Variant report

Variant	nsv524627
Chromosome Location	chr12:65082330-65091031
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:65088130-65088354	K562	blood:	n/a	n/a
2	ARID3A	chr12:65089997-65090224	HepG2	liver:	n/a	n/a
3	ATF2	chr12:65085269-65085765	GM12878	blood:	n/a	n/a
4	ATF2	chr12:65085160-65085810	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:65085069-65085805	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:65090526-65090697	K562	blood:	n/a	n/a
7	BCL3	chr12:65083316-65083543	GM12878	blood:	n/a	n/a
8	BHLHE40	chr12:65087958-65088164	K562	blood:	n/a	n/a
9	CEBPB	chr12:65087157-65087413	K562	blood:	n/a	n/a
10	CEBPB	chr12:65087208-65087399	A549	lung:	n/a	n/a
11	CHD1	chr12:65085294-65085720	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr12:65085184-65085674	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr12:65090320-65090470	GM06990	blood:	n/a	n/a
14	CTCF	chr12:65090300-65090450	HVMF	connective:	n/a	chr12:65090311-65090332
15	CTCF	chr12:65090240-65090390	Hela-S3	cervix:	n/a	chr12:65090311-65090332
16	CTCF	chr12:65090273-65090402	SK-N-SH_RA	brain:	n/a	chr12:65090311-65090332
17	CTCF	chr12:65088584-65088681	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr12:65090320-65090470	K562	blood:	n/a	n/a
19	CTCF	chr12:65090025-65090651	HCT-116	colon:	n/a	chr12:65090311-65090332
20	CTCF	chr12:65090240-65090390	HepG2	liver:	n/a	chr12:65090311-65090332
21	CTCF	chr12:65090260-65090410	AG04449	skin:	n/a	chr12:65090311-65090332
22	CTCF	chr12:65090300-65090450	RPTEC	kidney:	n/a	chr12:65090311-65090332
23	CTCF	chr12:65090260-65090410	AoAF	blood vessel:	n/a	chr12:65090311-65090332
24	CTCF	chr12:65090260-65090410	HRPEpiC	eye:	n/a	chr12:65090311-65090332
25	CTCF	chr12:65090260-65090410	BE2_C	brain:	n/a	chr12:65090311-65090332
26	CTCF	chr12:65090160-65090310	AG04450	lung:	n/a	n/a
27	CTCF	chr12:65090220-65090370	SAEC	small airway:	n/a	chr12:65090311-65090332
28	CTCF	chr12:65090240-65090390	HCPEpiC	choroid plexus:	n/a	chr12:65090311-65090332
29	CTCF	chr12:65090280-65090430	HRPEpiC	eye:	n/a	chr12:65090311-65090332
30	CTCF	chr12:65088520-65088670	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr12:65090294-65090431	GM12878	blood:	n/a	chr12:65090311-65090332
32	CTCF	chr12:65090232-65090398	Lung_OC	lung:	n/a	chr12:65090311-65090332
33	CTCF	chr12:65090300-65090450	HFF	foreskin:	n/a	chr12:65090311-65090332
34	CTCF	chr12:65090260-65090410	HPF	lung:	n/a	chr12:65090311-65090332
35	CTCF	chr12:65090280-65090430	AG10803	skin:	n/a	chr12:65090311-65090332
36	CTCF	chr12:65090241-65090430	Medullo	brain:	n/a	chr12:65090311-65090332
37	CTCF	chr12:65090260-65090410	HA-sp	spinal cord:	n/a	chr12:65090311-65090332
38	CTCF	chr12:65088590-65088790	GM12878	blood:	n/a	n/a
39	CTCF	chr12:65090220-65090370	HCFaa	heart:	n/a	chr12:65090311-65090332
40	CTCF	chr12:65090231-65090437	LNCaP	prostate:	n/a	chr12:65090311-65090332
41	CTCF	chr12:65090240-65090390	BJ	skin:	n/a	chr12:65090311-65090332
42	CTCF	chr12:65090220-65090370	A549	lung:	n/a	chr12:65090311-65090332
43	CTCF	chr12:65090260-65090410	MCF-7	breast:	n/a	chr12:65090311-65090332
44	CTCF	chr12:65090320-65090470	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr12:65090300-65090450	AG04449	skin:	n/a	chr12:65090311-65090332
46	CTCF	chr12:65088503-65088725	K562	blood:	n/a	n/a
47	CTCF	chr12:65088540-65088690	AG04450	lung:	n/a	n/a
48	CTCF	chr12:65090056-65090535	A549	lung:	n/a	chr12:65090311-65090332
49	CTCF	chr12:65090280-65090430	NB4	blood:	n/a	chr12:65090311-65090332
50	CTCF	chr12:65088540-65088690	HBMEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:65088718-65088768	MCF10A-Er-Src	breast:	n/a
