Variant report

Variant	nsv428494
Chromosome Location	chr6:114666307-114774841
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	chr6:114719700-114720055	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:114697785-114698182	HepG2	liver:	n/a	n/a
3	ATF2	chr6:114742286-114742964	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:114684060-114684545	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:114725720-114726354	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:114742313-114742815	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:114740396-114740716	GM12878	blood:	n/a	n/a
8	ATF2	chr6:114740228-114740801	GM12878	blood:	n/a	n/a
9	ATF2	chr6:114684024-114684508	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:114682017-114682038	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:114684132-114684582	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr6:114740282-114740635	GM12878	blood:	n/a	chr6:114740550-114740558
13	BATF	chr6:114740453-114740646	GM12878	blood:	n/a	chr6:114740550-114740558
14	BCL11A	chr6:114740306-114740650	GM12878	blood:	n/a	chr6:114740537-114740546
15	BCL11A	chr6:114740341-114740587	GM12878	blood:	n/a	chr6:114740537-114740546
16	BCL3	chr6:114740370-114740686	GM12878	blood:	n/a	chr6:114740537-114740546
17	BHLHE40	chr6:114740465-114740913	GM12878	blood:	n/a	n/a
18	BRCA1	chr6:114740396-114740411	GM12878	blood:	n/a	n/a
19	CEBPB	chr6:114667692-114667939	A549	lung:	n/a	chr6:114667826-114667837 chr6:114667825-114667836 chr6:114667827-114667836 chr6:114667827-114667836 chr6:114667825-114667838 chr6:114667827-114667836 chr6:114667827-114667836
20	CEBPB	chr6:114667725-114667986	Hela-S3	cervix:	n/a	chr6:114667826-114667837 chr6:114667825-114667836 chr6:114667827-114667836 chr6:114667827-114667836 chr6:114667825-114667838 chr6:114667827-114667836 chr6:114667827-114667836
21	CEBPB	chr6:114700947-114701083	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:114740451-114740890	Hela-S3	cervix:	n/a	chr6:114740826-114740835 chr6:114740824-114740837 chr6:114740824-114740837 chr6:114740826-114740837
23	CEBPB	chr6:114719715-114719925	HepG2	liver:	n/a	chr6:114719840-114719851
24	CEBPB	chr6:114667671-114668013	HepG2	liver:	n/a	chr6:114667826-114667837 chr6:114667825-114667836 chr6:114667827-114667836 chr6:114667827-114667836 chr6:114667825-114667838 chr6:114667827-114667836 chr6:114667827-114667836
25	CEBPB	chr6:114719661-114720027	HepG2	liver:	n/a	chr6:114719840-114719851
26	CEBPB	chr6:114704925-114705162	HepG2	liver:	n/a	chr6:114705023-114705034 chr6:114705021-114705038
27	CEBPB	chr6:114667647-114668013	IMR90	lung:	n/a	chr6:114667826-114667837 chr6:114667825-114667836 chr6:114667827-114667836 chr6:114667827-114667836 chr6:114667825-114667838 chr6:114667827-114667836 chr6:114667827-114667836
28	CEBPB	chr6:114740419-114740988	HepG2	liver:	n/a	chr6:114740826-114740835 chr6:114740824-114740837 chr6:114740824-114740837 chr6:114740826-114740837
29	CEBPB	chr6:114711303-114711381	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr6:114719688-114719966	H1-hESC	embryonic stem cell:	n/a	chr6:114719840-114719851
31	CEBPB	chr6:114667657-114668041	MCF-7	breast:	n/a	chr6:114667826-114667837 chr6:114667825-114667836 chr6:114667827-114667836 chr6:114667827-114667836 chr6:114667825-114667838 chr6:114667827-114667836 chr6:114667827-114667836
32	CEBPZ	chr6:114703847-114703925	HepG2	liver:	n/a	n/a
33	CHD1	chr6:114741717-114742852	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr6:114753670-114753678	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD1	chr6:114746849-114747456	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:114751679-114751945	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr6:114753659-114753690	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr6:114711315-114711705	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr6:114740402-114740739	GM12878	blood:	n/a	n/a
40	CREB1	chr6:114740278-114740842	GM12878	blood:	n/a	n/a
41	CTBP2	chr6:114683698-114684418	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:114747265-114747276	GM10248	blood:	n/a	n/a
43	CTCF	chr6:114729026-114729225	GM12878	blood:	n/a	n/a
44	CTCF	chr6:114758187-114758246	GM20000	blood:	n/a	n/a
45	CTCF	chr6:114729083-114729225	Medullo	brain:	n/a	n/a
46	CTCF	chr6:114723100-114723250	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr6:114708485-114708498	GM20000	blood:	n/a	n/a
