Variant report

Variant	nsv896004
Chromosome Location	chr10:112834763-112842961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:112835928-112836256	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:112836293-112836298	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr10:112835859-112836195	GM12878	blood:	n/a	n/a
4	BHLHE40	chr10:112836018-112836051	GM12878	blood:	n/a	n/a
5	BRCA1	chr10:112837094-112837268	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr10:112839602-112839860	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:112835911-112836210	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr10:112836738-112836921	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr10:112836615-112837339	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr10:112837851-112838588	H1-hESC	embryonic stem cell:	n/a	n/a
11	CREB1	chr10:112835906-112836229	A549	lung:	n/a	n/a
12	CTBP2	chr10:112835669-112837158	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr10:112836440-112836590	RPTEC	kidney:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
14	CTCF	chr10:112836463-112836572	H1-hESC	embryonic stem cell:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
15	CTCF	chr10:112835828-112836262	GM12878	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060 chr10:112835841-112835850
16	CTCF	chr10:112836270-112836374	GM19240	blood:	n/a	n/a
17	CTCF	chr10:112835960-112836110	HCT-116	colon:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
18	CTCF	chr10:112836414-112836593	SK-N-SH_RA	brain:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
19	CTCF	chr10:112836600-112836750	HCM	heart:	n/a	chr10:112836706-112836719
20	CTCF	chr10:112835980-112836130	A549	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
21	CTCF	chr10:112835918-112836200	Lung_OC	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
22	CTCF	chr10:112835886-112836222	A549	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
23	CTCF	chr10:112836470-112836574	LNCaP	prostate:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
24	CTCF	chr10:112835771-112836264	H1-hESC	embryonic stem cell:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060 chr10:112835841-112835850
25	CTCF	chr10:112835960-112836110	A549	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
26	CTCF	chr10:112836460-112836610	SK-N-SH_RA	brain:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
27	CTCF	chr10:112835780-112836448	H1-hESC	embryonic stem cell:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060 chr10:112835841-112835850
28	CTCF	chr10:112835980-112836130	AG10803	skin:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
29	CTCF	chr10:112835960-112836110	GM12864	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
30	CTCF	chr10:112836463-112836582	NHEK	skin:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
31	CTCF	chr10:112835887-112836281	MCF-7	breast:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
32	CTCF	chr10:112835937-112836153	SK-N-SH_RA	brain:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
33	CTCF	chr10:112835960-112836110	GM12869	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
34	CTCF	chr10:112835980-112836130	SAEC	small airway:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
35	CTCF	chr10:112835980-112836130	Caco-2	colon:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
36	CTCF	chr10:112835834-112836250	A549	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060 chr10:112835841-112835850
37	CTCF	chr10:112835891-112836421	GM12891	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
38	CTCF	chr10:112835820-112836196	K562	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060 chr10:112835841-112835850
39	CTCF	chr10:112836400-112836550	HCM	heart:	n/a	chr10:112836519-112836537 chr10:112836522-112836531 chr10:112836522-112836535
40	CTCF	chr10:112838540-112838690	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr10:112835865-112836355	GM19238	blood:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
42	CTCF	chr10:112835926-112836151	Hela-S3	cervix:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
43	CTCF	chr10:112836323-112836331	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:112836380-112836530	HMF	breast:	n/a	n/a
45	CTCF	chr10:112835960-112836110	HPF	lung:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
46	CTCF	chr10:112835841-112836228	T-47D	breast:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060 chr10:112835841-112835850
47	CTCF	chr10:112835929-112836147	HepG2	liver:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
48	CTCF	chr10:112835980-112836130	HVMF	connective:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
49	CTCF	chr10:112835916-112836182	LNCaP	prostate:	n/a	chr10:112836045-112836053 chr10:112836035-112836048 chr10:112836044-112836065 chr10:112836042-112836060
50	CTCF	chr10:112836465-112836474	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:112842008-112842058	NB4	blood:	n/a
2	chr10:112842008-112842058	NB4	blood:	n/a
3	chr10:112836688-112836738	HCT-116	colon:	n/a
4	chr10:112836785-112836835	ProgFib	skin:	n/a
5	chr10:112839446-112839496	RPTEC	kidney:	n/a
6	chr10:112836471-112836521	SKMC	muscle:	n/a
7	chr10:112836785-112836835	ECC-1	luminal epithelium:	n/a
8	chr10:112836724-112836774	LNCaP	prostate:	n/a
9	chr10:112836780-112836830	ovcar-3	ovarian:	n/a
10	chr10:112836609-112836659	H1-hESC	embryonic stem cell:	embryo
