Variant report

Variant	nsv566140
Chromosome Location	chr14:105347488-105359556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:1221)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr14:105358499-105358699	K562	blood:	n/a	n/a
2	CHD1	chr14:105348520-105348722	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr14:105359253-105359389	K562	blood:	n/a	n/a
4	CTCF	chr14:105359248-105359251	K562	blood:	n/a	n/a
5	CTCF	chr14:105359300-105359450	GM12871	blood:	n/a	n/a
6	CTCF	chr14:105359200-105359350	K562	blood:	n/a	chr14:105359252-105359265
7	CTCF	chr14:105359299-105359356	K562	blood:	n/a	n/a
8	CTCF	chr14:105359220-105359370	HUVEC	blood vessel:	n/a	chr14:105359252-105359265
9	CTCF	chr14:105348240-105348390	BE2_C	brain:	n/a	n/a
10	CTCF	chr14:105359280-105359430	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr14:105359240-105359390	HCPEpiC	choroid plexus:	n/a	chr14:105359252-105359265
12	CTCF	chr14:105351775-105351837	GM12891	blood:	n/a	n/a
13	CTCF	chr14:105359260-105359394	GM12891	blood:	n/a	n/a
14	CTCF	chr14:105356572-105356620	GM20000	blood:	n/a	n/a
15	CTCF	chr14:105359339-105359347	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr14:105359260-105359410	NB4	blood:	n/a	n/a
17	CTCF	chr14:105357228-105357249	GM19239	blood:	n/a	n/a
18	CTCF	chr14:105359291-105359370	H1-hESC	embryonic stem cell:	n/a	n/a
19	EGR1	chr14:105350955-105351130	K562	blood:	n/a	n/a
20	EGR1	chr14:105357086-105357555	K562	blood:	n/a	n/a
21	EGR1	chr14:105351246-105351530	K562	blood:	n/a	n/a
22	EGR1	chr14:105356650-105357085	K562	blood:	n/a	n/a
23	ELF1	chr14:105355220-105355668	GM12878	blood:	n/a	n/a
24	FOXA1	chr14:105348707-105348990	T-47D	breast:	n/a	n/a
25	GATA3	chr14:105348440-105348697	MCF-7	breast:	n/a	n/a
26	HMGN3	chr14:105358476-105358669	K562	blood:	n/a	n/a
27	HMGN3	chr14:105348889-105349103	K562	blood:	n/a	n/a
28	JUND	chr14:105348545-105348933	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr14:105348158-105348339	NB4	blood:	n/a	chr14:105348200-105348210 chr14:105348240-105348250
30	MAZ	chr14:105348624-105348972	K562	blood:	n/a	n/a
31	MAZ	chr14:105348744-105349002	Hela-S3	cervix:	n/a	n/a
32	MAZ	chr14:105359096-105359343	K562	blood:	n/a	n/a
33	MXI1	chr14:105347438-105349130	SK-N-SH	brain:	n/a	n/a
34	MYC	chr14:105349732-105349740	MCF-7	breast:	n/a	n/a
35	MYC	chr14:105348213-105348215	NB4	blood:	n/a	n/a
36	MYC	chr14:105348861-105348874	MCF-7	breast:	n/a	n/a
37	NANOG	chr14:105348672-105348978	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr14:105355795-105356278	K562	blood:	n/a	n/a
39	POLR2A	chr14:105356576-105356748	ProgFib	skin:	n/a	n/a
40	POLR2A	chr14:105358846-105358891	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr14:105358802-105358814	HepG2	liver:	n/a	n/a
42	POLR2A	chr14:105354436-105354577	K562	blood:	n/a	n/a
43	POLR2A	chr14:105358747-105358791	HepG2	liver:	n/a	n/a
44	POLR2A	chr14:105357493-105360907	K562	blood:	n/a	n/a
45	POLR2A	chr14:105359238-105359511	K562	blood:	n/a	n/a
46	POLR2A	chr14:105359170-105359189	K562	blood:	n/a	n/a
47	POLR2A	chr14:105354776-105355448	K562	blood:	n/a	n/a
48	POLR2A	chr14:105359059-105359077	K562	blood:	n/a	n/a
49	POLR2A	chr14:105359234-105359437	K562	blood:	n/a	n/a
50	POLR2A	chr14:105358817-105360627	K562	blood:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105349776-105349826	SKMC	muscle:	n/a
2	chr14:105349776-105349826	SKMC	muscle:	n/a
3	chr14:105350697-105350747	HL-60	blood:	n/a
4	chr14:105352845-105352895	SKMC	muscle:	n/a
5	chr14:105349455-105349505	GM19239	blood:	n/a
6	chr14:105349455-105349505	PFSK-1	brain:	n/a
7	chr14:105350290-105350340	Hela-S3	cervix:	n/a
8	chr14:105350290-105350340	BE2_C	brain:	n/a
9	chr14:105354267-105354317	HepG2	liver:	n/a
10	chr14:105356083-105356133	HCPEpiC	choroid plexus:	n/a
11	chr14:105355938-105355988	Caco-2	colon:	n/a
12	chr14:105347803-105347853	AG04449	skin:	fetal
13	chr14:105357477-105357527	H1-hESC	embryonic stem cell:	embryo
14	chr14:105355938-105355988	CMK	blood:	n/a
15	chr14:105354267-105354317	T-47D	breast:	n/a
16	chr14:105349455-105349505	Jurkat	blood:	n/a
17	chr14:105350432-105350482	T-47D	breast:	n/a
18	chr14:105350915-105350965	H1-hESC	embryonic stem cell:	embryo
19	chr14:105354267-105354317	NHBE	bronchial:	n/a
