Variant report

Variant	nsv555444
Chromosome Location	chr11:74200739-74221170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:708)
CpG islands
(count:734)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:74216773-74216973	K562	blood:	n/a	n/a
2	ARID3A	chr11:74215901-74216250	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:74204029-74204748	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:74204099-74204316	K562	blood:	n/a	n/a
5	ARID3A	chr11:74204983-74205036	K562	blood:	n/a	n/a
6	ATF1	chr11:74208008-74208186	K562	blood:	n/a	n/a
7	ATF1	chr11:74204083-74204482	K562	blood:	n/a	n/a
8	ATF2	chr11:74203903-74204454	GM12878	blood:	n/a	n/a
9	ATF3	chr11:74216010-74216336	K562	blood:	n/a	n/a
10	ATF3	chr11:74204217-74204573	A549	lung:	n/a	chr11:74204218-74204227
11	ATF3	chr11:74204088-74204706	K562	blood:	n/a	chr11:74204218-74204227
12	ATF3	chr11:74204133-74204626	A549	lung:	n/a	chr11:74204218-74204227
13	BACH1	chr11:74204020-74205247	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr11:74203802-74204331	A549	lung:	n/a	chr11:74204218-74204231
15	BCL3	chr11:74203866-74204879	A549	lung:	n/a	chr11:74204218-74204231
16	BCLAF1	chr11:74204065-74204612	GM12878	blood:	n/a	chr11:74204218-74204231
17	BHLHE40	chr11:74216577-74216764	K562	blood:	n/a	n/a
18	BHLHE40	chr11:74204099-74205115	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:74204074-74204921	K562	blood:	n/a	n/a
20	BRCA1	chr11:74204012-74204159	HepG2	liver:	n/a	n/a
21	BRCA1	chr11:74204639-74204901	HepG2	liver:	n/a	n/a
22	BRCA1	chr11:74204032-74204904	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr11:74213705-74214089	K562	blood:	n/a	n/a
24	CBX3	chr11:74215836-74216400	K562	blood:	n/a	n/a
25	CBX3	chr11:74203927-74204814	K562	blood:	n/a	n/a
26	CCNT2	chr11:74204008-74204925	K562	blood:	n/a	chr11:74204218-74204227
27	CEBPB	chr11:74203801-74205280	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:74203981-74204586	MCF-7	breast:	n/a	n/a
29	CEBPB	chr11:74214067-74214330	HepG2	liver:	n/a	chr11:74214200-74214211 chr11:74214202-74214211
30	CEBPB	chr11:74214029-74214245	A549	lung:	n/a	chr11:74214200-74214211 chr11:74214202-74214211
31	CEBPB	chr11:74204126-74204906	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:74203717-74204402	K562	blood:	n/a	n/a
33	CEBPB	chr11:74203817-74204233	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:74204172-74204919	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:74216080-74216358	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr11:74216054-74216352	A549	lung:	n/a	n/a
37	CEBPB	chr11:74203792-74204852	K562	blood:	n/a	n/a
38	CEBPB	chr11:74203900-74204894	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr11:74203874-74204385	A549	lung:	n/a	n/a
40	CEBPB	chr11:74216477-74216775	K562	blood:	n/a	n/a
41	CEBPB	chr11:74203806-74204895	A549	lung:	n/a	n/a
42	CEBPB	chr11:74214028-74214260	IMR90	lung:	n/a	chr11:74214200-74214211 chr11:74214202-74214211
43	CEBPB	chr11:74216072-74216375	IMR90	lung:	n/a	n/a
44	CEBPB	chr11:74210009-74210167	K562	blood:	n/a	n/a
45	CEBPB	chr11:74204711-74204942	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPD	chr11:74204592-74204885	HepG2	liver:	n/a	n/a
47	CEBPD	chr11:74204238-74204973	HepG2	liver:	n/a	n/a
48	CHD2	chr11:74203971-74204934	GM12878	blood:	n/a	n/a
49	CHD2	chr11:74204737-74204944	K562	blood:	n/a	n/a
50	CHD2	chr11:74204005-74205296	Hela-S3	cervix:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:74207624-74207674	RPTEC	kidney:	n/a
2	chr11:74204163-74204213	ProgFib	skin:	n/a
3	chr11:74207624-74207674	RPTEC	kidney:	n/a
4	chr11:74204163-74204213	ProgFib	skin:	n/a
5	chr11:74204613-74204663	GM12878	blood:	n/a
6	chr11:74204105-74204155	NHDF-neo	bronchial:	n/a
7	chr11:74204840-74204890	GM19239	blood:	n/a
8	chr11:74204835-74204885	HCF	heart:	n/a
9	chr11:74204835-74204885	GM12878	blood:	n/a
10	chr11:74204613-74204663	NH-A	brain:	n/a
11	chr11:74204835-74204885	HEEpiC	esophagus:	n/a
12	chr11:74204975-74205025	K562	blood:	n/a
13	chr11:74204902-74204952	SKMC	muscle:	n/a
14	chr11:74204613-74204663	Jurkat	blood:	n/a
15	chr11:74204105-74204155	HCT-116	colon:	n/a
16	chr11:74204105-74204155	HCF	heart:	n/a
17	chr11:74204163-74204213	HMEC	breast:	n/a
18	chr11:74204917-74204967	HNPCEpiC	eye:	n/a
19	chr11:74204163-74204213	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:74207624-74207674	HUVEC	blood vessel:	n/a
21	chr11:74207624-74207674	CMK	blood:	n/a
