Variant report

Variant	esv1798974
Chromosome Location	chr3:133949713-133973731
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:133961597-133961797	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:133969629-133969983	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:133969054-133969120	HepG2	liver:	n/a	n/a
4	BACH1	chr3:133969712-133970099	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr3:133969581-133969850	GM12878	blood:	n/a	chr3:133969655-133969671 chr3:133969583-133969599
6	BHLHE40	chr3:133969724-133969911	K562	blood:	n/a	n/a
7	BHLHE40	chr3:133958649-133958694	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:133968690-133969026	GM12878	blood:	n/a	n/a
9	BRCA1	chr3:133969220-133969279	HepG2	liver:	n/a	n/a
10	BRCA1	chr3:133956176-133956180	H1-hESC	embryonic stem cell:	n/a	n/a
11	BRCA1	chr3:133969713-133970025	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr3:133965512-133965818	K562	blood:	n/a	n/a
13	CCNT2	chr3:133968957-133970062	K562	blood:	n/a	chr3:133969152-133969161
14	CCNT2	chr3:133950007-133950220	K562	blood:	n/a	n/a
15	CEBPB	chr3:133970585-133970828	A549	lung:	n/a	n/a
16	CEBPB	chr3:133970621-133971116	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:133969792-133970177	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:133969880-133970152	K562	blood:	n/a	n/a
19	CEBPB	chr3:133970534-133970850	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:133961540-133961929	A549	lung:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
21	CEBPB	chr3:133961473-133962019	MCF-7	breast:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
22	CEBPB	chr3:133961514-133961945	IMR90	lung:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
23	CEBPB	chr3:133961556-133961886	A549	lung:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
24	CEBPB	chr3:133961512-133961931	HepG2	liver:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
25	CEBPB	chr3:133961497-133962053	MCF-7	breast:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
26	CEBPB	chr3:133969603-133970155	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:133970524-133970877	K562	blood:	n/a	n/a
28	CEBPB	chr3:133950022-133950304	K562	blood:	n/a	n/a
29	CEBPB	chr3:133961537-133961923	HepG2	liver:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
30	CEBPB	chr3:133965905-133966190	A549	lung:	n/a	n/a
31	CEBPB	chr3:133969823-133970097	A549	lung:	n/a	n/a
32	CEBPB	chr3:133950032-133950354	K562	blood:	n/a	n/a
33	CEBPB	chr3:133970531-133971120	HepG2	liver:	n/a	n/a
34	CEBPB	chr3:133961255-133962088	Hela-S3	cervix:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
35	CEBPB	chr3:133961536-133961921	K562	blood:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
36	CEBPB	chr3:133969767-133970076	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr3:133961430-133961965	ECC-1	luminal epithelium:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
38	CEBPB	chr3:133961542-133961906	HepG2	liver:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
39	CEBPB	chr3:133965866-133966197	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:133961554-133961984	A549	lung:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
41	CEBPB	chr3:133969777-133970150	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr3:133961558-133961951	ECC-1	luminal epithelium:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
43	CEBPB	chr3:133969818-133970104	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:133961364-133962118	HCT-116	colon:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
45	CEBPB	chr3:133961651-133961784	K562	blood:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
46	CEBPB	chr3:133971674-133971952	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:133961327-133962201	HCT-116	colon:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
48	CEBPB	chr3:133961593-133961841	HepG2	liver:	n/a	chr3:133961725-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961736 chr3:133961727-133961738
49	CEBPB	chr3:133970544-133970756	K562	blood:	n/a	n/a
50	CEBPB	chr3:133965920-133966161	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133969591-133969641	AoSMC	blood vessel:	n/a
2	chr3:133969591-133969641	AoSMC	blood vessel:	n/a
3	chr3:133969058-133969108	H1-hESC	embryonic stem cell:	embryo
4	chr3:133962408-133962458	U87	brain:	n/a
5	chr3:133966275-133966325	SKMC	muscle:	n/a
6	chr3:133956516-133956566	T-47D	breast:	n/a
7	chr3:133968920-133968970	HMEC	breast:	n/a
8	chr3:133969914-133969964	HCM	heart:	n/a
9	chr3:133966275-133966325	AoSMC	blood vessel:	n/a
