Variant report

Variant	nsv534854
Chromosome Location	chr1:9964726-10001012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:972)
CpG islands
(count:1282)
Chromatin interactive
region (count:66)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:9974263-9974911	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:9968964-9969571	K562	blood:	n/a	n/a
3	ARID3A	chr1:9989033-9989889	K562	blood:	n/a	n/a
4	ARID3A	chr1:9989523-9990446	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:9994301-9994619	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:9970695-9970819	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:9968951-9969165	HepG2	liver:	n/a	n/a
8	ATF1	chr1:9970493-9971422	K562	blood:	n/a	n/a
9	ATF2	chr1:9970617-9971222	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:9969181-9969567	GM12878	blood:	n/a	n/a
11	ATF2	chr1:9970540-9970995	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr1:9970600-9971045	GM12878	blood:	n/a	n/a
13	BACH1	chr1:9970746-9971154	K562	blood:	n/a	n/a
14	BACH1	chr1:9970429-9970935	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCLAF1	chr1:9970115-9970387	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:9974156-9974813	HepG2	liver:	n/a	n/a
17	BHLHE40	chr1:9969252-9969364	K562	blood:	n/a	n/a
18	BHLHE40	chr1:9989429-9989911	K562	blood:	n/a	n/a
19	BHLHE40	chr1:9970173-9971293	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:9989478-9989762	HepG2	liver:	n/a	n/a
21	BHLHE40	chr1:9969601-9969700	K562	blood:	n/a	n/a
22	BHLHE40	chr1:9970155-9971363	K562	blood:	n/a	n/a
23	BHLHE40	chr1:9996970-9997179	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:9970489-9971059	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr1:9970706-9970857	HepG2	liver:	n/a	n/a
26	BRCA1	chr1:9970969-9971108	GM12878	blood:	n/a	n/a
27	CBX3	chr1:9970443-9971432	K562	blood:	n/a	n/a
28	CBX3	chr1:9989384-9989836	K562	blood:	n/a	n/a
29	CCNT2	chr1:9969816-9971351	K562	blood:	n/a	chr1:9970031-9970040
30	CEBPB	chr1:9970478-9971222	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr1:9990073-9990434	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:9990048-9990310	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:9990133-9990389	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:9990109-9990358	K562	blood:	n/a	n/a
35	CEBPB	chr1:9976307-9976425	K562	blood:	n/a	n/a
36	CEBPB	chr1:9989882-9990441	K562	blood:	n/a	n/a
37	CEBPB	chr1:9990082-9990352	IMR90	lung:	n/a	n/a
38	CEBPB	chr1:9975082-9975401	HepG2	liver:	n/a	chr1:9975239-9975250
39	CEBPB	chr1:9989526-9990451	K562	blood:	n/a	n/a
40	CEBPB	chr1:9972022-9972143	K562	blood:	n/a	n/a
41	CEBPB	chr1:9986072-9986185	K562	blood:	n/a	n/a
42	CEBPB	chr1:9974402-9974635	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:9989557-9990430	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:9994172-9994411	HepG2	liver:	n/a	chr1:9994236-9994247
45	CEBPB	chr1:9970470-9970595	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:9988853-9989000	HepG2	liver:	n/a	chr1:9988874-9988885
47	CEBPB	chr1:9972471-9972899	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:9970641-9971458	GM12878	blood:	n/a	n/a
49	CEBPB	chr1:9975211-9975305	IMR90	lung:	n/a	chr1:9975239-9975250
50	CEBPB	chr1:9990096-9990338	HepG2	liver:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:9970789-9970839	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:9970789-9970839	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:9992130-9992180	H1-hESC	embryonic stem cell:	embryo
4	chr1:9973750-9973800	RPTEC	kidney:	n/a
5	chr1:9970789-9970839	HCPEpiC	choroid plexus:	n/a
6	chr1:9992130-9992180	A549	lung:	n/a
7	chr1:9970659-9970709	Hepatocyte	liver:	n/a
8	chr1:9970789-9970839	GM12892	blood:	n/a
9	chr1:9969424-9969474	AoSMC	blood vessel:	n/a
10	chr1:9970993-9971043	HepG2	liver:	n/a
11	chr1:9982553-9982603	A549	lung:	n/a
12	chr1:9971115-9971165	GM19239	blood:	n/a
13	chr1:9969906-9969956	PANC-1	pancreas:	n/a
14	chr1:9969906-9969956	BJ	skin:	n/a
15	chr1:9970659-9970709	AG09319	gingival:	n/a
16	chr1:9970773-9970823	Jurkat	blood:	n/a
17	chr1:9970042-9970092	HCF	heart:	n/a
18	chr1:9970633-9970683	MCF10A-Er-Src	breast:	n/a
19	chr1:9970633-9970683	ECC-1	luminal epithelium:	n/a
20	chr1:9982553-9982603	Hepatocyte	liver:	n/a
21	chr1:9970659-9970709	NB4	blood:	n/a
22	chr1:9970659-9970709	AG09309	skin:	n/a
