Variant report

Variant	nsv520609
Chromosome Location	chr1:223931411-223947081
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:673)
CpG islands
(count:611)
Chromatin interactive
region (count:45)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:223938930-223939189	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:223937010-223937124	K562	blood:	n/a	n/a
3	ATF3	chr1:223936810-223937218	A549	lung:	n/a	n/a
4	BACH1	chr1:223936431-223937118	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:223936096-223936303	GM12878	blood:	n/a	chr1:223936201-223936212 chr1:223936202-223936212
6	BATF	chr1:223936084-223936283	GM12878	blood:	n/a	chr1:223936201-223936212 chr1:223936202-223936212
7	BCL3	chr1:223936819-223937394	A549	lung:	n/a	n/a
8	BCLAF1	chr1:223936796-223937109	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:223936856-223937013	K562	blood:	n/a	n/a
10	BHLHE40	chr1:223936619-223937095	GM12878	blood:	n/a	n/a
11	BRCA1	chr1:223946954-223947154	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr1:223936347-223936575	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr1:223936416-223937187	K562	blood:	n/a	n/a
14	CCNT2	chr1:223936570-223937163	K562	blood:	n/a	n/a
15	CEBPB	chr1:223935519-223936069	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:223935689-223935997	A549	lung:	n/a	n/a
17	CEBPB	chr1:223935623-223936433	A549	lung:	n/a	n/a
18	CEBPB	chr1:223938995-223939307	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:223933529-223933765	IMR90	lung:	n/a	n/a
20	CHD1	chr1:223936538-223937022	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:223939573-223939588	HepG2	liver:	n/a	n/a
22	CHD2	chr1:223936109-223937115	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr1:223946933-223947137	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr1:223936786-223937016	K562	blood:	n/a	n/a
25	CREB1	chr1:223936767-223937124	A549	lung:	n/a	n/a
26	CTCF	chr1:223936940-223937090	AG04449	skin:	n/a	n/a
27	CTCF	chr1:223937000-223937150	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:223936940-223937090	GM12874	blood:	n/a	n/a
29	CTCF	chr1:223946999-223947433	K562	blood:	n/a	n/a
30	CTCF	chr1:223936930-223937135	HepG2	liver:	n/a	n/a
31	CTCF	chr1:223947012-223947017	K562	blood:	n/a	n/a
32	CTCF	chr1:223937220-223937370	HepG2	liver:	n/a	n/a
33	CTCF	chr1:223936960-223937110	GM12870	blood:	n/a	n/a
34	CTCF	chr1:223936848-223937163	GM19238	blood:	n/a	n/a
35	CTCF	chr1:223946911-223947464	K562	blood:	n/a	n/a
36	CTCF	chr1:223943840-223943990	Caco-2	colon:	n/a	n/a
37	CTCF	chr1:223936877-223937192	T-47D	breast:	n/a	n/a
38	CTCF	chr1:223936855-223937153	GM12891	blood:	n/a	n/a
39	CTCF	chr1:223943800-223943950	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:223936980-223937130	BE2_C	brain:	n/a	n/a
41	CTCF	chr1:223936566-223937572	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr1:223937377-223937384	LNCaP	prostate:	n/a	n/a
43	CTCF	chr1:223943820-223943970	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:223943800-223943950	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr1:223936980-223937130	NHEK	skin:	n/a	n/a
46	CTCF	chr1:223937000-223937150	GM12869	blood:	n/a	n/a
47	CTCF	chr1:223943841-223943957	K562	blood:	n/a	n/a
48	CTCF	chr1:223936920-223937070	NHEK	skin:	n/a	n/a
49	CTCF	chr1:223936980-223937130	GM12874	blood:	n/a	n/a
50	CTCF	chr1:223936980-223937130	HPF	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223933792-223933842	HCF	heart:	n/a
2	chr1:223933792-223933842	HCF	heart:	n/a
3	chr1:223937043-223937093	RPTEC	kidney:	n/a
4	chr1:223934864-223934914	K562	blood:	n/a
5	chr1:223936799-223936849	GM12878	blood:	n/a
6	chr1:223933792-223933842	CMK	blood:	n/a
7	chr1:223936812-223936862	ovcar-3	ovarian:	n/a
8	chr1:223936838-223936888	LNCaP	prostate:	n/a
9	chr1:223937043-223937093	HEK293	kidney:	embryo
10	chr1:223936799-223936849	HIPEpiC	eye:	n/a
11	chr1:223933792-223933842	AG10803	skin:	n/a
12	chr1:223936343-223936393	NT2-D1	testis:	n/a
13	chr1:223934864-223934914	AG09319	gingival:	n/a
14	chr1:223937196-223937246	LNCaP	prostate:	n/a
15	chr1:223933792-223933842	BE2_C	brain:	n/a
16	chr1:223937196-223937246	HUVEC	blood vessel:	n/a
17	chr1:223936812-223936862	SKMC	muscle:	n/a
18	chr1:223936343-223936393	AG10803	skin:	n/a
19	chr1:223936838-223936888	BJ	skin:	n/a
20	chr1:223936812-223936862	HCT-116	colon:	n/a