10	chr3:133969914-133969964	PANC-1	pancreas:	n/a
11	chr3:133970158-133970208	A549	lung:	n/a
12	chr3:133968920-133968970	GM12891	blood:	n/a
13	chr3:133956516-133956566	NB4	blood:	n/a
14	chr3:133969058-133969108	AG09319	gingival:	n/a
15	chr3:133969591-133969641	NT2-D1	testis:	n/a
16	chr3:133969914-133969964	GM12878	blood:	n/a
17	chr3:133956516-133956566	ovcar-3	ovarian:	n/a
18	chr3:133966275-133966325	HMEC	breast:	n/a
19	chr3:133962408-133962458	HMEC	breast:	n/a
20	chr3:133956516-133956566	Hela-S3	cervix:	n/a
21	chr3:133970158-133970208	HL-60	blood:	n/a
22	chr3:133969058-133969108	ovcar-3	ovarian:	n/a
23	chr3:133966275-133966325	PANC-1	pancreas:	n/a
24	chr3:133970158-133970208	GM12892	blood:	n/a
25	chr3:133956516-133956566	PANC-1	pancreas:	n/a
26	chr3:133969914-133969964	NHBE	bronchial:	n/a
27	chr3:133969591-133969641	HIPEpiC	eye:	n/a
28	chr3:133966275-133966325	RPTEC	kidney:	n/a
29	chr3:133968920-133968970	Jurkat	blood:	n/a
30	chr3:133969921-133969971	Jurkat	blood:	n/a
31	chr3:133970158-133970208	CMK	blood:	n/a
32	chr3:133962408-133962458	ECC-1	luminal epithelium:	n/a
33	chr3:133969058-133969108	HEK293	kidney:	embryo
34	chr3:133970158-133970208	SKMC	muscle:	n/a
35	chr3:133969278-133969328	PANC-1	pancreas:	n/a
36	chr3:133969058-133969108	NHDF-neo	bronchial:	n/a
37	chr3:133969921-133969971	GM19239	blood:	n/a
38	chr3:133956516-133956566	U87	brain:	n/a
39	chr3:133966275-133966325	HRPEpiC	eye:	n/a
40	chr3:133966275-133966325	NHBE	bronchial:	n/a
41	chr3:133969921-133969971	Hepatocyte	liver:	n/a
42	chr3:133969914-133969964	ovcar-3	ovarian:	n/a
43	chr3:133973256-133973306	AG09309	skin:	n/a
44	chr3:133969921-133969971	NHDF-neo	bronchial:	n/a
45	chr3:133969278-133969328	GM19239	blood:	n/a
46	chr3:133969914-133969964	HCT-116	colon:	n/a
47	chr3:133973256-133973306	HIPEpiC	eye:	n/a
48	chr3:133969591-133969641	SK-N-SH	brain:	n/a
49	chr3:133962408-133962458	HCF	heart:	n/a
50	chr3:133966275-133966325	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:133959513..133961967-chr3:133961988..133964183,2	MCF-7	breast:
2	chr3:133955309..133957526-chr3:133961542..133964023,3	K562	blood:
3	chr3:133970647..133972912-chr3:133975711..133978069,2	MCF-7	breast:
4	chr3:133970945..133973560-chr3:133978440..133980451,2	MCF-7	breast:
5	chr3:22413816..22414336-chr3:133969155..133969870,2	HCT-116	colon:
6	chr3:133969851..133972992-chr3:133976680..133979913,3	K562	blood:
7	chr3:133951157..133954155-chr3:133956985..133958917,3	MCF-7	breast:
8	chr3:133954849..133956381-chr3:134017446..134019848,2	MCF-7	breast:
9	chr3:133956480..133959518-chr3:133968010..133971200,3	MCF-7	breast:
10	chr3:133967562..133971327-chr3:134067822..134072418,4	MCF-7	breast:
11	chr3:133969854..133971498-chr3:134203715..134206373,2	K562	blood:
12	chr3:133969091..133969747-chr7:35839773..35840580,2	Hela-S3	cervix:
13	chr12:102091137..102092560-chr3:133969061..133970004,4	Hela-S3	cervix:
14	chr12:15942011..15942548-chr3:133969611..133970273,2	Hela-S3	cervix:
15	chr3:133958163..133961151-chr3:133961211..133962762,2	K562	blood:
16	chr3:133961848..133963508-chr3:133970974..133972912,2	K562	blood:
17	chr3:133966207..133969204-chr3:134075829..134077344,2	MCF-7	breast:
18	chr3:133969194..133969719-chr3:136470769..136471350,2	Hela-S3	cervix:
19	chr3:133946454..133948337-chr3:133962958..133965127,2	K562	blood:
20	chr3:133925826..133929174-chr3:133972868..133975223,3	MCF-7	breast:
21	chr3:133952476..133954777-chr3:133957594..133959346,2	K562	blood:
22	chr19:10206614..10207226-chr3:133969204..133969782,2	NB4	blood:
23	chr3:133968058..133969986-chr3:134093152..134094854,2	MCF-7	breast:
24	chr3:133967100..133970573-chr3:133973529..133976629,4	MCF-7	breast:
25	chr3:133959235..133962152-chr3:133965404..133967966,3	K562	blood:
26	chr3:133958163..133961151-chr3:133961211..133962762,2	K562	blood:
27	chr3:133959513..133961967-chr3:133961988..133964183,2	MCF-7	breast:
28	chr3:133969328..133972317-chr3:134030794..134032589,3	MCF-7	breast:
29	chr3:133961848..133963508-chr3:133970974..133972912,2	K562	blood:
30	chr3:133959235..133962152-chr3:133965404..133967966,3	K562	blood:
31	chr3:133960747..133964572-chr3:133967986..133970740,5	MCF-7	breast:
32	chr3:133952476..133954777-chr3:133957594..133959346,2	K562	blood:
33	chr3:133948864..133950989-chr3:133968171..133969773,2	MCF-7	breast:
34	chr3:133970115..133972265-chr3:133986843..133989271,2	MCF-7	breast:
35	chr3:133966982..133969357-chr3:134203200..134205519,3	MCF-7	breast:
36	chr3:133951157..133954155-chr3:133956985..133958917,3	MCF-7	breast:
