Variant report

Variant	nsv564908
Chromosome Location	chr14:65015655-65017474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:549)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:65016898-65017108	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr14:65016989-65017055	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr14:65015808-65016025	H1-hESC	embryonic stem cell:	n/a	chr14:65015925-65015936
4	CEBPB	chr14:65015867-65016107	HepG2	liver:	n/a	chr14:65015925-65015936
5	CEBPB	chr14:65015748-65016753	Hela-S3	cervix:	n/a	chr14:65015925-65015936
6	CEBPB	chr14:65015764-65016119	IMR90	lung:	n/a	chr14:65015925-65015936
7	CEBPB	chr14:65015798-65015979	K562	blood:	n/a	chr14:65015925-65015936
8	CHD2	chr14:65016418-65016760	Hela-S3	cervix:	n/a	chr14:65016637-65016647 chr14:65016625-65016635
9	CTCF	chr14:65016700-65016850	Caco-2	colon:	n/a	n/a
10	CTCF	chr14:65016770-65016855	MCF-7	breast:	n/a	n/a
11	CTCF	chr14:65016804-65016844	NHEK	skin:	n/a	n/a
12	CTCF	chr14:65016700-65016850	GM12875	blood:	n/a	n/a
13	CTCF	chr14:65016435-65016712	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr14:65016680-65016830	GM12874	blood:	n/a	n/a
15	CTCF	chr14:65016751-65016885	MCF-7	breast:	n/a	n/a
16	CTCF	chr14:65016799-65016800	NHEK	skin:	n/a	n/a
17	CTCF	chr14:65016680-65016830	GM12866	blood:	n/a	n/a
18	CTCF	chr14:65016738-65016905	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:65016824-65016860	H1-hESC	embryonic stem cell:	n/a	n/a
20	E2F1	chr14:65016451-65016831	Hela-S3	cervix:	n/a	n/a
21	E2F6	chr14:65016523-65016748	K562	blood:	n/a	n/a
22	E2F6	chr14:65016431-65016947	H1-hESC	embryonic stem cell:	n/a	n/a
23	E2F6	chr14:65016482-65017304	H1-hESC	embryonic stem cell:	n/a	n/a
24	ELK1	chr14:65016551-65016763	Hela-S3	cervix:	n/a	n/a
25	ELK4	chr14:65016252-65016764	Hela-S3	cervix:	n/a	n/a
26	FOS	chr14:65015820-65016038	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr14:65015767-65016082	MCF10A-Er-Src	breast:	n/a	n/a
28	GTF2F1	chr14:65015787-65016676	Hela-S3	cervix:	n/a	n/a
29	GTF2F1	chr14:65016574-65016616	H1-hESC	embryonic stem cell:	n/a	n/a
30	HA-E2F1	chr14:65016336-65016984	MCF-7	breast:	n/a	n/a
31	HA-E2F1	chr14:65016447-65016870	Hela-S3	cervix:	n/a	n/a
32	JUND	chr14:65015843-65016032	HepG2	liver:	n/a	n/a
33	MAFK	chr14:65016509-65016826	Hela-S3	cervix:	n/a	n/a
34	MAFK	chr14:65015949-65016077	HepG2	liver:	n/a	chr14:65015979-65015993 chr14:65015976-65015991
35	MAFK	chr14:65015787-65016232	Hela-S3	cervix:	n/a	chr14:65015979-65015993 chr14:65015976-65015991
36	MAFK	chr14:65015832-65016078	HepG2	liver:	n/a	chr14:65015979-65015993 chr14:65015976-65015991
37	MAX	chr14:65016460-65016902	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAX	chr14:65016547-65016833	NB4	blood:	n/a	n/a
39	MAX	chr14:65016522-65016824	K562	blood:	n/a	n/a
40	MAX	chr14:65016921-65017121	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr14:65016344-65016854	Hela-S3	cervix:	n/a	n/a
42	MAX	chr14:65016400-65017057	MCF-7	breast:	n/a	n/a
43	MAX	chr14:65016468-65017093	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr14:65016507-65016901	A549	lung:	n/a	n/a
45	MAX	chr14:65016382-65016914	A549	lung:	n/a	n/a
46	MAZ	chr14:65016516-65016783	Hela-S3	cervix:	n/a	n/a
47	MXI1	chr14:65016419-65016767	Hela-S3	cervix:	n/a	n/a
48	MYC	chr14:65016593-65016596	MCF-7	breast:	n/a	n/a
49	MYC	chr14:65016602-65016887	MCF-7	breast:	n/a	n/a
50	MYC	chr14:65016747-65016857	MCF-7	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:65016545-65016595	AoSMC	blood vessel:	n/a
2	chr14:65016545-65016595	NHBE	bronchial:	n/a
3	chr14:65017091-65017141	LNCaP	prostate:	n/a
4	chr14:65016258-65016308	CMK	blood:	n/a
5	chr14:65016517-65016567	HL-60	blood:	n/a
6	chr14:65015998-65016048	AG09309	skin:	n/a
7	chr14:65016802-65016852	HIPEpiC	eye:	n/a
8	chr14:65016591-65016641	K562	blood:	n/a
9	chr14:65016802-65016852	HCM	heart:	n/a
10	chr14:65016595-65016645	GM12892	blood:	n/a
11	chr14:65016591-65016641	GM12891	blood:	n/a
12	chr14:65016545-65016595	GM12891	blood:	n/a
13	chr14:65016545-65016595	PANC-1	pancreas:	n/a
14	chr14:65016595-65016645	NT2-D1	testis:	n/a
15	chr14:65016595-65016645	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:65016595-65016645	GM12891	blood:	n/a
17	chr14:65016602-65016652	GM06990	blood:	n/a
18	chr14:65016802-65016852	A549	lung:	n/a
19	chr14:65015998-65016048	BJ	skin:	n/a
20	chr14:65016258-65016308	AG04450	lung:	fetal
21	chr14:65016545-65016595	Hela-S3	cervix:	n/a
22	chr14:65016258-65016308	Caco-2	colon:	n/a
23	chr14:65015998-65016048	IMR90	lung:	fetal
24	chr14:65017091-65017141	MCF-7	breast:	n/a
25	chr14:65016602-65016652	NT2-D1	testis:	n/a
26	chr14:65016595-65016645	HCT-116	colon:	n/a
27	chr14:65016258-65016308	LNCaP	prostate:	n/a
28	chr14:65016517-65016567	U87	brain:	n/a
29	chr14:65017091-65017141	GM12892	blood:	n/a
30	chr14:65016591-65016641	AG09309	skin:	n/a
31	chr14:65016595-65016645	SK-N-MC	brain:	n/a
32	chr14:65016802-65016852	SK-N-MC	brain:	n/a
