Variant report

Variant	esv1810385
Chromosome Location	chr6:35758072-35766871
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	BHLHE40	chr6:35765017-35765289	K562	blood:	n/a	n/a
2	BHLHE40	chr6:35758607-35758807	HepG2	liver:	n/a	n/a
3	BHLHE40	chr6:35760699-35760763	K562	blood:	n/a	n/a
4	CEBPB	chr6:35758467-35758814	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr6:35758561-35758682	HepG2	liver:	n/a	n/a
6	CEBPB	chr6:35762562-35762885	K562	blood:	n/a	n/a
7	CEBPB	chr6:35758405-35758921	A549	lung:	n/a	n/a
8	CEBPB	chr6:35758448-35758812	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr6:35758461-35758817	K562	blood:	n/a	n/a
10	CEBPB	chr6:35758444-35758768	MCF-7	breast:	n/a	n/a
11	CEBPB	chr6:35758462-35758824	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:35758454-35758819	A549	lung:	n/a	n/a
13	CEBPB	chr6:35758463-35758813	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:35758455-35758789	K562	blood:	n/a	n/a
15	CTCF	chr6:35765740-35765890	GM12864	blood:	n/a	n/a
16	CTCF	chr6:35766010-35766063	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr6:35760300-35760450	AG04449	skin:	n/a	n/a
18	CTCF	chr6:35760640-35760790	GM12868	blood:	n/a	n/a
19	E2F4	chr6:35759420-35759424	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F6	chr6:35761233-35761368	K562	blood:	n/a	chr6:35761248-35761260
21	E2F6	chr6:35761154-35761630	H1-hESC	embryonic stem cell:	n/a	chr6:35761248-35761260
22	E2F6	chr6:35766297-35766870	H1-hESC	embryonic stem cell:	n/a	n/a
23	E2F6	chr6:35761091-35761480	H1-hESC	embryonic stem cell:	n/a	chr6:35761248-35761260
24	E2F6	chr6:35766372-35766946	H1-hESC	embryonic stem cell:	n/a	n/a
25	EGR1	chr6:35765030-35765252	K562	blood:	n/a	n/a
26	EGR1	chr6:35763349-35763621	K562	blood:	n/a	chr6:35763477-35763491 chr6:35763478-35763491 chr6:35763479-35763490 chr6:35763479-35763490 chr6:35763479-35763488
27	ELF1	chr6:35764865-35765253	GM12878	blood:	n/a	n/a
28	FOXA1	chr6:35764086-35764407	T-47D	breast:	n/a	n/a
29	FOXA1	chr6:35764145-35764400	T-47D	breast:	n/a	n/a
30	GTF2F1	chr6:35765022-35765053	H1-hESC	embryonic stem cell:	n/a	n/a
31	GTF2F1	chr6:35766681-35766722	H1-hESC	embryonic stem cell:	n/a	n/a
32	GTF2F1	chr6:35763645-35763723	K562	blood:	n/a	n/a
33	JUN	chr6:35765331-35765335	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAFF	chr6:35758034-35758157	K562	blood:	n/a	n/a
35	MAFF	chr6:35762658-35762770	HepG2	liver:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
36	MAFF	chr6:35762574-35762875	K562	blood:	n/a	chr6:35762725-35762739 chr6:35762719-35762737
37	MAFK	chr6:35762557-35762899	K562	blood:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
38	MAFK	chr6:35762562-35762855	HepG2	liver:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
39	MAFK	chr6:35762633-35762864	Hela-S3	cervix:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
40	MAFK	chr6:35758054-35758231	HepG2	liver:	n/a	n/a
41	MAFK	chr6:35762579-35762870	HepG2	liver:	n/a	chr6:35762726-35762736 chr6:35762726-35762735 chr6:35762722-35762742 chr6:35762721-35762736 chr6:35762725-35762739
42	MAX	chr6:35761205-35761542	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr6:35765792-35766276	H1-hESC	embryonic stem cell:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
44	MAX	chr6:35761223-35761454	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr6:35765943-35766141	K562	blood:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
46	MAX	chr6:35761196-35761505	K562	blood:	n/a	n/a
47	MAX	chr6:35766531-35766863	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
48	MAX	chr6:35766425-35766854	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738
49	MAX	chr6:35765902-35766195	K562	blood:	n/a	chr6:35766039-35766048 chr6:35766038-35766048 chr6:35766038-35766049 chr6:35766039-35766048 chr6:35766040-35766047
50	MAX	chr6:35766413-35766899	H1-hESC	embryonic stem cell:	n/a	chr6:35766728-35766738

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:35765215-35765265	HMEC	breast:	n/a
2	chr6:35765093-35765143	PrEC	prostate:	n/a
3	chr6:35765589-35765639	RPTEC	kidney:	n/a
4	chr6:35764958-35765008	GM12891	blood:	n/a
5	chr6:35765215-35765265	NH-A	brain:	n/a
6	chr6:35765589-35765639	A549	lung:	n/a
7	chr6:35765146-35765196	Caco-2	colon:	n/a
8	chr6:35765146-35765196	MCF10A-Er-Src	breast:	n/a
9	chr6:35764958-35765008	K562	blood:	n/a
10	chr6:35765589-35765639	HCF	heart:	n/a
11	chr6:35764958-35765008	SK-N-SH_RA	brain:	n/a
12	chr6:35765215-35765265	BJ	skin:	n/a
13	chr6:35762844-35762894	Hela-S3	cervix:	n/a
14	chr6:35765146-35765196	AG04450	lung:	fetal
15	chr6:35765093-35765143	K562	blood:	n/a
16	chr6:35766051-35766101	CMK	blood:	n/a
17	chr6:35765215-35765265	NT2-D1	testis:	n/a
18	chr6:35765215-35765265	RPTEC	kidney:	n/a
19	chr6:35765146-35765196	NT2-D1	testis:	n/a
20	chr6:35766051-35766101	NHBE	bronchial:	n/a
21	chr6:35765093-35765143	HRCEpiC	kidney:	n/a
22	chr6:35765093-35765143	LNCaP	prostate:	n/a
23	chr6:35765176-35765226	H1-hESC	embryonic stem cell:	embryo
24	chr6:35765215-35765265	AG04450	lung:	fetal
25	chr6:35764958-35765008	Jurkat	blood:	n/a
26	chr6:35766051-35766101	NH-A	brain:	n/a