22	chr11:74204902-74204952	HEK293	kidney:	embryo
23	chr11:74204987-74205037	HIPEpiC	eye:	n/a
24	chr11:74204163-74204213	MCF-7	breast:	n/a
25	chr11:74204917-74204967	GM12892	blood:	n/a
26	chr11:74204163-74204213	NT2-D1	testis:	n/a
27	chr11:74204835-74204885	NH-A	brain:	n/a
28	chr11:74204902-74204952	ProgFib	skin:	n/a
29	chr11:74204613-74204663	SKMC	muscle:	n/a
30	chr11:74204105-74204155	GM12878	blood:	n/a
31	chr11:74204835-74204885	AG04450	lung:	fetal
32	chr11:74204163-74204213	GM12878	blood:	n/a
33	chr11:74207624-74207674	HEEpiC	esophagus:	n/a
34	chr11:74204840-74204890	HepG2	liver:	n/a
35	chr11:74204840-74204890	HL-60	blood:	n/a
36	chr11:74204338-74204388	HUVEC	blood vessel:	n/a
37	chr11:74204917-74204967	PrEC	prostate:	n/a
38	chr11:74204613-74204663	NHDF-neo	bronchial:	n/a
39	chr11:74204840-74204890	BE2_C	brain:	n/a
40	chr11:74204835-74204885	HepG2	liver:	n/a
41	chr11:74204987-74205037	ECC-1	luminal epithelium:	n/a
42	chr11:74204163-74204213	SAEC	small airway:	n/a
43	chr11:74204902-74204952	HRPEpiC	eye:	n/a
44	chr11:74204840-74204890	HMEC	breast:	n/a
45	chr11:74204835-74204885	HRE	kidney:	n/a
46	chr11:74204840-74204890	HRPEpiC	eye:	n/a
47	chr11:74204835-74204885	GM06990	blood:	n/a
48	chr11:74204338-74204388	ECC-1	luminal epithelium:	n/a
49	chr11:74204987-74205037	HAEpiC	amniotic membrane:	n/a
50	chr11:74204338-74204388	U87	brain:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:74203316..74206013-chr11:74301160..74305311,5	MCF-7	breast:
2	chr11:74175244..74178880-chr11:74203216..74205739,4	MCF-7	breast:
3	chr11:74203931..74204800-chr22:40742102..40742878,2	NB4	blood:
4	chr1:145382677..145383294-chr11:74204286..74204811,2	Hela-S3	cervix:
5	chr1:17222169..17223164-chr11:74203977..74204800,2	HCT-116	colon:
6	chr11:74212022..74214778-chr11:74214834..74217303,2	K562	blood:
7	chr11:74196620..74198242-chr11:74204138..74205722,2	K562	blood:
8	chr11:74185351..74193647-chr11:74202565..74206845,12	MCF-7	breast:
9	chr11:74202987..74205917-chr11:75525143..75527102,2	MCF-7	breast:
10	chr11:74200976..74203933-chr11:74257256..74259577,2	MCF-7	breast:
11	chr11:74204220..74206114-chr11:74206623..74210457,3	MCF-7	breast:
12	chr11:74204283..74204932-chr13:48611614..48612146,2	Hela-S3	cervix:
13	chr11:74175411..74179003-chr11:74201966..74206100,6	MCF-7	breast:
14	chr11:74203221..74207585-chr11:74212498..74217761,7	K562	blood:
15	chr10:126106993..126107608-chr11:74204160..74204849,2	Hela-S3	cervix:
16	chr11:74204457..74206567-chr11:74218836..74220561,2	MCF-7	breast:
17	chr11:74204273..74205120-chr12:108955828..108956400,2	Hela-S3	cervix:
18	chr11:74204304..74205190-chr11:78285459..78286026,2	Hela-S3	cervix:
19	chr11:74203709..74204682-chr11:75526078..75526626,2	Hela-S3	cervix:
20	chr11:74202077..74207497-chr11:74219080..74223707,5	MCF-7	breast:
21	chr11:74176347..74178704-chr11:74203526..74206053,3	K562	blood:
22	chr11:74196733..74198968-chr11:74202003..74205722,4	K562	blood:
23	chr11:74171843..74173907-chr11:74203180..74205587,3	MCF-7	breast:
24	chr11:74204313..74206449-chr16:3506549..3509156,2	MCF-7	breast:
25	chr11:74204211..74205020-chr16:74734088..74734697,2	Hela-S3	cervix:
26	chr11:74199497..74201596-chr11:74201884..74204811,3	K562	blood:
27	chr11:74202594..74206347-chr11:74211663..74216525,7	K562	blood:
28	chr11:74204361..74206263-chr11:74214624..74217236,3	MCF-7	breast:
29	chr11:74212022..74214778-chr11:74214834..74217303,2	K562	blood:
30	chr11:74164577..74165120-chr11:74214878..74215449,2	MCF-7	breast:
31	chr11:74204339..74204947-chr12:7052537..7053170,2	Hela-S3	cervix:
32	chr11:74202819..74206685-chr11:74211078..74218962,13	MCF-7	breast:
33	chr11:74172990..74175155-chr11:74199456..74202165,2	K562	blood:
34	chr11:74204419..74204973-chr6:123110245..123110887,2	Hela-S3	cervix:
35	chr1:185286539..185287111-chr11:74204400..74204998,2	Hela-S3	cervix:
36	chr11:74203150..74205819-chr11:74301632..74306352,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000254837	TF binding region
POLD3	TF binding region
ENSG00000254974	TF binding region
LIPT2	TF binding region
ENSG00000254837	CpG island
POLD3	CpG island
ENSG00000254974	CpG island
LIPT2	CpG island
ENSG00000175536	chromatin interactions
ENSG00000077514	chromatin interactions
ENSG00000122390	chromatin interactions
ENSG00000255507	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000254974	chromatin interactions