37	chr3:133955309..133957526-chr3:133961542..133964023,3	K562	blood:
38	chr3:133969506..133971460-chr3:134202147..134204798,2	K562	blood:
39	chr3:133965027..133966647-chr3:134091891..134094278,2	MCF-7	breast:
40	chr3:133971742..133973681-chr3:133989273..133991521,2	MCF-7	breast:

Variant related genes	Relation type
RYK	TF binding region
RYK	CpG island
ENSG00000260633	chromatin interactions
ENSG00000163785	chromatin interactions
ENSG00000228878	chromatin interactions
ENSG00000111666	chromatin interactions
ENSG00000118007	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000130812	chromatin interactions
ENSG00000129055	chromatin interactions
ENSG00000151789	chromatin interactions
ENSG00000214289	chromatin interactions
ENSG00000151491	chromatin interactions
ENSG00000114019	chromatin interactions
ENSG00000182923	chromatin interactions
ENSG00000240006	chromatin interactions

Extended variants
information (count: 864 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4339087	chr3:133949713-133949714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538899600	chr3:133949714-133949715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs149791558	chr3:133949723-133949724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538550360	chr3:133949768-133949769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377758966	chr3:133949775-133949776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528523124	chr3:133949794-133949795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572250166	chr3:133949837-133949838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs534849645	chr3:133949872-133949873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577871602	chr3:133949884-133949885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574959264	chr3:133949893-133949894	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7614434	chr3:133949913-133949914	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190904685	chr3:133949916-133949917	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552422128	chr3:133949969-133949970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs9809556	chr3:133949974-133949975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs376422543	chr3:133950037-133950038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547038571	chr3:133950038-133950039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs559654650	chr3:133950051-133950052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528772560	chr3:133950053-133950054	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146248074	chr3:133950070-133950071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs4295144	chr3:133950092-133950093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs76505532	chr3:133950106-133950107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139332091	chr3:133950132-133950133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144094195	chr3:133950134-133950135	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538659628	chr3:133950136-133950137	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4312630	chr3:133950150-133950151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529129720	chr3:133950152-133950153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552487891	chr3:133950214-133950215	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146528941	chr3:133950290-133950291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557801938	chr3:133950422-133950423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs149100371	chr3:133950516-133950517	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371768863	chr3:133950644-133950645	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs568285101	chr3:133950662-133950663	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537145653	chr3:133950689-133950690	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs142062431	chr3:133950716-133950717	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs565857383	chr3:133950745-133950746	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs151135506	chr3:133950757-133950758	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545754320	chr3:133950779-133950780	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552968127	chr3:133950832-133950833	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs573152000	chr3:133950834-133950835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs542125019	chr3:133950908-133950909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs542829286	