27	chr6:35765146-35765196	HRCEpiC	kidney:	n/a
28	chr6:35764958-35765008	AG09319	gingival:	n/a
29	chr6:35765589-35765639	HL-60	blood:	n/a
30	chr6:35765215-35765265	HIPEpiC	eye:	n/a
31	chr6:35766051-35766101	GM12878	blood:	n/a
32	chr6:35765093-35765143	HAEpiC	amniotic membrane:	n/a
33	chr6:35762844-35762894	AG09309	skin:	n/a
34	chr6:35765589-35765639	GM12878	blood:	n/a
35	chr6:35765146-35765196	AG09319	gingival:	n/a
36	chr6:35765093-35765143	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:35766021-35766071	HCT-116	colon:	n/a
38	chr6:35766051-35766101	ProgFib	skin:	n/a
39	chr6:35766051-35766101	U87	brain:	n/a
40	chr6:35765093-35765143	IMR90	lung:	fetal
41	chr6:35765093-35765143	PANC-1	pancreas:	n/a
42	chr6:35764958-35765008	MCF10A-Er-Src	breast:	n/a
43	chr6:35765215-35765265	Hepatocyte	liver:	n/a
44	chr6:35764958-35765008	PrEC	prostate:	n/a
45	chr6:35765589-35765639	HNPCEpiC	eye:	n/a
46	chr6:35762844-35762894	BE2_C	brain:	n/a
47	chr6:35765146-35765196	HCF	heart:	n/a
48	chr6:35762844-35762894	ECC-1	luminal epithelium:	n/a
49	chr6:35766021-35766071	Caco-2	colon:	n/a
50	chr6:35765176-35765226	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:35742984..35745597-chr6:35763979..35765844,2	MCF-7	breast:
2	chr6:35760015..35761880-chr6:35763280..35765561,2	K562	blood:
3	chr6:35747942..35750162-chr6:35760132..35762411,2	MCF-7	breast:
4	chr6:35762307..35765078-chr6:35772426..35774241,2	MCF-7	breast:
5	chr6:35753847..35759789-chr6:35762486..35768711,9	K562	blood:
6	chr6:35753638..35758618-chr6:35762629..35767095,7	K562	blood:
7	chr6:35753638..35758618-chr6:35762629..35767095,7	K562	blood:
8	chr6:35762283..35764266-chr6:35764644..35767426,2	MCF-7	breast:
9	chr6:35762091..35764853-chr6:35765476..35768100,2	MCF-7	breast:
10	chr6:35753847..35759789-chr6:35762486..35768711,9	K562	blood:
11	chr6:35762091..35764853-chr6:35765476..35768100,2	MCF-7	breast:
12	chr6:35760846..35763760-chr6:36163836..36166432,2	K562	blood:

Variant related genes	Relation type
CLPS	TF binding region
CLPS	CpG island
ENSG00000204140	chromatin interactions
ENSG00000197753	chromatin interactions
ENSG00000137392	chromatin interactions
ENSG00000096070	chromatin interactions
ENSG00000246982	chromatin interactions
ENSG00000196748	chromatin interactions

Extended variants
information (count: 523 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534326425	chr6:35758074-35758075	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs552895810	chr6:35758076-35758077	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574344480	chr6:35758088-35758089	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535221896	chr6:35758104-35758105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs9462114	chr6:35758108-35758109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs9470096	chr6:35758142-35758143	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs75895388	chr6:35758143-35758144	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565440755	chr6:35758210-35758211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191214217	chr6:35758251-35758252	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs79235746	chr6:35758268-35758269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541350529	chr6:35758271-35758272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs144736349	chr6:35758284-35758285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs9462115	chr6:35758334-35758335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2395636	chr6:35758342-35758343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1409613	chr6:35758353-35758354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs4434466	chr6:35758388-35758389	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552354283	chr6:35758400-35758401	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372428635	chr6:35758441-35758442	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs115849572	chr6:35758452-35758453	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs116279820	chr6:35758468-35758469	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546577245	chr6:35758495-35758496	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568078066	chr6:35758583-35758584	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115590886	chr6:35758587-35758588	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556657798	chr6:35758621-35758622	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs574944564	chr6:35758638-35758639	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370470175	chr6:35758639-35758640	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559146730	chr6:35758667-35758668	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs148521236	chr6:35758680-35758681	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs1831031	chr6:35758696-35758697	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs386700155	chr6:35758703-35758704	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373008857	chr6:35758705-35758706	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs142842291	chr6:35758731-35758732	