2	chr12:65082713-65082763	GM19239	blood:	n/a
3	chr12:65088718-65088768	HUVEC	blood vessel:	n/a
4	chr12:65082713-65082763	RPTEC	kidney:	n/a
5	chr12:65088718-65088768	HPAEpiC	pulmonary alveolar:	n/a
6	chr12:65088718-65088768	AG09319	gingival:	n/a
7	chr12:65082713-65082763	GM12891	blood:	n/a
8	chr12:65082713-65082763	GM12878	blood:	n/a
9	chr12:65082713-65082763	Hepatocyte	liver:	n/a
10	chr12:65088718-65088768	HCT-116	colon:	n/a
11	chr12:65082713-65082763	AG09319	gingival:	n/a
12	chr12:65088718-65088768	IMR90	lung:	fetal
13	chr12:65082713-65082763	HCM	heart:	n/a
14	chr12:65088718-65088768	AG04450	lung:	fetal
15	chr12:65088718-65088768	ovcar-3	ovarian:	n/a
16	chr12:65082713-65082763	HIPEpiC	eye:	n/a
17	chr12:65082713-65082763	PrEC	prostate:	n/a
18	chr12:65088718-65088768	GM12891	blood:	n/a
19	chr12:65088718-65088768	GM12892	blood:	n/a
20	chr12:65088718-65088768	ECC-1	luminal epithelium:	n/a
21	chr12:65088718-65088768	Hepatocyte	liver:	n/a
22	chr12:65082713-65082763	NHBE	bronchial:	n/a
23	chr12:65088718-65088768	HRE	kidney:	n/a
24	chr12:65088718-65088768	GM12878	blood:	n/a
25	chr12:65082713-65082763	HCT-116	colon:	n/a
26	chr12:65082713-65082763	U87	brain:	n/a
27	chr12:65082713-65082763	NB4	blood:	n/a
28	chr12:65082713-65082763	ProgFib	skin:	n/a
29	chr12:65088718-65088768	HL-60	blood:	n/a
30	chr12:65088718-65088768	HRPEpiC	eye:	n/a
31	chr12:65088718-65088768	K562	blood:	n/a
32	chr12:65088718-65088768	PrEC	prostate:	n/a
33	chr12:65082713-65082763	HMEC	breast:	n/a
34	chr12:65088718-65088768	Jurkat	blood:	n/a
35	chr12:65082713-65082763	CMK	blood:	n/a
36	chr12:65088718-65088768	HCM	heart:	n/a
37	chr12:65082713-65082763	A549	lung:	n/a
38	chr12:65088718-65088768	HNPCEpiC	eye:	n/a
39	chr12:65088718-65088768	BE2_C	brain:	n/a
40	chr12:65088718-65088768	BJ	skin:	n/a
41	chr12:65082713-65082763	Caco-2	colon:	n/a
42	chr12:65082713-65082763	ECC-1	luminal epithelium:	n/a
43	chr12:65088718-65088768	LNCaP	prostate:	n/a
44	chr12:65088718-65088768	NT2-D1	testis:	n/a
45	chr12:65082713-65082763	PANC-1	pancreas:	n/a
46	chr12:65088718-65088768	SK-N-SH_RA	brain:	n/a
47	chr12:65082713-65082763	SKMC	muscle:	n/a
48	chr12:65082713-65082763	HepG2	liver:	n/a
49	chr12:65082713-65082763	HRE	kidney:	n/a
50	chr12:65082713-65082763	MCF10A-Er-Src	breast:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:65071734..65074838-chr12:65083895..65087734,4	MCF-7	breast:
2	chr12:65014921..65016651-chr12:65088874..65091449,2	MCF-7	breast:
3	chr12:65082042..65085864-chr12:65087016..65092187,5	K562	blood:
4	chr12:64942909..64943588-chr12:65088552..65089201,2	MCF-7	breast:
5	chr12:65081919..65084016-chr12:65085608..65087815,2	MCF-7	breast:
6	chr12:65001559..65004124-chr12:65084616..65086462,2	MCF-7	breast:
7	chr12:65081919..65084016-chr12:65085608..65087815,2	MCF-7	breast:
8	chr12:65018895..65020884-chr12:65086015..65088325,2	MCF-7	breast:
9	chr12:65082782..65085440-chr12:65086852..65090149,3	MCF-7	breast:
10	chr12:65002975..65007733-chr12:65085361..65090240,7	K562	blood:
11	chr12:65002182..65006670-chr12:65087134..65093452,10	MCF-7	breast:
12	chr12:65001714..65006897-chr12:65088342..65093997,11	MCF-7	breast:
13	chr12:65002305..65005095-chr12:65090588..65092916,2	K562	blood:
14	chr12:65004226..65005800-chr12:65083088..65085035,2	MCF-7	breast:
15	chr12:64943293..64944014-chr12:65088905..65089680,2	MCF-7	breast:
16	chr12:65002687..65005159-chr12:65085153..65088192,5	MCF-7	breast:
17	chr12:65082782..65085440-chr12:65086852..65090149,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNS-3	chr12:65089971-65090330	NONHSAT029160