ENSG00000136143	chromatin interactions
ENSG00000198382	chromatin interactions
ENSG00000254837	chromatin interactions
ENSG00000175538	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000065154	chromatin interactions
ENSG00000136003	chromatin interactions
ENSG00000273004	chromatin interactions
ENSG00000136159	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000137513	chromatin interactions
ENSG00000255444	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000239900	chromatin interactions
ENSG00000207005	chromatin interactions
ENSG00000262621	chromatin interactions
ENSG00000172594	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:748 , 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	rs601904	chr11:74200739-74200740	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12792003	chr11:74200765-74200766	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571741106	chr11:74200832-74200833	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs189921998	chr11:74200871-74200872	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs543531977	chr11:74200873-74200874	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs1145664	chr11:74200889-74200890	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs550659497	chr11:74200958-74200959	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs377058863	chr11:74200961-74200962	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs536590830	chr11:74201069-74201070	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs536237879	chr11:74201159-74201160	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs553621274	chr11:74201166-74201167	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs11602790	chr11:74201183-74201184	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs538828574	chr11:74201242-74201243	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs557455274	chr11:74201261-74201262	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs182552982	chr11:74201311-74201312	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs141757397	chr11:74201365-74201366	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs556726734	chr11:74201375-74201376	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs573570291	chr11:74201382-74201383	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs589970	chr11:74201436-74201437	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs555899710	chr11:74201440-74201441	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs559664506	chr11:74201460-74201461	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs1280087	chr11:74201474-74201475	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs545188113	chr11:74201485-74201486	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs528790276	chr11:74201502-74201503	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs565385916	chr11:74201505-74201506	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs376762820	chr11:74201509-74201510	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs530863947	chr11:74201524-74201525	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs115139258	chr11:74201542-74201543	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs567594167	chr11:74201564-74201565	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs557382422	chr11:74201577-74201578	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs530090465	chr11:74201581-74201582	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs544951070	chr11:74201594-74201595	Weak transcription Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs546919364	chr11:74201603-74201604	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs566799016	chr11:74201750-74201751	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs373257816	chr11:74201766-74201767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs73500317	chr11:74201852-74201853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552314746	chr11:74201863-74201864	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569104054	chr11:74201893-74201894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536784190	chr11:74201927-74201928	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs557000134	chr11:74201933-74201934	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573582001	chr11:74201949-74201950	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs536216591	chr11:74201972-74201973	