33	chr14:65016602-65016652	NB4	blood:	n/a
34	chr14:65015998-65016048	RPTEC	kidney:	n/a
35	chr14:65016602-65016652	ProgFib	skin:	n/a
36	chr14:65016595-65016645	U87	brain:	n/a
37	chr14:65016591-65016641	HUVEC	blood vessel:	n/a
38	chr14:65016591-65016641	HCT-116	colon:	n/a
39	chr14:65017091-65017141	BE2_C	brain:	n/a
40	chr14:65017091-65017141	HUVEC	blood vessel:	n/a
41	chr14:65017091-65017141	GM12891	blood:	n/a
42	chr14:65016802-65016852	HMEC	breast:	n/a
43	chr14:65017091-65017141	Hepatocyte	liver:	n/a
44	chr14:65016517-65016567	AG04449	skin:	fetal
45	chr14:65016545-65016595	Hepatocyte	liver:	n/a
46	chr14:65016591-65016641	HEK293	kidney:	embryo
47	chr14:65015998-65016048	H1-hESC	embryonic stem cell:	embryo
48	chr14:65016545-65016595	NT2-D1	testis:	n/a
49	chr14:65015998-65016048	Caco-2	colon:	n/a
50	chr14:65016802-65016852	Caco-2	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:65017028..65018763-chr14:65046297..65047824,2	MCF-7	breast:
2	chr14:64971147..64972847-chr14:65015662..65018406,2	MCF-7	breast:
3	chr14:65006007..65010466-chr14:65011368..65016510,6	MCF-7	breast:
4	chr14:65005138..65007971-chr14:65016762..65019337,2	MCF-7	breast:
5	chr14:65005373..65008937-chr14:65014849..65020282,8	MCF-7	breast:
6	chr14:65006961..65009286-chr14:65016299..65018796,2	K562	blood:
7	chr14:65015799..65018122-chr20:55818007..55820214,2	MCF-7	breast:
8	chr14:64969437..64972776-chr14:65017251..65021474,5	MCF-7	breast:

No data

Variant related genes	Relation type
PPP1R36	TF binding region
PPP1R36	CpG island
ENSG00000126804	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000126803	chromatin interactions
ENSG00000259116	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7149152	chr14:65015655-65015656	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147678994	chr14:65015672-65015673	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs200771121	chr14:65015720-65015721	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs34740996	chr14:65015722-65015723	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs143379588	chr14:65015723-65015724	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs544765961	chr14:65015776-65015777	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs556830987	chr14:65015777-65015778	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs142254696	chr14:65015789-65015790	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs180863692	chr14:65015797-65015798	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs367735905	chr14:65015807-65015808	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs560587392	chr14:65015833-65015834	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs113560817	chr14:65015841-65015842	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs550096949	chr14:65015950-65015951	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs569741511	chr14:65015981-65015982	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs146238444	chr14:65015997-65015998	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs73267790	chr14:65015998-65015999	Enhancers Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs576912795	chr14:65016015-65016016	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs571740989	chr14:65016061-65016062	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs185478788	chr14:65016068-65016069	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs201635414	chr14:65016091-65016092	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs138655448	chr14:65016099-65016100	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs189887455	chr14:65016100-65016101	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs149290857	chr14:65016143-65016144	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs556854307	chr14:65016191-65016192	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs76880483	chr14:65016194-65016195	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs545534469	chr14:65016244-65016245	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs565154752	chr14:65016325-65016326	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs7154937	chr14:65016335-65016336	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs369147747	chr14:65016520-65016521	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs12323549	chr14:65016572-65016573	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs529736074	chr14:65016605-65016606	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs549520782	chr14:65016616-65016617	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs183220356	chr14:65016618-65016619	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs532327153	chr14:65016625-65016626	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs552313774	chr14:65016631-65016632	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs113220995	chr14:65016672-65016673	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs565914774	chr14:65016694-65016695	