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RASSF3	hsa-miR-124-3p	chr12:65090380-65090386
2	RASSF3	hsa-miR-18a-5p	chr12:65088837-65088859

Variant related genes	Relation type
ENSG00000268028	TF binding region
ENSG00000268028	CpG island
ENSG00000207546	chromatin interactions
ENSG00000268028	chromatin interactions
ENSG00000256670	chromatin interactions
ENSG00000153179	chromatin interactions

Extended variants
information (count: 371 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs508792	chr12:65082330-65082331	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34507087	chr12:65082407-65082408	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs562781203	chr12:65082432-65082433	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73119785	chr12:65082475-65082476	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs693179	chr12:65082484-65082485	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs564750095	chr12:65082492-65082493	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs367591850	chr12:65082509-65082510	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571791202	chr12:65082566-65082567	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs527339161	chr12:65082592-65082593	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs538992552	chr12:65082593-65082594	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192989194	chr12:65082594-65082595	Weak transcription Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139228520	chr12:65082617-65082618	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549191694	chr12:65082625-65082626	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs1690260	chr12:65082644-65082645	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs572421345	chr12:65082661-65082662	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559261170	chr12:65082662-65082663	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs150012298	chr12:65082679-65082680	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376715855	chr12:65082687-65082688	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571562890	chr12:65082706-65082707	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147691181	chr12:65082726-65082727	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs1690261	chr12:65082738-65082739	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs12832292	chr12:65082765-65082766	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs536436196	chr12:65082766-65082767	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75857175	chr12:65082767-65082768	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs562398785	chr12:65082777-65082778	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs576259119	chr12:65082798-65082799	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544978667	chr12:65082799-65082800	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112159224	chr12:65082863-65082864	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs571697908	chr12:65082877-65082878	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540670373	chr12:65082889-65082890	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560626231	chr12:65082940-65082941	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377037669	chr12:65082986-65082987	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs117947873	chr12:65082987-65082988	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111761430	chr12:65083000-65083001	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34526895	chr12:65083001-65083002	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143445590	chr12:65083010-65083011	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs76448737	chr12:65083023-65083024	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs10688391	chr12:65083026-65083027	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78944443	chr12:65083045-65083046	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184881608	chr12:65083047-65083048	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562958666	chr12:65083099-65083100	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs74764260	chr12:65083116-65083117	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs551781078	chr12:65083130-65083131	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs144803223	chr12:65083168-65083169	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534163730	chr12:65083172-65083173	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547847962	chr12:65083177-65083178	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567729961	chr12:65083228-65083229	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188371145	chr12:65083237-65083238	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs147966708	chr12:65083272-65083273	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576167181	chr12:65083297-65083298	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:65068400-65087200	Weak transcription	Liver	Liver
2	chr12:65070000-65085200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr12:65070000-65092400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:65075000-65108400	Weak transcription	NH-A	brain
5	chr12:65075200-65087400	Weak transcription	HMEC	breast
6	chr12:65075400-65088600	Weak transcription	Esophagus	oesophagus
7	chr12:65077000-65085000	Weak transcription	Hela-S3	cervix
8	chr12:65077000-65086800	Weak transcription	Osteobl	bone
9	chr12:65077000-65091800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr12:65077200-65082600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr12:65077200-65085000	Weak transcription	Fetal Kidney	kidney
12	chr12:65077200-65088200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr12:65077200-65088600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr12:65077200-65091800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr12:65077200-65106800	Weak transcription	Brain Hippocampus Middle	brain
16	chr12:65077400-65085200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:65077400-65088600	Weak transcription	Ovary	ovary
18	chr12:65077400-65091800	Weak transcription	Brain Anterior Caudate	brain
19	chr12:65077400-65114800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:65077600-65091800	Weak transcription	Brain Substantia Nigra	brain
21	chr12:65078200-65083000	Strong transcription	Fetal Intestine Small	intestine
22	chr12:65078400-65083000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:65078400-65083400	Strong transcription	GM12878-XiMat	blood
24	chr12:65078400-65083600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr12:65078400-65084400	Strong transcription	Fetal Muscle Trunk	muscle
26	chr12:65078600-65088600	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr12:65078600-65089200	Strong transcription	Primary B cells from peripheral blood	blood
28	chr12:65078600-65092200	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr12:65078800-65092400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
30	chr12:65079000-65082800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr12:65079000-65083000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr12:65079000-65083400	Strong transcription	Fetal Intestine Large	intestine
33	chr12:65079000-65083400	Strong transcription	Dnd41	blood
34	chr12:65079000-65092000	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr12:65079200-65083600	Genic enhancers	Primary T cells from cord blood	blood
36	chr12:65079200-65091600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
37	chr12:65079200-65092200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr12:65079800-65082400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr12:65079800-65087800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr12:65080000-65113600	Weak transcription	Colonic Mucosa	Colon
41	chr12:65080200-65085600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr12:65080800-65082800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr12:65080800-65082800	Genic enhancers	Fetal Muscle Leg	muscle
44	chr12:65081000-65082600	Genic enhancers	Primary B cells from cord blood	blood
45	chr12:65081000-65082600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr12:65081000-65082800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
47	chr12:65081200-65082400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:65081200-65082400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr12:65081200-65082400	Enhancers	HSMM	muscle
50	chr12:65081200-65082400	Enhancers	NHDF-Ad	bronchial

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