chr3:133950918-133950919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561938079	chr3:133951023-133951024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140211641	chr3:133951031-133951032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562205676	chr3:133951039-133951040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543131760	chr3:133951075-133951076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563435037	chr3:133951096-133951097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146966039	chr3:133951103-133951104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116729874	chr3:133951152-133951153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199999503	chr3:133951159-133951160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534323830	chr3:133951217-133951218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133877800-133950200	Weak transcription	Small Intestine	intestine
2	chr3:133895000-133950000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:133895000-133950200	Weak transcription	Gastric	stomach
4	chr3:133919000-133950600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:133920800-133950200	Weak transcription	Aorta	Aorta
6	chr3:133920800-133950200	Weak transcription	Spleen	Spleen
7	chr3:133920800-133950600	Weak transcription	Hela-S3	cervix
8	chr3:133930000-133950000	Weak transcription	NHDF-Ad	bronchial
9	chr3:133930000-133950400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:133930000-133954600	Weak transcription	Brain Cingulate Gyrus	brain
11	chr3:133930200-133950000	Weak transcription	HSMM	muscle
12	chr3:133930200-133950200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr3:133930200-133950600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr3:133930200-133955000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr3:133930200-133968000	Weak transcription	Fetal Kidney	kidney
16	chr3:133930400-133950200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr3:133930600-133957800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr3:133931400-133950200	Weak transcription	Dnd41	blood
19	chr3:133932400-133951000	Weak transcription	NHLF	lung
20	chr3:133933600-133950000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:133934600-133950400	Weak transcription	Brain Hippocampus Middle	brain
22	chr3:133935400-133954600	Weak transcription	HUVEC	blood vessel
23	chr3:133938400-133950000	Weak transcription	Primary T cells from cord blood	blood
24	chr3:133938400-133950000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:133938800-133955200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:133939000-133949800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:133939000-133950000	Weak transcription	HSMMtube	muscle
28	chr3:133941000-133950200	Weak transcription	Primary B cells from peripheral blood	blood
29	chr3:133941000-133954600	Weak transcription	Duodenum Mucosa	Duodenum
30	chr3:133941000-133954800	Weak transcription	Fetal Intestine Large	intestine
31	chr3:133941000-133961600	Weak transcription	Esophagus	oesophagus
32	chr3:133941200-133950200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:133941200-133950200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr3:133941200-133950400	Weak transcription	Placenta	Placenta
35	chr3:133941400-133950000	Weak transcription	Thymus	Thymus
36	chr3:133941400-133950800	Weak transcription	HepG2	liver
37	chr3:133941400-133957200	Weak transcription	Fetal Stomach	stomach
38	chr3:133941400-133967400	Weak transcription	Fetal Muscle Leg	muscle
39	chr3:133942000-133951000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr3:133942000-133952600	Weak transcription	Brain Angular Gyrus	brain
41	chr3:133943000-133950800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr3:133943200-133954600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:133943400-133950200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr3:133943400-133950200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr3:133943400-133950200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr3:133943400-133950200	Weak transcription	Colon Smooth Muscle	Colon
47	chr3:133943400-133950400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr3:133943400-133950400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr3:133943400-133961800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr3:133943600-133950200	Weak transcription	Primary T cells fromperipheralblood	blood

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