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs146544195	chr6:35758750-35758751	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182522383	chr6:35758759-35758760	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563776839	chr6:35758765-35758766	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs186030376	chr6:35758777-35758778	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61127901	chr6:35758821-35758822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs397792534	chr6:35758835-35758836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369418142	chr6:35758836-35758837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs59928722	chr6:35758839-35758840	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141461369	chr6:35758866-35758867	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs115528048	chr6:35758870-35758871	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2766591	chr6:35758882-35758883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs370792798	chr6:35758930-35758931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568234564	chr6:35758933-35758934	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs6907802	chr6:35758934-35758935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9462117	chr6:35758940-35758941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143878660	chr6:35758941-35758942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs539193925	chr6:35758945-35758946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557545956	chr6:35758967-35758968	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35755400-35765600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:35755600-35758600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:35757000-35760400	Weak transcription	Pancreas	Pancrea
4	chr6:35757800-35759000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:35758400-35758600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:35758600-35758800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:35758800-35760400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:35760400-35760600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:35760400-35760600	Enhancers	Pancreas	Pancrea
10	chr6:35760400-35761600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr6:35760600-35760800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:35760600-35760800	Flanking Active TSS	Pancreas	Pancrea
13	chr6:35760600-35760800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
14	chr6:35760600-35762600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:35760800-35761200	Enhancers	Pancreas	Pancrea
16	chr6:35761200-35761400	Active TSS	Pancreas	Pancrea
17	chr6:35761200-35761600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr6:35761400-35761600	Flanking Active TSS	Pancreas	Pancrea
19	chr6:35761600-35762400	Active TSS	Pancreas	Pancrea
20	chr6:35762200-35762400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:35762200-35765200	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr6:35762400-35764000	Transcr. at gene 5' and 3'	Pancreas	Pancrea
23	chr6:35762600-35763000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:35762800-35763000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:35762800-35763600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:35763000-35772800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr6:35763400-35763600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:35763600-35773000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:35764000-35765600	Active TSS	Pancreas	Pancrea
30	chr6:35765600-35766000	Flanking Active TSS	Pancreas	Pancrea
31	chr6:35765600-35766200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr6:35765600-35766600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr6:35765800-35766000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr6:35765800-35766000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr6:35765800-35766200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:35765800-35766800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr6:35765800-35767400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:35766000-35766200	Bivalent Enhancer	HepG2	liver
39	chr6:35766000-35766800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr6:35766000-35766800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr6:35766000-35766800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:35766000-35768200	Enhancers	Pancreas	Pancrea
43	chr6:35766200-35769200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:35766400-35767000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:35766400-35767000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr6:35766600-35766800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr6:35766600-35767000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr6:35766600-35767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr6:35766600-35767200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr6:35766600-35772800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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