48	CTCF	chr6:114729080-114729230	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr6:114744774-114744825	GM13976	blood:	n/a	n/a
50	CTCF	chr6:114768995-114769071	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114697971-114698021	Jurkat	blood:	n/a
2	chr6:114751873-114751923	ovcar-3	ovarian:	n/a
3	chr6:114707054-114707104	AG04450	lung:	fetal
4	chr6:114697971-114698021	SK-N-MC	brain:	n/a
5	chr6:114707054-114707104	GM12891	blood:	n/a
6	chr6:114751873-114751923	MCF10A-Er-Src	breast:	n/a
7	chr6:114697971-114698021	BE2_C	brain:	n/a
8	chr6:114741679-114741729	GM06990	blood:	n/a
9	chr6:114751873-114751923	SK-N-MC	brain:	n/a
10	chr6:114725242-114725292	SKMC	muscle:	n/a
11	chr6:114697971-114698021	HCT-116	colon:	n/a
12	chr6:114741679-114741729	HUVEC	blood vessel:	n/a
13	chr6:114697971-114698021	NHDF-neo	bronchial:	n/a
14	chr6:114707054-114707104	Hepatocyte	liver:	n/a
15	chr6:114751873-114751923	K562	blood:	n/a
16	chr6:114741679-114741729	Hela-S3	cervix:	n/a
17	chr6:114751873-114751923	U87	brain:	n/a
18	chr6:114725242-114725292	RPTEC	kidney:	n/a
19	chr6:114725242-114725292	GM06990	blood:	n/a
20	chr6:114725242-114725292	GM12892	blood:	n/a
21	chr6:114697971-114698021	BJ	skin:	n/a
22	chr6:114751873-114751923	HCM	heart:	n/a
23	chr6:114751873-114751923	NHBE	bronchial:	n/a
24	chr6:114751873-114751923	HEEpiC	esophagus:	n/a
25	chr6:114697971-114698021	HCF	heart:	n/a
26	chr6:114751873-114751923	HL-60	blood:	n/a
27	chr6:114741679-114741729	AG10803	skin:	n/a
28	chr6:114725242-114725292	CMK	blood:	n/a
29	chr6:114725242-114725292	ECC-1	luminal epithelium:	n/a
30	chr6:114707054-114707104	MCF10A-Er-Src	breast:	n/a
31	chr6:114707054-114707104	HepG2	liver:	n/a
32	chr6:114751873-114751923	HRE	kidney:	n/a
33	chr6:114697971-114698021	SAEC	small airway:	n/a
34	chr6:114697971-114698021	H1-hESC	embryonic stem cell:	embryo
35	chr6:114707054-114707104	ovcar-3	ovarian:	n/a
36	chr6:114697971-114698021	HIPEpiC	eye:	n/a
37	chr6:114697971-114698021	GM12891	blood:	n/a
38	chr6:114725242-114725292	PANC-1	pancreas:	n/a
39	chr6:114751873-114751923	HMEC	breast:	n/a
40	chr6:114725242-114725292	NB4	blood:	n/a
41	chr6:114707054-114707104	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:114741679-114741729	SK-N-SH	brain:	n/a
43	chr6:114751873-114751923	LNCaP	prostate:	n/a
44	chr6:114697971-114698021	NHBE	bronchial:	n/a
45	chr6:114707054-114707104	H1-hESC	embryonic stem cell:	embryo
46	chr6:114751873-114751923	Hela-S3	cervix:	n/a
47	chr6:114725242-114725292	U87	brain:	n/a
48	chr6:114725242-114725292	NH-A	brain:	n/a
49	chr6:114707054-114707104	CMK	blood:	n/a
50	chr6:114741679-114741729	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:114699357..114700992-chr6:114703215..114705730,2	K562	blood:
2	chr6:114662119..114667220-chr6:114669334..114673077,6	MCF-7	breast:
3	chr6:114670440..114672596-chr6:114674899..114677569,2	MCF-7	breast:
4	chr6:114684479..114687440-chr6:114692233..114694827,2	MCF-7	breast:
5	chr6:114699357..114700992-chr6:114703215..114705730,2	K562	blood:
6	chr6:114716541..114719212-chr6:114721790..114724337,2	MCF-7	breast:
7	chr6:114684479..114687440-chr6:114692233..114694827,2	MCF-7	breast:
8	chr6:114662119..114667220-chr6:114669334..114673077,6	MCF-7	breast:
9	chr6:114716541..114719212-chr6:114721790..114724337,2	MCF-7	breast:
10	chr6:114662992..114664998-chr6:114748035..114750370,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCKS-5	chr6:114770131-114770195	ENSG00000228624
2	lnc-MARCKS-5	chr6:114736766-114736776	XLOC_005441
3	lnc-HS3ST5-3	chr6:114670647-114671812	NONHSAT114609
4	lnc-MARCKS-5	chr6:114736744-114736776	XLOC_005441
5	lnc-HS3ST5-7	chr6:114730053-114731474	NONHSAT114610
6	lnc-MARCKS-5	chr6:114666846-114667056	NONHSAT114607
7	lnc-MARCKS-5	chr6:114727807-114727832	ENSG00000228624
8	lnc-MARCKS-5	chr6:114692756-114692856	ENSG00000228624
9	lnc-MARCKS-5	chr6:114692756-114692850	NONHSAT114608
10	lnc-MARCKS-5	chr6:114770131-114770195	XLOC_005441
11	lnc-MARCKS-5	chr6:114759133-114759230	ENSG00000228624
12	lnc-MARCKS-5	chr6:114770080-114770195	NONHSAT114614
13	lnc-MARCKS-5	chr6:114770124-114770195	ENSG00000228624
14	lnc-MARCKS-5	chr6:114770131-114770195	ENSG00000228624
15	lnc-MARCKS-5	chr6:114770131-114770195	XLOC_005441
16	lnc-MARCKS-5	chr6:114746776-114746836	ENSG00000228624
17	lnc-HS3ST5-7	chr6:114744178-114745122	NONHSAT114610

Variant related genes	Relation type
DNAJA1P4	TF binding region