23	chr1:9970659-9970709	MCF10A-Er-Src	breast:	n/a
24	chr1:9970639-9970689	T-47D	breast:	n/a
25	chr1:9967849-9967899	T-47D	breast:	n/a
26	chr1:9968130-9968180	PrEC	prostate:	n/a
27	chr1:9969906-9969956	H1-hESC	embryonic stem cell:	embryo
28	chr1:9971115-9971165	HRCEpiC	kidney:	n/a
29	chr1:9970653-9970703	K562	blood:	n/a
30	chr1:9970993-9971043	HCM	heart:	n/a
31	chr1:9970639-9970689	GM12891	blood:	n/a
32	chr1:9971115-9971165	NHDF-neo	bronchial:	n/a
33	chr1:9970773-9970823	HCPEpiC	choroid plexus:	n/a
34	chr1:9969906-9969956	SAEC	small airway:	n/a
35	chr1:9968130-9968180	Jurkat	blood:	n/a
36	chr1:9982553-9982603	AG09309	skin:	n/a
37	chr1:9971115-9971165	RPTEC	kidney:	n/a
38	chr1:9970653-9970703	HMEC	breast:	n/a
39	chr1:9970639-9970689	HUVEC	blood vessel:	n/a
40	chr1:9967849-9967899	RPTEC	kidney:	n/a
41	chr1:9970773-9970823	PFSK-1	brain:	n/a
42	chr1:9970636-9970686	NT2-D1	testis:	n/a
43	chr1:9967849-9967899	GM12878	blood:	n/a
44	chr1:9970773-9970823	K562	blood:	n/a
45	chr1:9969424-9969474	AG04449	skin:	fetal
46	chr1:9970789-9970839	HAEpiC	amniotic membrane:	n/a
47	chr1:9967849-9967899	HRPEpiC	eye:	n/a
48	chr1:9970257-9970307	GM12878	blood:	n/a
49	chr1:9999765-9999815	HMEC	breast:	n/a
50	chr1:9969647-9969697	RPTEC	kidney:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:9968980..9971143-chr1:10091275..10094032,2	MCF-7	breast:
2	chr1:9951877..9953921-chr1:9969781..9972106,2	K562	blood:
3	chr1:9598357..9600468-chr1:9996244..9998759,2	K562	blood:
4	chr1:9927613..9929212-chr1:9967136..9969117,2	K562	blood:
5	chr1:9970332..9972521-chr1:9987991..9990638,3	K562	blood:
6	chr1:9970359..9972833-chr1:9979234..9983583,5	K562	blood:
7	chr1:9969786..9972785-chr1:9998354..10000528,2	K562	blood:
8	chr1:9970652..9971321-chr1:186343842..186344380,2	Hela-S3	cervix:
9	chr1:9943715..9945341-chr1:9996740..9998512,2	K562	blood:
10	chr1:9934948..9935494-chr1:9974131..9974751,2	MCF-7	breast:
11	chr1:9970587..9972464-chr1:10010441..10012006,2	K562	blood:
12	chr1:9979462..9981194-chr1:9999339..10001219,2	K562	blood:
13	chr1:9948830..9950649-chr1:9965085..9967755,2	K562	blood:
14	chr1:9983752..9986427-chr1:10003479..10005012,2	K562	blood:
15	chr1:9884699..9887504-chr1:9972988..9975946,2	K562	blood:
16	chr1:9935000..9935869-chr1:9974774..9975319,2	MCF-7	breast:
17	chr1:9942309..9944442-chr1:9963388..9967082,3	K562	blood:
18	chr1:9971162..9973726-chr1:9979028..9981341,2	MCF-7	breast:
19	chr1:9882877..9885289-chr1:9969259..9970898,2	MCF-7	breast:
20	chr1:9923513..9926464-chr1:9996887..9999846,2	K562	blood:
21	chr1:9998207..10001225-chr1:10001288..10004124,5	MCF-7	breast:
22	chr1:9963836..9965578-chr1:9968398..9970356,2	MCF-7	breast:
23	chr1:9979666..9982180-chr1:9989888..9991989,2	K562	blood:
24	chr1:9970332..9972521-chr1:9989080..9990638,2	K562	blood:
25	chr1:9968711..9972372-chr1:9974326..9978702,4	MCF-7	breast:
26	chr1:9969356..9971879-chr1:10474323..10477073,2	K562	blood:
27	chr1:9969188..9972816-chr1:10001560..10005397,4	MCF-7	breast:
28	chr1:9969032..9972214-chr1:9991997..9995260,4	K562	blood:
29	chr1:9979462..9981194-chr1:9999339..10001219,2	K562	blood:
30	chr1:9987221..9989617-chr1:10002378..10005088,3	K562	blood:
31	chr1:9968043..9973723-chr1:10001891..10008599,10	K562	blood:
32	chr1:9968103..9970707-chr1:9972255..9974509,2	MCF-7	breast:
33	chr1:9950543..9952376-chr1:9989570..9991778,2	K562	blood:
34	chr1:9935001..9935634-chr1:9989098..9989618,2	K562	blood:
35	chr1:9969076..9970759-chr1:9993245..9994949,2	K562	blood:
36	chr1:9969199..9972073-chr1:10003014..10005092,3	MCF-7	breast:
37	chr1:9958455..9962584-chr1:9963252..9967560,5	MCF-7	breast:
38	chr1:9979666..9982180-chr1:9989888..9991989,2	K562	blood:
39	chr1:9970314..9973220-chr1:10093612..10095585,2	K562	blood:
40	chr1:9982335..9985252-chr1:10003262..10005012,2	K562	blood:
41	chr1:9991529..9996345-chr1:10001160..10004231,6	K562	blood:
42	chr1:9948461..9950463-chr1:9972142..9973829,2	K562	blood:
43	chr1:9992820..9997928-chr1:9999758..10004449,8	K562	blood:
44	chr1:9969329..9971047-chr1:10093028..10095066,2	K562	blood:
45	chr1:9937606..9938358-chr1:9974492..9975167,2	MCF-7	breast:
46	chr1:9790874..9793270-chr1:9967778..9969493,2	K562	blood:
47	chr1:9776353..9779413-chr1:9969324..9972333,3	K562	blood:
48	chr1:9965927..9968463-chr1:9968735..9971514,3	MCF-7	breast:
49	chr1:9963862..9967458-chr1:9967663..9970423,5	K562	blood:
50	chr1:9969022..9974825-chr1:10002123..10006220,12	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTNNBIP1-1	chr1:9986451-9987467	NONHSAT000825

No data

Variant related genes	Relation type
NMNAT1	TF binding region
ENSG00000228150	TF binding region
CTNNBIP1	TF binding region
LZIC	TF binding region
NMNAT1	CpG island
ENSG00000228150	CpG island
CTNNBIP1	CpG island
LZIC	CpG island
ENSG00000110756	chromatin interactions
ENSG00000202415	chromatin interactions
ENSG00000178585	chromatin interactions
ENSG00000228150	chromatin interactions
ENSG00000142657	chromatin interactions
ENSG00000162441	chromatin interactions
ENSG00000171603	chromatin interactions
ENSG00000171612	chromatin interactions
ENSG00000173614	chromatin interactions
ENSG00000130939	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000171608	chromatin interactions

Extended variants
information (count: 1273 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556444015	chr1:9964786-9964787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577786613	chr1:9964842-9964843	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79165370	chr1:9964886-9964887	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs149068496	chr1:9964892-9964893	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs145732525	chr1:9964948-9964949	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527408766	chr1:9964971-9964972	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147777169	chr1:9964986-9964987	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540871127	chr1:9965020-9965021	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs77661536	chr1:9965037-9965038	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531216026	chr1:9965190-9965191	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141389307	chr1:9965205-9965206	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs552738263	chr1:9965239-9965240	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577877344	chr1:9965285-9965286	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147012273	chr1:9965305-9965306	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116256906	chr1:9965354-9965355	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs544929987	chr1:9965374-9965375	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2486084	chr1:9965425-9965426	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs139132204	chr1:9965487-9965488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs72858068	chr1:9965489-9965490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs78303386	chr1:9965498-9965499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77819805	chr1:9965499-9965500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530449732	chr1:9965506-9965507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567605337	chr1:9965567-9965568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543823588	chr1:9965573-9965574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562193249	chr1:9965629-9965630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529403753	chr1:9965641-9965642	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs61785600	chr1:9965646-9965647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75643266	chr1:9965648-9965649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs188426541	chr1:9965679-9965680	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148070903	chr1:9965708-9965709	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577951704	chr1:9965710-9965711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538826250	chr1:9965740-9965741	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548052521	chr1:9965756-9965757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12737902	chr1:9965779-9965780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368034514	chr1:9965783-9965784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559643335	chr1:9965784-9965785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554389064	chr1:9965785-9965786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs572034205	chr1:9965800-9965801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533699247	chr1:9965815-9965816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12723530	chr1:9965825-9965826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12723540	