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs7156953	chr14:65016702-65016703	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs147817006	chr14:65016720-65016721	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs141338206	chr14:65016721-65016722	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs567652176	chr14:65016725-65016726	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs369642002	chr14:65016740-65016741	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs373435160	chr14:65016752-65016753	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs570297554	chr14:65016765-65016766	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs539000130	chr14:65016776-65016777	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs375518915	chr14:65016818-65016819	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs112052589	chr14:65016876-65016877	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs540719542	chr14:65016882-65016883	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs368531469	chr14:65016921-65016922	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs548546466	chr14:65016939-65016940	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Hematopoietic stem cell	20738155	CNVD
Cancer	17440070	CNVD
Intracranial arachnoid cysts	20187927	CNVD

Chromatin state (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65008600-65016200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:65009000-65016200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:65009400-65016600	Weak transcription	Gastric	stomach
4	chr14:65009600-65016200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr14:65010400-65015800	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr14:65010400-65015800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr14:65010400-65016600	Weak transcription	Aorta	Aorta
8	chr14:65011200-65015800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:65011400-65015800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr14:65011400-65016000	Weak transcription	NHDF-Ad	bronchial
11	chr14:65011600-65016000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr14:65011600-65016000	Weak transcription	Colon Smooth Muscle	Colon
13	chr14:65011600-65016000	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr14:65011600-65016000	Weak transcription	NHLF	lung
15	chr14:65011600-65016200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:65011800-65015800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr14:65012000-65016000	Weak transcription	Brain Cingulate Gyrus	brain
18	chr14:65012000-65016200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:65012000-65016200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr14:65012000-65016600	Weak transcription	Brain Angular Gyrus	brain
21	chr14:65012200-65016000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr14:65013600-65016200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr14:65013800-65016600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr14:65015400-65016000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr14:65015400-65016200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr14:65015400-65016200	Enhancers	Brain Anterior Caudate	brain
27	chr14:65015400-65016200	Enhancers	Brain Substantia Nigra	brain
28	chr14:65015400-65016200	Enhancers	Hela-S3	cervix
29	chr14:65015400-65016200	Enhancers	NHEK	skin
30	chr14:65015600-65016000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr14:65015600-65016200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr14:65015600-65016200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:65015600-65016200	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr14:65015600-65016400	Enhancers	Brain Hippocampus Middle	brain
35	chr14:65015600-65016400	Enhancers	Psoas Muscle	Psoas
36	chr14:65015800-65016000	Bivalent Enhancer	Primary T cells from cord blood	blood
37	chr14:65015800-65016200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr14:65015800-65016200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
39	chr14:65015800-65016200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
40	chr14:65015800-65016200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:65015800-65016200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr14:65015800-65016200	Enhancers	Rectal Mucosa Donor 29	rectum
43	chr14:65015800-65016200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr14:65015800-65016200	Enhancers	Stomach Mucosa	stomach
45	chr14:65015800-65016400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
46	chr14:65015800-65016400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr14:65015800-65016400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr14:65015800-65016400	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr14:65015800-65016400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr14:65015800-65016400	Enhancers	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links