HS3ST5	TF binding region
ENSG00000228624	TF binding region
DNAJA1P4	CpG island
HS3ST5	CpG island
ENSG00000228624	CpG island
ENSG00000249853	chromatin interactions
ENSG00000218089	chromatin interactions
THBS1	miRNA target sites
YARS2	miRNA target sites
AHNAK2	miRNA target sites
TLK1	miRNA target sites
ZC3HAV1	miRNA target sites
UBE2D3	miRNA target sites
MXI1	miRNA target sites

Extended variants
information (count: 3735 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:3735 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532085788	chr6:114666321-114666322	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs552498528	chr6:114666388-114666389	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs547389622	chr6:114666421-114666422	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs565503107	chr6:114666453-114666454	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536554590	chr6:114666472-114666473	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554893178	chr6:114666478-114666479	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139173514	chr6:114666536-114666537	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537284107	chr6:114666582-114666583	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs34868381	chr6:114666630-114666631	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs142971479	chr6:114666668-114666669	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187173590	chr6:114666674-114666675	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200302485	chr6:114666769-114666770	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs117360518	chr6:114666772-114666773	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553341544	chr6:114666796-114666797	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574838649	chr6:114666837-114666838	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs112446349	chr6:114666853-114666854	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs542240168	chr6:114666859-114666860	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs75608190	chr6:114666865-114666866	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs549613564	chr6:114666904-114666905	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs191447334	chr6:114666905-114666906	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs543628415	chr6:114666938-114666939	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs564900322	chr6:114666939-114666940	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs532247623	chr6:114666945-114666946	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs547133370	chr6:114666964-114666965	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs62444081	chr6:114666977-114666978	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs62444082	chr6:114666979-114666980	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs559022401	chr6:114667014-114667015	Weak transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs182133095	chr6:114667096-114667097	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs556779468	chr6:114667141-114667142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs60232257	chr6:114667217-114667218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs111763475	chr6:114667312-114667313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571897706	chr6:114667394-114667395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35633522	chr6:114667460-114667461	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs188849464	chr6:114667469-114667470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570917135	chr6:114667508-114667509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114051249	chr6:114667651-114667652	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs149641607	chr6:114667693-114667694	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs574976976	chr6:114667697-114667698	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs557606913	chr6:114667707-114667708	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs535884728	chr6:114667766-114667767	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs557369559	chr6:114667780-114667781	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs576424439	chr6:114667867-114667868	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs543315145	chr6:114667877-114667878	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565095845	