chr1:9965836-9965837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542664649	chr1:9965858-9965859	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141732444	chr1:9965866-9965867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180890859	chr1:9965884-9965885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs12723693	chr1:9965886-9965887	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs150147522	chr1:9965912-9965913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565158011	chr1:9965928-9965929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532498649	chr1:9965934-9965935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs74224889	chr1:9966013-9966014	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79912646	chr1:9966037-9966038	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1557 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9949400-9967600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr1:9951600-9969000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr1:9958000-9968800	Weak transcription	Fetal Stomach	stomach
4	chr1:9958800-9969000	Weak transcription	Hela-S3	cervix
5	chr1:9959000-9964800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:9960800-9967800	Weak transcription	Thymus	Thymus
7	chr1:9960800-9969400	Weak transcription	Aorta	Aorta
8	chr1:9961000-9964800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr1:9961000-9965000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:9961000-9967600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:9961000-9968800	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr1:9961000-9969000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr1:9961000-9969200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:9961200-9969000	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr1:9961400-9965600	Enhancers	Left Ventricle	heart
16	chr1:9961400-9969000	Weak transcription	Primary B cells from cord blood	blood
17	chr1:9961600-9968800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr1:9961600-9968800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr1:9961800-9968000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr1:9962000-9965000	Weak transcription	HMEC	breast
21	chr1:9962000-9967600	Weak transcription	Brain Germinal Matrix	brain
22	chr1:9962000-9968800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:9962000-9968800	Weak transcription	Small Intestine	intestine
24	chr1:9962000-9969000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr1:9962000-9969000	Weak transcription	Fetal Brain Female	brain
26	chr1:9962200-9964800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:9962200-9964800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:9962200-9965000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:9962200-9965000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:9962200-9966600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:9962200-9966600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:9962200-9967800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr1:9962200-9967800	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:9962200-9968800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr1:9962200-9969000	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr1:9962400-9964800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:9962400-9965000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr1:9962400-9965000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:9962400-9965000	Weak transcription	K562	blood
40	chr1:9962400-9967600	Weak transcription	Esophagus	oesophagus
41	chr1:9962400-9968800	Weak transcription	Fetal Intestine Small	intestine
42	chr1:9962400-9969000	Weak transcription	Fetal Thymus	thymus
43	chr1:9962400-9969000	Weak transcription	Spleen	Spleen
44	chr1:9962400-9969200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr1:9962600-9966800	Weak transcription	Duodenum Mucosa	Duodenum
46	chr1:9962600-9967400	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr1:9962600-9967600	Weak transcription	Pancreas	Pancrea
48	chr1:9962600-9968800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:9962600-9968800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:9962600-9969000	Weak transcription	Brain Angular Gyrus	brain

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