6:166720997-166721047	HCF	heart:	n/a
10	chr6:166720749-166720799	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:166722060-166722110	A549	lung:	n/a
12	chr6:166721644-166721694	HMEC	breast:	n/a
13	chr6:166722060-166722110	U87	brain:	n/a
14	chr6:166720997-166721047	SK-N-MC	brain:	n/a
15	chr6:166722060-166722110	MCF-7	breast:	n/a
16	chr6:166722053-166722103	PFSK-1	brain:	n/a
17	chr6:166720749-166720799	HUVEC	blood vessel:	n/a
18	chr6:166722165-166722215	H1-hESC	embryonic stem cell:	embryo
19	chr6:166722165-166722215	NHDF-neo	bronchial:	n/a
20	chr6:166722165-166722215	ovcar-3	ovarian:	n/a
21	chr6:166720433-166720483	T-47D	breast:	n/a
22	chr6:166722062-166722112	HCM	heart:	n/a
23	chr6:166722060-166722110	BJ	skin:	n/a
24	chr6:166720997-166721047	HRE	kidney:	n/a
25	chr6:166722060-166722110	GM12892	blood:	n/a
26	chr6:166722053-166722103	AG04449	skin:	fetal
27	chr6:166722248-166722298	HRCEpiC	kidney:	n/a
28	chr6:166720433-166720483	ECC-1	luminal epithelium:	n/a
29	chr6:166722773-166722823	GM19239	blood:	n/a
30	chr6:166720433-166720483	PANC-1	pancreas:	n/a
31	chr6:166722165-166722215	NT2-D1	testis:	n/a
32	chr6:166722248-166722298	AG09309	skin:	n/a
33	chr6:166721644-166721694	A549	lung:	n/a
34	chr6:166720749-166720799	HepG2	liver:	n/a
35	chr6:166722062-166722112	BE2_C	brain:	n/a
36	chr6:166722058-166722108	HepG2	liver:	n/a
37	chr6:166720997-166721047	HCPEpiC	choroid plexus:	n/a
38	chr6:166720997-166721047	BJ	skin:	n/a
39	chr6:166721644-166721694	Caco-2	colon:	n/a
40	chr6:166721644-166721694	HCPEpiC	choroid plexus:	n/a
41	chr6:166721759-166721809	NHBE	bronchial:	n/a
42	chr6:166721759-166721809	HIPEpiC	eye:	n/a
43	chr6:166720749-166720799	GM12891	blood:	n/a
44	chr6:166721155-166721205	CMK	blood:	n/a
45	chr6:166722773-166722823	Jurkat	blood:	n/a
46	chr6:166721644-166721694	AG04450	lung:	fetal
47	chr6:166721759-166721809	SK-N-SH_RA	brain:	n/a
48	chr6:166722053-166722103	HRPEpiC	eye:	n/a
49	chr6:166722058-166722108	HRCEpiC	kidney:	n/a
50	chr6:166720997-166721047	NB4	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166722484..166724020-chr6:166795532..166798475,2	K562	blood:
2	chr6:166722651..166724604-chr6:166784233..166785851,2	K562	blood:
3	chr6:166722635..166726585-chr6:166755013..166756920,3	K562	blood:
4	chr6:166722256..166724406-chr6:166752301..166754007,2	MCF-7	breast:
5	chr6:166719852..166722547-chr6:166755922..166758056,2	K562	blood:

No data

Variant related genes	Relation type
PRR18	TF binding region
PRR18	CpG island
ENSG00000261420	chromatin interactions
ENSG00000198818	chromatin interactions
ENSG00000060762	chromatin interactions

Extended variants
information (count: 124 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:124 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	rs75291681	chr6:166720830-166720831	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
30	rs200347308	chr6:166720860-166720861	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
31	rs141594777	chr6:166720862-166720863	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
32	rs566981011	chr6:166720901-166720902	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
33	rs534030399	chr6:166720933-166720934	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
34	rs555771783	chr6:166720951-166720952	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
35	rs373872044	chr6:166720966-166720967	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
36	rs151246255	chr6:166720983-166720984	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
37	rs537800335	chr6:166720997-166720998	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
38	rs556456266	chr6:166721028-166721029	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs577902206	chr6:166721048-166721049	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs372264427	chr6:166721073-166721074	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375458610	chr6:166721103-166721104	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200995730	chr6:166721108-166721109	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs13204594	chr6:166721211-166721212	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs201295448	chr6:166721220-166721221	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7757150	chr6:166721224-166721225	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs200470806	chr6:166721248-166721249	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369396640	chr6:166721252-166721253	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544192282	chr6:166721262-166721263	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562802984	chr6:166721265-166721266	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533053957	chr6:166721283-166721284	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent Enhancer	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:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166718800-166722600	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr6:166719200-166722400	Active TSS	Brain Substantia Nigra	brain
3	chr6:166719400-166720400	Bivalent Enhancer	Adipose Nuclei	Adipose
4	chr6:166719400-166720400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
5	chr6:166719400-166720400	Active TSS	Brain Inferior Temporal Lobe	brain
6	chr6:166719400-166722400	Active TSS	Brain Cingulate Gyrus	brain
7	chr6:166719800-166720600	Enhancers	Liver	Liver
8	chr6:166719800-166720800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
9	chr6:166719800-166722400	Bivalent Enhancer	Fetal Brain Male	brain
10	chr6:166720000-166720600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
11	chr6:166720000-166720600	Bivalent Enhancer	Fetal Brain Female	brain
12	chr6:166720000-166720800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:166720000-166720800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
14	chr6:166720000-166720800	Bivalent Enhancer	Fetal Lung	lung
15	chr6:166720200-166720400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
16	chr6:166720200-166720400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
17	chr6:166720200-166720400	Flanking Active TSS	Gastric	stomach
18	chr6:166720200-166720400	Flanking Bivalent TSS/Enh	HepG2	liver
19	chr6:166720200-166720600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr6:166720200-166720600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:166720200-166720600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
22	chr6:166720200-166720600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
23	chr6:166720200-166720600	Bivalent Enhancer	Colonic Mucosa	Colon
24	chr6:166720200-166720600	Enhancers	Pancreas	Pancrea
25	chr6:166720200-166720800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
26	chr6:166720200-166720800	Bivalent Enhancer	Lung	lung
27	chr6:166720200-166721000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
28	chr6:166720200-166721000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:166720200-166722000	Active TSS	GM12878-XiMat	blood
30	chr6:166720200-166722200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
31	chr6:166720200-166722400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
32	chr6:166720400-166720600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr6:166720400-166720600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr6:166720400-166720600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:166720400-166720600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
36	chr6:166720400-166720600	Bivalent Enhancer	Primary B cells from cord blood	blood
37	chr6:166720400-166720600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
38	chr6:166720400-166720600	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
39	chr6:166720400-166720600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
40	chr6:166720400-166720600	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
41	chr6:166720400-166720600	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr6:166720400-166720600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr6:166720400-166720600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:166720400-166720600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
45	chr6:166720400-166720600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
46	chr6:166720400-166720600	Bivalent/Poised TSS	Esophagus	oesophagus
47	chr6:166720400-166720600	Bivalent Enhancer	Fetal Intestine Large	intestine
48	chr6:166720400-166720600	Enhancers	Gastric	stomach
49	chr6:166720400-166720600	Bivalent/Poised TSS	Ovary	ovary
50	chr6:166720400-166720600	Bivalent Enhancer	Stomach Mucosa	stomach

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