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs553318631	chr11:74202012-74202013	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs573132571	chr11:74202024-74202025	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs617989	chr11:74202033-74202034	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs575433182	chr11:74202097-74202098	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs575387405	chr11:74202189-74202190	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs544414246	chr11:74202201-74202202	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs146232858	chr11:74202220-74202221	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs530065745	chr11:74202231-74202232	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	21364760	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74191400-74204000	Weak transcription	Ovary	ovary
2	chr11:74192400-74203200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr11:74197000-74203800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:74197200-74203000	Weak transcription	K562	blood
5	chr11:74197200-74203200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr11:74197200-74204200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:74197600-74203200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:74197600-74203200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:74197600-74203200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr11:74197600-74204000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr11:74197800-74202800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr11:74198200-74203400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr11:74198200-74204000	Weak transcription	Lung	lung
14	chr11:74198200-74204000	Weak transcription	Pancreas	Pancrea
15	chr11:74198400-74203200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr11:74198400-74204000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:74198800-74203200	Weak transcription	Brain Anterior Caudate	brain
18	chr11:74199000-74203200	Weak transcription	Placenta	Placenta
19	chr11:74199600-74202200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr11:74199600-74204000	Weak transcription	HepG2	liver
21	chr11:74200000-74202000	Weak transcription	Liver	Liver
22	chr11:74200000-74203400	Weak transcription	Fetal Intestine Large	intestine
23	chr11:74200200-74203200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr11:74200400-74201800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:74200400-74203200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:74200400-74203200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr11:74200400-74204200	Weak transcription	Spleen	Spleen
28	chr11:74200600-74202200	Strong transcription	Primary T cells from cord blood	blood
29	chr11:74200600-74203200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr11:74200600-74203200	Weak transcription	HUVEC	blood vessel
31	chr11:74200600-74204000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr11:74200800-74203400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:74200800-74203800	Weak transcription	Psoas Muscle	Psoas
34	chr11:74200800-74204000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr11:74201000-74203400	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr11:74201000-74203400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr11:74201000-74204000	Weak transcription	Aorta	Aorta
38	chr11:74201200-74204000	Weak transcription	Right Atrium	heart
39	chr11:74201200-74204200	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr11:74201600-74202000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr11:74201600-74203400	Weak transcription	Fetal Kidney	kidney
42	chr11:74201600-74203800	Weak transcription	Right Ventricle	heart
43	chr11:74201600-74204000	Weak transcription	Brain Angular Gyrus	brain
44	chr11:74201800-74202800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:74201800-74203200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr11:74201800-74204000	Weak transcription	Osteobl	bone
47	chr11:74202000-74202200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr11:74202000-74203200	Strong transcription	Liver	Liver
49	chr11:74202000-74203600	Weak transcription	Brain Hippocampus Middle	brain
50	chr11:74202200-74202400	Enhancers	Primary monocytes fromperipheralblood	blood

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