20	chr14:105356083-105356133	NHBE	bronchial:	n/a
21	chr14:105349455-105349505	IMR90	lung:	fetal
22	chr14:105354889-105354939	Caco-2	colon:	n/a
23	chr14:105354889-105354939	LNCaP	prostate:	n/a
24	chr14:105354267-105354317	SAEC	small airway:	n/a
25	chr14:105350290-105350340	H1-hESC	embryonic stem cell:	embryo
26	chr14:105350432-105350482	HRPEpiC	eye:	n/a
27	chr14:105350290-105350340	NT2-D1	testis:	n/a
28	chr14:105355938-105355988	AG10803	skin:	n/a
29	chr14:105349607-105349657	K562	blood:	n/a
30	chr14:105356083-105356133	Hela-S3	cervix:	n/a
31	chr14:105355938-105355988	SKMC	muscle:	n/a
32	chr14:105352845-105352895	HL-60	blood:	n/a
33	chr14:105350432-105350482	HCPEpiC	choroid plexus:	n/a
34	chr14:105350432-105350482	IMR90	lung:	fetal
35	chr14:105352634-105352684	AG10803	skin:	n/a
36	chr14:105354267-105354317	AG09319	gingival:	n/a
37	chr14:105354889-105354939	SKMC	muscle:	n/a
38	chr14:105349776-105349826	Hela-S3	cervix:	n/a
39	chr14:105350697-105350747	AG10803	skin:	n/a
40	chr14:105357477-105357527	PFSK-1	brain:	n/a
41	chr14:105349455-105349505	SKMC	muscle:	n/a
42	chr14:105349776-105349826	HCF	heart:	n/a
43	chr14:105352634-105352684	Hepatocyte	liver:	n/a
44	chr14:105349607-105349657	AG09319	gingival:	n/a
45	chr14:105352884-105352934	HEK293	kidney:	embryo
46	chr14:105350697-105350747	K562	blood:	n/a
47	chr14:105358567-105358617	RPTEC	kidney:	n/a
48	chr14:105352884-105352934	HRE	kidney:	n/a
49	chr14:105356083-105356133	GM12878	blood:	n/a
50	chr14:105352634-105352684	GM06990	blood:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105348765..105350400-chr14:105351876..105353640,2	MCF-7	breast:
2	chr14:105219031..105220671-chr14:105346376..105348521,2	MCF-7	breast:
3	chr14:105330091..105337184-chr14:105346220..105351503,12	MCF-7	breast:
4	chr14:105347472..105352873-chr14:105360965..105365202,8	MCF-7	breast:
5	chr14:105349215..105352197-chr14:105846638..105849114,2	K562	blood:
6	chr14:105348429..105351330-chr14:105352853..105355749,4	MCF-7	breast:
7	chr14:105353091..105355273-chr14:105361625..105363258,2	K562	blood:
8	chr14:105347000..105348818-chr14:105354613..105356174,2	K562	blood:
9	chr14:105232900..105235354-chr14:105346063..105347686,2	K562	blood:
10	chr14:105279959..105283279-chr14:105346411..105348850,3	MCF-7	breast:
11	chr14:105348765..105350400-chr14:105351876..105353640,2	MCF-7	breast:
12	chr14:105340925..105344300-chr14:105357578..105360032,4	MCF-7	breast:
13	chr14:105348429..105351330-chr14:105352853..105355749,4	MCF-7	breast:
14	chr14:105347470..105350764-chr14:105354861..105357572,3	MCF-7	breast:
15	chr14:105347000..105348818-chr14:105354613..105356174,2	K562	blood:
16	chr14:105348832..105350459-chr14:105350760..105352328,2	K562	blood:
17	chr14:105348832..105350459-chr14:105350760..105352328,2	K562	blood:
18	chr14:105271769..105274271-chr14:105354431..105356106,2	MCF-7	breast:
19	chr14:105354054..105356669-chr14:105361595..105363882,2	MCF-7	breast:
20	chr14:105359445..105362307-chr14:105370488..105372774,2	MCF-7	breast:
21	chr14:105346924..105348500-chr14:105353592..105356174,2	K562	blood:
22	chr14:105350985..105352976-chr14:105358068..105360801,2	K562	blood:
23	chr14:105347470..105350764-chr14:105354861..105357572,3	MCF-7	breast:
24	chr14:105346924..105348500-chr14:105353592..105356174,2	K562	blood:
25	chr14:105329866..105333084-chr14:105347618..105350775,5	MCF-7	breast:
26	chr14:105247569..105249557-chr14:105347096..105349716,2	K562	blood:
27	chr14:105337782..105339687-chr14:105357084..105359181,2	MCF-7	breast:
28	chr14:105358507..105360165-chr14:105487372..105489405,2	K562	blood:
29	chr14:105343975..105346931-chr14:105350690..105354607,3	K562	blood:
30	chr14:105349366..105351471-chr14:105398354..105401032,2	MCF-7	breast:
31	chr14:105351476..105354651-chr14:105359301..105361618,3	K562	blood:
32	chr14:105345637..105347359-chr14:105353237..105355891,2	MCF-7	breast:
33	chr14:105353151..105355417-chr14:105358751..105361227,2	K562	blood:
34	chr14:105346758..105349135-chr14:105488164..105490065,2	MCF-7	breast:

No data

Variant related genes	Relation type
CEP170B	TF binding region
CEP170B	CpG island
ENSG00000099814	chromatin interactions
ENSG00000184990	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000166428	chromatin interactions