11	chr10:112836724-112836774	MCF10A-Er-Src	breast:	n/a
12	chr10:112836780-112836830	NHDF-neo	bronchial:	n/a
13	chr10:112836609-112836659	HCF	heart:	n/a
14	chr10:112837240-112837290	HCM	heart:	n/a
15	chr10:112836681-112836731	GM12891	blood:	n/a
16	chr10:112839302-112839352	NH-A	brain:	n/a
17	chr10:112842008-112842058	Jurkat	blood:	n/a
18	chr10:112836785-112836835	HCPEpiC	choroid plexus:	n/a
19	chr10:112839302-112839352	AG09319	gingival:	n/a
20	chr10:112837537-112837587	HMEC	breast:	n/a
21	chr10:112835859-112835909	GM06990	blood:	n/a
22	chr10:112839446-112839496	ovcar-3	ovarian:	n/a
23	chr10:112836471-112836521	MCF-7	breast:	n/a
24	chr10:112834861-112834911	NHDF-neo	bronchial:	n/a
25	chr10:112842008-112842058	AG09319	gingival:	n/a
26	chr10:112836681-112836731	HUVEC	blood vessel:	n/a
27	chr10:112835859-112835909	BJ	skin:	n/a
28	chr10:112838983-112839033	AG10803	skin:	n/a
29	chr10:112838983-112839033	HRE	kidney:	n/a
30	chr10:112838078-112838128	A549	lung:	n/a
31	chr10:112839302-112839352	HMEC	breast:	n/a
32	chr10:112839446-112839496	ECC-1	luminal epithelium:	n/a
33	chr10:112842008-112842058	K562	blood:	n/a
34	chr10:112836688-112836738	CMK	blood:	n/a
35	chr10:112836471-112836521	HMEC	breast:	n/a
36	chr10:112834861-112834911	MCF-7	breast:	n/a
37	chr10:112839446-112839496	AG04450	lung:	fetal
38	chr10:112836688-112836738	NB4	blood:	n/a
39	chr10:112842008-112842058	SK-N-SH	brain:	n/a
40	chr10:112836681-112836731	HAEpiC	amniotic membrane:	n/a
41	chr10:112836185-112836235	HPAEpiC	pulmonary alveolar:	n/a
42	chr10:112838983-112839033	GM12892	blood:	n/a
43	chr10:112836785-112836835	Jurkat	blood:	n/a
44	chr10:112842008-112842058	T-47D	breast:	n/a
45	chr10:112836609-112836659	LNCaP	prostate:	n/a
46	chr10:112836724-112836774	PANC-1	pancreas:	n/a
47	chr10:112836609-112836659	PANC-1	pancreas:	n/a
48	chr10:112835859-112835909	HRCEpiC	kidney:	n/a
49	chr10:112836471-112836521	NHBE	bronchial:	n/a
50	chr10:112842008-112842058	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:112837126..112840004-chr10:112842044..112844644,2	K562	blood:
2	chr10:112835556..112836368-chr10:113357671..113358964,3	MCF-7	breast:
3	chr10:112837126..112840004-chr10:112842044..112844644,2	K562	blood:
4	chr10:112835905..112836784-chr10:113041082..113041711,3	MCF-7	breast:
5	chr10:112835831..112836588-chr10:112967176..112967740,2	MCF-7	breast:
6	chr10:112835910..112836421-chr10:113083278..113083990,2	MCF-7	breast:
7	chr10:112835558..112836069-chr10:112858564..112859533,2	MCF-7	breast:

Variant related genes	Relation type
ADRA2A	TF binding region
ADRA2A	CpG island

Extended variants
information (count: 299 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35844011	chr10:112834763-112834764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188299869	chr10:112834813-112834814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551037733	chr10:112834861-112834862	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs76778667	chr10:112834919-112834920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs550413845	chr10:112834937-112834938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs180704518	chr10:112834969-112834970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs569556390	chr10:112834998-112834999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571955088	chr10:112835009-112835010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12246561	chr10:112835109-112835110	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs11195418	chr10:112835159-112835160	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs375266585	chr10:112835232-112835233	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534547938	chr10:112835235-112835236	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs553218422	chr10:112835268-112835269	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376499008	chr10:112835289-112835290	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs542346081	chr10:112835315-112835316	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs563633960	chr10:112835332-112835333	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372198555	chr10:112835345-112835346	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs367715570	chr10:112835350-112835351	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs575590310	chr10:112835379-112835380	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs566105210	chr10:112835398-112835399	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs546475373	chr10:112835461-112835462	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs564655531	chr10:112835504-112835505	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs34733173	chr10:112835586-112835587	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs521674	chr10:112835590-112835591	Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs138566637	chr10:112835643-112835644	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs186490369	chr10:112835687-112835688	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554594964	chr10:112835697-112835698	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs529696129	chr10:112835747-112835748	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs562845730	chr10:112835770-112835771	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs371450801	chr10:112835786-112835787	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs375762938	chr10:112835828-112835829	