21	chr1:223936508-223936558	GM06990	blood:	n/a
22	chr1:223940656-223940706	HIPEpiC	eye:	n/a
23	chr1:223934864-223934914	SKMC	muscle:	n/a
24	chr1:223933792-223933842	HepG2	liver:	n/a
25	chr1:223936508-223936558	SAEC	small airway:	n/a
26	chr1:223936508-223936558	T-47D	breast:	n/a
27	chr1:223936799-223936849	HEK293	kidney:	embryo
28	chr1:223936812-223936862	SK-N-SH_RA	brain:	n/a
29	chr1:223940656-223940706	Hela-S3	cervix:	n/a
30	chr1:223936812-223936862	MCF10A-Er-Src	breast:	n/a
31	chr1:223936812-223936862	K562	blood:	n/a
32	chr1:223937043-223937093	K562	blood:	n/a
33	chr1:223936799-223936849	Hepatocyte	liver:	n/a
34	chr1:223936812-223936862	HepG2	liver:	n/a
35	chr1:223934864-223934914	BJ	skin:	n/a
36	chr1:223934864-223934914	HAEpiC	amniotic membrane:	n/a
37	chr1:223936343-223936393	SAEC	small airway:	n/a
38	chr1:223937043-223937093	Hela-S3	cervix:	n/a
39	chr1:223936343-223936393	GM06990	blood:	n/a
40	chr1:223936812-223936862	NHBE	bronchial:	n/a
41	chr1:223937043-223937093	GM06990	blood:	n/a
42	chr1:223937196-223937246	SAEC	small airway:	n/a
43	chr1:223936343-223936393	AG09309	skin:	n/a
44	chr1:223933792-223933842	SKMC	muscle:	n/a
45	chr1:223936812-223936862	HIPEpiC	eye:	n/a
46	chr1:223936508-223936558	RPTEC	kidney:	n/a
47	chr1:223933792-223933842	HEK293	kidney:	embryo
48	chr1:223937043-223937093	SK-N-MC	brain:	n/a
49	chr1:223936799-223936849	A549	lung:	n/a
50	chr1:223936799-223936849	HPAEpiC	pulmonary alveolar:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:223918981..223919488-chr1:223936544..223937377,2	K562	blood:
2	chr1:223899768..223900540-chr1:223936575..223937471,3	K562	blood:
3	chr1:223941213..223943613-chr1:223960905..223963587,2	K562	blood:
4	chr1:223936472..223939236-chr1:224031329..224033727,2	K562	blood:
5	chr1:223924785..223927259-chr1:223936900..223938830,2	K562	blood:
6	chr1:223884772..223887549-chr1:223936018..223938654,2	MCF-7	breast:
7	chr1:223937050..223939736-chr1:223946719..223949161,2	K562	blood:
8	chr1:223899607..223901005-chr1:223936533..223937452,13	MCF-7	breast:
9	chr1:223940271..223942442-chr1:223944013..223946177,2	K562	blood:
10	chr1:223937050..223939736-chr1:223946719..223949161,2	K562	blood:
11	chr1:223936854..223938919-chr1:223960180..223962303,2	K562	blood:
12	chr1:223886106..223889532-chr1:223933715..223936535,3	K562	blood:
13	chr1:223903418..223905687-chr1:223928822..223931791,2	MCF-7	breast:
14	chr1:223898965..223904523-chr1:223935616..223939096,7	MCF-7	breast:
15	chr1:223940335..223944037-chr1:223947483..223951720,4	K562	blood:
16	chr1:223908483..223912094-chr1:223930572..223933646,3	MCF-7	breast:
17	chr1:223935650..223937154-chr1:223966505..223968008,2	MCF-7	breast:
18	chr1:223895463..223896414-chr1:223936797..223937493,2	MCF-7	breast:
19	chr1:223907255..223908800-chr1:223930400..223932243,2	MCF-7	breast:
20	chr1:223886322..223888614-chr1:223940802..223943504,2	K562	blood:
21	chr1:223885662..223886577-chr1:223936613..223937522,3	MCF-7	breast:
22	chr1:223888703..223890245-chr1:223939416..223941061,2	K562	blood:
23	chr1:223929603..223931458-chr1:223939312..223941787,2	K562	blood:
24	chr1:223931041..223933395-chr1:223937050..223938620,2	K562	blood:
25	chr1:223886105..223888614-chr1:223940802..223943504,3	K562	blood:
26	chr1:223937037..223939857-chr1:223940065..223944617,5	K562	blood:
27	chr1:223884441..223887114-chr1:223935723..223937532,2	MCF-7	breast:
28	chr1:223891679..223894044-chr1:223943117..223944759,2	MCF-7	breast:
29	chr1:223915826..223918177-chr1:223937169..223939533,2	K562	blood:
30	chr1:223899274..223906539-chr1:223934896..223938666,15	MCF-7	breast:
31	chr1:223885511..223886611-chr1:223936562..223937549,9	K562	blood:
32	chr1:223900571..223903093-chr1:223940555..223942413,2	K562	blood:
33	chr1:223931292..223932836-chr1:224033167..224035727,2	K562	blood:
34	chr1:223900092..223902158-chr1:223929992..223931627,2	K562	blood:
35	chr1:223887852..223890245-chr1:223935483..223937346,2	MCF-7	breast:
36	chr1:223902474..223903675-chr1:223936616..223937446,3	MCF-7	breast:
37	chr1:223899613..223901021-chr1:223936548..223937320,7	MCF-7	breast:
38	chr1:223937021..223937991-chr1:223946905..223947482,2	K562	blood:
39	chr1:223897059..223902247-chr1:223935403..223939761,6	K562	blood:
40	chr1:223900402..223903093-chr1:223939885..223943104,3	K562	blood:
41	chr1:223888227..223888814-chr1:223936381..223937102,2	MCF-7	breast:
42	chr1:223931041..223933395-chr1:223937050..223938620,2	K562	blood:
43	chr1:223925259..223927259-chr1:223937310..223938830,2	K562	blood:
44	chr1:223885792..223886704-chr1:223936418..223937470,7	MCF-7	breast:
45	chr1:223901725..223903941-chr1:223941728..223943865,2	MCF-7	breast:

No data

Variant related genes	Relation type
CAPN2	TF binding region
CAPN2	CpG island
ENSG00000162909	chromatin interactions
ENSG00000143514	chromatin interactions

Extended variants
information (count: 698 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1222138	chr1:223931411-223931412	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190984603	chr1:223931450-223931451	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs151160044	chr1:223931522-223931523	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs28370049	chr1:223931626-223931627	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs28370050	chr1:223931636-223931637	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs1222137	chr1:223931648-223931649	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs116739091	chr1:223931649-223931650	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568930948	chr1:223931652-223931653	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs536911232	chr1:223931665-223931666	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs558437481	chr1:223931694-223931695	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs368336554	chr1:223931712-223931713	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534513310	chr1:223931781-223931782	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs183076282	chr1:223931785-223931786	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186794828	chr1:223931797-223931798	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs61729462	chr1:223931800-223931801	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369599821	chr1:223931862-223931863	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs372591359	chr1:223931866-223931867	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs375820403	chr1:223931867-223931868	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563242004	chr1:223931882-223931883	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139777234	chr1:223931914-223931915	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs369956165	chr1:223931930-223931931	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372469023	chr1:223931959-223931960	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs373083391	chr1:223931987-223931988	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189695844	chr1:223931991-223931992	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs530389722	chr1:223932008-223932009	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs564623437	chr1:223932045-223932046	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528824153	chr1:223932052-223932053	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550470355	chr1:223932060-223932061	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs546865639	chr1:223932084-223932085	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112239533	chr1:223932102-223932103	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs535862632	chr1:223932168-223932169	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs28370051	chr1:223932181-223932182	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201970381	chr1:223932183-223932184	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs6682412	chr1:223932185-223932186	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs571583889	chr1:223932201-223932202	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183117059	chr1:223932225-223932226	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532390596	chr1:223932226-223932227	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs1222136	chr1:223932229-223932230	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs556112273	chr1:223932235-223932236	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77992974	chr1:223932243-223932244	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6674541	chr1:223932250-223932251	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs58609178	chr1:223932305-223932306	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs565995372	