chr6:114667886-114667887	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs577014031	chr6:114667903-114667904	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs541213262	chr6:114667950-114667951	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs116467833	chr6:114667959-114667960	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs572755918	chr6:114667970-114667971	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs9481441	chr6:114667999-114668000	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs111408750	chr6:114668004-114668005	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Acute myeloid leukemia	19651600	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114665000-114666400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr6:114665200-114666600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:114665200-114667600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:114665400-114667200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:114665400-114667800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:114665600-114666600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr6:114665600-114666600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:114665600-114667000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:114665800-114666600	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:114665800-114666800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr6:114665800-114667000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:114665800-114667000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr6:114666000-114666400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr6:114666000-114666400	Enhancers	Brain Anterior Caudate	brain
15	chr6:114666200-114666400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr6:114666200-114666400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:114666200-114666400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:114666200-114666400	Enhancers	Brain Hippocampus Middle	brain
19	chr6:114666200-114666400	Enhancers	Esophagus	oesophagus
20	chr6:114666200-114666600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr6:114666200-114666600	Enhancers	Fetal Brain Male	brain
22	chr6:114666200-114666800	Enhancers	Muscle Satellite Cultured Cells	--
23	chr6:114666200-114667200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:114666400-114666600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr6:114666400-114666600	Enhancers	Rectal Smooth Muscle	rectum
26	chr6:114666400-114666800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:114666600-114667000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr6:114666600-114681800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr6:114667000-114667400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr6:114667000-114667800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr6:114667000-114680600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:114667000-114681600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr6:114667200-114668200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:114667400-114668000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr6:114667800-114668000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr6:114667800-114668000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:114668000-114668600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr6:114668200-114668800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:114668600-114668800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr6:114668800-114681800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr6:114669000-114669200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:114675800-114676400	Enhancers	Fetal Heart	heart
43	chr6:114675800-114676800	Enhancers	HSMMtube	muscle
44	chr6:114679000-114686400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:114679400-114680000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:114679800-114680000	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr6:114680000-114681400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr6:114680000-114681600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:114680400-114680600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr6:114680600-114680800	Enhancers	ES-I3 Cell Line	embryonic stem cell

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