ENSG00000259067	chromatin interactions
ENSG00000179364	chromatin interactions

Extended variants
information (count: 724 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2582558	chr14:105347488-105347489	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533827198	chr14:105347509-105347510	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs536562380	chr14:105347534-105347535	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs192304144	chr14:105347545-105347546	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553506872	chr14:105347554-105347555	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs566953269	chr14:105347558-105347559	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576806998	chr14:105347618-105347619	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs539406388	chr14:105347637-105347638	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559017696	chr14:105347644-105347645	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574844396	chr14:105347676-105347677	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs118083700	chr14:105347688-105347689	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs113295573	chr14:105347714-105347715	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561102665	chr14:105347754-105347755	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs187927239	chr14:105347812-105347813	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs111860167	chr14:105347837-105347838	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191363179	chr14:105347851-105347852	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs143073561	chr14:105347853-105347854	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs546157192	chr14:105347854-105347855	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184278931	chr14:105347906-105347907	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558219809	chr14:105347940-105347941	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187143823	chr14:105347950-105347951	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs568310464	chr14:105347963-105347964	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs192321121	chr14:105347964-105347965	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs527475121	chr14:105347995-105347996	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs4983391	chr14:105348013-105348014	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs77494727	chr14:105348018-105348019	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs556087584	chr14:105348020-105348021	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs4983392	chr14:105348021-105348022	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs4983393	chr14:105348039-105348040	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2582557	chr14:105348051-105348052	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs560253315	chr14:105348061-105348062	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs574731382	chr14:105348154-105348155	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs72700183	chr14:105348160-105348161	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546026466	chr14:105348168-105348169	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554002937	chr14:105348195-105348196	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs577233211	chr14:105348207-105348208	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs545888357	chr14:105348215-105348216	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562825549	chr14:105348216-105348217	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs531735803	chr14:105348218-105348219	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185324654	chr14:105348223-105348224	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs561950130	chr14:105348231-105348232	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147459934	chr14:105348247-105348248	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs148496061	chr14:105348257-105348258	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570467371	chr14:105348258-105348259	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs370237946	chr14:105348259-105348260	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200558464	chr14:105348270-105348271	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs72700184	chr14:105348271-105348272	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569357517	chr14:105348285-105348286	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs61323993	chr14:105348334-105348335	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs72700185	chr14:105348338-105348339	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD

Chromatin state (count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105333400-105349200	Weak transcription	Small Intestine	intestine
2	chr14:105334200-105351600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:105334400-105348600	Weak transcription	Fetal Brain Male	brain
4	chr14:105339400-105348600	Weak transcription	Fetal Kidney	kidney
5	chr14:105339400-105356400	Strong transcription	Fetal Intestine Small	intestine
6	chr14:105339600-105353400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr14:105339600-105363000	Weak transcription	NH-A	brain
8	chr14:105340000-105353200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:105340000-105357200	Weak transcription	NHDF-Ad	bronchial
10	chr14:105340000-105363600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr14:105340800-105348800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:105340800-105349000	Weak transcription	Stomach Mucosa	stomach
13	chr14:105341200-105350400	Strong transcription	NHLF	lung
14	chr14:105341600-105348200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr14:105342200-105348400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr14:105342400-105348000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:105342400-105348400	Strong transcription	NHEK	skin
18	chr14:105342800-105349400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr14:105342800-105356000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:105342800-105356200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr14:105343000-105347800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:105343000-105356000	Strong transcription	Fetal Intestine Large	intestine
23	chr14:105343000-105356200	Strong transcription	Fetal Brain Female	brain
24	chr14:105343200-105348200	Strong transcription	Gastric	stomach
25	chr14:105343200-105348800	Strong transcription	Rectal Mucosa Donor 29	rectum
26	chr14:105343200-105351800	Weak transcription	Hela-S3	cervix
27	chr14:105343400-105347600	Strong transcription	Adipose Nuclei	Adipose
28	chr14:105343400-105347600	Strong transcription	HMEC	breast
29	chr14:105343400-105348200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr14:105343400-105348400	Strong transcription	Placenta Amnion	Placenta Amnion
31	chr14:105343400-105350600	Strong transcription	Duodenum Mucosa	Duodenum
32	chr14:105343400-105355600	Strong transcription	Colonic Mucosa	Colon
33	chr14:105343600-105347600	Strong transcription	Brain Germinal Matrix	brain
34	chr14:105343600-105350600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr14:105343600-105350600	Strong transcription	Stomach Smooth Muscle	stomach
36	chr14:105343600-105356200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr14:105343800-105356200	Strong transcription	Lung	lung
38	chr14:105344200-105348000	Strong transcription	Aorta	Aorta
39	chr14:105344200-105348200	Strong transcription	Liver	Liver
40	chr14:105344200-105348400	Strong transcription	Sigmoid Colon	Sigmoid Colon
41	chr14:105344200-105356000	Strong transcription	Pancreas	Pancrea
42	chr14:105344400-105347600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr14:105344400-105350400	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr14:105345000-105348200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:105345000-105349200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:105345000-105353200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr14:105345800-105349400	Weak transcription	Osteobl	bone
48	chr14:105346000-105348000	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr14:105346600-105347600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:105346600-105347600	Genic enhancers	HSMM	muscle

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