chr1:223932315-223932316	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28370052	chr1:223932329-223932330	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558276851	chr1:223932337-223932338	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1222135	chr1:223932338-223932339	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs140839723	chr1:223932360-223932361	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188200210	chr1:223932365-223932366	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564146392	chr1:223932368-223932369	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs144876817	chr1:223932399-223932400	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223915400-223933000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:223915400-223933000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:223915400-223936200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr1:223915800-223931600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr1:223916600-223932600	Weak transcription	Fetal Brain Female	brain
6	chr1:223919200-223935600	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr1:223919200-223936200	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr1:223921200-223932800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr1:223921200-223936000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:223921600-223932800	Weak transcription	Liver	Liver
11	chr1:223921600-223936600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr1:223921800-223933400	Weak transcription	Brain Angular Gyrus	brain
13	chr1:223921800-223935600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:223921800-223936000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:223922200-223934600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr1:223922200-223935600	Weak transcription	Fetal Brain Male	brain
17	chr1:223922800-223931600	Weak transcription	Brain Germinal Matrix	brain
18	chr1:223922800-223934800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr1:223923000-223931800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr1:223925200-223934600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:223925400-223931800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:223925400-223931800	Weak transcription	Ovary	ovary
23	chr1:223925400-223934800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:223926800-223931600	Weak transcription	Hela-S3	cervix
25	chr1:223926800-223932800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr1:223927400-223933000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:223927600-223931600	Weak transcription	Brain Hippocampus Middle	brain
28	chr1:223927800-223931600	Weak transcription	Colon Smooth Muscle	Colon
29	chr1:223927800-223935400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
30	chr1:223928000-223932800	Weak transcription	Esophagus	oesophagus
31	chr1:223928000-223933200	Weak transcription	Psoas Muscle	Psoas
32	chr1:223928000-223935400	Weak transcription	Small Intestine	intestine
33	chr1:223928000-223935600	Weak transcription	Right Atrium	heart
34	chr1:223928000-223936400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr1:223928200-223933400	Weak transcription	K562	blood
36	chr1:223928400-223936200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr1:223928800-223931600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr1:223928800-223932000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:223929000-223931800	Weak transcription	Aorta	Aorta
40	chr1:223929000-223934800	Weak transcription	Fetal Kidney	kidney
41	chr1:223929400-223931600	Enhancers	Left Ventricle	heart
42	chr1:223929400-223932200	Genic enhancers	A549	lung
43	chr1:223929800-223931800	Genic enhancers	Muscle Satellite Cultured Cells	--
44	chr1:223929800-223935200	Weak transcription	Fetal Heart	heart
45	chr1:223930000-223931800	Weak transcription	Placenta	Placenta
46	chr1:223930000-223933000	Weak transcription	Stomach Mucosa	stomach
47	chr1:223930000-223935000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr1:223930200-223932800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr1:223930200-223934800	Strong transcription	Fetal Stomach	stomach
50	chr1:223930200-223935000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood

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