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs569834607	chr10:112835893-112835894	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs114777841	chr10:112835897-112835898	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs190927797	chr10:112835913-112835914	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs570619079	chr10:112835942-112835943	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs79481725	chr10:112835992-112835993	Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs113214539	chr10:112836155-112836156	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs182317442	chr10:112836186-112836187	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs35187985	chr10:112836193-112836194	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs557220961	chr10:112836223-112836224	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs7089069	chr10:112836264-112836265	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545913078	chr10:112836284-112836285	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564522319	chr10:112836299-112836300	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371648330	chr10:112836308-112836309	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs573432713	chr10:112836342-112836343	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs76931336	chr10:112836402-112836403	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs540531932	chr10:112836449-112836450	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs1800544	chr10:112836503-112836504	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs146171437	chr10:112836506-112836507	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs547856804	chr10:112836563-112836564	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:591 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112829800-112835600	Weak transcription	Pancreas	Pancrea
2	chr10:112831400-112835600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:112834400-112835400	Enhancers	Fetal Brain Female	brain
4	chr10:112835400-112835600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:112835400-112835600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:112835400-112835600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
7	chr10:112835400-112835600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:112835400-112835600	Bivalent Enhancer	Brain Hippocampus Middle	brain
9	chr10:112835400-112835600	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr10:112835400-112835600	Enhancers	Ovary	ovary
11	chr10:112835400-112835800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
12	chr10:112835400-112835800	Enhancers	Fetal Brain Male	brain
13	chr10:112835400-112835800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr10:112835400-112836000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
15	chr10:112835400-112836000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr10:112835400-112836000	Flanking Active TSS	Fetal Brain Female	brain
17	chr10:112835400-112836000	Bivalent Enhancer	Fetal Heart	heart
18	chr10:112835400-112837000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr10:112835400-112838000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr10:112835600-112835800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:112835600-112835800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr10:112835600-112835800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:112835600-112835800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
24	chr10:112835600-112835800	Bivalent Enhancer	Primary B cells from cord blood	blood
25	chr10:112835600-112835800	Bivalent Enhancer	Primary T cells from cord blood	blood
26	chr10:112835600-112835800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
27	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
28	chr10:112835600-112835800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
29	chr10:112835600-112835800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
30	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:112835600-112835800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr10:112835600-112835800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr10:112835600-112835800	Bivalent Enhancer	Liver	Liver
35	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
36	chr10:112835600-112835800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
37	chr10:112835600-112835800	Bivalent/Poised TSS	Colonic Mucosa	Colon
38	chr10:112835600-112835800	Bivalent Enhancer	Colon Smooth Muscle	Colon
39	chr10:112835600-112835800	Bivalent Enhancer	Fetal Lung	lung
40	chr10:112835600-112835800	Bivalent Enhancer	Fetal Muscle Leg	muscle
41	chr10:112835600-112835800	Bivalent Enhancer	Fetal Stomach	stomach
42	chr10:112835600-112835800	Flanking Active TSS	Ovary	ovary
43	chr10:112835600-112835800	Enhancers	Pancreas	Pancrea
44	chr10:112835600-112835800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
45	chr10:112835600-112835800	Flanking Active TSS	Right Atrium	heart
46	chr10:112835600-112835800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
47	chr10:112835600-112835800	Bivalent/Poised TSS	HSMM	muscle
48	chr10:112835600-112836000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr10:112835600-112836000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr10:112835600-112836000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung

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